In Vivo Brain Glutathione: History
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Contributor:
Luca Pasquini
,
Antonio Napolitano
,
,
Martina Lucignani
,
Francesco Dellepiane
,
Emiliano Visconti

Glutathione (GSH) is an important antioxidant implicated in several physiological functions, including the oxidation−reduction reaction balance and brain antioxidant defense against endogenous and exogenous toxic agents. Altered brain GSH levels may reflect inflammatory processes associated with several neurologic disorders. An accurate and reliable estimation of cerebral GSH concentrations could give a clear and thorough understanding of its metabolism within the brain, thus providing a valuable benchmark for clinical applications. 

  • glutathione (GSH)
  • magnetic resonance spectroscopy (MRS)
  • neurological disorders

1. Introduction

Glutathione (GSH) is an antioxidant metabolite originating from glutamic acid (Glu), cysteine (Cys), and Glycine (Gly) amino acids, globally present in all mammalian cells [1]. Among its many roles, GSH is mainly implicated in oxidation−reduction reactions, acting as a protector against endogenous and exogenous toxic agents like reactive oxygen species (ROS) and reactive nitrogen species (RNS) [2]. Changes in the GSH brain concentration from oxidative stress may reflect inflammatory processes and mitochondrial dysfunction associated with biological aging [3] and pathological conditions [4][5]. In particular, as high levels of ROS may lead to cerebral tissue damage, the altered GSH concentration of specific brain areas has been described in several neurologic disorders, including epilepsy [6][7], multiple sclerosis [8][9], Alzheimer’s disease [10], Parkinson’s disease [11][12], and psychiatric disorders [13][14][15][16]. In order to provide a clear and thorough understating of GSH metabolism within the brain, an accurate and reliable estimation of cerebral concentrations needs to be performed. The quantification of GSH brain levels was first attempted ex vivo from autoptic specimens, by means of liquid chromatography with UV detection and spectroscopic techniques [17][18][19]. GSH biosynthesis and metabolism were also tested in vitro, where different cell culture models were investigated to assess oxidative stress levels from blood and cerebrospinal fluids [20][21]. More recently, in vivo GSH measurements were obtained using proton magnetic resonance spectroscopy (MRS), a powerful non-invasive technique for brain metabolite quantification. Although widely used for GSH detection in both animals and humans [22], MRS presents several technical challenges, mostly related to the low GSH brain concentration and severe spectral overlapping between metabolites with different peak intensities [23]. Many MRS techniques have been developed for GSH concentration assessment, with a high methodologic heterogeneity, which may limit a comparative evaluation of the results provided by different studies. For this reason, the literature is still lacking a comprehensive and detailed description of the GSH normal levels within different specific brain areas. This information appears crucial for the interpretation of GSH findings in the normal brain and neurologic disorders, providing a valuable benchmark for clinical applications.

2. GSH Metabolism

GSH is abundant in the brain, with a high concentration in non-neuronal cells, mostly neuropil and white matter tracts, with the exception of some cerebellar neurons, such as granule cells and Purkinje cells [22]. Within the brain, GSH is synthesized from the essential amino acids Glu, Cys, and Gly in a two-step reaction catalyzed by ATP-dependent enzymes. In the first step, Glu is combined with Cys by γ-glutamylcysteine synthetase (or glutamate−cysteine ligase (GCL) EC 6.3.2.2) to form γ-Glu−Cys. This dipeptide is further combined with Gly by glutathione synthetase (GS; EC 6.3.2.3) to produce GSH [1]. GSH catabolism is realized through hydrolysis by γ-glutamyltransferase (γGT; EC 2.3.2.2), which is located in the cell membranes of many cells throughout the body. In the brain, γGT is located in non-neuronal cells, mostly ependymal cells, and secondarily in Schwann and glial cells [22]. GSH metabolism is summarized in Figure 1. GSH fulfills its antioxidant role through two main mechanisms: (1) direct non-enzymatic reaction with free radicals such as superoxide (O2−), NO, or hydroxide (OH−), and by (2) acting as a reducing agent in the presence of glutathione peroxidase (GP), by donating an electron to H2O2, leading to the formation of H2O, O2, and glutathione disulfide (GSSG) [1]. In turn, glutathione reductase (GR) regenerates GSH by transferring an electron from NADPH to GSSG (Figure 1). This enzyme is mostly expressed in oligodendrocytes, microglia, and neurons, with a lower expression in astrocytes [22]. Another major role of GSH is the detoxification and removal of xenobiotics and other endogenous compounds, that are conjugated with GSH by glutathione-S-transferase to be exported from the cell through multidrug resistance pumps (MRPs), the main GSH transporters [22][24]. Furthermore, GSH is a cofactor of various enzymes. For example, the glyoxalase enzyme system catalyzes the detoxification of ketoaldehyde methylglyoxal (a very reactive molecule that mediates protein denaturation) to D-lactate with the participation of GSH [22].
Figure 1. Glutathione (GSH) metabolism within the nervous tissue. GSH is synthesized in the cytoplasm of neurons and glia from essential amino acids, and catabolized through hydrolysis in the cell membranes. GSH acts as a reducing agent by donating an electron to H2O2, leading to the formation of H2O, O2, and glutathione disulfide (GSSG), which is regenerated by glutathione reductase (GR) from NADPH. The transportation of GSH and essential metabolites is regulated by different transporters across cell membranes. Cys—cysteine; glu—glutamate; gln—glycine; met—methionine; homocys—homocysteine; MPR—multidrug resistance pump; γGT—γ-glutamyltransferase; γ-glucys—γ-glutamylcysteine; EAAT—excitatory amino acid transporter; SNAT—sodium-coupled neutral amino acid transporter; ASC—alanine, serine, and cysteine transport system.

3. Brain Areas GSH Concentration and MRS techniques

The MRS acquisition sequence used to sample brain GSH 'in vivo' is a decisive step, as the metabolite concentrations could be different when selecting edited or unedited techniques. Dhamala showed strongly correlated GSH measures between SPECIAL and PRESS techniques, while a weak correlation occurred between MEGA-PRESS and both SPECIAL and PRESS [25]. Similarly, Nezhad reported a significant difference in GSH concentration estimates when comparing MEGA-PRESS with PRESS [26]. Moreover, the study showed more sensibility in edited (MEGA-PRESS) compared with unedited sequences (PRESS) when identifying differences between two brain area concentrations (i.e., anterior cingulate cortex and occipital cortex) only with MEGA-PRESS. As GSH detection has the potential to provide a better understanding of the oxidation−reduction balance in the human brain, several examples of both edited and unedited techniques have been reported in the literature, where VOI were placed in different brain areas, with sizes ranging from 15 mm3 [27] to 30 cm3 [9][28]. A comprehensive description of the GSH detection studies has been reported. Researchers reported GSH concentration within the different brain areas investigated for HC subjects found in the literature (Table 1). Particularly, Table 1 reports the number of HC participants and the corresponding mean age, together with the main evidence found for each study. The definition of standard reference GSH values within the different brain areas reported could lead to a better interpretation of the altered GSH levels recorded in subjects with neurological disorders, with insight into the possible role of GSH as a biomarker and therapeutic target. Referring to the reliability previously discussed and the sensibility of MEGA-PRESS, the most reliable GSH detected values were those of studies that used this technique in brain area analysis through a comparison between groups and in clinical applications [3][10][29][30][31][32][33][34][35][36][37][38].
Table 1. Number of healthy control subjects, the corresponding age, and GSH concentration measured in the brain areas, type of scanner, method, site of voxels for the GSH measurements, and the results reported in the studies.
Ref HC Participants Age
(Range or Mean ± SD)		 Scanner Method Site of Detection
(VOI Dimension and Brain Area)		 GSH Concentration (HC) Results
[39] Phantoms   3 T GE + 8 channels head coil Edited: MEGA-PRESS TR/TE = 1800/131 ms + LCModel
Unedited: PRESS TR/TE = 3000/30 ms + LCModel		     MEGA-PRESS appears more precise at a lower GSH concentration
[40] Phantoms + 10 HC 26 ± 3.3 3 T Siemens + 32 channels head coil Edited: MEGA-PRESS TR/TE = 2000/120 ms + Gannet
Unedited: PRESS TR/TE = 2000/30 ms SPECIAL TR/TE = 2000/8 ms
PR-STEAM TR/TE = 2000/6.5 ms + LCModel		 24 cm3 in MFC MEGA-PRESS 1.87 ± 0.36 mM PRESS: 1.69 ± 0.13 mM SPECIAL = 2.3 ± 027 mM
PR-STEAM: 2.29 ± 0.16 mM		 Reliability comparison shows more reproducible GSH measurements for unedited sequences
(only for highest values, above 3 mM)
[23] Phantoms + 5 HC 24–36;
30 ± 3		 3 T Siemens + 32 channels head coil Unedited: PRESS TR/TE = 2000/30 ms + CNN for GSH quantification 20 × 20 × 20 mm3 in left FC GSH/tNAA = ~0.07–0.15 Implementation of a robust method for GSH quantification in MRS using CNN
[41] Phantoms + 4 HC 30–45 7 T Siemens + 32 channels head coil Unedited: 2D-COSY TR/TE = 2000/20 ms 25 × 25 × 25 mm3 in OC GSH/Cr = 0.05 ± 0.01 Non-uniformly weighted sampling (NUWS) sequences produced a higher SNR
[42] Phantoms + 13 HC 28 ± 9 3 T Magnex Scientific Edited: Multiple Quantum Chemical Shift Imaging + Levenberg−Marquardt least square minimization algorithm 40 × 40 × 40 mm3 in FPC 1.2 ± 0.16 mmol/Kg DQC filtering-based chemical shift imaging of GSH at 3T implementation
[43] Phantoms + 6 HC 34 ± 13 3 T Siemens/Philips/GE/Canon + 32 channels head coil Edited: MEGA-PRESS TR/TE = 2000/80 ms + Gannet 27 cm3 in MCC GSH/Cr = 0.045 ± 0.013 (Philips scanner)
GSH/Cr = 0.051 ± 0.007 (Siemens scanner)		 In vivo GSH/Cr ratio shows relatively low variations between scanners using the universal sequence
[44] Phantoms + 10 HC 32.6 ± 8.8 3 T Philips + 32 channels head coil Edited: MEGA-PRESS TR/TE = 2000/120 ms
MEGA-PRIAM TR/TE = 2000/120 ms + Gannet		 33 × 33 × 33 mm3 in left and right FC MEGA-PRESS:
2.61 ± 0.50 i.u. (left FC)
2.95 ± 0.65 i.u. (right FC)
MEGA-PRIAM
2.44 ± 0.60 i.u. (left FC)
2.81 ± 0.67 i.u. (right FC)		 No significant difference between MEGA-PRESS and MEGA-PRIAM in GSH estimates
[45] Phantoms + 5 HC + simulations 31 ± 8 3 T Philips + 32 channels head coil Edited: MEGA-PRESS TR/TE = 2000/120 ms + Gannet 36 × 36 × 36 mm3 in midline PC GSH integrals normalized by the sum of the
integrals from each subject averaged across all subjects ~0.4–0.5		 TE of 120 ms appears to be optimal for in vivo GSH detection
[26] Phantoms + 7 HC 23–35 3 T Philips + 8 channels head coil Edited: MEGA-PRESS TR/TE = 2000/130 ms + AMARES
Unedited: PRESS TR/TE = 2000/35 ms + jMRUI		 40 × 25 × 25 mm3 in ACC and 30 × 30 × 30 mm3 in OC MEGA-PRESS:
3.2 ± 0.6 mM (ACC)
1.4 ± 0.4 mM (OC)
PRESS:
2.8 ± 0.3 mM (ACC)
2.5 ± 0.7 mM. (OC)		 Physiological concentrations (<4 mM) of GSH cannot be reliably quantified from PRESS spectra at 3 T
[46] Phantoms + 9 HC 25 4 T Varian INOVA Edited: MEGA-PRESS TR/TE = 4000/60 ms + LCModel 30 × 30 × 30 mm3 in OC 1.3 ± 0.2 µmol/g GSH concentration estimation
[47] Phantoms + 2 HC 18–32 1.5 T Philips Edited: DQC
Unedited: PRESS		 15.6–17.4 cm3   DQC filter for the selective in vivo detection of GSH in the human brain presentation
[48] Phantoms + 10 HC 34.7 ± 8.8 3 T Philips + 32 channels head coil Edited: MEGA-PRESS TR/TE = 2000/80 ms
HERMES TR/TE = 2000/80 ms + Gannet		 30 × 30 × 30 mm3 in Ins   SNR of the HERMES spectra is similar to those
of MEGA-PRESS, with the benefit of saving half the acquisition time
[49] Phantoms + 6 HC + simulations N.D 7 T Philips Unedited: asymmetric PRESS TE1/TE2 = 37/63 ms
STEAM TR/TE = 2500/14–74 ms + LCModel		 25 × 30 × 30 mm3 in MPFC   Optimization of the TE delays in asymmetric PRESS enables the separation of GSH without editing
[50] Phantoms + 8 HC + simulations 32 ± 11 7 T Siemens + 32 channels head coil Unedited: asymmetric PRESS TR/TE = 3000/3.9 ms 20 × 20 × 20 mm3 in MPFC and FC GSH/tCr = 0.216 ± 0.02 (MPFC) GSH/tCr = 0.27 ± 0.03 (FC); Glu and Gln higher in GM. GSH and Gln have a similar concentration (20–27% of Cr)
[51] 6 HC 22–26 3 T/7 T Siemens Unedited: SPECIAL TR/TE = 4000/6 ms + LCModel 20 × 20 × 20 mm3 in OC 1.4 ± 0.11 mmol/Kg (3 T); 1.3 ± 0.2 mmol/Kg (7 T) SPECIAL with ultrashort TEs resulted in a high SNR and allow to reduce RF power requirements and improve chemical shift displacement errors
[25] 15 HC 24.9 ± 3.5 3 T Siemens + 32 channels head coil Edited: MEGA-PRESS TR/TE = 3200/68 ms + LCModel
Unedited: SPECIAL TR/TE = 3200/8.5 ms + LCModel		 30 × 30 × 20 mm3 in DLPC and M1 MEGA-PRESS:
0.5–3 mmol/L (M1)
3–4 mmol/L (DLPC)
SPECIAL:
1.3–2.4 mmol/L (M1 and DLPC)		 GSH levels detected with reasonably good precision using SPECIAL, but poor precision using MEGA-PRESS
[27] 21 HC 32.2 ± 8.1 3 T Siemens + quadrature head coil Unedited: SPECIAL TR/TE = 3000/6 ms + LCModel 15 × 15 × 15 mm3 in left A 1.03 ± 0.38 mmol/L (CRLBs: 24 ± 11 only in 16/21 HC) Only in a small portion of the acquired spectra GSH passed the CRLB threshold of 20%
[52] 18 HC N.D. 3 T Siemens Unedited: PRESS TR/TE = 2000/30 ms + LCModel 25 × 25 × 15 mm3 in SMA ~2.2–2.6 mmol/Kg No difference in GSH concentration recorded between HC and PSP
[53] 22 HC 12–14 3 T Siemens Unedited: 2D J-resolved PRESS TR/TE = 2000/22 ms + LCModel 20 × 20 × 30 mm3 in RACC   GSH variation factor results of 8.6 ± 4.1%, significant Pearson correlation (0.821) resulted between test and retest
[54] 63 HC 40–60 3 T Siemens Unedited: 2D J-resolved MRS TR/TE = 2000/31–229 ms + ProFit 19 cm3 in RACC GSH/H20 = 0.003–0.004 GSH significantly increased for HC receiving supplements when compared with the placebo
[9] 5 HC 32 ± 8 7 T Agilent + 8 channels head coil Edited: JDE semi-LASER TR/TE = 3200/72 ms + LCModel
Unedited: STEAM TR/TE = 3000/10 ms + LCModel		 30 × 30 × 30 mm3 for JDE semi-LASER and 20 × 20 × 20 mm3 for STEAM in midline OC 1.34 ± 0.13 mM (JDE semi-LASER)
2.15 ± 0.16 mM (STEAM)		 Better reliability results (in terms of Coefficient of variation CV) for JDE semi-LASER when compared to STEAM
[55] 21 HC Neonates 1.5 T GE Unedited: PRESS TR/TE = 3000/20 ms + LCModel 29 × 10 × 11 mm3 in WM; 11 × 24 × 11 in Th; 22 × 13 × 15 in GM 2.1 ± 0.7 mmol/Kg (WM)
2.4 ± 0.8 mmol/Kg (Th)
2.5 ± 0.5 mmol/Kg (GM)		 Absolute brain GSH content in premature infants at term was not considerably different from that in fullterm infants
[28] 5 HC 25–32 3 T Siemens + quadrature head coil Edited: DQF TR/TE = 3000/70 ms 30 × 30 × 30 mm3 in left and right PC 0.91 ± 0.16 mM (left PC) 0.89 ± 0.16 mM (right PC) Sequence shown to be
invariant to phase difference between excitation and DQF
generating pulse.
[56] 10 HC 26.1 ± 9 3 T Siemens Unedited: STEAM TR/TE = 2000/6.5 ms + LCModel 6 cm3 in ACC and PCC 2.74 ± 0.2 i.u. (ACC)
2.07 ± 0.0025 i.u. (PCC)		 Good reliability results in terms of coefficient of variation CV (<10%)
[57] 60 HC 60–85 3 T Siemens Edited: Multiple Quantum Chemical Shift Imaging + Levenberg−Marquardt least square minimization algorithm 50 × 50 × 30 mm3 in FC and PC 1.27 ± 0.32 mmol/Kg (FC)
1.28 ± 0.27 mmol/Kg (PC)		 glutathione concentrations in brain regions were positively correlated with milk servings
[58] 18 HC Neonates 3 T Philips Edited: HERMES TRT/E = 2000/80 ms + Gannet 31 × 25 × 20 mm3 in Th and ACC 0.55–0.7 i.u. (ACC)
0.5–0.58 i.u (Th)		 lower GSH levels in Th compared to the ACC and higher GSH levels in the ACC following tissue-correction
[59] 20 HC 21–35;
29 ± 5		 3 T Philips + 32 channel head coil Edited: HERMES TRT/E = 2000/80 ms + LCModel 25 × 25 × 25 mm3 in MACC GSH/tCr = 0.18 ± 0.04 HERMES showed to be more sensitive to motion, as variability of spectral quality measures were observed for GSH when only retrospective outlier removal was applied.
[60] 40 HC   3 T Philips Edited: HERMES TRT/E = 2000/80 ms + Gannet Ranging from 30 × 30 × 30 to 36 × 36 × 36 mm3 in medial PC   The multi step Frequency and Phase Correction approach (msFPC) results in improved correction of frequency/phase errors in multiplexed GABA-/GSH-edited MRS experiments.
[61] 67 HC 8–12 3 T Philips Edited: HERMES TR/TE = 2000/80 ms + Gannet 30 × 30 × 30 mm3 in right SM, SMA, and right Ins 0.56 ± 0.14 i.u. (SM)
0.57 ± 0.15 i.u. (SMA)
0.69 ± 0.19 i.u. (Ins)		 Robust Spectral Registration (rSR) reduced more subtraction artifacts than the multistep method
[62] 12 HC 25 ± 2.5 3 T Siemens + 32 channel head coil Edited:MEGA-PRESS TR/TE = 2000/120 ms
HERMES TRT/E = 2000/80 ms + Gannet		 30 × 25 × 25 mm3 in DACC 1.96 ± 0.49 i.u. (MEGA-PRESS)
3.95 ± 0.44 i.u. (HERMES)		 MEGA-PRESS provide more reproducible GSH (in terms of CV%) quantification compared to HERMES
[63] 4 HC 47.3 ± 5.6 3 T GE Edited: MEGA-PRESS TR/TE = 2000/80 ms 30 × 30 × 30 mm3 in PC 2 mM Phantoms confirm GSH MEGA-PRESS signal and that GSSG would be undetectable at concentrations expected in vivo
[64] 9 HC 23 4 T Varian INOVA Edited: DWE with MEGA-PRESS TR/TE = 4500/112 ms + LCModel 30 × 30 × 30 mm3 in midsagittal OC 0.8 ± 0.1 µmol/g Double editing did not compromise sensitivity
[3] 44 HC (22 young + 22 elderly) Young = 20.4 ± 1.4
Elderly = 76.6 ± 6.1		 4 T Varian INOVA Edited: DWE with MEGA-PRESS TR/TE = 4500/122 ms + LCModel 30 × 30 × 30 mm3 in midsagittal OC Young = 0.31 ± 0.05 i.u.
Elderly = 0.20 ± 0.08 i.u.		 Elderly subjects had a lower GSH concentration than younger subjects
[32] 12 HC   4 T Varian INOVA Edited: DWE with MEGA-PRESS TR/TE = 4500/102 ms + LCModel 30 × 30 × 30 mm3 in OC 0.7–0.9 µmol/g GSH concentration remains costant after intravenous vitamin C infusion
[29] 11 HC 61.5 ± 10.5 3 T GE + 8 channels head coil Edited: MEGA-PRESS TR/TE = 1500/68 ms + in-house software developed in MATLAB 20 × 25 × 25 mm3 in PG and MC GSH/W = 1.6 ± 0.4 × 10−3 i.u. (MC) Significantly lower GSH in ALS patients when compared with HC
[31] 11 HC 30 ± 11 3 T Philips Edited: MEGA-PRESS TR/TE = 2000/131 ms 50 × 30 × 30 mm3 in PC 1.20 ± 0.14 mM Optimal TE = 130 ms. Stroke patients not significantly different from HC
[65] 10 HC 18–65 3 T Edited: MEGA-PRESS TR/TE = 1500/68 ms 30 × 30 × 20 mm3 in OC   Anhedonia and GSH negatively correlated
[66] 13 HC 18–45 3 T GE Edited: MEGA-PRESS TR/TE = 1500/68 ms 30 × 30 × 20 mm3 in OC   No differences between HC and CFS patients
[34] 44 HC (25 males and 19 females) 23.6 ± 2.1 3 T Philips Edited: MEGA-PRESS TR/TE = 2500/120 ms 2.5 cm3 in FC PC, Hyp and C ~20–22 a.u. (FC females)
~15–22 a.u. (FC males)
~30 a.u. (PC females)
~17–25 a.u. (PC males)
~15 a.u. (Hyp females)
~15 a.u. (Hyp males)
~14–17 a.u. (C females)
~10–15 a.u. (C males)		 Higher GSH in young, gender matched parietal cortex hippocampus vs. older patients
[10] 21 HC 65 ± 5 3 T Philips Edited: MEGA-PRESS TR/TE = 2500/120 ms + KALPANA 15–16 cm3 in FP Hyp 1.12 ± 0.18 mmol/L (FC)
1.02 ± 0.17 mmol/L (Hyp)		 Significant reductions in GSH in both the frontal cortex and hippocampus in disease
[35] 17 HC 38.8 ± 13.1 3 T GE Edited: MEGA-PRESS TR/TE = 1800/68 ms + LCModel 25 × 40 × 30 mm3 in DLPC
28 × 30 × 25 mm3 in ACC		 GSH/Cr = 0.11 ± 0.03 (ACC)
GSH/Cr = 0.11 ± 0.03 (left DLPC);		 Higher GSH in patients
[30] 16 HC 21–41; 30 ± 7.2 3 T GE + standard quadrature coil Edited: MEGA-PRESS TR/TE = 1500/94 ms + GE software 28 × 30 × 22 mm3 in PMPC 0.928 ± 0.24 mM No significant differences between GSH concentration of HC and patients
[3] 14 HC 32 ± 10 7 T Magnex Scientific Unedited: STEAM TR/TE = 5000/8 ms + LCModel Ranging from 6 × 6 × 13 to 20 × 20 × 20 mm3 in FWM, LS, PCC, OC, P, SN, and CV Ranging from 0.50 ± 0.1 μmol/g (OC) to 1.2 ± 0.2 μmol/g (CV) Lower GSH concentration in elderly subjects than in younger subjects
[67] 10 HC 25 ± 3 7 T Philips + 16 channels head coil Unedited: STEAM TR/TE = 3000/15 ms + LCModel 20 × 20 × 20 mm3 in OC 2.28 ± 0.1 µmol/g GSH increased during visual stimulation
[68] 10 HC 20 ± 3 4 T Varian INOVA Edited: MEGA-PRESS TR/TE = 4500/68 ms + LCModel
Unedited: STEAM TR/TE = 4500/5 ms + LCModel		 17 cm3 in ACC and 8 cm3 in OC 1.6 ± 0.4 µmol/g (ACC)
1.6 ± 0.2 µmol/g (OC)		 Validation of glutathione quantitation from the STEAM spectra
[7] 10 HC 20–70;
39.2 ± 15.3		 7 T Siemens + 32 channels head coil STEAM TR/TE = 8500 (9 subjects)−9300 (1 subject)/6 ms + LCModel 20 × 20 × 20 mm3 in PCC/precuneus 1.9 ± 0.3 mmol/L GSH levels higher in IGE (idiopathic generalized epilepsy) compared with HC
[69] 8 HC 19–53;
28.4 ± 10.7		 1.5 T Philips + birdcage head coil PRESS + DCQ (double quantum coherence) filtering 25 × 25 × 25 cm3 POC GSH/H2O = 2.3 ± 0.9 × 10−5 (right POC)
2.5 ± 1.2 × 10−5 (left POC)		 GSH/water ratio significantly reduced in both hemisphere Ins epileptic patients compared with HC
[70] 7 HC 6–17 3 T Siemens + 32 channels head coil PRESS TR/TE = 1980/30 ms + LCModel variable from 3 to 8 cm3 in the right gangliocapsular region 2.0 ± 0.5 mM Higher levels of brain GSH in KD patients compared with HC
[71] 17 HC   7 T and 3 T Siemens + 16 channels head coil (7 T) MEGA-PRESS TR/TE = 2000/68 ms 3.5 × 2.5 × 2.3 cm3 in left or right M1 (3 T and 7 T) and pons (3 T)   No significative difference in brain GSH between ALS patients and HC using 3 T scanner
[29] 11 HC 58.5 ± 6.6 3 T GE + 8 channels head coil PRESS with J-edited spin echo method TR/TE 1500/68 ms single voxel on primary motor cortex (M1) GSH/H2O = 1.6 ± 0.5 × 10−3
GSH/Cr 1.9 ± 0.8 × 10−2		 Reduced GSH in ALS patients compared with HC
[72] 15 HC 55–75 3 T GE + 8 channels head coil PRESS with J-edited spin echo method TR/TE 1500/68 ms 2.5 × 2.5 × 2.5 cm3 PCC and precuneus   GSH reduction with increased levels of amyloidosis
[34] 85 HC males
26.4 ± 3.0;
females 23.6 ± 2.1		 3 T Philips + 32 channels head coil MEGA-PRESS TR/TE = 2500/120 ms 2.5 × 2.5 × 2.5 cm3 in several brain regions   Female HC have higher GSH levels compared to male HC with a specific distribution pattern
[73] 29 HC 18–50 3 T GE PRESS TR/TE = 3000/30 ms + LCM model 20 × 20 × 15 mm3 in BG and 16 × 24 × 20 mm3 in DMPFC 2–3 mM (DMPFC and BG) No difference between GSH levels in ASD patients and HC
[37] 40 HC 18–30 3 T Philips + 32 channels head coil MEGA-PRESS TR/TE = 2048/68 ms 3 × 3 × 3 cm3 in five different regions (OC, left/right MT, TC, and PC) Occipital 6.91 (0.68) i.u.
Left MT+ 5.51 (0.86) i.u.
Right MT+ 6.59 (0.67) i.u.
Temporal 7.17 (0.93) i.u.
Parietal 5.17 (0.59) i.u		 No difference in GLX metabolites between ASD patients and HC
[15] 12 HC 50–84; 61.5 ± 4.9 3 T GE + 8 channel head coil PRESS TR/TE = 2000/35 ms + LCModel 20 × 20 × 20 mm3 in ACC GSH/Cr = 0.22 ± 0.06 Increased GSH in patients with depressive symptoms
[74] 17 HC 20–29 3 T GE + 8 channel head coil PRESS TR/TE = 2000/35 ms + LCModel 20 × 20 × 20 mm3 in ACC 1.47 ± 0.47 i.u. Less GSH in the ACC of patients with high risk of alcohol abuse
[14] 49 HC 18–30 3 T GE + 8 channel head coil PRESS TR/TE = 2000/35 ms + LCModel 20 × 20 × 20 mm3 in ACC and 1.5 × 3.0 × 1.0 in left Hyp   Decreased ACC-GSH with tobacco use in patients with bipolar disorder. No differences in GSH levels with alcohol use
[75] 25 HC   3 T GE + 8 channel head coil PRESS TR/TE = 2000/35 ms + LCModel 320 × 20 × 20 mm3 in ACC   Distinct neurometabolic profiles are evident in young people with major psychiatric disorders
[24] 45 HC   7 T Philips STEAM TR/TE = 2000/17 ms + LCModel 20 × 18 × 25 mm3 in ACC, 40 × 12 × 18 mm3 in left Ins, 20 × 22 × 20 mm3 in OC 1.75 ± 0.31 mM (ACC)
1.72 ± 0.20 mM (left Ins)
1.5 ± 0.17 mM (OC)		 Reduced GSH in ACC of patients with schizophrenia
[76] 25 HC 34.0 ± 12.3 3 T Siemens + 32 channels head coil 2DJ PRESS 20 × 20 × 20 mm3 in PCC GSH/Cr = 0.25 Lower GSH/Cr in PCC of patients with obsessive compulsive disorder
[33] 26 HC 22.77 ± 4.05 3 T GE + 8 channel head coil MEGA-PRESS TR/TE = 1500/68 ms 20 × 40 × 30 mm3 in MPFC GSH/H2O = 0.0015–0.0018 No difference in GSH levels between HC and patients at a clinical high risk for psychosis
[36] 9 HC 22.56 ± 2.35 3 T GE + 8 channel head coil MEGA-PRESS TR/TE = 1500/68 ms 4.5 × 2.5 × 2.5 mm3 in striatum GSH/H2O = 1.10 ± 0.10 × 10−3 Striatal GSH deficit in patients with a first episode of psychosis
[35] 17 HC 40.4 ± 12.3 3 T GE + 8 channel head coil MEGA-PRESS TR/TE = 1800/68 ms + LCModel 28 × 30 × 25 mm3 in ACC and 25 × 40 × 30 mm3 in DPLFC GSH/Cr = 0.11 ± 0.03 (ACC) Higher GSH levels in PTSD patients
[77] 41 HC 56–80; 68.7 ± 5.8 3 T GE + 8 channel head coil PRESS TR/TE = 2000/35 ms + LCModel 20 × 20 × 20 mm3 in ACC   Elevated ratios of GSH in subjects with mild cognitive impairment
[78] 18 HC 15–29 3 T GE PRESS TE 30 ms + LCModel 2 cm in both TC 1.5–2 mM GSH levels significantly higher in patients with a first episode of psychosis

This entry is adapted from the peer-reviewed paper 10.3390/antiox10091407

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