From diabetes to renal aging: the therapeutic potential of adiponectin

J Physiol Biochem. 2021 May;77(2):205-214. doi: 10.1007/s13105-021-00790-4. Epub 2021 Feb 8.

Abstract

Nowadays, the complications related to diabetes, such as nephropathy, cardiovascular problems, and aging, are highly being considered. Renal cell aging is affected by various mechanisms of inflammation, oxidative stress, and basement membrane thickening, which are significant causes of renal dysfunction in diabetes. Due to recent studies, adiponectin plays a key role in diabetes-related kidney diseases as a fat-derived hormone. In diabetes, reduced adiponectin levels are associated to renal cell aging. Oxidative stress and related signaling pathways are the main routes in which adiponectin may be effective to decline diabetes-associated aging. Therefore, adiponectin signaling in target tissues becomes one of the research areas of interest in metabolism and clinical medicine. Studies on adiponectin signaling will increase our understanding of adiponectin role in diabetes-linked diseases as well as shortening life span conditions which may guide the design of antidiabetic and anti-aging drugs.

Keywords: Adiponectin; Aging; Diabetes; Kidney; Oxidative stress.

Publication types

  • Review

MeSH terms

  • AMP-Activated Protein Kinases / genetics
  • AMP-Activated Protein Kinases / metabolism
  • Adiponectin / genetics*
  • Adiponectin / metabolism
  • Aging
  • Animals
  • Diabetes Mellitus, Type 2 / drug therapy
  • Diabetes Mellitus, Type 2 / genetics*
  • Diabetes Mellitus, Type 2 / metabolism
  • Diabetes Mellitus, Type 2 / pathology
  • Diabetic Nephropathies / drug therapy
  • Diabetic Nephropathies / genetics*
  • Diabetic Nephropathies / metabolism
  • Diabetic Nephropathies / pathology
  • Gene Expression Regulation
  • Humans
  • Hypoglycemic Agents / therapeutic use
  • Kidney / drug effects
  • Kidney / metabolism
  • Kidney / pathology
  • Metabolic Networks and Pathways / genetics
  • Obesity / drug therapy*
  • Obesity / genetics*
  • Obesity / metabolism
  • Obesity / pathology
  • Oxidative Stress
  • PPAR alpha / genetics
  • PPAR alpha / metabolism
  • Receptors, Adiponectin / genetics*
  • Receptors, Adiponectin / metabolism
  • Signal Transduction

Substances

  • ADIPOQ protein, human
  • Adiponectin
  • Hypoglycemic Agents
  • PPAR alpha
  • PPARA protein, human
  • Receptors, Adiponectin
  • AMP-Activated Protein Kinases