Gastrointestinal Peptides as Therapeutic Targets to Mitigate Obesity and Metabolic Syndrome.
Kleopatra AlexiadouTricia Mei-Mei TanPublished in: Current diabetes reports (2020)
Clinical trials have proven that the widely used GLP-1 analogues have pleotropic effects beyond those on weight and glucose metabolism and appear to confer favourable cardiovascular and renal outcomes. However, GLP-1 analogues alone do not deliver sufficient efficacy for the treatment of obesity, being limited by their dose-dependent gastrointestinal side effects. Novel dual agonists for GLP-1/glucagon and GLP-1/GIP are being developed by the pharmaceutical industry and have demonstrated some promising results for weight loss and improvement in glycaemia over and above GLP-1 analogues. Triagonists (for example GLP-1/GIP/glucagon) are currently in pre-clinical or early clinical development. Gastrointestinal hormones possess complementary effects on appetite, energy expenditure, and glucose metabolism. We highlight the idea that combinations of these hormones may represent the way forward in obesity and diabetes therapeutics.
Keyphrases
- weight loss
- metabolic syndrome
- bariatric surgery
- insulin resistance
- type diabetes
- roux en y gastric bypass
- clinical trial
- weight gain
- glycemic control
- gastric bypass
- molecular docking
- high fat diet induced
- cardiovascular disease
- body mass index
- small molecule
- skeletal muscle
- randomized controlled trial
- adipose tissue
- combination therapy
- smoking cessation
- amino acid
- structure activity relationship
- phase iii