பயோமெடிக்கல் சயின்சஸ் ஜர்னல்

• ஜர்னல் ஹோம்
• காப்பகம்
ஆசிரியர்கள்
• ஆசிரியர் வழிகாட்டுதல்கள்
• கையெழுத்துப் பிரதியை சமர்ப்பிக்கவும்
விவரம்
• நோக்கம் மற்றும் நோக்கம்
• வெளியீட்டு நெறிமுறைகள்
• சக மதிப்பாய்வு செயல்முறை
• காப்புரிமை
• எங்களை தொடர்பு கொள்ள

சுருக்கம்

Effect of Chromium Picolinate and Melatonin either in Single or in a Combination in Alloxan Induced Male Wistar Rats

Zephy Doddigarla, Iqbal Parwez, Subuhi Abidi and Jamal Ahmad

Background: Diabetes Mellitus (DM) is an endocrine disorder due to improper secretion of insulin or action of insulin regardless of hyperglycemia in the body. Reactive oxygen species (ROS) play a major role in the development of insulin resistance and DM.
Objective: The present study, designed to assess the role of chemically induced ROS and also the effect of chromium picolinate (CrPic) and melatonin (Mel) alone or in combination (CrPic+Mel) along with ROS on insulin resistance, blood glucose, lipid, and oxidative stress variables in alloxan induced Wistar rats. Methods: Male Wistar rats have been categorized into five groups and group consists of six rats. Group I served as untreated, while group II, III, IV, and V, were treated with alloxan (AID), alloxan+CrPic (AID+CrPic), alloxan+Mel (AID+Mel), and alloxan+CrPic+Mel (AID+CrPic+Mel) respectively.
Results: Insulin resistance was greatly increased in group AID rats compared with untreated rats. A similar increase was seen in blood glucose, total cholesterol, and triacylglycerols compared between group II and untreated (P<0.05). Significant differences were observed when group group III, group IV, and group V rats were compared with group II rats in blood glucose and lipid variables (P<0.05). But prominent significant differences were observed between group group II and group IV experimental rats in serum levels of zinc, malondialdehyde, nitric oxide, superoxide dismutase, catalase, and glutathione (P<0.05) respectively. Histopathological findings suggest that the Mel and CrPic+Mel treated rats had normal renal tubular architecture compared with group II rats. Relatively normal architecture of liver and pancreas was observed in alloxan rats treated with Mel and CrPic+Mel.
Conclusion: CrPic and Mel alone or in a combination prevented pathological alterations in the serum and in tissues due to their anti-hyperglycemic, insulinsensitizing, anti-dyslipidemia, and antioxidant activity, but Mel alone was most effective.