Affiliations 

  • 1 School of Medicine, Xiamen University, Xiamen, 361102, Fujian Province, China; School of Traditional Chinese Medicine, Xiamen University, Malaysia
  • 2 School of Medicine, Xiamen University, Xiamen, 361102, Fujian Province, China
  • 3 Department of Traditional Chinese Medicine, First Affiliated Hospital of Xiamen University, China
  • 4 Liver Disease Center, Xiamen Hospital of Traditional Chinese Medicine, Xiamen, 361009, Fujian Province, China; School of Traditional Chinese Medicine, Beijing University of Chinese Medicine, Beijing, China. Electronic address: 13850005898@163.com
  • 5 School of Medicine, Xiamen University, Xiamen, 361102, Fujian Province, China; School of Traditional Chinese Medicine, Xiamen University, Malaysia. Electronic address: adong@xmu.edu.cn
J Therm Biol, 2024 Jan;119:103799.
PMID: 38342042 DOI: 10.1016/j.jtherbio.2024.103799

Abstract

Epidemiological evidence shows that diabetic patients are susceptible to high temperature weather, and brown adipose tissue (BAT) activity is closely related to type 2 diabetes (T2DM). Activation of BAT under cold stress helps improve T2DM. However, the impact of high temperature on the activity of BAT is still unclear. The study aimed to investigate the impact of heat stress on glucose and lipid metabolism in T2DM mice by influencing BAT activity. High-fat feeding and injecting streptozotocin (STZ) induced model of T2DM mice. All mice were randomly divided into three groups: a normal(N) group, a diabetes (DM) group and a heat stress diabetes (DMHS) group. The DMHS group received heat stress intervention for 3 days. Fasting blood glucose, fasting serum insulin and blood lipids were measured in all three groups. The activity of BAT was assessed by using quantitative real-time PCR (qRT-PCR), electron microscopy, and PET CT. Furthermore, the UHPLC-Q-TOF MS technique was employed to perform metabolomics analysis of BAT on both DM group and DMHS group. The results of this study indicated that heat stress aggravated the dysregulation of glucose and lipid metabolism, exacerbated mitochondrial dysfunction in BAT and reduced the activity of BAT in T2DM mice. This may be related to the abnormal accumulation of branched-chain amino acids (BCAAs) in the mitochondria of BAT.

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.