Adipocyte function and the development of cardiometabolic disease. (21st October 2021)
- Record Type:
- Journal Article
- Title:
- Adipocyte function and the development of cardiometabolic disease. (21st October 2021)
- Main Title:
- Adipocyte function and the development of cardiometabolic disease
- Authors:
- Giroud, Maude
Jodeleit, Henrika
Prentice, Kacey J.
Bartelt, Alexander - Abstract:
- Abstract: Obesity is a medical disorder caused by multiple mechanisms of dysregulated energy balance. A major consequence of obesity is an increased risk to develop diabetes, diabetic complications and cardiovascular disease. While a better understanding of the molecular mechanisms linking obesity, insulin resistance and cardiovascular disease is needed, translational research of the human pathology is hampered by the available cellular and rodent model systems. Major barriers are the species‐specific differences in energy balance, vascular biology and adipose tissue physiology, especially related to white and brown adipocytes, and adipose tissue browning. In rodents, non‐shivering thermogenesis is responsible for a large part of energy expenditure, but humans possess much less thermogenic fat, which means temperature is an important variable in translational research. Mouse models with predisposition to dyslipidaemia housed at thermoneutrality and fed a high‐fat diet more closely reflect human physiology. Also, adipocytes play a key role in the endocrine regulation of cardiovascular function. Adipocytes secrete a variety of hormones, lipid mediators and other metabolites that directly influence the local microenvironment as well as distant tissues. This is specifically apparent in perivascular depots, where adipocytes modulate vascular function and inflammation. Altogether, these mechanisms highlight the critical role of adipocytes in the development of cardiometabolicAbstract: Obesity is a medical disorder caused by multiple mechanisms of dysregulated energy balance. A major consequence of obesity is an increased risk to develop diabetes, diabetic complications and cardiovascular disease. While a better understanding of the molecular mechanisms linking obesity, insulin resistance and cardiovascular disease is needed, translational research of the human pathology is hampered by the available cellular and rodent model systems. Major barriers are the species‐specific differences in energy balance, vascular biology and adipose tissue physiology, especially related to white and brown adipocytes, and adipose tissue browning. In rodents, non‐shivering thermogenesis is responsible for a large part of energy expenditure, but humans possess much less thermogenic fat, which means temperature is an important variable in translational research. Mouse models with predisposition to dyslipidaemia housed at thermoneutrality and fed a high‐fat diet more closely reflect human physiology. Also, adipocytes play a key role in the endocrine regulation of cardiovascular function. Adipocytes secrete a variety of hormones, lipid mediators and other metabolites that directly influence the local microenvironment as well as distant tissues. This is specifically apparent in perivascular depots, where adipocytes modulate vascular function and inflammation. Altogether, these mechanisms highlight the critical role of adipocytes in the development of cardiometabolic disease. Abstract : Abstract figure legend While cardiometabolic health is associated with adipose tissue browning and beneficial adipokine profiles, obesity leads to adipose tissue whitening, inflammation and atherosclerosis. … (more)
- Is Part Of:
- Journal of physiology. Volume 600:Number 5(2022)
- Journal:
- Journal of physiology
- Issue:
- Volume 600:Number 5(2022)
- Issue Display:
- Volume 600, Issue 5 (2022)
- Year:
- 2022
- Volume:
- 600
- Issue:
- 5
- Issue Sort Value:
- 2022-0600-0005-0000
- Page Start:
- 1189
- Page End:
- 1208
- Publication Date:
- 2021-10-21
- Subjects:
- adipocyte -- cardiovascular disease -- lipids -- obesity -- thermogenesis
Physiology -- Periodicals
612.005 - Journal URLs:
- http://jp.physoc.org/ ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1113/JP281979 ↗
- Languages:
- English
- ISSNs:
- 0022-3751
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5039.000000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 21828.xml