GSH and Diabetes
Dietary glutathione protects rats from diabetic
nephropathy and neuropathy.
Ueno Y, Kizaki M, Nakagiri R, Kamiya T, Sumi H, Osawa T. [J Nutr. 2002
May;132(5):897-900.] The aim of this study was to examine the involvement of
oxidative stress in the progression of kidney dysfunction and neuropathy in
diabetes and to evaluate the potential usefulness of glutathione (GSH) in
diabetes. Diabetic rats were treated with 1 g/100 g GSH as a dietary supplement.
GSH significantly suppressed the diabetes-induced increase in urinary
8-hydroxy-2'-deoxyguanosine, one of the markers of oxidative stress. It also
prevented the diabetes-induced increases in albumin and creatinine in urine. The
diabetes-induced increase in the tail flick reaction time to thermal stimuli
also was normalized by treatment with dietary GSH. In conclusion, GSH treatment
can beneficially affect STZ-induced diabetic rats, with preservation of in vivo
renal and neural function. This suggests a potential usefulness of dietary GSH
treatment to reduce diabetic complications.
Glutathione in overweight
patients with poorly controlled type 2 diabetes
Aaseth J and Stoa-Birketvedt G. [Journal of Trace Elements in Experimental
Medicine]. 2000; volume 13, number 1, pages 105-111. "Therapeutic trials with
antioxidants that can regenerate the intracellular level of GSH [glutathione]
are scarce but promising."
Influence of reduced glutathione infusion on glucose metabolism in patients
with non-insulin-dependent diabetes mellitus
De Mattia G, Bravi MC, and others. [Metabolism 1998
Aug;47(8):993-7.] "In conclusion, our data support the hypothesis that abnormal
intracellular GSH redox status plays an important role in reducing insulin
sensitivity in NIDDM patients. Accordingly, intravenous GSH [glutathione]
infusion significantly increased both intraerythrocytic GSH/GSSG ratio and total
glucose uptake in the same patients."
Reduction of oxidative stress by oral N-acetyl-L-cysteine treatment decreases
plasma soluble vascular cell adhesion molecule-1 concentrations in non-obese,
non-dyslipideaemic, normotensive, patients with non-insulin-dependent diabetes
De Mattia G, Bravi MC and others. [Diabetologia 1998
Nov;41(11):1392-6.] "NAC therapy could be valuable in other clinical situations
in which GSH deficiency or oxidative stress plays a role in disease pathology,
e.g. rheumatoid arthritis, Parkinson's disease, hepatitis, liver cirrhosis,
septic shock and diabetes. Our data indicate that the vascular endothelium is
activated in non-insulin dependent diabetes. Antioxidant treatment
counterbalanced such endothelial activation. Thus, antioxidant agents might
protect against oxidant-related upregulation of endothelial adhesion molecules
and slow down the progression of vascular damage in non-insulin dependent
diabetes."
Glutathione in human plasma: Decline in
association with aging, age- related macular degeneration, and diabetes
Samiec PS, Drews-Botsch C, and
others. [Free Radic Biol Med 1998 Mar 15;24(5):699-704.] Analyses of whole
blood GSH showed that GSH was significantly lower in diabetic cases compared to
the other groups, but did not reveal any difference associated with age or ARMD.
In contrast, GSSG in whole blood was significantly higher in the older groups
compared to the younger controls. The results suggest that in studies of
age-related pathologies, oxidation of GSH may be a more important parameter than
a decline in pool size, while in specific pathologies such as diabetes, both
oxidation and a decline in pool size may be important.
Intracellular reduced glutathione content in
normal and type 2 diabetic erythrocytes: effect of insulin and (-)epicatechin
Rizvi SI, Zaid MA. [J Physiol Pharmacol 2001 Sep;52(3):483-8] Since
oxidative stress has been implicated in the development of diabetic
complications and GSH plays an important role in protection against oxidative
damages, we have studied the in vitro effect of (-)epicatechin and insulin on
the reduced glutathione content in normal and type 2 diabetic erythrocytes. The
GSH content was significantly lower in type 2 diabetic patients as compared to
normal individuals. In vitro insulin treatment resulted in increase in the GSH
content in both normal and type 2 diabetic erythrocytes. (-)Epicatechin also
resulted in an increase in erythrocyte GSH content in both normal and type 2
diabetic erythrocytes. Although the exact mechanism by which (-)epicatechin
causes elevation of erythrocyte GSH is not clear nevertheless this finding may
have important therapeutic implications. A higher content of dietary flavanoids
may thus protect diabetic patients against long-term complications.
Apoptosis and oxidative status
in peripheral blood mononuclear cells of diabetic patients
Graber R, Farine JC, and others. [Apoptosis. 1999; volume 4, number
4, pages 263- 270.]
Hyperglycemia in diabetic rats reduces the glutathione content in the aortic
tissue
Tachi Y, Okuda Y, Bannai C, Bannai S,
Shinohara M, Shimpuku H, Yamashita K, Ohura K. [Life Sci 2001 Jul
20;69(9):1039-47] The glutathione redox cycle plays a major role in scavenging
hydrogen peroxide (H2O2) under physiological conditions. Recently, we
demonstrated that a high glucose concentration in the culture medium reduced the
level of H2O2 scavenging activity of human vascular smooth muscle cells (hVSMCs).
We also showed that a high glucose concentration reduced the intracellular
glutathione (GSH) content and the rate of uptake of cystine, which itself is a
rate-limiting factor that maintains the GSH level. In the present study, we
investigated whether the hyperglycemic condition in diabetic rats impairs the
glutathione content in the aortic tissue in vivo. We demonstrated in vivo that
the hyperglycemic condition in STZ-induced diabetic Wistar rats and OLETF rats
reduced the GSH content in aortic tissue. This suggested reduced glutathione
redox cycle function of aorta.
Association of Glutathione Peroxidase
Activity with Insulin Resistance and Dietary Fat Intake during Normal Pregnancy
Xinhua Chen, Theresa O. Scholl, Maria J. Leskiw, Melissa R. Donaldson and T.
Peter Stein [ The Journal of Clinical Endocrinology & Metabolism Vol. 88,
No. 12 5963-5968] Glutathione peroxidase (GPx) is one of the most important
antioxidant enzymes in humans. We studied the relationship between erythrocyte
GPx activity and fasting serum insulin, plasma glucose, and C-peptide, estimates
of insulin resistance from the homeostasis model of assessment as well as
dietary fat intake in 408 normotensive nondiabetic pregnant women from Camden,
NJ. In conclusion, we demonstrated that normal pregnancy is associated with
increased GPx activity and insulin resistance. There are ethnic differences in
antioxidant response and dietary fat intake. Our findings suggest a potential
link among antioxidant defenses, insulin resistance, and dietary fat intake.
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