TY - JOUR
T1 - A Synthetic ERR Agonist Alleviates Metabolic Syndrome
AU - Billon, Cyrielle
AU - Schoepke, Emmalie
AU - Avdagic, Amer
AU - Chatterjee, Arindam
AU - Butler, Andrew A.
AU - Elgendy, Bahaa
AU - Walker, John K.
AU - Burris, Thomas P.
N1 - Publisher Copyright:
Copyright © 2024 by The American Society for Pharmacology and Experimental Therapeutics.
PY - 2024/2/1
Y1 - 2024/2/1
N2 - Physical exercise induces physiologic adaptations and is effective at reducing the risk of premature death from all causes. Pharmacological exercise mimetics may be effective in the treatment of a range of diseases including obesity and metabolic syndrome. Previously, we described the development of SLU-PP-332, an agonist for the estrogen-related receptor (ERR)a, b, and c nuclear receptors that activates an acute aerobic exercise program. Here we examine the effects of this exercise mimetic in mouse models of obesity and metabolic syndrome. Diet-induced obese or ob/ob mice were administered SLU-PP-332, and the effects on a range of metabolic parameters were assessed. SLU-PP-332 administration mimics exercise-induced benefits on whole-body metabolism in mice including increased energy expenditure and fatty acid oxidation. These effects were accompanied by decreased fat mass accumulation. Additionally, the ERR agonist effectively reduced obesity and improved insulin sensitivity in models of metabolic syndrome. Pharmacological activation of ERR may be an effective method to treat metabolic syndrome and obesity.
AB - Physical exercise induces physiologic adaptations and is effective at reducing the risk of premature death from all causes. Pharmacological exercise mimetics may be effective in the treatment of a range of diseases including obesity and metabolic syndrome. Previously, we described the development of SLU-PP-332, an agonist for the estrogen-related receptor (ERR)a, b, and c nuclear receptors that activates an acute aerobic exercise program. Here we examine the effects of this exercise mimetic in mouse models of obesity and metabolic syndrome. Diet-induced obese or ob/ob mice were administered SLU-PP-332, and the effects on a range of metabolic parameters were assessed. SLU-PP-332 administration mimics exercise-induced benefits on whole-body metabolism in mice including increased energy expenditure and fatty acid oxidation. These effects were accompanied by decreased fat mass accumulation. Additionally, the ERR agonist effectively reduced obesity and improved insulin sensitivity in models of metabolic syndrome. Pharmacological activation of ERR may be an effective method to treat metabolic syndrome and obesity.
UR - http://www.scopus.com/inward/record.url?scp=85182956628&partnerID=8YFLogxK
U2 - 10.1124/jpet.123.001733
DO - 10.1124/jpet.123.001733
M3 - Article
C2 - 37739806
AN - SCOPUS:85182956628
SN - 0022-3565
VL - 388
SP - 232
EP - 240
JO - Journal of Pharmacology and Experimental Therapeutics
JF - Journal of Pharmacology and Experimental Therapeutics
IS - 2
ER -