Hypoglycaemic activity of biosynthesized copper oxide nanoparticles in alloxan-induced diabetic Wister rats

Endocrinol Diabetes Metab. 2023 May;6(3):e423. doi: 10.1002/edm2.423. Epub 2023 Apr 10.

Abstract

Background: Diabetes mellitus (DM) is a metabolic disorder that affects the body's ability to produce or use insulin. This study evaluated the hypoglycaemic activity of biosynthesized copper oxide nanoparticles (CuO-NPs) in alloxan-induced diabetic Wister rats.

Methods: CuO-NPs were synthesized via the green route and characterized using different analytical tools. Diabetes was induced intraperitoneally using 90 mg/kg body weight of alloxan monohydrate in albino rats. Thirty (30) rats were randomly divided into 5 groups of 6 rats each and orally treated for 21 days. Groups I and II were treated with 300 mg/kg bwt Cereus hildmannianus extract and CuO-NPs, respectively. Groups III and IV received 5 mg/kg bwt of Glibenclamide and 2 mL of normal saline, respectively, while Group V was left untreated as the diabetic control. Blood glucose (BG) levels and body weight changes were monitored at 3- and 7-day intervals, respectively, throughout 21-day treatment period. Lipid profiles, enzyme assays and histopathological studies of the liver were also carried out.

Results: Spheroidal tenorite phase of CuO-NPs with a crystallite size of 62.57 nm, surface area (20.64 m2 /g) and a UV-maximum absorption at 214.27 nm was formed. The diabetic rats treated with 300 mg/kg bwt CuO-NPs had the highest BG lowering ability (from 482.75 ± 27.70 to 124.50 ± 2.50 mg/dL). A significant difference (p < 0.05) in weight gain and serum enzymes was also observed in the CuO-NPs treated group compared with other groups. The CuO-NPs-treated group had a significant increase (p < 0.05) in HDL-cholesterol and a decrease in total cholesterol, triglycerides, LDL-cholesterol and VLDL-cholesterol compared with other groups.

Conclusion: The green synthesized CuO-NPs nanoparticles significantly reduced (p < 0.05) blood glucose levels in rats and other associated indices and could serve as drug lead in the treatment of diabetes.

Keywords: Alloxan monohydrate; Histoarchitecture; biosynthesis; copper oxide nanoparticles; diabetes mellitus.

MeSH terms

  • Alloxan / adverse effects
  • Animals
  • Blood Glucose
  • Body Weight
  • Cholesterol, HDL
  • Copper / adverse effects
  • Diabetes Mellitus, Experimental* / drug therapy
  • Hypoglycemic Agents / adverse effects
  • Nanoparticles*
  • Oxides / adverse effects
  • Plant Extracts / adverse effects
  • Rats
  • Rats, Wistar

Substances

  • Hypoglycemic Agents
  • cupric oxide
  • cuprous oxide
  • Copper
  • Alloxan
  • Blood Glucose
  • Plant Extracts
  • Cholesterol, HDL
  • Oxides