Omentin roles in physiology and pathophysiology: an up-to-date comprehensive review.
Aida A HusseinNoha A AhmedHader I SakrTarek AtiaOsama M AhmedPublished in: Archives of physiology and biochemistry (2023)
Omentin (intelectin) was first detected in the visceral omental adipose tissue. It has mainly two isoforms, omentin-1 and -2, with isoform-1 being the main form in human blood. It possesses insulin-sensitizing, anti-inflammatory, anti-atherogenic, cardio-protective, and oxidative stress-decreasing effects. Omentin's cardiovascular protective actions are caused by the improved endothelial cell survival and function, increased endothelial nitric oxide synthase (eNOS) and nitric oxide (NO) bioavailability, enhanced vascular smooth muscle cells (VSMCs) relaxation with reduced proliferation, decreased inflammation, and suppressed oxidative stress. Omentin may also have a potential role in different cancer types and rheumatic diseases. Thus, omentin is an excellent therapeutic target in many diseases, including diabetes mellitus (DM), metabolic syndrome (MetS), cardiovascular diseases (CVDs), inflammatory diseases, and cancer. This review demonstrates the physiological functions of omentin in ameliorating insulin resistance (IR), vascular function, and inflammation and its possible share in managing obesity-linked diseases, such as metabolic disorders, DM, and cardiovascular conditions.
Keyphrases
- oxidative stress
- insulin resistance
- nitric oxide synthase
- nitric oxide
- metabolic syndrome
- adipose tissue
- endothelial cells
- vascular smooth muscle cells
- type diabetes
- glycemic control
- papillary thyroid
- high fat diet
- cardiovascular disease
- skeletal muscle
- anti inflammatory
- squamous cell
- diabetic rats
- induced apoptosis
- squamous cell carcinoma
- hydrogen peroxide
- cardiovascular risk factors
- angiotensin ii
- cell proliferation
- single molecule
- coronary artery disease
- weight gain
- childhood cancer
- physical activity
- cardiovascular events