Effect of angiotensin II blockade on cardiac hypertrophy and remodelling: a review
- PMID: 8583480
Effect of angiotensin II blockade on cardiac hypertrophy and remodelling: a review
Abstract
Activation of the renin-angiotensin system both systemically and locally seems to be of importance for cardiovascular hypertrophy and remodelling. The octapeptide angiotensin II definitively plays a central role. In the reversal, for example, of left ventricular hypertrophy, so far the most important independent risk factor for an adverse outcome, blocking of the renin-angiotensin system with ACE inhibition has been shown to be particularly effective. In cardiac tissue, however, ACE inhibition has been suggested to inhibit only a fraction of angiotensin II formed, indicating that other enzymatic pathways can be of importance. From a theoretical point of view a more complete blockade of the angiotensin II type 1 receptor would offer a more effective attenuation of the unfavourable effect of angiotensin II. Experimentally, losartan, a novel selective angiotensin II receptor type 1 antagonist has been shown to decrease cardiac hypertrophic response in models of both hypertension and volume cardiac hypertrophy as well as reverse hypertrophy in spontaneously hypertensive rats. TCV-116, another selective angiotensin II antagonist, also effectively reverses cardiac hypertophy and interstitial fibrosis in the rat. The only report so far regarding the effect of angiotensin II blockade on cardiac hypertrophy in essential hypertension suggests a more favourable short-term effect on cardiac hypertrophy for the same blood pressure reduction with losartan compared with atenolol in a small population of mild to moderate hypertensives. In the perspective of the well-established positive effects of ACE inhibition on the remodelling process in the remaining viable myocardium after myocardial infarction, involving myocyte hypertrophy, interstitial fibrosis and progressive dilatation, it is reassuring that angiotensin II blockade has been shown to perform equally well as ACE inhibition after experimental coronary ligation. In summary, the development of cardiovascular hypertrophy in hypertension is a serious prognostic indicator and selective angiotensin II blockade is a new anti-hypertensive treatment modality with promising properties, especially for prevention and reversal of cardiac hypertrophy including pathological fibrosis and cardiac remodelling after myocardial infarction. Thus, taking into account the shortcomings of today's anti-hypertensive treatment to achieve normalisation of excessive cardiovascular morbidity and mortality, as well as the seemingly great importance of the renin-angiotensin system for hypertension-induced functional and structural abnormalities, a therapy based on a specific All antagonist could offer obvious advantages in a high risk hypertensive patient with cardiovascular hypertrophy. This hypothesis will be investigated in a large prospective trial (Losartan Intervention For End-point reduction in hypertension: The LIFE Study).
Similar articles
-
The future role of losartan.J Hum Hypertens. 1995 Nov;9 Suppl 5:S55-8. J Hum Hypertens. 1995. PMID: 8583483 Review.
-
Discovery of losartan, the first angiotensin II receptor antagonist.J Hum Hypertens. 1995 Nov;9 Suppl 5:S3-18. J Hum Hypertens. 1995. PMID: 8583479 Review.
-
The Losartan Intervention For Endpoint reduction (LIFE) in Hypertension study: rationale, design, and methods. The LIFE Study Group.Am J Hypertens. 1997 Jul;10(7 Pt 1):705-13. Am J Hypertens. 1997. PMID: 9234823 Clinical Trial.
-
[Losartan and the LIFE-study. Antihypertensive treatment with AT1-receptor antagonist].Tidsskr Nor Laegeforen. 1996 Feb 10;116(4):504-7. Tidsskr Nor Laegeforen. 1996. PMID: 8644056 Review. Norwegian.
-
The diversified pharmacology of angiotensin II-receptor blockade.Blood Press Suppl. 1996;2:53-61. Blood Press Suppl. 1996. PMID: 8913541 Review.
Cited by
-
Effect of telmisartan on the regression of the left ventricular hypertrophy in the patients of essential hypertension.J Clin Diagn Res. 2013 Jul;7(7):1352-5. doi: 10.7860/JCDR/2013/5416.3127. Epub 2013 Jul 1. J Clin Diagn Res. 2013. PMID: 23998064 Free PMC article.
-
Clinical pharmacokinetics of vasodilators. Part I.Clin Pharmacokinet. 1998 Jun;34(6):457-82. doi: 10.2165/00003088-199834060-00003. Clin Pharmacokinet. 1998. PMID: 9646008 Review.
-
Valsartan. A review of its pharmacology and therapeutic use in essential hypertension.Drugs. 1997 Aug;54(2):299-311. doi: 10.2165/00003495-199754020-00009. Drugs. 1997. PMID: 9257084 Review.
-
The Effects of Hydroalchoholic Extract of Teucrium polium L. on Hypertension Induced by Angiotensin II in Rats.Int J Prev Med. 2014 Oct;5(10):1255-60. Int J Prev Med. 2014. PMID: 25400883 Free PMC article.
-
Decreased fetal cardiac output in pregnant women with severe SARS-Cov-2 infection.Echocardiography. 2022 Jun;39(6):803-810. doi: 10.1111/echo.15367. Epub 2022 May 20. Echocardiography. 2022. PMID: 35596234 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Medical
Miscellaneous