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The discovery and biological effects of apelin, a new vasodilator substance and a member of the renin-angiotensin system. Apelin interacts with its receptor apj and has various functions including lowering blood pressure, regulating heart and blood vessel contraction, insulin secretion, and pituitary hormone release. The imbalance between apelin and angiotensin ii may contribute to hypertension and heart diseases such as heart failure, coronary heart disease, and atrial fibrillation. Apelin is also expressed in obesity and related diseases, and can inhibit the release of vasopressin, affecting kidney disease.
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Apelin Signaling Pathway
There are many substances that relax blood vessels in the body, such as NO, prostacyclin, vasoactive intestinal peptide, etc. Recently, another vasodilator substance, Apelin, has been discovered. In 1993, Carroll et al. discovered a protein similar in structure to angiotensin II type 1 receptor, named angiotensin type 1 receptor-associated protein, also known as APJ, which belongs to the G-protein coupled family. In 1998, Tatemoto et al. extracted the APJ endogenous ligand named Apelin from bovine gastric secretion, which is a new adipocytokine and forms an Apelin/APJ system with APJ. Apelin is homologous to angiotensin II (AngII) and is a new member of the renin-angiotensin system (RAS). Apelin has many biological effects such as lowering blood pressure, regulating heart and blood vessel contraction, insulin secretion, pituitary hormone release, and humoral balance.
The Apelin/APJ system together with AngII-AT1 antagonism maintains blood pressure homeostasis, and the imbalance between the two may be an important factor in the development of hypertension. Recently, studies have found that Apelin may be associated with heart diseases such as heart failure, coronary heart disease, atrial fibrillation, and as a new adipokine, Apelin is expressed in obesity with insulin resistance, regulation of fatty insulin axis and obesity-related diseases (such as hypertension, type 2 diabetes, etc.). In addition, Apelin can also inhibit the release of vasopressin, which has a diuretic effect, and has a certain relationship with kidney disease.
Apelin family
Carroll et al. found that Apelin mRNA was expressed in the mammary gland, lung, cardiovascular, brain, kidney, testis, ovary and skeletal muscle of rats, and expressed in the breast and lung, vascular endothelium, adipose tissue and gastric parietal cells. In humans, Apelin is mainly expressed in vascular endothelial cells of heart, kidney and lung, and is less expressed in cardiomyocytes, lung, kidney, adrenal secretory cells, vascular smooth muscle cells, adipose tissue, and nerve cells. The human apelin gene is located on chromosome Xq25-26 and consists of three exons and two introns.
https://www.creative-diagnostics.com/apelin-signaling-pathway.htm