Is the β 3 -Adrenoceptor a Valid Target for the Treatment of Obesity and/or Type 2 Diabetes?
Haneen S DwaibMartin Christian MichelPublished in: Biomolecules (2023)
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.
Keyphrases
- type diabetes
- body weight
- adipose tissue
- insulin resistance
- high fat diet induced
- glycemic control
- metabolic syndrome
- clinical trial
- weight loss
- cardiovascular disease
- public health
- weight gain
- high fat diet
- body mass index
- quality improvement
- adverse drug
- blood glucose
- smoking cessation
- open label
- fatty acid
- replacement therapy
- wound healing