Adrenomedullin ameliorates palmitic acid-induced insulin resistance through PI3K/Akt pathway in adipocytes

Acta Diabetol. 2022 May;59(5):661-673. doi: 10.1007/s00592-021-01840-5. Epub 2022 Jan 3.

Abstract

Aims: White adipose tissue (WAT) dysfunction has been associated with adipose tissue low-grade inflammation and oxidative stress leading to insulin resistance (IR). Adrenomedullin (ADM), an endogenous active peptide considered as an adipokine, is associated with adipocytes function.

Methods: We evaluated the protective effects of ADM against IR in 3T3-L1 adipocytes treated by palmitic acid (PA) and in visceral white adipose tissue (vWAT) of obese rats fed with high-fat diet.

Results: We found that endogenous protein expressions of ADM and its receptor in PA-treated adipocytes were markedly increased. PA significantly induced impaired insulin signaling by affecting phosphatidylinositol 3-kinase (PI3K)-protein kinase B (Akt) axis and glucose transporter-4 (GLUT-4) levels, whereas ADM pretreatment enhanced insulin signaling PI3K/Akt and GLUT-4 membrane protein levels, decreased pro-inflammatory cytokines tumor necrosis factor α (TNFα), interleukin-1β (IL-1β) and IL-6 levels, and improved oxidative stress accompanied with reduced reactive oxygen species (ROS) levels and increased anti-oxidant enzymes manganese superoxide dismutase 2 (SOD2), glutathione peroxidase (GPx1) and catalase (CAT) protein expressions. Furthermore, ADM treatment not only improved IR in obese rats, but also effectively restored insulin signaling, and reduced inflammation and oxidative stress in vWAT of obese rats.

Conclusions: This study demonstrates a prevention potential of ADM against obesity-related metabolic disorders, due to its protective effects against IR, inflammation and oxidative stress in adipocytes.

Keywords: Adrenomedullin; Inflammation; Insulin resistance; Oxidative stress; PI3K/Akt pathway.

MeSH terms

  • Adipocytes / metabolism
  • Adrenomedullin / metabolism
  • Adrenomedullin / pharmacology
  • Animals
  • Inflammation / metabolism
  • Insulin / metabolism
  • Insulin Resistance*
  • Obesity / metabolism
  • Palmitic Acid / pharmacology
  • Phosphatidylinositol 3-Kinase / metabolism
  • Phosphatidylinositol 3-Kinase / pharmacology
  • Phosphatidylinositol 3-Kinases / metabolism
  • Proto-Oncogene Proteins c-akt* / metabolism
  • Rats

Substances

  • Insulin
  • Adrenomedullin
  • Palmitic Acid
  • Phosphatidylinositol 3-Kinase
  • Proto-Oncogene Proteins c-akt