Biochemical profiling of lead-intoxicated impaired lipid metabolism and its amelioration using plant-based bioactive compound

Environ Sci Pollut Res Int. 2022 Aug;29(40):60414-60425. doi: 10.1007/s11356-022-20069-5. Epub 2022 Apr 14.

Abstract

The aim of this study was to investigate the lead (Pb)-induced lipid metabolism impairment and its amelioration using plant-based therapeutic interventions. Pb-induced hepatotoxicity can disturb the normal levels of natural antioxidant enzymes including glutathione (GSH) and superoxide dismutase (SOD) exerting a crucial impact on membrane unsaturated fatty acids (FA), hence leading to lipid peroxidation. Furthermore, Pb toxicity can also alter the regulation of various hormones involved in the synthesis of 3-hydroxy-methyl glutaryl CoA (HMG-CoA reductase), leading to an impairment in normal levels of serum cholesterol and other associated conjugated lipid molecules such HDL-cholesterol, LDL-cholesterol and VLDL-cholesterol. In this study, the lipoprotein fractions, cholesterol, triglyceride (TGs) and biomarkers of liver functions were estimated by employing respective assay kits. The levels of antioxidant enzymes, FFAs and HMG-CoA reductase were determined by employing sandwich ELISA method. The administration of PbAc in experimental rats induced a significant disturbance in lipid profile (P < 0.05) accompanying a significant reduction in natural antioxidant defence system (P < 0.05). The significant alteration in the levels of serum antioxidant enzymes can lead to membrane lipid peroxidation that is reflected by a significantly (P < 0.05) high level of serum MDA in PbAc-induced experimental rats. However, the administration of resveratrol proved therapeutically effective in the treatment of Pb toxicity. Overall, the results of this study accompanying histopathological examination had proved the ameliorating effect of resveratrol in Pb-induced lipid metabolism impairment by adopting vitamin C as a standard therapeutic intervention.

Keywords: Pb toxicity; antioxidant enzymes; hepatotoxicity; lipid peroxidation; lipid profile; therapeutic intervention.

MeSH terms

  • Animals
  • Antioxidants* / metabolism
  • Cholesterol / metabolism
  • Glutathione / metabolism
  • Lead / metabolism
  • Lipid Metabolism*
  • Lipid Peroxidation
  • Lipids
  • Liver
  • Rats
  • Resveratrol / pharmacology
  • Superoxide Dismutase / metabolism

Substances

  • Antioxidants
  • Lipids
  • Lead
  • Cholesterol
  • Superoxide Dismutase
  • Glutathione
  • Resveratrol