Effects of hypothyroidism on the mesenteric and omental adipose tissue in rats

Mol Cell Endocrinol. 2019 Jun 15:490:88-99. doi: 10.1016/j.mce.2019.04.011. Epub 2019 Apr 17.

Abstract

To characterize the influence of hypothyroidism on the endocrine activity of mesenteric and omental adipose tissue (MOAT) and the peripheral regulation of energy balance (EB) in rats, we analyzed food intake (FI); basal metabolic rate (BMR); locomotor activity; body weight (BW); serum hormone concentrations and the expression of their receptors in MOAT. We evaluated the morphology and differentiation of adipocytes. Hypothyroidism decreased FI, BMR and BW. The percentage of visceral white adipose tissue (WAT) depots and the morphology of adipocytes were similar to euthyroid rats. Serum leptin and adiponectin expression in MOAT were altered by hypothyroidism. The expression of Perilipin 1, HSL, UCP1 and PRDM16 was significantly lower in MOAT of hypothyroid animals. Hypothyroidism in rats leads to a compensated EB by inducing a white adipocyte dysfunction and a decrease in BW, BMR, FI and adipokine secretions without changing the percentage of WAT depots and the morphology of the MOAT.

Keywords: Adipokines; Adipose tissue; Energy balance; Hormonal patterns; Hypothyroidism.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adipocytes / metabolism
  • Adipokines / blood
  • Adipose Tissue / pathology*
  • Adipose Tissue, White / metabolism
  • Adipose Tissue, White / pathology
  • Animals
  • Basal Metabolism
  • Biomarkers / metabolism
  • Body Weight
  • Corticosterone / metabolism
  • Eating
  • Fatty Acids / metabolism
  • Female
  • Glucose / metabolism
  • Hypothyroidism / blood
  • Hypothyroidism / pathology*
  • Insulin / metabolism
  • Mesentery / pathology*
  • Motor Activity
  • Omentum / pathology*
  • Ovary / metabolism
  • Propylthiouracil / pharmacology
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Rats, Sprague-Dawley

Substances

  • Adipokines
  • Biomarkers
  • Fatty Acids
  • Insulin
  • RNA, Messenger
  • Propylthiouracil
  • Glucose
  • Corticosterone