Related Experiment Video
Updated: May 31, 2026

Measuring the Rate of Lipolysis in Ex Vivo Murine Adipose Tissue and Primary Preadipocytes Differentiated In Vitro
Published on: March 17, 2023
Inflammation inhibits GPR81 expression in adipose tissue
Kenneth R Feingold1, Arthur Moser, Judy K Shigenaga
1Metabolism Section (111F), Department of Veterans Affairs Medical Center, University of California San Francisco, 4150 Clement Street, San Francisco, CA 94121, USA. kenneth.feingold@ucsf.edu
Inflammation significantly reduces G protein-coupled receptor 81 (GPR81) expression in mouse adipose tissue. This finding is relevant for understanding metabolic disorders and inflammation.
Area of Science:
- Metabolic research
- Inflammation studies
- Adipose tissue biology
Background:
- G protein-coupled receptor 81 (GPR81) is activated by lactate, inhibiting lipolysis.
- Understanding GPR81 regulation in adipose tissue is crucial for metabolic health.
Purpose of the Study:
- To investigate the impact of inflammatory stimuli on GPR81 expression in mouse adipose tissue.
- To explore the relationship between inflammation and GPR81 levels in metabolic conditions.
Main Methods:
- Mice were treated with inflammatory agents like lipopolysaccharide (LPS), zymosan, or turpentine.
- GPR81 mRNA levels were quantified using real-time PCR.
- In vitro studies involved treating 3T3-L1 adipocytes with cytokines.
Main Results:
- LPS, zymosan, and turpentine treatments decreased GPR81 mRNA levels in mouse adipose tissue.
- No significant change in GPR81 expression was observed in adipocytes treated with cytokines.
- GPR81 expression was reduced in ob/ob mice, a model for type 2 diabetes with inflammation.
Conclusions:
- Inflammatory conditions lead to a decrease in GPR81 expression within adipose tissue.
- These findings suggest a link between inflammation, GPR81 regulation, and metabolic dysfunction.
More Related Videos
Related Concept Videos
GPCRs Regulate Adenylyl Cylase Activity
Two...
TGF - β Signaling Pathway
Inflammation
GPCR Desensitization
Glucagon-like Receptor Agonists
GLP-1, when administered in high doses intravenously, triggers insulin secretion, inhibits glucagon release, slows gastric emptying, reduces food intake, and restores normal insulin secretion. However, its rapid inactivation by the...
Regulation of Food Intake

