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Is the β 3 -Adrenoceptor a Valid Target for the Treatment of Obesity and/or Type 2 Diabetes?

ORCID
0000-0002-2514-2617
Affiliation
Department of Clinical Nutrition and Dietetics, Palestine Ahliya University, Bethlehem P.O. Box 1041, Palestine;
Dwaib, Haneen S.;
ORCID
0000-0003-4161-8467
Affiliation
Department of Pharmacology, University Medical Center, Johannes Gutenberg University, Langenbeckstr. 1, 55131 Mainz, Germany
Michel, Martin C.

β 3 -Adrenoceptors mediate several functions in rodents that could be beneficial for the treatment of obesity and type 2 diabetes. This includes promotion of insulin release from the pancreas, cellular glucose uptake, lipolysis, and thermogenesis in brown adipose tissue. In combination, they lead to a reduction of body weight in several rodent models including ob/ob mice and Zucker diabetic fatty rats. These findings stimulated drug development programs in various pharmaceutical companies, and at least nine β 3 -adrenoceptor agonists have been tested in clinical trials. However, all of these projects were discontinued due to the lack of clinically relevant changes in body weight. Following a concise historical account of discoveries leading to such drug development programs we discuss species differences that explain why β 3 -adrenoceptors are not a meaningful drug target for the treatment of obesity and type 2 diabetes in humans.

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