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Expression of hepatic antioxidant enzymes in non-obese type-2 diabetic Goto-Kakizaki rats

Authors
Ryu, Chang SeonOh, Soo JinOh, Jung MinLee, Sang YoonKwak, Hui ChanYun, Kang UkLee, Ji-YoonPark, Song-KyuKim, Bong-HeeMa, Jin YeulKim, Sang Kyum
Issue Date
Oct-2014
Publisher
PHARMACEUTICAL SOC KOREA
Keywords
Non-obese diabetes; GK rat; Antioxidant enzymes; Glutathione S-transferase; Oxidative stress
Citation
ARCHIVES OF PHARMACAL RESEARCH, v.37, no.10, pp.1345 - 1353
Indexed
SCIE
SCOPUS
KCI
Journal Title
ARCHIVES OF PHARMACAL RESEARCH
Volume
37
Number
10
Start Page
1345
End Page
1353
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/97211
DOI
10.1007/s12272-013-0267-3
ISSN
0253-6269
Abstract
Diabetes mellitus and its complications have been attributed in part to oxidative stress, against which antioxidant enzymes constitute a major protective mechanism. The present study was performed to investigate the effects of early stage type 2 diabetes in the absence of obesity and liver damage on hepatic antioxidant enzyme expression and oxidative stress using 9-week-old Goto-Kakizaki (GK) rats. Hepatic total antioxidant capacity determined by total oxygen radical scavenging capacity and lipid peroxidation determined by malondialdehyde in plasma and liver were not significantly different between normal Wistar rats and GK rats. These results indicated that oxidative stress is not evident in these type 2 diabetic rats. Hepatic expression levels of antioxidant enzymes, including superoxide dismutase-1, catalase, glutathione peroxidase and reductase, thioredoxin-1, mu- and pi-class glutathione S-transferase (GST), and the gamma-glutamylcysteine ligase catalytic subunit, were not different between normal rats and GK rats. But, hepatic level and activity of alpha-class GST were decreased and peroxiredoxin-1 level was increased in GK rats, suggesting that upregulation of peroxiredoxin-1 compensates for downregulation of alpha-class GST. These results suggest that alpha-class GST and peroxiredoxin-1 in liver can be altered during the early stages of type 2 diabetes in the absence of obesity and severe oxidative stress.
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