Increased oxidative stress, inflammation and fibrosis in perirenal adipose tissue of patients with cortisol-producing adenoma

Adipocyte. 2019 Dec;8(1):347-356. doi: 10.1080/21623945.2019.1690834.

Abstract

Although much is known about that corticosteroids affect the functions of adipose tissues, little genetic information is available for perirenal adipose tissue (peri-N) from patients with cortisol-producing adenoma (CPA). We conducted microarray analysis of peri-N from patients with CPA by using an Affymetrix human U133 plus 2.0 array. We also analysed the inflammation, fibrosis and oxidative stress in vitro. Compared with normotension (NT) group, CPA group has significantly higher protein levels of TNFα, IL-6, fibronectin (FN) and collagen I (COLI). The protein level of NADPH oxidase 4 (Nox4) significantly increased, while nuclear factor erythroid 2-related factor 2 (Nrf2) and hemeoxygenase-1 (HO-1) levels were significantly reduced in the CPA group. Dexamethasone markedly induced fibrosis and adipogenesis-related gene expression in predifferentiated stromal vascular fraction (SVF) cells, 3T3-L1 preadipocytes and brown preadipocytes. Chronic exposure to endogenous glucocorticoids due to CPA increases peri-N oxidative stress, inflammation and fibrosis, which may contribute to the metabolic disturbances associated with hypercortisolism in these patients.

Keywords: Cushing’s syndrome; adipose tissue; fibrosis; inflammation; microarray; oxidative stress.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 3T3-L1 Cells
  • ACTH-Secreting Pituitary Adenoma / genetics*
  • ACTH-Secreting Pituitary Adenoma / metabolism
  • ACTH-Secreting Pituitary Adenoma / pathology
  • Adenoma / genetics*
  • Adenoma / metabolism
  • Adenoma / pathology
  • Adipose Tissue / metabolism
  • Adult
  • Animals
  • Collagen Type I / genetics*
  • Collagen Type I / metabolism
  • Female
  • Fibronectins / genetics*
  • Fibronectins / metabolism
  • Fibrosis
  • Gene Expression Regulation
  • Heme Oxygenase-1 / metabolism
  • Humans
  • Male
  • Mice
  • Middle Aged
  • NADPH Oxidase 4 / metabolism
  • NF-E2-Related Factor 2 / metabolism
  • Oligonucleotide Array Sequence Analysis / methods*
  • Oxidative Stress
  • Tumor Necrosis Factor-alpha / genetics*
  • Tumor Necrosis Factor-alpha / metabolism
  • Young Adult

Substances

  • Collagen Type I
  • Fibronectins
  • NF-E2-Related Factor 2
  • NFE2L2 protein, human
  • TNF protein, human
  • Tumor Necrosis Factor-alpha
  • HMOX1 protein, human
  • Heme Oxygenase-1
  • NADPH Oxidase 4
  • NOX4 protein, human

Grants and funding

This work was supported by the National Natural Science Foundation of China Grants 81870612, 81628004, 31400992 and 81470047, and Guangdong Science and Technology Project 2019A1515011997.