Perivascular Adipose Tissue: History
View Latest Version
Please note this is an old version of this entry, which may differ significantly from the current revision.
Subjects: Biology
Contributor:
Huige Li

Perivascular adipose tissue (PVAT) is the connective tissue surrounding most of the systemic blood vessels. PVAT is now recognized as an important endocrine tissue that maintains vascular homeostasis. Healthy PVAT has anticontractile, anti-inflammatory, and antioxidative roles. Vascular oxidative stress is an important pathophysiological event in cardiometabolic complications of obesity, type 2 diabetes, and hypertension. Accumulating data from both humans and experimental animal models suggests that PVAT dysfunction is potentially linked to cardiovascular diseases, and associated with augmented vascular inflammation, oxidative stress, and arterial remodeling. Reactive oxygen species produced from PVAT can be originated from mitochondria, nicotinamide adenine dinucleotide phosphate (NADPH) oxidases, and uncoupled endothelial nitric oxide synthase. PVAT can also sense vascular paracrine signals and response by secreting vasoactive adipokines. Therefore, PVAT may constitute a novel therapeutic target for the prevention and treatment of cardiovascular diseases.

  • perivascular adipose tissue
  • oxidative stress
  • sirtuin 1
  • endothelial nitric oxide synthase
  • metabolic diseases
  • cardiovascular diseases

1. Introduction

Perivascular adipose tissue (PVAT) is the ectopic fat depot that surrounds large arteries and veins, small and resistance vessels, and skeletal muscle microvessels [1]. In recent decades, PVAT has been revealed as an important endocrine tissue that maintains vascular homeostasis. The role of PVAT in vascular function was first described by the observation that PVAT diminishes agonists-induced contractile responses in the Sprague–Dawley rat aortae in vitro [2]. PVAT exerts an anticontractile effect on vessels in both rodents and humans [3][4]. It is currently known that PVAT regulates vascular function via endocrine and paracrine mechanisms by releasing various factors, including adipokines, cytokines/chemokines, reactive oxygen species, nitric oxide, and hydrogen sulphide (H2S) [1]. These factors may enter the media and reach the endothelial layer of blood vessels either by direct diffusion or via the vasa vasorum or the small media conduit networks connecting the medial layer with the underlying adventitia [5][6][7]. These adipose tissue-secreted factors include both proinflammatory and anti-inflammatory vasoactive molecules. These PVAT-derived factors modulate various complex processes, including vascular inflammation and oxidative stress, vascular tone, and smooth muscle proliferation and migration [8][9].
Obesity, with respect to its growing frequency worldwide, has become a major public health concern and a burden to developed countries [10]. Obesity is also known as a critical risk factor for most cardiovascular diseases [11]. Accumulating data from both humans and experimental animal models suggests that the dysfunction of PVAT is involved in obesity-related cardiovascular complications, such as endothelial dysfunction, atherosclerosis, or hypertension [12][13][14]. An ‘obesity triad’ consisting of PVAT hypoxia, inflammation, and oxidative stress is proposed as the central mechanism in obesity-induced PVAT dysfunction [1]. Among the triad, vascular oxidative stress is an important pathophysiological event in cardiometabolic complications, including obesity, type 2 diabetes, and hypertension. During oxidative stress, the production of oxidants (e.g., reactive oxygen species, ROS) exceeds antioxidant defense mechanisms, leading to a redox imbalance [15]. In normal conditions, homeostatic ROS play a critical role as secondary messengers in various intracellular signaling pathways in both innate and adaptive immune responses [16]. ROS from PVAT can originate from the mitochondria, nicotinamide adenine dinucleotide phosphate (NADPH) oxidase, and uncoupled endothelial nitic oxide synthase (eNOS) [15]. An abnormal generation of ROS by PVAT emerges as a potential pathophysiological mechanism underlying vascular injury. The anticontractile effect of PVAT is attenuated after the augmentation of oxidative stress [4]. Therefore, PVAT could be a potential therapeutic antioxidant target for the prevention and treatment of cardiovascular diseases.

2. PVAT Modulates Vascular Function

The vascular wall of blood vessels is composed of three layers: tunica adventitia, tunica media, and tunica intima. The tunica intima, the inner layer, is a single layer of flattened, polygonal endothelial cells that rest on basal lamina and loose connective tissues, while the tunica media (especially in arteries) mainly consists of vascular smooth muscle cells (VSMC). The adventitia mainly contains connective tissue [17]. PVAT can be found outside the adventitial layer surrounding most of the systemic blood vessels, including large arteries and veins, small and resistance vessels, and skeletal muscle microvessels. Other microvasculature and the cerebral vasculature are free of PVAT [5][8].
The endothelium has long been recognized as an important regulator of vascular tone by releasing vasoactive factors that modulate VSMC contractility. Endothelium can release both vasodilating (such as endothelium-derived hyperpolarizing factors (EDHF), prostaglandin (PGI2), and nitric oxide (NO)) and vasoconstricting factors (such as endothelin-1 (ET-1) and thromboxane A2 (TXA2)). The endothelium can control the vascular tone by balancing the release of these vasoactive molecules [18]. It is well known that endothelium dysfunction is a major factor in the pathogenesis of many cardiovascular diseases, including hypertension and atherosclerosis [19], as well as metabolic syndrome and diabetes [20][21]. The importance of the endothelium in vascular function is undebatable; however, it is now known that it is not the sole significant regulator of the vascular tone.
The crosstalk between PVAT and the blood vessel is vital for normal vascular function (Figure 1). The modulation of the vascular function by PVAT has been demonstrated by its inhibiting effect on vascular contraction to various agonists in both rodents and humans [3][4]. PVAT exerts anti-contractile function through the release of various PVAT-derived relaxing factors (PVRFs), previously known as the adventitium-derived relaxing factors (ADRFs) [22]. Although it is still unclear how PVRFs exert their anti-contractile effects, a number of potential PVRFs have been suggested, including leptin and adiponectin [23], hydrogen sulphide (H2S) [24], hydrogen peroxide (H2O2) [19], prostaglandins [25][26], NO [27], and angiotensin (Ang) 1–7 [28]. Currently, it is hypothesized that PVAT modulates vascular function through two distinct mechanisms: an endothelium-dependent mechanism through a transferable PVRF and the stimulation of NO release from the endothelium, and an endothelium-independent mechanism through the generation of H2O2 [27]. The transferable PVRFs modulate the release of endothelial NO and the subsequent activation of potassium (K+) channels to facilitate vascular relaxation. On the other hand, the non-transferable anticontractile property of PVAT may involve the generation of H2O2. A recent study suggests that the mitochondria of PVAT are important sources of O2− and H2O2, which are continuously generated in response to contractile stimuli. PVAT regulates the relaxation and contraction of VSMC [29], while ROS may act as important mediators of PVAT anticontractile effects by direct actions in the VSMC [30].
Antioxidants 09 00574 g001 550
Figure 1. The crosstalk between perivascular adipose tissue (PVAT) and the blood vessel modulates vascular function. PVAT releases vasoactive molecules. H2S is synthesized in PVAT and induces vascular smooth muscle cell (VSMC) hyperpolarization. Leptin activates eNOS and stimulates H2S production, which lead to endothelium-dependent vasodilatation. H2S released from endothelium and PVAT functions as an endothelium-derived hyperpolarizing factor (EDHF) and activates endothelial K+ channels. The resulting hyperpolarization of endothelial cells can be transmitted to VSMC. NO and H2O2 released from PVAT can elicit vasodilatation by activating soluble guanylyl cyclase (sGC). Adiponectin produced by PVAT stimulates NO production in PVAT and in endothelial cells and induces VSMC hyperpolarization. Ang 1–7 acts on endothelial cells and stimulates endothelial NO production. Vasodilating prostaglandins released from PVAT can act on VSMC and stimulate vasorelaxation. Reactive oxygen species (ROS) produced from nicotinamide adenine dinucleotide phosphate (NADPH) oxidases in PVAT can cause contractile response in VSMC via the mitogen-activated protein kinase/extracellular signal-regulated kinase (MAPK/ERK) pathway. Other potential PVAT-derived contracting factors have been suggested, including chemerin, calpastatin, and norepinephrine. Antioxidant enzymes SOD and catalase in PVAT can detoxify ROS to produce H2O2, which can stimulate vasodilation. Cytokines released from PVAT, including TNF-α, MCP-1 and TGF-β can lead to VSMC proliferation. MAPK/ERK, mitogen-activated protein kinase/extracellular signal-regulated kinase; Ang, angiotensin; eNOS, endothelial nitric oxide synthase; SOD, superoxide dismutase; TNF-α, tumor necrosis factor-α; MCP-1, monocyte chemotactic protein-1; TGF-β, transforming growth factor-β; H2S, hydrogen sulphide; VSMC, vascular smooth muscle cells.
In addition to PVRF, recent studies have also demonstrated that PVAT can secrete PVAT-derived contracting factors (PVCFs), which modulate vasoconstriction [31][32][33]. Studies in rats have shown that both PVRFs and PVCFs can modulate local vascular tone through endothelium-dependent or endothelium-independent effects, by as-of-yet underdetermined mechanisms [25][34]. Currently, a number of potential PVCFs have been suggested, including chemerin [35], calpastatin [36], norepinephrine (NE) [37], AngII, and ROS [38]. Also, upon perivascular nerve stimulation, PVAT may produce superoxide (O2−) mediated by NADPH oxidases, which enhances the arterial contractile response. This enhancement of contractile effect involves the activation of tyrosine kinase and the mitogen-activated protein kinase/extracellular signal-regulated kinase (MAPK/ERK) pathway. Moreover, the contractile effects of PVAT are regulated by other antioxidant enzymes including SOD (superoxide dismutase) and catalase. Both Mn-SOD and CuZn-SOD are expressed in PVAT [25][38]. When stimulated by NE, the expression of Mn-SOD is increased and the expression of catalase is decreased in PVAT, which induces the generation of O2− in PVAT [30].
It is hypothesized that mitochondria-derived ROS in PVAT modulates vascular reactivity. The uncoupling of mitochondria and the removal of H2O2 increase the NE-induced contraction in vessel rings surrounded with PVAT [30]. Perivascular nerve activation by electric field stimulation (EFS) increases O2− generation in isolated PVAT, which is attenuated by an inhibition of NADPH oxidases. Treatment with apocynin and diphenyleneiodonium chloride (DPI) to inhibit NADPH oxidases attenuates the contractile response to EFS in the vessel rings with PVAT [38]. Also, exogenous O2− augments the contractile response to EFS and to phenylephrine in vessel rings without PVAT [38]. Therefore, ROS in PVAT may act as a pivotal signaling molecule in regulating the contraction of VSMC.
A recent study has shown that the anticontractile effects of PVAT can be mediated by vasoactive amines such as dopamine, NE, and serotonin, which can be uptaken and metabolized in PVAT. Monoamine oxidase A/B (MAO-A/B, which catalyzes the oxidative deamination of vasoactive amine) and semicarbazide-sensitive amine oxidase (SSAO, which catalyzes the production of H2O2 and ammonia) are presented in PVAT, which is responsible for the metabolism of these vasoactive amines. In rat mesenteric arteries, the inhibition of MAO and SSAO, or the inhibition of norepinephrine transporter (NET) with nisoxetine reduced PVAT’s anticontractile effect in response to NE-induced vasocontraction. Furthermore, sympathetic stimulation can trigger the release of adiponectin via β3-adrenoceptor activation in PVAT [39]. Moreover, PVAT can also prevent noradrenaline-induced vasocontraction, by acting as a reservoir of noradrenaline and preventing it from reaching the vessel wall [39]. These studies suggest that PVAT possesses various underdetermined mechanisms, in addition to releasing vasoactive factors, to regulate the vascular function.

3. Obesity-Linked PVAT Dysfunction

Over the past few decades, the prevalence of obesity has doubled worldwide, with a concomitant increase in associated cardiovascular diseases [40]. Obesity has a variety of adverse effects on the cardiovascular system [41]. Although obese patients have a higher risk of developing hypertension, cardiomyopathy, and stroke, endothelial dysfunction is not always evident in in vitro studies. In fact, the dysfunction of PVAT, but not obesity itself, is responsible for obesity-induced vascular disorders. The anticontractile effects of PVAT are attenuated in obese mice compared to lean mice [12][42][43]. When PVAT is removed from the vessel, the anticontractile responses to vasodilators are not different between obese and lean mice, suggesting that obesity does not directly impair the intrinsic vascular bed reactivity but rather the PVAT function [44]. Moreover, mesenteric arteries incubated with PVAT surrounding the thoracic aorta region of aorta from HFD-fed rats show reduced endothelium-dependent relaxation compared to those incubated with aortic PVAT from rats on a standard chow diet [45]. Therefore, it is likely that PVAT dysfunction is related to the development of obesity-associated vascular complications.
Inflammation and oxidative stress in PVAT alter the anticontractile effects under obese conditions (Figure 2). HFD feeding significantly increases the mass of PVAT and the number of hypertrophic adipocytes, and results in WAT characteristics of PVAT in rodents [45]. Obesity may cause inflammation in WAT-like PVAT, characterized by the infiltration of macrophage and dendritic cells with the high expression of inflammatory adipokines and cytokines, including leptin, MCP-1, tumor necrosis factor alpha (TNF-α) [46], and IL-6 [47], while the expression of the anti-inflammatory adipokine adiponectin is reduced in obese PVAT [48]. Obesity-induced PVAT inflammation also stimulates the generation of O2− and H2O2 by NADPH oxidases, which promote aortic wall procontractile activity. The inactivation of O2−, dismutation of mitochondrial-derived H2O2, or uncoupling of oxidative phosphorylation can reduce phenylephrine-induced vasocontraction in vessel rings surrounded by PVAT from HFD-fed mice [12][42]. HFD-fed mice also show a reduced expression of SOD3 and glutathione levels in mesenteric PVAT [47]. Also, the anticontractile effects of PVAT are impaired in mice lacking IL-18 specifically in PVAT. Moreover, these mice show increased amount of WAT-like PVAT accompanied with deformed mitochondria and decreased Mn-SOD expression [49]. Obese mice lacking TNF-α receptors in PVAT have reduced H2O2 generation and sensitivity to phenylephrine-induced vasocontraction, suggesting that oxidative stress significantly contributes to the procontractile shift of PVAT [42].
Antioxidants 09 00574 g002 550
Figure 2. Mechanisms of PVAT dysfunction in diet-induced obesity. High-fat diet (HFD)-induced adipocyte hypertrophy leads to hypoxia and the production of pro-inflammatory cytokines and chemokines, the activation of NADPH oxidases, and the downregulation of antioxidant enzymes (e.g., superoxide dismutase and peroxiredoxin-1) and non-enzymatic antioxidants (e.g., glutathione). Infiltrating immune cells potentiate PVAT inflammation and oxidative stress. Chronic hyperleptinaemia leads to vascular leptin resistance (loss of leptin-induced vasodilatation) and the potentiation of PVAT inflammation. Long-term obesity decreases PVAT H2S production by downregulating CSE expression. The upregulation of arginases leads to L-arginine deficiency and eNOS uncoupling (enhanced superoxide production and reduced NO production by eNOS). PVAT adiponectin expression is reduced in obesity, likely due to a downregulation of PPARγ. Normally, NO stimulates adiponectin secretion and adiponectin increases PVAT NO production. This positive feedback mechanism is impaired in obesity. CSE, cystathionine gamma-lyase; H2S, hydrogen sulphide; PPARγ, peroxisome proliferator-activated receptors gamma; eNOS, endothelial nitric oxide synthase. Reproduced from Xia et al. 2017 [1] under the terms of the Creative Commons Attribution-Noncommercial License.
Aldose reductase is an enzyme of the aldoketo reductase super-family that catalyzes the conversion of glucose to sorbitol in the polyol pathway of glucose metabolism, which also depletes the antioxidant glutathione system due to the scavenging of NADPH, thereby increasing the production of ROS [50]. PVAT of diabetic rats exhibits higher levels of markers of oxidative stress including augmented malonaldehyde and aldose reductase activity, which are associated with reduced antioxidant protection [51]. In addition, increased Ang II levels may induce ROS production during obesity in systemic and related adipose tissue including PVAT [52]. eNOS uncoupling and increased O2− generation are proposed to contribute to the PVAT-induced endothelial dysfunction in obese mice [43]. The impaired anticontractile effects of PVAT upon HFD feeding are not only dependent on the endothelium but are also a consequence of reduced NO bioavailability due to L-arginine deficiency and eNOS uncoupling in WAT-like PVAT [43][53]. L-arginine supplementation and arginase inhibition could reverse obesity-induced vascular dysfunction ex vivo [43]. In a human study, CuZn-SOD, peroxiredoxin-1, and adiponectin expressions are reduced in obese subjects compared to healthy subjects [53]. The anti-contractility of aortic rings with normal PVAT is improved when incubated with SOD, catalase, or TNF-α, while the anticontractile effect is attenuated when aortic rings with obese PVAT are incubated with anti-TNF-α antibodies or free radical scavengers [53].
PVAT inflammation could be related to hypoxia. Hypoxia stimulates the production of inflammatory cytokines and chemokines from PVAT and infiltrating macrophages [4]. In obesity, adipocytes become hypertrophic, leading to inadequate perfusion and consequent local hypoxia. Hypoxia-inducible factor alpha (HIF-1α), a key mediator of hypoxia, is increased in the adipose tissue of obese subjects [54]. HIF-1 α is responsible for the stimulation of inflammatory mediator production, such as TNF-α and IL-6, and for suppressing the expression of adiponectin [55]. Incubation with TNF-α and IL-6 in PVAT leads to the attenuation of the anticontractile effects of PVAT, while the induction of hypoxia also causes inflammation and the loss of the anti-contractile function of PVAT [4]. This hypoxia-induced PVAT dysfunction can be normalized by in vitro incubation with either anti-TNF-α antibody, anti-IL-6 antibody, or by catalase and SOD antagonists. From these observations, PVAT loses its anticontractile properties after the increase of oxidative stress during obesity. In addition, obesity related PVAT dysfunction, increased inflammation, and oxidative stress are critical features in atherogenesis. Atherosclerotic lesions are characterized by the activation of NADPH oxidases, as well as increased eNOS uncoupling and O2− generation [56]. The combination of oxidative stress and inflammation creates a vicious cycle that is further supported by a variety of metabolic and genetic risk factors leading to atherogenesis [57]. Therefore, increased oxidative stress in PVAT is a critical link between obesity and vascular complications.

This entry is adapted from the peer-reviewed paper 10.3390/antiox9070574

References

  1. Xia, N.; Li, H. The role of perivascular adipose tissue in obesity-induced vascular dysfunction. Br. J. Pharmacol. 2017, 174, 3425–3442.
  2. Soltis, E.E.; Cassis, L.A. Influence of perivascular adipose tissue on rat aortic smooth muscle responsiveness. Clin. Exp. Hypertens. Part A Theory Pract. 1991, 13, 277–296.
  3. Gao, Y.-J.; Zeng, Z.-H.; Teoh, K.; Sharma, A.M.; Abouzahr, L.; Cybulsky, I.; Lamy, A.; Semelhago, L.; Lee, R.M. Perivascular adipose tissue modulates vascular function in the human internal thoracic artery. J. Thorac. Cardiovasc. Surg. 2005, 130, 1130–1136.
  4. Greenstein, A.S.; Khavandi, K.; Withers, S.B.; Sonoyama, K.; Clancy, O.; Jeziorska, M.; Laing, I.; Yates, A.P.; Pemberton, P.W.; Malik, R.A. Local inflammation and hypoxia abolish the protective anticontractile properties of perivascular fat in obese patients. Circulation 2009, 119, 1661.
  5. Gil-Ortega, M.; Somoza, B.; Huang, Y.; Gollasch, M.; Fernández-Alfonso, M.S. Regional differences in perivascular adipose tissue impacting vascular homeostasis. Trends Endocrinol. Metab. 2015, 26, 367–375.
  6. Gräbner, R.; Lötzer, K.; Döpping, S.; Hildner, M.; Radke, D.; Beer, M.; Spanbroek, R.; Lippert, B.; Reardon, C.A.; Getz, G.S. Lymphotoxin β receptor signaling promotes tertiary lymphoid organogenesis in the aorta adventitia of aged ApoE−/− mice. J. Exp. Med. 2009, 206, 233–248.
  7. Campbell, K.A.; Lipinski, M.J.; Doran, A.C.; Skaflen, M.D.; Fuster, V.; McNamara, C.A. Lymphocytes and the adventitial immune response in atherosclerosis. Circ. Res. 2012, 110, 889–900.
  8. Brown, N.K.; Zhou, Z.; Zhang, J.; Zeng, R.; Wu, J.; Eitzman, D.T.; Chen, Y.E.; Chang, L. Perivascular adipose tissue in vascular function and disease: A review of current research and animal models. Arterioscler. Thromb. Vasc. Biol. 2014, 34, 1621–1630.
  9. Omar, A.; Chatterjee, T.K.; Tang, Y.; Hui, D.Y.; Weintraub, N.L. Proinflammatory phenotype of perivascular adipocytes. Arterioscler. Thromb. Vasc. Biol. 2014, 34, 1631–1636.
  10. Collaborators, G.O. Health effects of overweight and obesity in 195 countries over 25 years. N. Engl. J. Med. 2017, 377, 13–27.
  11. Lavie, C.J.; Milani, R.V.; Ventura, H.O. Obesity and cardiovascular disease: Risk factor, paradox, and impact of weight loss. J. Am. Coll. Cardiol. 2009, 53, 1925–1932.
  12. Ketonen, J.; Shi, J.; Martonen, E.; Mervaala, E. Periadventitial adipose tissue promotes endothelial dysfunction via oxidative stress in diet-induced obese C57Bl/6 mice. Circ. J. 2010, 74, 1479–1487.
  13. Qi, X.-Y.; Qu, S.-L.; Xiong, W.-H.; Rom, O.; Chang, L.; Jiang, Z.-S. Perivascular adipose tissue (PVAT) in atherosclerosis: A double-edged sword. Cardiovasc. Diabetol. 2018, 17, 1–20.
  14. Zou, L.; Wang, W.; Liu, S.; Zhao, X.; Lyv, Y.; Du, C.; Su, X.; Geng, B.; Xu, G. Spontaneous hypertension occurs with adipose tissue dysfunction in perilipin-1 null mice. Biochim. Biophys. Acta (BBA)-Mol. Basis Dis. 2016, 1862, 182–191.
  15. Sena, C.M.; Leandro, A.; Azul, L.; Seiça, R.; Perry, G. Vascular oxidative stress: Impact and therapeutic approaches. Front. Physiol. 2018, 9, 1668.
  16. Sies, H. Hydrogen peroxide as a central redox signaling molecule in physiological oxidative stress: Oxidative eustress. Redox Biol. 2017, 11, 613–619.
  17. Man, W.; Wang, Y. Age-associated arterial remodelling. EC Cardiol. 2017, 4, 137–164.
  18. Félétou, M.; Vanhoutte, P.M. Endothelium-derived hyperpolarizing factor: Where are we now? Arterioscler. Thromb. Vasc. Biol. 2006, 26, 1215–1225.
  19. Zaborska, K.; Wareing, M.; Austin, C. Comparisons between perivascular adipose tissue and the endothelium in their modulation of vascular tone. Br. J. Pharmacol. 2017, 174, 3388–3397.
  20. Kim, J.-A.; Montagnani, M.; Koh, K.K.; Quon, M.J. Reciprocal relationships between insulin resistance and endothelial dysfunction: Molecular and pathophysiological mechanisms. Circulation 2006, 113, 1888–1904.
  21. Avogaro, A.; Albiero, M.; Menegazzo, L.; de Kreutzenberg, S.; Fadini, G.P. Endothelial dysfunction in diabetes: The role of reparatory mechanisms. Diabetes Care 2011, 34, S285–S290.
  22. Chang, L.; Milton, H.; Eitzman, D.T.; Chen, Y.E. Paradoxical roles of perivascular adipose tissue in atherosclerosis and hypertension. Circ. J. 2012, 77, 11–18.
  23. Fésüs, G.; Dubrovska, G.; Gorzelniak, K.; Kluge, R.; Huang, Y.; Luft, F.C.; Gollasch, M. Adiponectin is a novel humoral vasodilator. Cardiovasc. Res. 2007, 75, 719–727.
  24. Wójcicka, G.; Jamroz-Wiśniewska, A.; Atanasova, P.; Chaldakov, G.N.; Chylińska-Kula, B.; Bełtowski, J. Differential effects of statins on endogenous H2S formation in perivascular adipose tissue. Pharmacol. Res. 2011, 63, 68–76.
  25. Awata, W.M.; Gonzaga, N.A.; Borges, V.F.; Silva, C.B.; Tanus-Santos, J.E.; Cunha, F.Q.; Tirapelli, C.R. Perivascular adipose tissue contributes to lethal sepsis-induced vasoplegia in rats. Eur. J. Pharmacol. 2019, 863, 172706.
  26. Ozen, G.; Topal, G.; Gomez, I.; Ghorreshi, A.; Boukais, K.; Benyahia, C.; Kanyinda, L.; Longrois, D.; Teskin, O.; Uydes-Dogan, B.S. Control of human vascular tone by prostanoids derived from perivascular adipose tissue. Prostaglandins Other Lipid Mediat. 2013, 107, 13–17.
  27. Gao, Y.J.; Lu, C.; Su, L.Y.; Sharma, A.; Lee, R. Modulation of vascular function by perivascular adipose tissue: The role of endothelium and hydrogen peroxide. Br. J. Pharmacol. 2007, 151, 323–331.
  28. Lee, R.M.; Lu, C.; Su, L.-Y.; Gao, Y.-J. Endothelium-dependent relaxation factor released by perivascular adipose tissue. J. Hypertens. 2009, 27, 782–790.
  29. Chang, L.; Garcia-Barrio, M.T.; Chen, Y.E. Perivascular Adipose Tissue Regulates Vascular Function by Targeting Vascular Smooth Muscle Cells. Arterioscler. Thromb. Vasc. Biol. 2020, 40, 1094–1109.
  30. Costa, R.M.; Filgueira, F.P.; Tostes, R.C.; Carvalho, M.H.C.; Akamine, E.H.; Lobato, N.S. H2O2 generated from mitochondrial electron transport chain in thoracic perivascular adipose tissue is crucial for modulation of vascular smooth muscle contraction. Vasc. Pharmacol. 2016, 84, 28–37.
  31. Chang, L.; Xiong, W.; Zhao, X.; Fan, Y.; Guo, Y.; Garcia-Barrio, M.; Zhang, J.; Jiang, Z.; Lin, J.D.; Chen, Y.E. Bmal1 in perivascular adipose tissue regulates resting-phase blood pressure through transcriptional regulation of angiotensinogen. Circulation 2018, 138, 67–79.
  32. Alberti, K.; Eckel, R.H.; Grundy, S.M.; Zimmet, P.Z.; Cleeman, J.I.; Donato, K.A.; Fruchart, J.-C.; James, W.P.T.; Loria, C.M.; Smith, S.C., Jr. Harmonizing the metabolic syndrome: A joint interim statement of the international diabetes federation task force on epidemiology and prevention; national heart, lung, and blood institute; American heart association; world heart federation; international atherosclerosis society; and international association for the study of obesity. Circulation 2009, 120, 1640–1645.
  33. Kumar, R.K.; Darios, E.S.; Burnett, R.; Thompson, J.M.; Watts, S.W. Fenfluramine-induced PVAT-dependent contraction depends on norepinephrine and not serotonin. Pharmacol. Res. 2019, 140, 43–49.
  34. Victorio, J.A.; Fontes, M.T.; Rossoni, L.V.; Davel, A.P. Different anti-contractile function and nitric oxide production of thoracic and abdominal perivascular adipose tissues. Front. Physiol. 2016, 7, 295.
  35. Watts, S.W.; Dorrance, A.M.; Penfold, M.E.; Rourke, J.L.; Sinal, C.J.; Seitz, B.; Sullivan, T.J.; Charvat, T.T.; Thompson, J.M.; Burnett, R. Chemerin connects fat to arterial contraction. Arterioscler. Thromb. Vasc. Biol. 2013, 33, 1320–1328.
  36. Owen, M.K.; Witzmann, F.A.; McKenney, M.L.; Lai, X.; Berwick, Z.C.; Moberly, S.P.; Alloosh, M.; Sturek, M.; Tune, J.D. Perivascular adipose tissue potentiates contraction of coronary vascular smooth muscle: Influence of obesity. Circulation 2013, 128, 9–18.
  37. Ayala-Lopez, N.; Martini, M.; Jackson, W.F.; Darios, E.; Burnett, R.; Seitz, B.; Fink, G.D.; Watts, S.W. Perivascular adipose tissue contains functional catecholamines. Pharmacol. Res. Perspect. 2014, 2, e00041.
  38. Gao, Y.-J.; Takemori, K.; Su, L.-Y.; An, W.-S.; Lu, C.; Sharma, A.M.; Lee, R.M. Perivascular adipose tissue promotes vasoconstriction: The role of superoxide anion. Cardiovasc. Res. 2006, 71, 363–373.
  39. Saxton, S.N.; Ryding, K.E.; Aldous, R.G.; Withers, S.B.; Ohanian, J.; Heagerty, A.M. Role of sympathetic nerves and adipocyte catecholamine uptake in the vasorelaxant function of perivascular adipose tissue. Arterioscler. Thromb. Vasc. Biol. 2018, 38, 880–891.
  40. Agha, M.; Agha, R. The rising prevalence of obesity: Part A: Impact on public health. Int. J. Surg. Oncol. 2017, 2, e17.
  41. Montero, D.; Walther, G.; Perez-Martin, A.; Roche, E.; Vinet, A. Endothelial dysfunction, inflammation, and oxidative stress in obese children and adolescents: Markers and effect of lifestyle intervention. Obes. Rev. 2012, 13, 441–455.
  42. Da Costa, R.M.; Fais, R.S.; Dechandt, C.R.; Louzada-Junior, P.; Alberici, L.C.; Lobato, N.S.; Tostes, R.C. Increased mitochondrial ROS generation mediates the loss of the anti-contractile effects of perivascular adipose tissue in high-fat diet obese mice. Br. J. Pharmacol. 2017, 174, 3527–3541.
  43. Xia, N.; Horke, S.; Habermeier, A.; Closs, E.I.; Reifenberg, G.; Gericke, A.; Mikhed, Y.; Münzel, T.; Daiber, A.; Förstermann, U. Uncoupling of endothelial nitric oxide synthase in perivascular adipose tissue of diet-induced obese mice. Arterioscler. Thromb. Vasc. Biol. 2016, 36, 78–85.
  44. Gil-Ortega, M.; Stucchi, P.; Guzmán-Ruiz, R.; Cano, V.; Arribas, S.; González, M.C.; Ruiz-Gayo, M.; Fernández-Alfonso, M.S.; Somoza, B. Adaptative nitric oxide overproduction in perivascular adipose tissue during early diet-induced obesity. Endocrinology 2010, 151, 3299–3306.
  45. Ma, L.; Ma, S.; He, H.; Yang, D.; Chen, X.; Luo, Z.; Liu, D.; Zhu, Z. Perivascular fat-mediated vascular dysfunction and remodeling through the AMPK/mTOR pathway in high-fat diet-induced obese rats. Hypertens. Res. 2010, 33, 446–453.
  46. Bailey-Downs, L.C.; Tucsek, Z.; Toth, P.; Sosnowska, D.; Gautam, T.; Sonntag, W.E.; Csiszar, A.; Ungvari, Z. Aging exacerbates obesity-induced oxidative stress and inflammation in perivascular adipose tissue in mice: A paracrine mechanism contributing to vascular redox dysregulation and inflammation. J. Gerontol. Ser. A Biomed. Sci. Med Sci. 2013, 68, 780–792.
  47. Gil-Ortega, M.; Condezo-Hoyos, L.; García-Prieto, C.F.; Arribas, S.M.; González, M.C.; Aranguez, I.; Ruiz-Gayo, M.; Somoza, B.; Fernández-Alfonso, M.S. Imbalance between pro and anti-oxidant mechanisms in perivascular adipose tissue aggravates long-term high-fat diet-derived endothelial dysfunction. PLoS ONE 2014, 9.
  48. Qiu, T.; Li, M.; Tanner, M.A.; Yang, Y.; Sowers, J.R.; Korthuis, R.J.; Hill, M.A. Depletion of dendritic cells in perivascular adipose tissue improves arterial relaxation responses in type 2 diabetic mice. Metabolism 2018, 85, 76–89.
  49. Li, W.; Jin, D.; Takai, S.; Hayakawa, T.; Ogata, J.; Yamanishi, K.; Yamanishi, H.; Okamura, H. Impaired function of aorta and perivascular adipose tissue in IL-18-deficient mice. Am. J. Physiol.-Heart Circ. Physiol. 2019, 317, H1142–H1156.
  50. Srivastava, S.K.; Yadav, U.C.; Reddy, A.B.; Saxena, A.; Tammali, R.; Shoeb, M.; Ansari, N.H.; Bhatnagar, A.; Petrash, M.J.; Srivastava, S. Aldose reductase inhibition suppresses oxidative stress-induced inflammatory disorders. Chem.-Biol. Interact. 2011, 191, 330–338.
  51. Azul, L.; Leandro, A.; Boroumand, P.; Klip, A.; Seiça, R.; Sena, C.M. Increased inflammation, oxidative stress and a reduction in antioxidant defense enzymes in perivascular adipose tissue contribute to vascular dysfunction in type 2 diabetes. Free Radic. Biol. Med. 2020, 146, 264–274.
  52. Ramalingam, L.; Menikdiwela, K.; LeMieux, M.; Dufour, J.M.; Kaur, G.; Kalupahana, N.; Moustaid-Moussa, N. The renin angiotensin system, oxidative stress and mitochondrial function in obesity and insulin resistance. Biochim. Biophys. Acta (BBA)-Mol. Basis Dis. 2017, 1863, 1106–1114.
  53. Aghamohammadzadeh, R.; Unwin, R.D.; Greenstein, A.S.; Heagerty, A.M. Effects of obesity on perivascular adipose tissue vasorelaxant function: Nitric oxide, inflammation and elevated systemic blood pressure. J. Vasc. Res. 2015, 52, 299–305.
  54. Cancello, R.; Henegar, C.; Viguerie, N.; Taleb, S.; Poitou, C.; Rouault, C.; Coupaye, M.; Pelloux, V.; Hugol, D.; Bouillot, J.-L. Reduction of macrophage infiltration and chemoattractant gene expression changes in white adipose tissue of morbidly obese subjects after surgery-induced weight loss. Diabetes 2005, 54, 2277–2286.
  55. Chen, B.; Lam, K.S.; Wang, Y.; Wu, D.; Lam, M.C.; Shen, J.; Wong, L.; Hoo, R.L.; Zhang, J.; Xu, A. Hypoxia dysregulates the production of adiponectin and plasminogen activator inhibitor-1 independent of reactive oxygen species in adipocytes. Biochem. Biophys. Res. Commun. 2006, 341, 549–556.
  56. Li, H.; Horke, S.; Förstermann, U. Vascular oxidative stress, nitric oxide and atherosclerosis. Atherosclerosis 2014, 237, 208–219.
  57. Packard, R.R.; Libby, P. Inflammation in atherosclerosis: From vascular biology to biomarker discovery and risk prediction. Clin. Chem. 2008, 54, 24–38.
More
© Text is available under the terms and conditions of the Creative Commons Attribution (CC BY) license; additional terms may apply. By using this site, you agree to the Terms and Conditions and Privacy Policy.
This entry is offline, you can click here to edit this entry!
ScholarVision Creations
Feedback