ACTION OF CAPPARIS-DECIDUA AGAINST ALLOXAN-INDUCED OXIDATIVE STRESS AND DIABETES IN RAT-TISSUES

Citation
P. Yadav et al., ACTION OF CAPPARIS-DECIDUA AGAINST ALLOXAN-INDUCED OXIDATIVE STRESS AND DIABETES IN RAT-TISSUES, Pharmacological research, 36(3), 1997, pp. 221-228
Citations number
28
Categorie Soggetti
Pharmacology & Pharmacy
Journal title
ISSN journal
10436618
Volume
36
Issue
3
Year of publication
1997
Pages
221 - 228
Database
ISI
SICI code
1043-6618(1997)36:3<221:AOCAAO>2.0.ZU;2-L
Abstract
Alloxan-induced diabetic rats were treated with insulin (i.p.) or with Capparis decidua powder as a hypoglycaemic agent mixed with diet. The effect was assessed on lipid peroxidation (LPO) and the antioxidant d efense system in rat tissues. The increased levels of blood glucose in diabetes produce superoxide anions and hydroxyl radicals in the prese nce of transition metal ions which cause oxidative damage to cell memb ranes. The heart tissue showed an increased lipid peroxidation (LPO) i n diabetic rats while no significant change was observed in the liver and kidney. The treatment with C. decidua lowered LPO in these tissues even more effectively than insulin-treated rats. The superoxide dismu tase (SOD) activity increased in the heart and kidneys in the diabetic group of rats probably to increase dismutation of superoxide anions. However, treatment with C. decidua decreased SOD activity in the liver and kidney and was comparable to control rats. Catalase (CAT) activit y was not significantly affected in any of the tissues in diabetic and insulin-treated animals, however, CAT activity markedly increased in tissues with C. decidua treatment. Total and Se-dependent glutathione peroxidase (GSH-Px) in the heart was markedly lowered in diabetic rats which recovered with insulin as well as with C. decidua treatment. Th e increase in GSH-Px and CAT activity with C. decidua treatment may lo wer H2O2 toxicity and reduce oxidative stress in diabetes. However, gl utathione (GSH) content in the heart and kidney and glutathione reduct ase (GSH-R) activity in all the tissues studied increased in diabetic rats while treatment with insulin lowered GSH content and GSH-R activi ty in these tissues. The treatment with C. decidua also decreased GSH- R activity in the kidney and heart which resulted in the decrease in G SH content in these tissues. The changes such as the increase in kidne y and heart SOD may be an adaptive response in order to neutralize sup eroxide anions. The increase in GSH content and GSH-R activity in the tissue are in response to neutralize superoxide anions and to countera ct oxidative stress in diabetes. Glutathione S-transferase (GST) was n ot significantly affected in diabetic rat tissue, however, heart GST i ncreased with antidiabetic treatments. The increase in glucose-6-phosp hate dehydrogenase (G6PDH) in the kidney and heart of diabetic rats su bsequently decreased with C. decidua treatment. The increase in G6PDH in tissues may increase NADPH generation required for GSH-R activity a nd GSH production. It is suggested that these changes initially counte ract the oxidative stress in diabetes, however, a gradual decrease in the antioxidative process may be one of the factors which results in c hronic diabetes. The data indicate that C. decidua may have potential use as an antidiabetic agent and in lowering oxidative stress in diabe tes. (C) 1997 The Italian Pharmacological Society.