A review on protective role of genistein against oxidative stress in diabetes and related complications

Chem Biol Interact. 2019 Sep 1:310:108665. doi: 10.1016/j.cbi.2019.05.031. Epub 2019 May 21.

Abstract

Diabetes mellitus (DM) is metabolism related problems that share the phenotype of hyperglycemia, which is triggered by a complicated interaction of hereditary and environmental elements. It is the main reason for end-stage renal disease (ESRD), amputations of the traumatic lower extremity, and grown-up visual impairment. It additionally inclines to neurodegenerative and cardiovascular sicknesses. With an expanding rate around the world, DM may be the main motive of morbidity and mortality within the foreseeable future. The objective of treatment for DM is to inhibit mortality and difficulties through normalizing blood glucose stage. Genistein, a naturally available soy isoflavone, is accounted for to have various medical advantages credited to numerous natural capacities. In the course of recent years, various examinations have shown that genistein has hostile to diabetic impacts, specifically, direct consequences for β-cell expansion, glucose-triggered insulin discharge, and safety towards apoptosis, unbiased of its functions as an estrogen receptor agonist, cancer prevention agent, or tyrosine kinase inhibitor. The present evaluation emphases on the promising molecular and biochemical paths associated with DM complications and, specifically, the multi-target method of genistein in diminishing diabetic neuropathy, nephropathy, and retinopathy.

Keywords: Diabetes mellitus; Genistein; Nephropathy; Neuropathy; Retinopathy.

Publication types

  • Review

MeSH terms

  • Animals
  • Diabetes Complications / drug therapy*
  • Diabetes Complications / metabolism
  • Diabetes Mellitus / drug therapy*
  • Diabetes Mellitus / metabolism
  • Diabetic Nephropathies / drug therapy
  • Diabetic Neuropathies / drug therapy
  • Diabetic Retinopathy / drug therapy
  • Genistein / pharmacology
  • Genistein / therapeutic use*
  • Humans
  • Oxidative Stress / drug effects*

Substances

  • Genistein