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Brazilian Attenuated Hyperglycemia, Dyslipidemia, and Prooxidant Status in Alloxan-Induced Diabetic Rats. | LitMetric

AI Article Synopsis

  • The ethanolic extract of EEMn was tested on diabetic rats for its potential health benefits, focusing on its effects on blood sugar and cholesterol levels.
  • EEMn (400 mg/kg) significantly lowered fasting and post-meal blood glucose, improved glucose tolerance, and decreased harmful lipids in diabetic rats.
  • Additionally, the study found that EEMn reduced oxidative stress markers in the liver and contained beneficial flavonoids like rutin and isoquercetin, suggesting it may offer protective cardiovascular effects.

Article Abstract

has been used popularly for several proposes, including diabetic. In an attempt to support medicinal value, the acute hypoglycemic, hypolipidemic, and antioxidant effects of the ethanolic extract of (EEMn 200 or 400 mg/kg b.w.) were evaluated in normal and alloxan-induced diabetic treated for 14 days. Serum biochemical and antioxidant analysis were performed at the end of experiment. Oral glucose tolerance test was performed at 10th and 15th days. Chromatographic analysis by HPLC-DAD of EEMn was performed. Insulin was used as positive control to glycemic metabolism as well as fenofibrate to lipid metabolism. EEMn (400 mg/kg/day) reduced fasting and postprandial glycaemia, improved oral glucose tolerance, and reduced lipolysis and proteolysis in diabetic rats. EEMn decreased the blood levels of total cholesterol and increased HDL level when compared to the diabetic control rats. At higher levels, EEMn reduced triglycerides and VLDL levels in diabetic rats. Also, EEMn reduced malondialdehyde and increased the reduced glutathione levels in liver of diabetic rats. Chromatographic analysis identified the presence of the flavonoids rutin, isoquercetin, and kaempferitrin. Acute EEMn treatment reduced hyperglycemia, improved oral glucose tolerance, and minimized dyslipidemia and oxidative stress leading to a reduction in atherogenic index in alloxan-induced diabetic rats.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5439258PMC
http://dx.doi.org/10.1155/2017/5275813DOI Listing

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