Urotensin-II receptor

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Urotensin-II receptor (UTR) is a G protein-coupled receptor that binds the peptide Urotensin II. This receptor is involved in a variety of physiological and pathological processes, making it a significant subject of research in the fields of cardiovascular disease, renal disease, and metabolic disorders. The Urotensin-II receptor is encoded by the gene UTS2R.

Structure[edit | edit source]

The Urotensin-II receptor is a member of the G protein-coupled receptor (GPCR) family, which is characterized by seven transmembrane domains. These receptors are known for their role in transducing extracellular signals through membrane activation. The UTR specifically binds to its ligand, Urotensin II, a cyclic peptide, which leads to a series of intracellular responses involving G proteins and downstream signaling pathways.

Function[edit | edit source]

The primary function of the Urotensin-II receptor is to mediate the effects of Urotensin II, which include vasoconstriction and vasodilation, depending on the vascular bed. This dual action makes it a potent regulator of blood pressure and blood flow. Additionally, UTR has been implicated in the pathogenesis of several diseases, including heart failure, hypertension, and diabetic nephropathy, due to its role in modulating vascular tone and promoting fibrosis.

Clinical Significance[edit | edit source]

Given its involvement in critical physiological processes, the Urotensin-II receptor has been studied as a potential therapeutic target for cardiovascular and renal diseases. Antagonists of the UTR have been explored for their therapeutic potential in treating conditions such as hypertension and heart failure. However, the development of drugs targeting the UTR has been challenging due to the complexity of its signaling pathways and the need for selective and potent inhibitors.

Research[edit | edit source]

Research on the Urotensin-II receptor has focused on understanding its signaling mechanisms, its role in disease, and the development of receptor antagonists as potential therapeutic agents. Studies have shown that blocking the UTR can lead to reduced blood pressure in animal models, suggesting a promising approach for treating hypertension. Additionally, research into the receptor's structure has provided insights into how it interacts with its ligand, Urotensin II, which is crucial for designing effective drugs.

Conclusion[edit | edit source]

The Urotensin-II receptor plays a critical role in cardiovascular and renal physiology and pathology. Its complex signaling mechanisms and involvement in various diseases make it an important target for research and drug development. Continued studies on the UTR are essential for understanding its function and for the development of new therapeutic strategies for treating cardiovascular and renal diseases.


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Contributors: Prab R. Tumpati, MD