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Antioxidant properties of date seeds extract (Phoenix dactylifera L.) in alloxan induced damage in rats.

R AbbassiM C PontesSabah DhibiL A M S Duarte FilhoS OthmaniHafsia BouzennaJackson Roberto Guedes da Silva AlmeidaN Hfaiedh
Published in: Brazilian journal of biology = Revista brasleira de biologia (2023)
The study was conducted to examine the antioxidant activity and evaluate the protective effects of the date seeds powder kentichi against alloxan-induced damage in the liver, kidney, and pancreas in diabetic's rats. Group 1: control group, that did not receive any treatment, Group 2: alloxan was injected intraperitoneally (120 mg/kg body weight) for two days (Diab), Group 3: treated only by date seeds powder added in the diet (300 g/kg) for 6 weeks (DSPK), Group 4: alloxan-diabetic rats treated with date seeds powder (300 g/kg) (DSPK + Diab). Estimations of biochemical parameters in blood were determined. TBARS, SOD, CAT, and GPx activities were determined. A histopathological study was done by immersing pieces of both organs in a fixative solution followed by paraffin hematoxylin-eosin staining. In addition, the antioxidant activities of DSPK were evaluated by DPPH radical scavenging activity, reducing power, and ABTS free radical scavenging. The results revealed that date seeds significantly decreased serum levels of glucose, cholesterol, triglycerides, urea, creatinine, T-protein, ALP, D-bili and T-bili levels. In addition, superoxide dismutase (SOD), catalase (CAT) and glutathione peroxidase (GPx) activities that had been reduced in liver, kidney, and pancreas of the treated group were restored by DSPK treatments and, therefore, the lipid peroxidation level was reduced in the liver, kidney and pancreas tissue compared to the control group. Additionally, the histological structure in these organs was restored after treatment with date seeds powder.
Keyphrases
  • diabetic rats
  • oxidative stress
  • body weight
  • type diabetes
  • anti inflammatory
  • amyotrophic lateral sclerosis
  • endothelial cells
  • hydrogen peroxide
  • binding protein
  • uric acid
  • nitric oxide