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Prenatal Hypoxia: Comparison
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Please note this is a comparison between Version 2 by Camila Xu and Version 1 by Hana Sutovska.

Prenatal hypoxia is a common complication in pregnancy, developing from various causes. Prenatal hypoxia during the prenatal period can interfere with the developmental trajectory and lead to developing hypertension in adulthood. Prenatal hypoxia is often associated with intrauterine growth restriction that interferes with metabolism and can lead to multilevel changes. 

  • prenatal hypoxia
  • prenatal programming
  • cardiovascular system

1. Introduction

The cardiovascular system is a dynamic system that can adapt to adverse conditions to maintain and satisfy homeostasis in the organism. Prolonged cardiovascular adaptations can result in the development of hypertension and other cardiovascular diseases in adulthood; however, hypertension can have its origins in the prenatal period when the cardiovascular system develops structurally and functionally [1]. This phenomenon observed in animals and humans is described as prenatal programming [2,3][2][3].
Prenatal programming is defined as a response to adverse factors acting during a critical prenatal period, leading to changes in the developmental trajectory with a permanent effect on the offspring’s adult phenotype [3]. Insults during the prenatal period lead to permanent structural or functional changes of the tissues and organs [3]. In general, if the prenatal factor acts during the early phase of an organ’s development, it leads to structural defects. In contrast, the action during the later phases of development affects functions [4]. The effect of prenatal insults on the foetus depends not only on the developmental stage but also on the type of insult. Consequently, some types of insults, such as various agents (warfarin, thalidomide, tetracycline, alcohol) and environmental factors of chemical (toxic metals), physical (ionising radiation) or biological origin (infection diseases), can disrupt the normal in utero development of the foetus and increase the risk of congenital disabilities, malformations, and in some cases, even death of the developing foetus [5].
Moderate effects on the foetus include high or low food availability, oxygen deficiency (hypoxia), maternal obesity, inadequate prenatal care, maternal stress, and maternal chronic diseases. The consequences of these factors can be identified during pregnancy screening and immediately after birth because they are often associated with a reduction in birth weight and asymmetric organ growth [6]. According to Barker’s theory, neonates with reduced birth weight have a higher incidence of stroke and coronary heart disease in adulthood [7]. A reduction in birth weight of neonates is the most accessible marker of poor in utero development. Indeed, many studies have recently explored an association between intrauterine growth restriction and an increased postnatal risk of cardiovascular diseases [8,9,10][8][9][10].
However, prenatal insults do not necessarily have to be manifested by low birth weight (Table 1) and still can lead to the programming of diseases in adulthood. This phenomenon is observed after exposure to prenatal hypoxia, which is a common complication in gravidity. In this case, neonates are born seemingly healthy, avoiding the early screening of diseases; however, due to prenatal hypoxia, the foetus has impaired endothelial function and undergoes oxidative stress [2[2][9][11],9,11], morphological changes in the heart and blood vessels [2,12][2][12] and changes in the activity of the autonomic nervous system [13[13][14],14], which is one of the key factors in the development of hypertension [15]. Prenatal hypoxia contributes to the development of hypertension, ischemic heart disease, coronary heart disease, heart failure, metabolic syndrome, and increased susceptibility to ischemic injury in humans [16,17][16][17].
Table 1. The effect of prenatal hypoxia on birth body weight.
Oxygen Duration; Time Animal Model Birth Body Weight Ref.
6.5% 1–20 ED; 8 h per day: 80 s hypoxia and 120 s normoxia; 18 cycles per hour Sprague Dawley rats ↓ [18]
7% 13–14 ED; 3 h Wistar rats ↓ [19]
7% 18 ED; 3 h Wistar rats = [20]
9% 15–21 ED; 6 h per day Sprague Dawley rats = [21]
9.5–10% 12, 24, 48, 120 h immediately prior to delivery at term Sprague Dawley rats ↓ [22]
10% 5–19 ED Sprague Dawley rats ↓ [23]
10% 5–20 ED Sprague Dawley rats ↓ [13,24,25,26,27][13][24][25][26][27
105–138 ED
sheep
↓
[
53
]
ED, embryonic day; NA, non-available; ↓, decreased birth body weight; =, no changes of the birth body weight in comparison with control group.
 
The most important signalling molecules that respond to changes in oxygen content are hypoxia-inducible factors (HIFs) from the family of heterodimeric transcription factors. The HIF transcription factor is composed of two subunits, α and β. Under normoxia, HIF-1α is rapidly degraded, but if the partial pressure of oxygen decreases, it is stabilized and accumulates in the cells. HIF-1α maintains oxygen homeostasis by regulating the expression of hundreds of genes and interacts with pathways involved in the regulation of the cardiovascular system, such as the chemoreflex, sympathetic drive [54], renin-angiotensin-aldosterone system (RAAS) [55][56], and local vessel wall components such as nitric oxide (NO) [57][58][59] and endothelin-1 [60][61]. Moreover, HIF directly interacts with the circadian clock because HIF-1α controls the expression of several canonical circadian genes and the response to hypoxia is gated by the circadian clock [62]. The relationship between the HIF and clock can be reciprocal, because in several experimental models, hypoxia was found to reduce the amplitude of circadian rhythms or their response to phase shifts [63].
The most important signalling molecules that respond to changes in oxygen content are hypoxia-inducible factors (HIFs) from the family of heterodimeric transcription factors. The HIF transcription factor is composed of two subunits, α and β. Under normoxia, HIF-1α is rapidly degraded, but if the partial pressure of oxygen decreases, it is stabilized and accumulates in the cells. HIF-1α maintains oxygen homeostasis by regulating the expression of hundreds of genes and interacts with pathways involved in the regulation of the cardiovascular system, such as the chemoreflex, sympathetic drive [54], renin-angiotensin-aldosterone system (RAAS) [55,56], and local vessel wall components such as nitric oxide (NO) [57,58,59] and endothelin-1 [60,61]. Moreover, HIF directly interacts with the circadian clock because HIF-1α controls the expression of several canonical circadian genes and the response to hypoxia is gated by the circadian clock [62]. The relationship between the HIF and clock can be reciprocal, because in several experimental models, hypoxia was found to reduce the amplitude of circadian rhythms or their response to phase shifts [63].

2. Prenatal Hypoxia

Prenatal hypoxia is a common complication in pregnancy, developing from various causes (Figure 1). In gravidity, prenatal hypoxia often occurs as a comorbidity of maternal diseases, such as hypertension, anaemia and respiratory diseases or as a consequence of poor maternal lifestyle, such as smoking, so-called preplacental hypoxia. Prenatal hypoxia can also develop as a consequence of morphological or functional changes in the placenta, such as failed remodelling of spiral arteries or metabolic reprogramming (uteroplacental hypoxia). Disturbed fetoplacental perfusion due to changes in foetal circulation or genetic anomalies in the circulatory system can lead to postplacental hypoxia [64].
Figure 1. Prenatal hypoxia as result of mother, placenta, and foetus and their effects on cardiovascular regulatory mechanisms in the foetus. Based on the level in which prenatal hypoxia occurs, it can be divided into preplacental hypoxia, uteroplacental hypoxia, and postplacental hypoxia. The foetus is able to compensate for oxygen deficiency and maintain homeostasis by the activation of regulatory mechanisms. The response of the foetus to prenatal hypoxia can also be modulated by the placenta and the mother. Changes in the set points of the cardiovascular regulatory mechanisms in the foetus increase susceptibility to hypertension in adulthood.

2.1. Foetus

Foetal blood is hypoxic compared with maternal blood. The foetal partial pressure of oxygen is reduced to 20–30 mmHg, while in the mother, the arterial partial pressure of oxygen is about 75–100 mmHg at sea level [65,66,67][65][66][67]. Nevertheless, the foetus can cope with up to a 50% (10–15 mmHg) reduction of the partial pressure of oxygen [68]. This has been well-described in sheep used as a common animal model of prenatal hypoxia. In sheep, during normoxia, the maternal partial pressure of oxygen is about 100 mmHg. In comparison, during hypoxia, it can decrease up to 35 mmHg, and the foetus can compensate for this condition. In the case of a sheep foetus, due to hypoxia, the oxygen saturation can decrease from 20 mmHg to 10.5 mmHg in the umbilical artery and from 34 mmHg to 15 mmHg in the umbilical vein [69]. A decrease of the partial pressure of oxygen in the foetus causes femoral vasoconstriction because of local and neurohumoral regulatory mechanisms [70], which can cooperate with the foetal, placental, or maternal regulations.
The adaptive response to hypoxia is a combination of the following five factors:
(1) Reflex response mediated by the chemoreflex and α1-adrenergic signalling in peripheral vessels [70,71,72][70][71][72]. Hypoxia also directly affects chromaffin cells in the adrenal medulla, thereby stimulating the release of catecholamines. Chromaffin cells of the adrenal medulla have a chemosensitive function until a sympathetic innervation develops between the adrenal glands and the central nervous system [73].
(2) An endocrine response that is involved in maintaining peripheral vasoconstriction and is activated within about 15 min of the onset of hypoxia, including angiotensin II (Ang II) and other vasoactive substances [71,74,75][71][74][75].
(3) Local components that respond to the direct effect of hypoxia at the tissue level. The vascular endothelium acts as a hypoxic sensor but also an effector system that releases NO [76], adenosine [77], and endothelin-1 [78], thus affecting the function of vascular smooth muscle.
(4) Placental vasoactive substances are released from the placenta into the foetus and can thus modulate the response to hypoxia. Such substances include adenosine [79], Ang II, thromboxane, endothelin, NO [80], glucocorticoids and others [81].
(5) Maternal factors that pass from the mother to the foetus. Environmental hypoxia, during which both the mother and the foetus are hypoxic, causes adaptive changes not only at the level of the foetus but also in the mother. Some of the mother’s adaptation mechanisms may also affect foetal development [81].
Activation of the described mechanisms as a response to prenatal hypoxia ensures sufficient blood flow to vital organs, such as the brain and heart, by peripheral vasoconstriction and reduction in oxygen consumption by the tissues and organs. WThe researchers further describe the effects of prenatal hypoxia on cardiovascular regulatory mechanisms: the chemoreflex, adenosine, NO, ROS, and RAAS, as well as the effects of prenatal hypoxia on morphological-functional changes in the heart, blood vessels, and kidneys (Table 2).
Table 2.
Effects of prenatal hypoxia on the regulatory mechanism of blood pressure.
Prenatal Hypoxia Type Animal Model Hypoxia Outcomes Ref.
Adenosine Arterial PaO2 15 mmHg; 1 h Sheep Foetal acidosis, mean arterial pressure increase, a transient heart rate decrease [77]
Hypoxia/anoxia;

20 or 60 min		 A1R+/+, A1R+/− and A1R−/− C57BL mice, hippocampal slices, isolated brainstem spinal cord Reduction in field excitatory postsynaptic potential [82]
10% O2;

7.5–10.5 ED		 A1AR+/+ and A1AR-deficient C57BL/6 mice Growth retardation, less stabilized HIF-1α protein and cardiac gene expression in A1AR−/− embryos [83]
10–12% O2; 30 min; 122–128 ED Western sheep Cortical blood flow increase, attenuated by a non-selective adenosine receptor antagonist [84]
NO, ROS 13% O2;

6–20 ED		 Wistar rats Foetus: aortic thickening, enhanced nitrotyrosine staining and increased cardiac HSP70 expression.

Adult offspring: impaired NO-dependent relaxation, increased myocardial contractility		 [2]
12% O2; for 4, 7, or 10 days; 58–62 ED Hartley-Duncan guinea pigs Increased eNOS mRNA in foetal ventricles, not altered K+-channel activation in response to acetylcholine-stimulated coronary dilation [59]
40–50% uteroplacental artery ligation; 25 ED New Zealand white rabbits Normal left and right ventricular thickness, increased vessel dilatation; HIF-1α, eNOS, p-eNOS, and iNOS induction suggesting increased NO and oxidative stress in the hearts [85]]
10% 15–20 ED Wistar rats
13% O2; most of gestation (prior to day 5) Wistar rats Maternal and placental oxidative stress—prevented by maternal treatment with vitamin C↓ [42][28,29][28][29]
10% from 121 ED–NA
13% O2; 6–20 EDsheep = [30]
Wistar rats Increased LF/HF HRV ratio and baroreflex gain—prevented by vitamin C [86] 10 ± 0.5% 5–20 ED Sprague Dawley rats
Acute: 10% O2; 0.5 h, 127 ± 1 ED; chronic: 10% O↓ 2; 105–138 ED Welsh Mountain sheep Mitochondria-derived oxidative stress, endothelial dysfunction and hypertension in adult offspring [[31]
53] 10.5% 15–20 ED; 4 h per day Sprague Dawley rats = [32]
6% O2; 0.5 h Welsh Mountain sheep Increased redistribution of blood flow and the glycemic and plasma catecholamine responses [87] 10.5% 4–21 ED Sprague Dawley rats ↓
14 ± 0.5% O2; 1–19 ED (embryos underwent euthanasia)[33]
Bovans Brown eggs Cardiac systolic dysfunction, impaired cardiac contractility and relaxability, increased cardiac sympathetic dominance, endothelial dysfunction in peripheral circulations [88] 10.5% 15–21 ED Sprague Dawley rats ↓ [34,[3435]][35]
Conceived, gestated, born and studied at Putre Research Station (3600 m above sea level) Sheep (neonates) Worsened carotid blood flow, vascular responses to potassium, serotonin, methacholine, and melatonin; diminished endothelial response via NO-independent mechanisms in isolated arteries [89 10.5% 11–17.5 ED BALB/c mice ↓ [36]
]
10.5% O2; 15–21 ED Sprague Dawley rats Revealed reprogramming of the mitochondrion [90] 10.5% last 15 days of gravidity guinea pigs ↓ [37]
10 ± 1% 7–21 ED; 3 h per day Sprague Dawley rats ↓ [
11% O2;

15–21 ED		 Sprague Dawley rats Male and female foetuses: increased oxidative stress in placentas; 7-month-old male and female offspring: cardiac diastolic dysfunction; 13-month-old female offspring: reduced vascular sensitivity to methacholine, 13-month-old male offspring: decreased vascular sensitivity to phenylephrine [91] 38]
13–14% O2;

6–20 ED		 Wistar rats Increased α1-adrenergic reactivity of the cardiovascular system, enhanced reactive hyperemia, sympathetic dominance, hypercontractility and diastolic dysfunction in the heart [92] 11% 15–21 ED rats ↓
7% O2; 2 h; 50–55 ED; foetal hearts were harvested at the end of hypoxia[39]
Guinea pigs Decreased heart ATP, lipid peroxides, 4-hydroxynonenal and malondialdehyde; increased apoptotic index, unremarkable foetal heart morphology, normal postpartum neonatal cardiac function and cerebral histology [93] 11.5% 13–20 ED Sprague Dawley rats ↓ [40]
Acute: 220–240 mmHg; 10,000 m above sea level; 4–5 min; 18 ED–delivery; chronic: 280–300 mmHg; 8000 m above sea level); 2 h; 14 ED–delivery C57BL/6 mice Acute hypoxia: decreased basal O2 consumption rate and intensity of oxidative phosphorylation by the brain mitochondria of newborn, the activation of the respiratory complex II; chronic hypoxia: increased basal O2 consumption rate and oxidative phosphorylation intensity [47] 12% 15–19 ED Sprague Dawley rats
RAAS 10.5% O2;

6–21 ED		= Sprague Dawley rats Foetal growth restriction, impaired trophoblast invasion and uteroplacental vascular remodeling, increased plasma ET-1 levels, prepro-ET-1 mRNA, ET-1 type A receptor and AT1 receptor in the kidney and placenta[41]
[78] 12% 14.5–21 ED CD-1 mice ↓ [11]
12% O2;

from 14.5 ED		 CD1 mice Weaning: both sexes: increased susceptibility to salt-induced cardiac fibrosis; male: renal fibrosis by high salt, increased renal renin mRNA;

12 months: both sexes: increased renal renin mRNA expression and concentrations, male: increased AT1a mRNA expression		 [94] 13% 6–20 ED Wistar rats = [2
10.5% O2;

4–21 ED		,12, Sprague Dawley rats42 Increased superoxide production and decreased SOD expression, enhanced NADPH4, but not NADPH1 or NADPH2 in foetal aortas; increased Ang II-mediated vessel contractions in foetal thoracic aortas blocked by losartan [33]][2][12][42]
13–14%
Acute isocapnic hypoxaemia (foetal PaO2 12–14 mmHg); 1 h; 110/114–124/128 ED6–20 ED Wistar rats = [ Sheep foetuses43]
No effects in foetal heart rate, mean arterial pressure, baro- or chemoreflexes, femoral blood flow, femoral vascular resistance or foetal growth [48] 14% 6–18 ED C57BL/J6 mice
Reflex= Aortic PaO2 12–15 mmHg without alterations in foetal PaCO2; 1 h; 124 ED Welsh Mountain sheep foetuses[44]
Transient bradycardia, femoral vasoconstriction and increases in plasma noradrenaline and adrenaline; the NO clamp: persisted bradycardia, greater peripheral vasoconstrictor and catecholaminergic responses—enhanced the chemoreflex sensitivity [70] 15% 19 ED–delivery; 10 min; 6 times per day
PaOSprague Dawley rats 2= [45]
15 mmHg;

137–144 ED		 Border Leicester Merino cross sheep Reduced and delayed the IA-type current [73] NA NA Jackson Black C-57 mice
Aortic PaO2 10–11 mmHg without alterations in foetal PaCO= 2[46]
; 1 h; 117–118 ED Sheep foetuses Bradycardia, increased arterial blood pressure, femoral vasoconstriction, blood glucose, lactate concentrations, plasma epinephrine and norepinephrine [95] 280–300 mmHg; 8000 m above sea level 14 ED–delivery; 2 h per day C57BL/6 mice = [
Foetal arterial oxygen saturation by 47.3% (uterine blood flow restriction); 118–126 ED47]
Sheep foetuses PaO2 13 mmHg 14 days sheep = [48]
Bradycardia, not in denervated foetuses, followed by a tachycardia; increased foetal heart rate in denervated foetuses; transiently increased foetal blood pressure in intact foetuses and decrease in denervated foetuses; increased cerebral blood flow in both intact and denervated foetuses; decreased carotid vascular resistance in denervated foetuses [96]
10% O2;

5–20 ED		 Sprague Dawley rats Decreased dopamine content in the carotid bodies; until 3 weeks after birth: hyperventilation and disturbed metabolism [31] 3820 m above sea level 30–120 ED sheep =
10% O2;

5–20 ED		[49 Sprague Dawley rats]
Evaluated resting ventilation and ventilatory response; periphery: reduced tyrosine hydroxylase activity within the first postnatal week and enhanced later; central areas: upregulated tyrosine hydroxylase activity within the first postnatal week and downregulated later 4000 m above sea level on first day, 5000 m above sea level on the second to fifth day 14–18 ED, 8 h per day rats ↓ [50]
[27] chronic anaemia NA sheep = [51]
9000 m above sea level; PaO2 42 mmHg 14–19 ED, once 4 h albino rats ↓ [52]
NA
ED, embryonic day; O2, oxygen; PaO2, partial pressure of O2; PaCO2, partial pressure of carbon dioxide; A1R, adenosine 1 receptor; HSP70, heat shock protein 70; ROS, reactive oxygen species; RAAS, renin-angiotensin-aldosterone system; NO, nitric oxide; HIF, hypoxia-inducible factor; eNOS, endothelial NO synthase; p-eNOS, phospho-eNOS; iNOS, inducible NO synthase; LF/HF, the ratio of low frequency to high frequency; HRV, heart rate variability; ET-1, endothelin-1; AT1, angiotensin II type 1 receptor; SOD, superoxide dismutase; NADPH, nicotinamide adenine dinucleotide phosphate oxidase; Ang II, angiotensin II.
 
 
 
Effects of prenatal hypoxia have been studied in different animal models, including chicken (hatching 21 days), mice (full-term 21 days), rats (full-term 22 days), guinea pigs (full-term 65 days) and sheep (full-term 147 days) [71,97][71][97] and each one has its advantages. Sheep have a relatively similar heart size compared with humans, allowing better observation of the changes in foetal cardiovascular parameters in utero. In contrast, mice and rats have smaller hearts than humans; however, they have a rapid reproduction rate, allowing a relatively fast observation of changes in the postnatal period. In addition, the use of mice in a prenatal hypoxia study allows the creation of knockouts to study selected regulatory mechanisms. The chicken embryo develops without direct humoral contacts with the mother, and the development can be easily manipulated [98]. Mice and rats are altricial species, and their development (e.g., nephrogenesis) continues after birth [99], whereas in precocial humans, sheep and guinea pigs, the development is terminated during the prenatal period [100]. The difference among animal models is also related to the time of organogenesis and the critical period of development, which can partially explain some interspecies variation in the foetal responses to prenatal hypoxia.

2.2. Placenta

Maternal and foetal blood do not mix, but their circulations are in close proximity in a newly formed fetomaternal interface, the placenta. This transient organ provides the environment for the exchange of nutrients and gases between the mother and the foetus and protects the foetus from deleterious environmental factors [134][101]. Oxygen crosses the placental barrier by simple diffusion down its concentration gradient, so the efficiency of its transport depends mostly on uterine blood flow, placental morphology, and placental metabolism [135][102]. During pregnancy, uteroplacental blood flow increases several times to meet foetal demands and, therefore, structural changes must constantly occur in the placenta [136,137][103][104]. If the placenta is exposed to adverse effects, such as hypoxia, its structure and function must change, thus sparing the developing foetus from oxygen deprivation [138][105]. On the other hand, when placental development is disturbed, the placental oxygen supply might become limited [43,139][43][106].
Placental function is linked to its structure. In humans, maternal spiral arteries deliver oxygenated blood into the space between placental chorionic villi, so the villous brush border membrane is washed directly by maternal blood. On the foetal side of the placenta, chorionic villi encompass foetal capillary networks. Maternal blood is thus separated from foetal circulation by several tissue layers [140][107]. Although some mammals have different numbers of barrier layers, the placental diffusing capacity remains similar among these species [141][108]. During the first trimester of human pregnancy, maternal spiral arteries are clogged with trophoblast cells derived from the developing embryo, resulting in fetoplacental hypoxia. At this stage, hypoxia is not pathological, on the contrary, it drives the placental and initial foetal development [142][109]. Meanwhile, clogged maternal arteries undergo physiological remodelling. This is a crucial process to ensure adequate placental perfusion throughout pregnancy, since foetal oxygenation depends strongly on uteroplacental blood flow. During physiological vascular conversion, the endothelial lining and vascular smooth muscle layer are replaced by fibrinoid, leading to vascular lumen enlargement. Remodelled vessels cannot respond to vasoactive substances to the degree they did before the remodelling [143][110], meaning that maternal blood flows into the intervillous space more continuously and under lower pressure [144][111]. Such low-resistance flow protects the chorionic villi and provides adequate time for the exchange of nutrients and gases. Moreover, the pressure difference between the intervillous space and foetal capillaries affects the thickness of the villous membrane, thus influencing the placental diffusing capacity [144][111].
Abnormal placental development with poor spiral artery remodelling can adversely affect placental haemodynamics and placental diffusing capacity [139,145][106][112] and lower foetal oxygenation may result from abnormal villous development [146][113]. Together, the inadequate conversion of spiral arteries along with abnormal villous development can cause placental insufficiency and jeopardize foetal development [145][112]. The shallow, or even absent, trophoblast invasion of spiral arteries is considered one of the causes of preeclampsia [147][114]. In preeclampsia, insufficiently remodelled spiral arteries still have a muscle layer [148[115][116],149], so they are more reactive to vasoactive substances [80]. In addition, insufficient remodelling can be accompanied by placental atherosis, which is characterized by fibrinoid necrosis of the vessel wall [150][117] and thrombosis [151][118], both contributing to uteroplacental ischaemia-reperfusion injury and subsequent oxidative stress [139][106]. As a result, intermittent placental perfusion is more frequent throughout the pregnancy than is normal [139][106]. The intermittent perfusion becomes a problem, especially towards the end of a pregnancy, when fetoplacental oxygen consumption is at its peak [148][115].
Placental vessels lack innervation, and their reactivity mostly results from locally produced substances [80]. Typically, if shear stress is high, placental endothelial cells produce NO, so placental vascular resistance decreases; however, in placental vessels from growth-restricted foetuses, the shear stress-induced vasodilation is impaired, resulting in a parallel increase in placental vascular resistance [136][103]. The strongest vasoconstrictor produced by preeclamptic placental tissue is probably thromboxane, but other local substances are involved, such as Ang II and endothelin. Placental vasoreactivity is amplified by decreased prostacyclin and prostaglandin E2 production [80]. Finally, the chronic increase in adenosine concentrations in preeclampsia stimulates the production of anti-angiogenic soluble fms-like tyrosine kinase-1, a non-membrane associated splice variant of receptor 1 for vascular endothelial growth factor (VEGF). It binds the angiogenic VEGF, decreasing its free circulating concentrations and reducing vessel growth and placental vasculature [152][119].
An inappropriate oxygen environment can induce changes in the placental structure, which might be beneficial for improving foetal oxygenation. A placental barrier can become thinner, capillary diameter increases and uteroplacental vascular resistance decreases, so a more efficient diffusion is achieved [138][105]. These changes are mediated by HIF-1α target genes and their proteins, such as VEGF and erythropoietin [153][120]. Moreover, hypoxia can stimulate the expression of arginase-2, an enzyme responsible for decreased NO production [136][103]. Higgins et al. demonstrated in a murine model that there is an oxygen threshold below which the placenta cannot compensate for the lack of oxygen and intrauterine growth restriction occurs. Their experiment showed that an inhalation of 13% O2 during pregnancy led to structural changes in the placenta (reduction of the thickness of the interhaemal membrane, increased labyrinth zone volume, reduced trophoblast volume, increased placental capacity for transport of nutrients and O2 to the foetus), which spared foetal growth. On the other hand, when pregnant dams inhaled 10% O2, the placental barrier became thicker and the exchange surface area was reduced, so the placental diffusing capacity was negatively affected, and foetal growth restriction occurred.
Along with structural changes, placental metabolism is also modified by hypoxia. The hypoxic placenta consumes less oxygen but increases glucose transport and uptake for anaerobic glycolysis. The placenta is susceptible to oxidative stress due to its high metabolic activity; however, with increasing foetal oxygen requirements and increased metabolic activity, the antioxidant capacity of the placenta gradually increases [154][121]. Such reprogramming can protect the foetus from growth restriction [155][122], but if the transplacental glucose transport is decreased and placental consumption is still increased, the foetus becomes hypoglycaemic, resulting in growth restriction [153,156][120][123]. Two other factors can affect placental metabolism: the stage of pregnancy when hypoxia occurs and maternal food intake [155][122]. Hypoxia can modulate maternal food intake, therefore, it might be difficult sometimes to distinguish whether the effects are due to a lack of oxygen or a lack of nutrients. The same applies for glucocorticoids; hypoxia can also induce glucocorticoid secretion [157][124]. A foetus is protected from maternal glucocorticoids by the placental enzyme 11β-hydroxysteroid dehydrogenase (11β-HSD) type 2, converting the biologically active cortisol to the inactive cortisone. Hypoxia reduces the expression of 11β-HSD type 2 [81] and thus allows more glucocorticoids to cross the placental barrier. In contrast, hypoxia does not affect the expression of 11β-HSD type 1, which converts inactive cortisone to active cortisol [158][125]. Many articles have analysed the effect of antenatal glucocorticoid exposure on the development of the foetal cardiovascular system [159][126]. Antenatal glucocorticoids have direct and mediated (Ang II, catecholamines) pressor and morphological effects, such as cardiomyocytes maturation as well as growth and differentiation of the smooth muscle and endothelial cells in vessels [160][127]. Based on these findings, the placenta integrates multiple signals to compensate for the foetal demands. Whether these adaptations are beneficial for the foetus depends not only on the severity of hypoxia but also on other factors that may buffer or amplify the effects of hypoxia.

2.3. Mother

The foetus is entirely dependent on maternal oxygen supply and therefore, maternal hypoxaemia strongly affects the foetus. Maternal hypoxaemia can arise from different aetiologies, which are related to maternal health conditions, such as maternal haematological disorders, chronic pulmonary disease, and heart disease, or various environmental factors. Hypoxia is usually studied by inhaling low oxygen air, which mimics the environment at high altitudes. Millions of people live permanently in high-altitude environments and are expected to be genetically well adapted. Indeed, women living in high altitudes have a more significant increase in uterine perfusion during gestation and because of that, better foetal outcomes [161][128]. Maternal health conditions can result in an insufficient oxygen supply, even when the mother herself is not hypoxic. In such cases, foetal hypoxia could be a consequence of reduced uteroplacental perfusion or increased fetoplacental metabolism.
Gestational diabetes is one of the most common complications of pregnancy. According to the studied population, its prevalence ranges from 1.7% to 11.6% [162][129]. During pregnancy, the maternal metabolism changes to ensure optimal foetal development, and a pregnant woman becomes insulin resistant to provide the foetus with a sufficient amount of glucose. When the pancreas of a hyperglycaemic pregnant woman cannot produce enough insulin to maintain glycaemia [163][130], more glucose passes through the placental barrier to the foetus, which becomes hyperglycaemic. Consequently, foetal hyperinsulinaemia develops with a consequent increase in size and metabolism of the foetus [164][131]. These changes are reflected in increased uteroplacental and foetal oxygen consumption [165][132], and if fetoplacental demands exceed the maternal oxygen supply, hypoxia occurs [166][133]. Moreover, gestational diabetes is associated with a changing “zigzag” pattern of heart rate variability in the foetus [167][134]. Similar changes were observed during the second stage of parturition when an overstretched or compressed umbilical cord occurred, or during reduced oxygen availability because of uterine contractions [167][134]. The observed changes suggest that heart rate variability and the “zigzag” profile may be used as an early marker of prenatal hypoxia and not only in pregnancies with gestational diabetes [167][134].
Haematological disorders. Epidemiological data show that every fifth pregnant woman is anaemic and in developing countries, the prevalence might even reach 75% [168][135]. During the first trimester, a woman’s blood volume starts to expand, followed by a later increase in red blood cell mass. These pregnancy-induced changes result in physiological anaemia [169][136]. Since iron is needed for red blood cell formation, its deficiency reduces the capacity of blood to carry oxygen [170][137]. Interestingly, compensatory changes may lead to paradoxically higher oxygen content in the umbilical cord [171][138]. Another example of haematological disorders may be an abnormal, rigid sickle shape of erythrocytes, observed in thalassemia [64].
Pulmonary complications. Pregnancy-induced changes may also contribute to the development of obstructive sleep apnoea, whose prevalence reaches up to 26% in late pregnancy because of a higher maternal body mass index [172][139]. Obstructive sleep apnoea is characterized by episodes of hypopnoea or even apnoea resulting in maternal intermittent hypoxaemia and hypercapnia [173][140]. Even though such a shortage of oxygen is not necessarily transmitted to the foetus [174][141], data indicate the association between obstructive sleep apnoea and adverse foetal growth [175][142]. Among other respiratory disorders, asthma is the most common during pregnancy, with a worldwide prevalence of 2–13% [176][143]. When airways are obstructed, ventilation becomes uneven, and maternal arterial oxygen saturation decreases [177][144]. Acute respiratory diseases such as bronchitis, and pneumonia can lead to maternal respiratory failure, represent a risk for the foetus, and are a common pulmonary problem during pregnancy [64].
Cardiac diseases occur in 1% of pregnant women [178][145]. Maternal cardiac output increases throughout a normal pregnancy until reaches more than 30% of the non-pregnant value [179][146]. This physiological change, accompanied by a decrease in systemic resistance, is necessary to ensure adequate foetal oxygenation. If a pregnant woman suffers from heart disease, the heart may not adapt to this increased load [180][147] leading to arrhythmias, heart failure [181][148], and pulmonary oedema. In such cases, insufficient gas exchange in maternal lungs causes hypoxaemia also in the foetus [180][147].
Lifestyle. Maternal hypoxia can also develop due to bad lifestyle habits, such as a high-fat diet, smoking, or alcohol consumption. Consumption of a high-fat diet is associated with lower uteroplacental perfusion. Moreover, if a high-fat diet is accompanied by maternal hyperinsulinaemia, it can result in placental dysfunction [182][149] and the placental oxygen transport it might become limited. Moreover, obese women are more susceptible to developing the above-mentioned diseases, such as gestational diabetes or obstructive sleep apnoea [183][150], which may further increase the risk of hypoxia. Active smoking causes a rapid increase in maternal pulse and blood pressure. These cardiovascular changes result from the action of serum catecholamines, whose concentration increases within a few minutes after smoking [184][151]. When the uterine vessels are constricted, uteroplacental blood flow might become temporarily limited, while maternal concentrations of carboxyhaemoglobin also increase, resulting in a lower oxygen supply for the foetus, thus making hypoxia even more pronounced [184][151]. A recent study showed that passive smoking might also cause foetal hypoxia [185][152]. Alcohol consumption results in placental oxidative stress and a subsequent decrease in NO availability [186][153]. Even drinking coffee during pregnancy could potentially affect foetal oxygenation by stimulating the maternal and placental renin-angiotensin system [187][154] and maternal catecholamine secretion [188][155].

References

  1. Bhatnagar, A. Environmental determinants of cardiovascular disease. Circ. Res. 2017, 121, 162–180.
  2. Giussani, D.A.; Camm, E.J.; Niu, Y.; Richter, H.G.; Blanco, C.E.; Gottschalk, R.; Blake, E.Z.; Horder, K.A.; Thakor, A.S.; Hansell, J.A.; et al. Developmental programming of cardiovascular dysfunction by prenatal hypoxia and oxidative stress. PLoS ONE 2012, 7, e31017.
  3. Kwon, E.J.; Kim, Y.J. What is fetal programming? A lifetime health is under the control of in utero health. Obstet. Gynecol. Sci. 2017, 60, 506–519.
  4. Brameld, J.M.; Buttery, P.J.; Dawson, J.M.; Harper, J.M.M. Nutritional and hormonal control of skeletal-muscle cell growth and differentiation. Proc. Nutr. Soc. 1998, 57, 207–217.
  5. Gilbert-Barness, E. Teratogenic causes of malformations. Ann. Clin. Lab. Sci. 2010, 40, 99–114.
  6. Armengaud, J.B.; Yzydorczyk, C.; Siddeek, B.; Peyter, A.C.; Simeoni, U. Intrauterine growth restriction: Clinical consequences on health and disease at adulthood. Reprod. Toxicol. 2021, 99, 168–176.
  7. Barker, D.J.P. The fetal and infant origins of adult disease. Br. Med. J. 1990, 301, 1111.
  8. Brain, K.L.; Allison, B.J.; Niu, Y.; Cross, C.M.; Itani, N.; Kane, A.D.; Herrera, E.A.; Skeffington, K.L.; Botting, K.J.; Giussani, D.A. Intervention against hypertension in the next generation programmed by developmental hypoxia. PLoS Biol. 2019, 17, e2006552.
  9. Chen, X.; Qi, L.; Fan, X.; Tao, H.; Zhang, M.; Gao, Q.; Liu, Y.; Xu, T.; Zhang, P.; Su, H.; et al. Prenatal hypoxia affected endothelium-dependent vasodilation in mesenteric arteries of aged offspring via increased oxidative stress. Hypertens. Res. 2019, 42, 863–875.
  10. Patterson, A.J.; Chen, M.; Xue, Q.; Xiao, D.; Zhang, L. Chronic Prenatal Hypoxia Induces Epigenetic Programming of PKCε Gene Repression in Rat Hearts. Circ. Res. 2010, 107, 365–373.
  11. Walton, S.L.; Singh, R.R.; Tan, T.; Paravicini, T.M.; Moritz, K.M. Late gestational hypoxia and a postnatal high salt diet programs endothelial dysfunction and arterial stiffness in adult mouse offspring. J. Physiol. 2016, 594, 1451–1463.
  12. Herrera, E.A.; Camm, E.J.; Cross, C.M.; Mullender, J.L.; Wooding, F.B.P.; Giussani, D.A. Morphological and Functional Alterations in the Aorta of the Chronically Hypoxic Fetal Rat. J. Vasc. Res. 2011, 49, 50–58.
  13. Peyronnet, J.; Dalmaz, Y.; Ehrström, M.; Mamet, J.; Roux, J.C.; Pequignot, J.M.; Thorén, P.H.; Lagercrantz, H. Long-lasting adverse effects of prenatal hypoxia on developing autonomic nervous system and cardiovascular parameters in rats. Pflugers Archiv. Eur. J. Physiol. 2002, 443, 858–865.
  14. Svitok, P.; Molcan, L.; Stebelova, K.; Vesela, A.; Sedlackova, N.; Ujhazy, E.; Mach, M.; Zeman, M. Prenatal hypoxia in rats increased blood pressure and sympathetic drive of the adult offspring. Hypertens. Res. 2016, 39, 501–505.
  15. Rook, W.; Johnson, C.D.; Coney, A.M.; Marshall, J.M. Prenatal hypoxia leads to increased muscle sympathetic nerve activity, sympathetic hyperinnervation, premature blunting of neuropeptide y signaling, and hypertension in adult life. Hypertension 2014, 64, 1321–1327.
  16. Ostadal, B.; Ostadalova, I.; Szarszoi, O.; Netuka, I.; Olejnickova, V.; Hlavackova, M. Sex-dependent effect of perinatal hypoxia on cardiac tolerance to oxygen deprivation in adults. Can. J. Physiol. Pharmacol. 2021, 99, 1–8.
  17. Giussani, D.A.; Davidge, S.T. Developmental programming of cardiovascular disease by prenatal hypoxia. J. Dev. Origins Health Dis. 2013, 4, 328–337.
  18. Iqbal, W.; Ciriello, J. Effect of maternal chronic intermittent hypoxia during gestation on offspring growth in the rat. Am. J. Obstet. Gynecol. 2013, 209, 564.e1–564.e9.
  19. Zhuravin, I.A.; Dubrovskaya, N.M.; Tumanova, N.L. Postnatal physiological development of rats after acute prenatal hypoxia. Neurosci. Behav. Physiol. 2004, 34, 809–816.
  20. Dubrovskaya, N.M.; Zhuravin, I.A. Ontogenetic characteristics of behavior in rats subjected to hypoxia on day 14 or day 18 of embryogenesis. Neurosci. Behav. Physiol. 2010, 40, 231–238.
  21. Hermans, R.H.M.; Longo, L.D.; Mcgivern, R.F. Decreased postnatal testosterone and corticosterone concentrations in rats following acute intermittent prenatal hypoxia without alterations in adult male sex behavior. Neurotoxicol. Teratol. 1994, 16, 201–206.
  22. Minior, V.K.; Levine, B.; Ferber, A.; Guller, S.; Divon, M.Y. Nucleated red blood cells as a marker of acute and chronic fetal hypoxia in a rat model. Rambam Maimonides Med. J. 2017, 8, e0025.
  23. Baud, O.; Daire, J.L.; Dalmaz, Y.; Fontaine, R.H.; Krueger, R.C.; Sebag, G.; Evrard, P.; Gressens, P.; Verney, C. Gestational hypoxia induces white matter damage in neonatal rats: A new model of periventricular leukomalacia. Brain Pathol. 2004, 14, 1–10.
  24. Joseph, V.; Mamet, J.; Lee, F.; Dalmaz, Y.; van Reeth, O. Prenatal hypoxia impairs circadian synchronisation and response of the biological clock to light in adult rats. J. Physiol. 2002, 543, 387–395.
  25. Mamet, J.; Peyronnet, J.; Roux, J.C.; Perrin, D.; Cottet-Emard, J.M.; Pequignot, J.M.; Lagercrantz, H.; Dalmaz, Y. Long-term prenatal hypoxia alters maturation of adrenal medulla in rat. Pediatr. Res. 2002, 51, 207–214.
  26. Perrin, D.; Mamet, J.; Scarna, H.; Roux, J.C.; Bérod, A.; Dalmaz, Y. Long-term prenatal hypoxia alters maturation of brain catecholaminergic systems and motor behavior in rats. Synapse 2004, 54, 92–101.
  27. Peyronnet, J.; Roux, J.C.; Mamet, J.; Perrin, D.; Lachuer, J.; Pequignot, J.M.; Dalmaz, Y. Developmental plasticity of the carotid chemoafferent pathway in rats that are hypoxic during the prenatal period. Eur. J. Neurosci. 2007, 26, 2865–2872.
  28. Camm, E.J.; Hansell, J.A.; Kane, A.D.; Herrera, E.A.; Lewis, C.; Wong, S.; Morrell, N.W.; Giussani, D.A. Partial contributions of developmental hypoxia and undernutrition to prenatal alterations in somatic growth and cardiovascular structure and function. Am. J. Obstet. Gynecol. 2010, 203, 495.e24–495.e34.
  29. Camm, E.J.; Martin-Gronert, M.S.; Wright, N.L.; Hansell, J.A.; Ozanne, S.E.; Giussani, D.A. Prenatal hypoxia independent of undernutrition promotes molecular markers of insulin resistance in adult offspring. FASEB J. 2011, 25, 420–427.
  30. Allison, B.J.; Brain, K.L.; Niu, Y.; Kane, A.D.; Herrera, E.A.; Thakor, A.S.; Botting, K.J.; Cross, C.M.; Itani, N.; Shaw, C.J.; et al. Altered cardiovascular defense to hypotensive stress in the chronically hypoxic fetus. Hypertension 2020, 76, 1195–1207.
  31. Peyronnet, J.; Roux, J.C.; Géloën, A.; Tang, L.Q.; Pequignot, J.M.; Lagercrantz, H.; Dalmaz, Y. Prenatal hypoxia, impairs the postnatal development of neural and functional chemoafferent pathway in rat. J. Physiol. 2000, 524, 525–537.
  32. Hermans, R.H.M.; Hunter, D.E.; Mcgivern, R.F.; Cain, C.D.; Longo, L.D. Behavioral sequelae in young rats of acute intermittent antenatal hypoxia. Neurotoxicol. Teratol. 1992, 14, 119–129.
  33. Zhu, X.; Gao, Q.; Tu, Q.; Zhong, Y.; Zhu, D.; Mao, C.; Xu, Z. Prenatal hypoxia enhanced angiotensin II-mediated vasoconstriction via increased oxidative signaling in fetal rats. Reprod. Toxicol. 2016, 60, 21–28.
  34. Li, G.; Bae, S.; Zhang, L. Effect of prenatal hypoxia on heat stress-mediated cardioprotection in adult rat heart. Am. J. Physiol. Heart Circ. Physiol. 2004, 286, H1712–H1719.
  35. Tong, W.; Chen, W.; Ostrowski, R.P.; Ma, Q.; Souvenir, R.; Zhang, L.; Zhang, J.H.; Tang, J. Maternal hypoxia increases the activity of MMPs and decreases the expression of TIMPs in the brain of neonatal rats. Dev. Neurobiol. 2010, 70, 182–194.
  36. Wang, K.C.W.; Larcombe, A.N.; Berry, L.J.; Morton, J.S.; Davidge, S.T.; James, A.L.; Noble, P.B. Foetal growth restriction in mice modifies postnatal airway responsiveness in an age and sex-dependent manner. Clin. Sci. 2018, 132, 273–284.
  37. Thompson, L.P.; Chen, L.; Polster, B.M.; Pinkas, G.; Song, H. Prenatal hypoxia impairs cardiac mitochondrial and ventricular function in guinea pig offspring in a sex-related manner. Am. J. Physiol. Regul. Integr. Comp. Physiol. 2018, 315, R1232–R1241.
  38. Wang, Z.; Huang, Z.; Lu, G.; Lin, L.; Ferrari, M. Hypoxia during pregnancy in rats leads to early morphological changes of atherosclerosis in adult offspring. Am. J. Physiol. Heart Circ. Physiol. 2009, 296, H1321–H1328.
  39. Bourque, S.L.; Gragasin, F.S.; Quon, A.L.; Mansour, Y.; Morton, J.S.; Davidge, S.T. Prenatal hypoxia causes long-term alterations in vascular endothelin-1 function in aged male, but not female, offspring. Hypertension 2013, 62, 753–758.
  40. Wang, K.C.W.; Morton, J.S.; Davidge, S.T.; Larcombe, A.N.; James, A.L.; Donovan, G.M.; Noble, P.B. Increased heterogeneity of airway Calibre in adult rats after hypoxia-induced intrauterine growth restriction. Respirology 2017, 22, 1329–1335.
  41. Vargas, V.E.; Gurung, S.; Grant, B.; Hyatt, K.; Singleton, K.; Myers, S.M.; Saunders, D.; Njoku, C.; Towner, R.; Myers, D.A. Gestational hypoxia disrupts the neonatal leptin surge and programs hyperphagia and obesity in male offspring in the sprague-dawley rat. PLoS ONE 2017, 12, e0185272.
  42. Richter, H.G.; Camm, E.J.; Modi, B.N.; Naeem, F.; Cross, C.M.; Cindrova-Davies, T.; Spasic-Boskovic, O.; Dunster, C.; Mudway, I.S.; Kelly, F.J.; et al. Ascorbate prevents placental oxidative stress and enhances birth weight in hypoxic pregnancy in rats. J. Physiol. 2012, 590, 1377–1387.
  43. Nuzzo, A.M.; Camm, E.J.; Sferruzzi-Perri, A.N.; Ashmore, T.J.; Yung, H.W.; Cindrova-Davies, T.; Spiroski, A.M.; Sutherland, M.R.; Logan, A.; Austin-Williams, S.; et al. Placental adaptation to early-onset hypoxic pregnancy and mitochondria-targeted antioxidant therapy in a rodent model. Am. J. Pathol. 2018, 188, 2704–2716.
  44. Hellgren, K.T.; Premanandhan, H.; Quinn, C.J.; Trafford, A.W.; Galli, G.L.J. Sex-dependent effects of developmental hypoxia on cardiac mitochondria from adult murine offspring. Free Rad. Biol. Med. 2021, 162, 490–499.
  45. Wang, R.; Xu, F.; Liu, J. prenatal hypoxia preconditioning improves hypoxic ventilatory response and reduces mortality in neonatal rats. J. Perinat. Med. 2008, 36, 161–167.
  46. Golan, H.; Kashtutsky, I.; Hallak, M.; Sorokin, Y.; Huleihel, M. Maternal hypoxia during pregnancy delays the development of motor reflexes in newborn mice. Dev. Neurosci. 2004, 26, 24–29.
  47. Urazov, D.; Astrakhanova, T.A.; Usenko, V.; Mishchenko, T.A.; Schelchkova, N.; Kravchenko, G.A.; Vedunova, V.; Mitroshina, E.V. New aspects of central nervous system adaptation to prenatal hypoxia. Sovremennye Tehnol. Med. 2018, 10, 60–68.
  48. Steyn, C.; Hanson, M.A. The effect of repeated acute hypoxaemia on fetal cardiovascular development in the sheep. J. Physiol. 1998, 512, 295–306.
  49. Kamitomo, M.; Longo, L.D.; Gilbert, R.D. Right and left ventricular function in fetal sheep exposed to long-term high-altitude hypoxemia. Am. J. Physiol. Heart Circ. Physiol. 1992, 262, H399–H405.
  50. Ostádalová, I.; Ostádal, B.; Kolár, F. Effect of prenatal hypoxia on contractile performance and responsiveness to Ca2+ in the isolated perinatal rat heart. Physiol. Res. Acad. Sci. Bohemoslov. 1995, 44, 135–137.
  51. Davis, L.E.; Hohimer, A.R. Hemodynamics and organ blood flow in fetal sheep subjected to chronic anemia. Am. J. Physiol. Regulat. Integr. Comp. Physiol. 1991, 261, R1542–R1548.
  52. Zubenko, S.I.; Yan, L.; Zhul’kov, M.O.; Lebed’ko, O.A.; Sazonova, E.N. Effects of antenatal hypoxia on tissue homeostasis in the myocardium of albino rats: Early and delayed consequences. Bull. Exp. Biol. Med. 2014, 157, 320–323.
  53. Botting, K.J.; Skeffington, K.L.; Niu, Y.; Allison, B.J.; Brain, K.L.; Itani, N.; Beck, C.; Logan, A.; Murray, A.J.; Murphy, M.P.; et al. Translatable mitochondria-targeted protection against programmed cardiovascular dysfunction. Sci. Adv. 2020, 6, eabb1929.
  54. Semenza, G.L.; Prabhakar, N.R. neural regulation of hypoxia-inducible factors and redox state drives the pathogenesis of hypertension in a rodent model of sleep apnea. J. Appl. Physiol. 2015, 119, 1152–1156.
  55. Huang, Y.; di Lorenzo, A.; Jiang, W.; Cantalupo, A.; Sessa, W.C.; Giordano, F.J. Hypoxia-inducible factor-1α in vascular smooth muscle regulates blood pressure homeostasis through a peroxisome proliferator-activated receptor-γ-angiotensin II receptor type 1 axis. Hypertension 2013, 62, 634–640.
  56. Zhu, Q.; Wang, Z.; Xia, M.; Li, P.L.; van Tassell, B.W.; Abbate, A.; Dhaduk, R.; Li, N. Silencing of hypoxia-inducible factor-1α gene attenuated angiotensin II-induced renal injury in sprague-dawley rats. Hypertension 2011, 58, 657–664.
  57. Chen, Y.F.; Wang, Z.H.; Chen, Z.K.; Lv, G.R.; Ferrari, M. Intermittent maternal hypoxia has an influence on regional expression of endothelial nitric oxide synthase in fetal arteries of rabbits. Pediatr. Res. 2013, 73, 706–712.
  58. Rood, K.; Lopez, V.; la Frano, M.R.; Fiehn, O.; Zhang, L.; Blood, A.B.; Wilson, S.M. Gestational hypoxia and programing of lung metabolism. Front. Physiol. 2019, 10, 1453.
  59. Thompson, L.P.; Aguan, K.; Pinkas, G.; Weiner, C.P. Chronic hypoxia increases the NO contribution of acetylcholine vasodilation of the fetal guinea pig heart. Am. J. Physiol. Regulat. Integr. Comp. Physiol. 2000, 279, R1813–R1820.
  60. Li, M.; Liu, Y.; Jin, F.; Sun, X.; Li, Z.; Liu, Y.; Fang, P.; Shi, H.; Jiang, X. Endothelin-1 induces hypoxia inducible factor 1α expression in pulmonary artery smooth muscle cells. FEBS Lett. 2012, 586.
  61. Yin, H.L.; Luo, C.W.; Dai, Z.K.; Shaw, K.P.; Chai, C.Y.; Wu, C.C. Hypoxia-inducible factor-1α, vascular endothelial growth factor, inducible nitric oxide synthase, and endothelin-1 expression correlates with angiogenesis in congenital heart disease. Kaohsiung J. Med. Sci. 2016, 32, 348–355.
  62. Wu, Y.; Tang, D.; Liu, N.; Xiong, W.; Huang, H.; Li, Y.; Ma, Z.; Zhao, H.; Chen, P.; Qi, X.; et al. Reciprocal regulation between the circadian clock and hypoxia signaling at the genome level in mammals. Cell Metab. 2017, 25, 73–85.
  63. Zlacká, J.; Zeman, M. Glycolysis under circadian control. Int. J. Molec. Sci. 2021, 22, 13666.
  64. Hutter, D.; Kingdom, J.; Jaeggi, E. Causes and mechanisms of intrauterine hypoxia and its impact on the fetal cardiovascular system: A review. Int. J. Pediatr. 2010, 2010, 1–9.
  65. Nye, G.A.; Ingram, E.; Johnstone, E.D.; Jensen, O.E.; Schneider, H.; Lewis, R.M.; Chernyavsky, I.L.; Brownbill, P. Human placental oxygenation in late gestation: Experimental and theoretical approaches. J. Physiol. 2018, 596, 5523–5534.
  66. Sharma, S.; Hashmi, M. Partial pressure of oxygen measurement. Antioxidants 2020, 9, 414.
  67. Vali, P.; Lakshminrusimha, S. The fetus can teach us: Oxygen and the pulmonary vasculature. Children 2017, 4, 67.
  68. Turner, J.M.; Mitchell, M.D.; Kumar, S.S. The physiology of intrapartum fetal compromise at term. Am. J. Obstet. Gynecol. 2020, 222, 17–26.
  69. Parer, J.T. The effect of acute maternal hypoxia on fetal oxygenation and the umbilical circulation in the sheep. Eur. J. Obstet. Gynecol. Reprod. Biol. 1980, 10, 125–136.
  70. Morrison, S.; Gardner, D.S.; Fletcher, A.J.W.; Bloomfield, M.R.; Giussani, D.A. Enhanced nitric oxide activity offsets peripheral vasoconstriction during acute hypoxaemia via chemoreflex and adrenomedullary actions in the sheep fetus. J. Physiol. 2003, 547, 283–291.
  71. Giussani, D.A. The fetal brain sparing response to hypoxia: Physiological mechanisms. J. Physiol. 2016, 594, 1215–1230.
  72. Kane, A.D.; Herrera, E.A.; Hansell, J.A.; Giussani, D.A. Statin treatment depresses the fetal defence to acute hypoxia via increasing nitric oxide bioavailability. J. Physiol. 2012, 590, 323–334.
  73. Rychkov, G.Y.; Adams, M.B.; McMillen, I.C.; Roberts, M.L. Oxygen sensing mechanisms are present in the chromaffin cells of the sheep adrenal medulla before birth. J. Physiol. 1998, 509, 887–893.
  74. Mao, C.; Hou, J.; Ge, J.; Hu, Y.; Ding, Y.; Zhou, Y.; Zhang, H.; Xu, Z.; Zhang, L. Changes of renal AT1/AT2 receptors and structures in ovine fetuses following exposure to long-term hypoxia. Am. J. Nephrol. 2010, 31, 141–150.
  75. Tang, J.; Li, N.; Chen, X.; Gao, Q.; Zhou, X.; Zhang, Y.; Liu, B.; Sun, M.; Xu, Z. Prenatal hypoxia induced dysfunction in cerebral arteries of offspring rats. J. Am. Heart Assoc. 2017, 6, e006630.
  76. Lane, S.L.; Doyle, A.S.; Bales, E.S.; Lorca, R.A.; Julian, C.G.; Moore, L.G. Increased uterine artery blood flow in hypoxic murine pregnancy is not sufficient to prevent fetal growth restriction. Biol. Reprod. 2020, 102, 660–670.
  77. Koos, B.J.; Chau, A.; Ogunyemi, D. Adenosine mediates metabolic and cardiovascular responses to hypoxia in fetal sheep. J. Physiol. 1995, 488, 761–766.
  78. Zhou, J.; Xiao, D.; Hu, Y.; Wang, Z.; Paradis, A.; Mata-Greenwood, E.; Zhang, L. Gestational hypoxia induces preeclampsia-like symptoms via heightened endothelin-1 signaling in pregnant rats. Hypertension 2013, 62, 599–607.
  79. Kurlak, L.O.; Williams, P.J.; Bulmer, J.N.; Broughton Pipkin, F.; Mistry, H.D. Placental expression of adenosine A2A receptor and hypoxia inducible factor-1 alpha in early pregnancy, term and pre-eclamptic pregnancies: Interactions with placental renin-angiotensin system. Placenta 2015, 36, 611–613.
  80. Benoit, C.; Zavecz, J.; Wang, Y. Vasoreactivity of chorionic plate arteries in response to vasoconstrictors produced by preeclamptic placentas. Placenta 2007, 28, 498–504.
  81. Cuffe, J.S.M.; Walton, S.L.; Singh, R.R.; Spiers, J.G.; Bielefeldt-Ohmann, H.; Wilkinson, L.; Little, M.H.; Moritz, K.M. Mid- to late term hypoxia in the mouse alters placental morphology, glucocorticoid regulatory pathways and nutrient transporters in a sex-specific manner. J. Physiol. 2014, 592, 3127–3141.
  82. Johansson, B.; Halldner, L.; Dunwiddie, T.V.; Masino, S.A.; Poelchen, W.; Giménez-Llort, L.; Escorihuela, R.M.; Fernández-Teruel, A.; Wiesenfeld-Hallin, Z.; Xu, X.J.; et al. Hyperalgesia, anxiety, and decreased hypoxic neuroprotection in mice lacking the adenosine A1 receptor. Proc. Natl. Acad. Sci. USA 2001, 98, 9407–9412.
  83. Wendler, C.C.; Amatya, S.; McClaskey, C.; Ghatpande, S.; Fredholm, B.B.; Rivkees, S.A. A1 adenosine receptors play an essential role in protecting the embryo against hypoxia. Proc. Natl. Acad. Sci. USA 2007, 104, 9697–9702.
  84. Blood, A.B.; Hunter, C.J.; Power, G.G. Adenosine mediates decreased cerebral metabolic rate and increased cerebral flow during acute moderate hypoxia in the near-term fetal sheep. J. Physiol. 2003, 553, 935–945.
  85. Figueroa, H.; Alvarado, C.; Cifuentes, J.; Lozano, M.; Rocco, J.; Cabezas, C.; Illanes, S.E.; Eixarch, E.; Hernández-Andrade, E.; Gratacós, E.; et al. Oxidative damage and nitric oxide synthase induction by surgical uteroplacental circulation restriction in the rabbit fetal heart. Prenat. Diagn. 2017, 37, 453–459.
  86. Kane, A.D.; Herrera, E.A.; Camm, E.J.; Giussani, D.A. Vitamin C prevents intrauterine programming of in vivo cardiovascular dysfunction in the rat. Circ. J. 2013, 77, 2604–2611.
  87. Thakor, A.S.; Allison, B.J.; Niu, Y.; Botting, K.J.; Serõn-Ferré, M.; Herrera, E.A.; Giussani, D.A. Melatonin modulates the fetal cardiovascular defense response to acute hypoxia. J. Pineal Res. 2015, 59, 80–90.
  88. Itani, N.; Skeffington, K.L.; Beck, C.; Niu, Y.; Giussani, D.A. Melatonin rescues cardiovascular dysfunction during hypoxic development in the chick embryo. J. Pineal Res. 2016, 60, 16–26.
  89. Herrera, E.A.; Macchiavello, R.; Montt, C.; Ebensperger, G.; Díaz, M.; Ramírez, S.; Parer, J.T.; Serõn-Ferré, M.; Reyes, R.V.; Llanos, A.J. Melatonin improves cerebrovascular function and decreases oxidative stress in chronically hypoxic lambs. J. Pineal Res. 2014, 57, 33–42.
  90. Gao, Y.; Dasgupta, C.; Huang, L.; Song, R.; Zhang, Z.; Zhang, L. Multi-omics integration reveals short and long-term effects of gestational hypoxia on the heart development. Cells 2019, 8, 1608.
  91. Aljunaidy, M.M.; Morton, J.S.; Kirschenman, R.; Phillips, T.; Case, C.P.; Cooke, C.-L.M.; Davidge, S.T. Maternal treatment with a placental-targeted antioxidant (MitoQ) impacts offspring cardiovascular function in a rat model of prenatal hypoxia. Pharmacol. Res. 2018, 134, 332–342.
  92. Spiroski, A.; Niu, Y.; Nicholas, L.M.; Austin-Williams, S.; Camm, E.J.; Sutherland, M.R.; Ashmore, T.J.; Skeffington, K.L.; Logan, A.; Ozanne, S.E.; et al. Mitochondria antioxidant protection against cardiovascular dysfunction programmed by early-onset gestational hypoxia. FASEB J. 2021, 35, e21446.
  93. Powell, S.R.; Mantell, L.L.; Garramone, V.; Drexler, S.; Teichberg, S. Acute effects of nonlethal in utero hypoxia on fetal guinea pig heart and lack of persistent cardiac or cerebral effects in the neonate. Biol. Neonate 2004, 86, 240–246.
  94. Walton, S.L.; Bielefeldt-Ohmann, H.; Singh, R.R.; Li, J.; Paravicini, T.M.; Little, M.H.; Moritz, K.M. Prenatal hypoxia leads to hypertension, renal renin-angiotensin system activation and exacerbates salt-induced pathology in a sex-specific manner. Sci. Rep. 2017, 7, 8241.
  95. Giussani, D.A.; Gardner, D.S.; Cox, D.T.; Fletcher, A.J.W. Purinergic contribution to circulatory, metabolic, and adrenergic responses to acute hypoxemia in fetal sheep. Am. J. Physiol. Regulat. Integr. Comp. Physiol. 2001, 280, R678–R685.
  96. Stein, P.; White, S.E.; Homan, J.; Hanson, M.A.; Bocking, A.D. Altered fetal cardiovascular responses to prolonged hypoxia after sinoaortic denervation. Am. J. Physiol. Regulat. Integr. Comp. Physiol. 1999, 276, R340–R346.
  97. DeSesso, J.M. Comparative gestational milestones in vertebrate development. In Developmental and Reproductive Toxicology; CRC Press: Boca Raton, FL, USA, 2016; pp. 107–152.
  98. Zeman, M.; Herichová, I. circadian melatonin production develops faster in birds than in mammals. Gen. Comp. Endocrinol. 2011, 172, 23–30.
  99. Sekulić, S.; Božić, K.; Bozić, A.; Borota, J.; Ćulić, M. Precocial rodents as new experimental model to study the effects of altered gravitational conditions on fetal development. Microgravity Sci. Technol. 2006, 18, 223–225.
  100. Carter, A.M. Animal models of human pregnancy and placentation: Alternatives to the mouse. Reproduction 2020, 160, R129–R143.
  101. Burton, G.J.; Fowden, A.L.; Thornburg, K.L. Placental origins of chronic disease. Physiol. Rev. 2016, 96, 1509–1565.
  102. Zamudio, S.; Torricos, T.; Fik, E.; Oyala, M.; Echalar, L.; Pullockaran, J.; Tutino, E.; Martin, B.; Belliappa, S.; Balanza, E.; et al. Hypoglycemia and the origin of hypoxia-induced reduction in human fetal growth. PLoS ONE 2010, 5, e8551.
  103. Morley, L.C.; Debant, M.; Walker, J.J.; Beech, D.J.; Simpson, N.A.B. Placental blood flow sensing and regulation in fetal growth restriction. Placenta 2021, 113, 23–28.
  104. Labarrere, C.A.; DiCarlo, H.L.; Bammerlin, E.; Hardin, J.W.; Kim, Y.M.; Chaemsaithong, P.; Haas, D.M.; Kassab, G.S.; Romero, R. Failure of physiologic transformation of spiral arteries, endothelial and trophoblast cell activation, and acute atherosis in the basal plate of the placenta. Am. J. Obstet. Gynecol. 2017, 216, 287.e1–287.e16.
  105. Cahill, L.S.; Rennie, M.Y.; Hoggarth, J.; Yu, L.X.; Rahman, A.; Kingdom, J.C.; Seed, M.; Macgowan, C.K.; Sled, J.G. Feto- and utero-placental vascular adaptations to chronic maternal hypoxia in the mouse. J. Physiol. 2018, 596, 3285–3297.
  106. Hung, T.-H.; Burton, G.J. Hypoxia and reoxygenation: A possible mechanism for placental oxidative stress in preeclampsia. Taiwan. J. Obstet. Gynecol. 2006, 45, 189–200.
  107. Ganapathy, V.; Prasad, P.D. Role of transporters in placental transfer of drugs. Toxicol. Appl. Pharmacol. 2005, 207, 381–387.
  108. Carter, A.M. Placental gas exchange and the oxygen supply to the fetus. In Comprehensive Physiology; Wiley: Hoboken, NJ, USA, 2015; Volume 5, pp. 1381–1403.
  109. James, J.L.; Stone, P.R.; Chamley, L.W. The regulation of trophoblast differentiation by oxygen in the first trimester of pregnancy. Hum. Reprod. Update 2006, 12, 137–144.
  110. Brosens, I.A. The utero-placental vessels at term—The distribution and extent of physiological changes. In Placental Vascularization and Blood Flow; Springer: Boston, MA, USA, 1988; pp. 61–67.
  111. Karimu, A.L.; Burton, G.J. The effects of maternal vascular pressure on the dimensions of the placental capillaries. BJOG: Int. J. Obstet. Gynaecol. 1994, 101, 57–63.
  112. Lyall, F.; Robson, S.C.; Bulmer, J.N. Spiral artery remodeling and trophoblast invasion in preeclampsia and fetal growth restriction relationship to clinical outcome. Hypertension 2013, 62, 1046–1054.
  113. Shchyogolev, A.I.; Dubova, E.A.; Pavlov, K.A.; Lyapin, V.M.; Kulikova, G.V.; Shmakov, R.G. Morphometric characteristics of terminal villi of the placenta in pre-eclampsia. Bull. Exp. Biol. Med. 2012, 154, 92–95.
  114. Phipps, E.A.; Thadhani, R.; Benzing, T.; Karumanchi, S.A. Pre-eclampsia: Pathogenesis, novel diagnostics and therapies. Nat. Rev. Nephrol. 2019, 15, 275–289.
  115. Burton, G.J.; Woods, A.W.; Jauniaux, E.; Kingdom, J.C.P. Rheological and physiological consequences of conversion of the maternal spiral arteries for uteroplacental blood flow during human pregnancy. Placenta 2009, 30, 473–482.
  116. Perez-Sepulveda, A.; Torres, M.J.; Khoury, M.; Illanes, S.E. Innate immune system and preeclampsia. Front. Immunol. 2014, 5, 244.
  117. Staff, A.C.; Fjeldstad, H.E.; Fosheim, I.K.; Moe, K.; Turowski, G.; Johnsen, G.M.; Alnaes-Katjavivi, P.; Sugulle, M. Failure of physiological transformation and spiral artery atherosis: Their roles in preeclampsia. Am. J. Obstet. Gynecol. 2020, 226, S895–S906.
  118. Brosens, I.; Renaer, M. On the pathogenesis of placental infarcts in pre-eclampsia. BJOG: Int. J. Obstet. Gynaecol. 1972, 79, 794–799.
  119. Iriyama, T.; Sun, K.; Parchim, N.F.; Li, J.; Zhao, C.; Song, A.; Hart, L.A.; Blackwell, S.C.; Sibai, B.M.; Chan, L.N.L.; et al. Elevated placental adenosine signaling contributes to the pathogenesis of preeclampsia. Circulation 2015, 131, 730–741.
  120. Zamudio, S. The placenta at high altitude. High Alt. Med. Biol. 2003, 4, 171–191.
  121. Jones, M.L.; Mark, P.J.; Lewis, J.L.; Mori, T.A.; Keelan, J.A.; Waddell, B.J. Antioxidant defenses in the rat placenta in late gestation: Increased labyrinthine expression of superoxide dismutases, glutathione peroxidase 3, and uncoupling Protein 21. Biol. Reprod. 2010, 83, 254–260.
  122. higgins, j.s.; vaughan, o.r.; fernandez de liger, e.; fowden, a.l.; sferruzzi-perri, a.n. placental phenotype and resource allocation to fetal growth are modified by the timing and degree of hypoxia during mouse pregnancy. J. Physiol. 2016, 594, 1341–1356.
  123. Illsley, N.P.; Caniggia, I.; Zamudio, S. Placental metabolic reprogramming: Do changes in the mix of energy-generating substrates modulate fetal growth? Int. J. Dev. Biol. 2010, 54, 409–419.
  124. Zoccal, D.B.; Bonagamba, L.G.H.; Antunes-Rodrigues, J.; Machado, B.H. Plasma corticosterone levels is elevated in rats submitted to chronic intermittent hypoxia. Auton. Neurosci. Basic Clin. 2007, 134, 115–117.
  125. Alfaidy, N.; Gupta, S.; DeMarco, C.; Caniggia, I.; Challis, J.R.G. Oxygen regulation of placental 11β-hydroxysteroid dehydrogenase 2: Physiological and pathological implications. J. Clin. Endocrinol. Metab. 2002, 87, 4797–4805.
  126. Benediktsson, R.; Lindsay, R.S.; Noble, J.; Seckl, J.R.; Edwards, C.R.W. Glucocorticoid exposure in utero: New model for adult hypertension. Lancet 1993, 341, 339–341.
  127. Jellyman, J.K.; Fletcher, A.J.W.; Fowden, A.L.; Giussani, D.A. Glucocorticoid maturation of fetal cardiovascular function. Trends Molec. Med. 2020, 26, 170–184.
  128. Julian, C.G.; Wilson, M.J.; Lopez, M.; Yamashiro, H.; Tellez, W.; Rodriguez, A.; Bigham, A.W.; Shriver, M.D.; Rodriguez, C.; Vargas, E.; et al. Augmented uterine artery blood flow and oxygen delivery protect andeans from altitude-associated reductions in fetal growth. Am. J. Physiol.-Regulat. Integr. Comp. Physiol. 2009, 296, R1564–R1575.
  129. Schneider, S.; Bock, C.; Wetzel, M.; Maul, H.; Loerbroks, A. The prevalence of gestational diabetes in advanced economies. J. Perinat. Med. 2012, 40, 511–520.
  130. Ngala, R.A.; Fondjo, L.A.; Gmagna, P.; Ghartey, F.N.; Awe, M.A. Placental peptides metabolism and maternal factors as predictors of risk of gestational diabetes in pregnant women. A case-control study. PLoS ONE 2017, 12, e0181613.
  131. MacFarlane, C.M.; Tsakalakos, N. Relative fetal hypoxia as a contributing factor to fetal macrosomia in diabetic pregnancy. Med. Hypotheses 1983, 11, 365–374.
  132. Philipps, A.F.; Dubin, J.W.; Matty, P.J.; Raye, J.R. Arterial hypoxemia and hyperinsulinemia in the chronically hyperglycemic fetal lamb. Pediatr. Res. 1982, 16, 653–658.
  133. Taricco, E.; Radaelli, T.; Rossi, G.; Nobile De Santis, M.S.; Bulfamante, G.P.; Avagliano, L.; Cetin, I. Effects of gestational diabetes on fetal oxygen and glucose levels in vivo. BJOG: Int. J. Obstet. Gynaecol. 2009, 116, 1729–1735.
  134. Tarvonen, M.; Hovi, P.; Sainio, S.; Vuorela, P.; Andersson, S.; Teramo, K. Intrapartal cardiotocographic patterns and hypoxia-related perinatal outcomes in pregnancies complicated by gestational diabetes mellitus. Acta Diabetol. 2021, 58, 1563–1573.
  135. Öztürk, M.; Öztürk, Ö.; Ulubay, M.; Karaşahin, E.; Özgürtaş, T.; Yenen, M.; Aydın, A.; Fıratlıgil, F.; Bodur, S. Gebeliğin Tanısı Ile Birlikte Saptanan Anemi Prevalansı. Turk Jinekoloji ve Obstetrik Dernegi Dergisi 2017, 14, 176–180.
  136. Horowitz, K.M.; Ingardia, C.J.; Borgida, A.F. Anemia in pregnancy. Clin. Lab. Med. 2013, 33, 281–291.
  137. Breymann, C. Iron deficiency anemia in pregnancy. Semin. Hematol. 2015, 52, 339–347.
  138. Watkins, V.Y.; Frolova, A.I.; Stout, M.J.; Carter, E.B.; Macones, G.A.; Cahill, A.G.; Raghuraman, N. The relationship between maternal anemia and umbilical cord oxygen content at delivery. Am. J. Obstet. Gynecol. MFM 2021, 3, 100270.
  139. Pien, G.W.; Pack, A.I.; Jackson, N.; Maislin, G.; Macones, G.A.; Schwab, R.J. Risk factors for sleep-disordered breathing in pregnancy. Thorax 2014, 69, 371–377.
  140. Malhotra, A.; White, D.P. Obstructive sleep apnoea. Lancet 2002, 360, 237–245.
  141. Almendros, I.; Martínez-Ros, P.; Farré, N.; Rubio-Zaragoza, M.; Torres, M.; Gutiérrez-Bautista, Á.J.; Carrillo-Poveda, J.M.; Sopena-Juncosa, J.J.; Gozal, D.; Gonzalez-Bulnes, A.; et al. Placental oxygen transfer reduces hypoxia-reoxygenation swings in fetal blood in a sheep model of gestational sleep apnea. J. Appl. Physiol. 2019, 127, 745–752.
  142. Warland, J.; Dorrian, J.; Morrison, J.L.; O’Brien, L.M. Maternal sleep during pregnancy and poor fetal outcomes: A scoping review of the literature with meta-analysis. Sleep Med. Rev. 2018, 41, 197–219.
  143. Bonham, C.A.; Patterson, K.C.; Strek, M.E. Asthma outcomes and management during pregnancy. Chest 2018, 153, 515–527.
  144. Waddell, J.A.; Emerson, P.A.; Gunstone, R.F. Hypoxia in bronchial asthma. Br. Med. J. 1967, 2, 402–404.
  145. Foeller, M.E.; Foeller, T.M.; Druzin, M. Maternal congenital heart disease in pregnancy. Obstet. Gynecol. Clin. N. Am. 2018, 45, 267–280.
  146. Meah, V.L.; Cockcroft, J.R.; Backx, K.; Shave, R.; Stöhr, E.J. Cardiac output and related haemodynamics during pregnancy: A series of meta-analyses. Heart 2016, 102, 518–526.
  147. Poole, J.H.; Spreen, D.T. Acute pulmonary edema in pregnancy. J. Perinatal Neonatal Nurs. 2005, 19, 316–331.
  148. Balci, A.; Sollie-Szarynska, K.M.; van der Bijl, A.G.L.; Ruys, T.P.E.; Mulder, B.J.M.; Roos-Hesselink, J.W.; van Dijk, A.P.J.; Wajon, E.M.C.J.; Vliegen, H.W.; Drenthen, W.; et al. Prospective validation and assessment of cardiovascular and offspring risk models for pregnant women with congenital heart disease. Heart 2014, 100, 1373–1381.
  149. Frias, A.E.; Morgan, T.K.; Evans, A.E.; Rasanen, J.; Oh, K.Y.; Thornburg, K.L.; Grove, K.L. Maternal high-fat diet disturbs uteroplacental hemodynamics and increases the frequency of stillbirth in a nonhuman primate model of excess nutrition. Endocrinology 2011, 152, 2456–2464.
  150. Dominguez, J.E.; Krystal, A.D.; Habib, A.S. Obstructive sleep apnea in pregnant women. Anesth. Analg. 2018, 127, 1167–1177.
  151. Quigley, M.E.; Sheehan, K.L.; Wilkes, M.M.; Yen, S.S.C. Effects of maternal smoking on circulating catecholamine levels and fetal heart rates. Am. J. Obstet. Gynecol. 1979, 133, 685–690.
  152. Levy, M.; Kovo, M.; Ben-Ezry, E.; Torem, M.; Shahaf, H.; Anchel, N.; Bar, J.; Schreiber, L.; Weiner, E. Passively inhaled tobacco smoke—Pregnancy and neonatal outcomes in correlation with placental histopathology. Placenta 2021, 112, 23–27.
  153. Bosco, C.; Diaz, E. Placental hypoxia and foetal development versus alcohol exposure in pregnancy. Alcohol Alcoholism 2012, 47, 109–117.
  154. Huang, J.; Zhou, S.; Ping, J.; Pan, X.; Liang, G.; Xu, D.; Kou, H.; Bao, C.; Wang, H. Role of P53-dependent placental apoptosis in the reproductive and developmental toxicities of caffeine in rodents. Clin. Exp. Pharmacol. Physiol. 2012, 39, 357–363.
  155. James, J.E. Maternal caffeine consumption and pregnancy outcomes: A narrative review with implications for advice to mothers and mothers-to-be. BMJ Evid. Based Med. 2021, 26, 114–115.
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