Cross-Regulation between Autophagy and Apoptosis Induced by Vitamin E and Lactobacillus Plantarum through Beclin-1 Network

Int J Mol Sci. 2022 Dec 4;23(23):15305. doi: 10.3390/ijms232315305.

Abstract

Autophagy and apoptosis are two important regulatory mechanisms for how the body can respond to diseases. This study was designed to investigate the protective actions of vitamin E (Vit-E) and lactobacillus plantarum (Lac-B) against mercuric chloride (HgCl2)-induced kidney injury. Thirty albino rats were divided into five groups: group 1 served as the normal group; rats in group 2 received high doses of HgCl2; rats in groups 3, 4 and 5 were given Vit-E, Lac-B and the combination of Vit-E and Lac-B, respectively along with HgCl2 for two weeks. HgCl2 provoked renal injury, manifested by elevation in serum urea, urea nitrogen and creatinine. Kidney levels of oxidative stress and inflammation were markedly increased post HgCl2 administration. Moreover, HgCl2 significantly elevated the gene expression levels of VCAM-1 and cystatin C, while podocin was downregulated. Additionally, it markedly decreased the protein expression of Beclin-1 and Bcl-2. Histopathological examination revealed massive degeneration with congested blood vessels following HgCl2 administration. Treatment with Vit-E or/and Lac-B restored the normal levels of the previously mentioned parameters, as well as improved the morphology of kidney tissues. Both Vit-E and Lac-B provided a protective effect against HgCl2-induced kidney damage by regulating autophagy and apoptosis.

Keywords: Beclin-1; Lactobacillus-plantarum; apoptosis; autophagy; vitamin E.

MeSH terms

  • Animals
  • Antioxidants / pharmacology
  • Apoptosis
  • Autophagy
  • Beclin-1 / metabolism
  • Kidney / metabolism
  • Lactobacillus plantarum* / metabolism
  • Mercuric Chloride / toxicity
  • Oxidative Stress
  • Rats
  • Urea / pharmacology
  • Vitamin E* / metabolism
  • Vitamin E* / pharmacology

Substances

  • Antioxidants
  • Beclin-1
  • Mercuric Chloride
  • Urea
  • Vitamin E

Grants and funding

This research received no external funding.