(2019) The potential therapeutic use of renin-angiotensin system inhibitors in the treatment of inflammatory diseases. Journal of Cellular Physiology. pp. 2277-2295. ISSN 0021-9541
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Abstract
Inflammation is a normal part of the immune response to injury or infection but its dysregulation promotes the development of inflammatory diseases, which cause considerable human suffering. Nonsteroidal anti-inflammatory agents are the most commonly prescribed agents for the treatment of inflammatory diseases, but they are accompanied by a broad range of side effects, including gastrointestinal and cardiovascular events. The renin-angiotensin system (RAS) is traditionally known for its role in blood pressure regulation. However, there is increasing evidence that RAS signaling is also involved in the inflammatory response associated with several disease states. Angiotensin II increases blood pressure by binding to angiotensin type 1 (AT(1)) receptor, and direct renin inhibitors, angiotensin-converting enzyme (ACE) inhibitors and AT(1) receptor blockers (ARBs) are clinically used as antihypertensive agents. Recent data suggest that these drugs also have anti-inflammatory effects. Therefore, this review summarizes these recent findings for the efficacy of two of the most widely used antihypertensive drug classes, ACE inhibitors and ARBs, to reduce or treat inflammatory diseases such as atherosclerosis, arthritis, steatohepatitis, colitis, pancreatitis, and nephritis.
Item Type: | Article |
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Keywords: | angiotensin receptor blockers angiotensin-converting enzyme inhibitors inflammatory diseases renin-angiotensin system converting enzyme-inhibitor ii type-1 receptor factor-kappa-b coronary atherosclerosis evaluation coa-reductase inhibition mouse colitis model e-deficient mice nonalcoholic steatohepatitis rat model rheumatoid-arthritis Cell Biology Physiology |
Divisions: | |
Page Range: | pp. 2277-2295 |
Journal or Publication Title: | Journal of Cellular Physiology |
Journal Index: | ISI |
Volume: | 234 |
Number: | 3 |
Identification Number: | https://doi.org/10.1002/jcp.27205 |
ISSN: | 0021-9541 |
Depositing User: | مهندس مهدی شریفی |
URI: | http://eprints.bmsu.ac.ir/id/eprint/2695 |
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