| First Author | Brede M | Year | 2001 |
| Journal | Regul Pept | Volume | 96 |
| Issue | 3 | Pages | 125-32 |
| PubMed ID | 11111018 | Mgi Jnum | J:83542 |
| Mgi Id | MGI:2662620 | Doi | 10.1016/s0167-0115(00)00168-3 |
| Citation | Brede M, et al. (2001) Transgenic mouse models of angiotensin receptor subtype function in the cardiovascular system. Regul Pept 96(3):125-32 |
| abstractText | Angiotensin II mediates is biological actions via different subtypes of G protein-coupled receptors, termed AT(1) and AT(2) receptors. In rodents, two AT(1) receptors have been identified, AT(1A) and AT(1B), whereas in humans a single AT(1) receptor exists. Recently, a number of transgenic animal models have been generated which overexpress or lack functional angiotensin II receptor subtypes. This review focuses on the physiological significance of angiotensin II receptor subtype diversity in the cardiovascular system. In the mouse, AT(1A) receptors are the major regulators of cardiovascular homeostasis by determining vascular tone and natriuresis. In addition, AT(1A) receptors mediate growth-stimulating signals in vascular and cardiac myocytes. AT(1B) receptors participate in blood pressure regulation, and their functions become apparent when the AT(1A) receptor gene is deleted. Deletion of the mouse gene for the AT(2) receptor subtype led to hypersensitivity to pressor and antinatriuretic effects of angiotensin II in vivo, suggesting that the AT(2) receptor subtype counteracts some of the biological effects of AT(1) receptor signalling. |
