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Cited by 219

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Changes in Hepatic Glutathione Metabolism in Diabetes

McLennan, Susan V, Heffernan, Scott, Wright, Lesley, Rae, Caroline, Fisher, Elizabeth, Yue, Dennis K, Turtle, John R·1991·Diabetes

Abstract

Glutathione is important in the regulation of the redox state, and a decline in its tissue level has often been considered to be indicative of increased oxidative stress in diabetes. In this study of diabetic rats, the level of hepatic glutathione was normal unless food intake was restricted. Thus, the previous report of a reduction in hepatic glutathione in diabetes is likely to be the result of food deprivation rather than diabetes alone. In contrast to changes characteristic of oxidative stress, the efflux of glutathione in bile from diabetic animals was significantly decreased, whereas hepatic mixed disulfides were unchanged, and the hepatic γ-glutamyltransferase activity was considerably increased. These changes were not reproduced by food deprivation. The decrease in biliary excretion of glutathione in diabetes may reflect an attempt to conserve glutathione by activation of the hepatic γ-glutamyl cycle. We conclude that the disturbances of glutathione metabolism in diabetes are not typical of those seen in oxidative stress or food restriction.

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Metadata

Authors
McLennan, S. V., Heffernan, S., Wright, L., Rae, C., Fisher, E., Yue, D. K., & Turtle, J. R.
Venue
Diabetes
Published
1991-03-01
Volume
40
Issue
3
Pages
344-348
ISSN
  • 0012-1797 (ISSN-L)
  • 1939-327X
OpenAlex
W2049909690
Cited by
219
References
0
FWCI
1.31
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: Changes in Hepatic Glutathione Metabolism in Diabetes. https://app.cochat.ai/papers/10.2337/diab.40.3.344
The paper
McLennan, S. V., Heffernan, S., Wright, L., Rae, C., Fisher, E., Yue, D. K., & Turtle, J. R. (1991). Changes in Hepatic Glutathione Metabolism in Diabetes. Diabetes. https://doi.org/10.2337/diab.40.3.344

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

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