Obesity

Obesity is an excessive accumulation of adipose tissue (body fat) which negatively impacts general health. A sedentary lifestyle and excessive calorie consumption are the most direct causes of obesity. However, polymorphisms in genes that influence appetite and metabolism are also believed to increase the risk of obesity. Long term obesity has been associated with the development of many diseases, including cardiovascular disorders, type-2 diabetes, liver disease, osteoarthritis, and thrombosis. R&D Systems offers a range of quality products to study the biological processes underlying obesity, including control of appetite, lipid and cholesterol metabolism, fatty acid transport, and other aspects of adipose tissue biology.

Key Obesity Research Targets 

5-HT1 Receptors 

5-HT2 Receptors

5-HT4 Receptors

5-HT5 Receptors

5-HT6 Receptors

5-HT7 Receptors

5-HT Transporters (SERT)

Adiponectin and Receptors

Adrenergic α Receptors 

Adrenergic β Receptor

Adrenergic Transporters (NET)

AMPK (AMP-activated Protein Kinases)

Apelin Receptors

Apolipoproteins

BDNF and Receptor

Bombesin Receptors 

C1qTNF

Calcitonin and Related Receptors

Cholecystokinin Receptors (CCK)

 

Fatty Acid Binding Proteins (FABPs)

Fatty Acid Transport Proteins (FATPs)

Free Fatty Acid Receptors 

FGF 

Galanin Receptors 

Ghrelin, Obestatin, and Receptors

Glucagon and Related Receptors

GPBA Receptors

IL-6 and Receptors

IL-11 and Receptor

Insulin and Insulin-like Receptors

Leptin and Receptor

Leukemia Inhibitory Factor (LIF) and Receptor

Lipases

 

Lipoprotein Receptors and Associated Proteins

Lipins (Phosphatidate Phosphatase)

Melanin-Concentrating Hormone (MCH) Receptors

Melanocortin (MC) Receptors 

Melatonin (MT) Receptors 

Neuropeptide FF/AF Receptors

Neuropeptide Y (NPY) and Receptors

Neurotensin Receptors 

NUAKs

Oncostatin M and Receptor

Opioid Receptors

Orexin Receptors 

Purinergic (P2Y) Receptors

Peroxisome Proliferator-Activated Receptors (PPARs)

SREBP

Stearoyl-CoA 9-Desaturase

Tachykinin Receptors

 

 

 

Background Information

 

Causes of Obesity

The most common cause of obesity is a combination of low energy expenditure and high caloric intake. Environmental factors play a role in some cases and numerous susceptibility genes have been identified, including agouti-related peptide (AgRP) 199G - A polymorphism, FTO, NPC1, leptin, leptin receptors (Ob-R), and prohormone convertase-1. Certain psychiatric illnesses are associated with obesity, as are some genetic syndromes including Prader-Wili syndrome and MOMO syndrome. In addition, obesity can be secondary to other conditions such as hypothyroidism, Cushing's syndrome and growth hormone deficiency.

Many endogenous peptides effect appetite and hence have an influence on energy intake. Peripheral hormones effecting appetite include ghrelin, adiponectin, leptin, insulin, peptide YY (3-36), pancreatic polypeptide, glucagon-like peptide 1 (GLP-1), oxyntomodulin, amylin, cholecystokinin and bombesin. Other peptides act centrally to control appetite and these include neuropeptide Y, AgRP, melanocortin, orexin, galanin, α-melanocyte-stimulating hormone (α-MSH), cocaine and amphetamine-related transcript (CART) and neurotensin (NT).

Therapeutics

Treatment for obesity is focused on decreasing caloric intake and increasing energy expenditure. However, pharmacological interventions are available and include orlistat, which inhibits pancreatic lipase to prevent uptake of fat from the diet, but has only a modest effect on weight. More recently launched, the GLP-1 agonist semaglutide and the dual GIP/GLP-1 receptor agonist tirzepatide have shown proved more efficacious for managing weight loss. 

The prevalence and economic burden resulting from obesity, means that novel pharmacological treatments are needed. Many are focusing on inhibiting the effects of orexigenic peptides and agonizing the effects of anorexigenic peptides to reduce appetite and subsequently reduce food intake. Current interest is focused on ghrelin receptor antagonists, peptide YY (3-36), amylin analogs and orexin 1 receptor (OX1) antagonists.