Literature DB >> 22527353

The kinin system in hypertensive pathophysiology.

Jagdish N Sharma1.   

Abstract

Cardiovascular diseases are the prime cause of death in the world. The kallikrein-kinin system has been implicated in the pathophysiology of the vascular smooth muscle and cardiac dysfunctions. In recent years, numerous observations obtained from clinical and experimental models of diabetes, hypertension, cardiac failure, ischemia, myocardial infarction and left ventricular hypertrophy, have suggested that the reduced activity of the local kallikrein-kinin system may be instrumental for the induction of cardiovascular-related diseases. The cardioprotective actions of the angiotensin-converting enzyme inhibitors are primarily dependent on protecting the kinin-forming components, which may cause regression of the left ventricular hypertrophy in hypertensive situations. The ability of kallikrein gene delivery to produce a wide spectrum of beneficial effects makes it an excellent candidate in treating hypertension, cardiovascular and renal diseases. In addition, stable kinin agonists may also be available in the future as therapeutic agents for cardiovascular and renal disorders.

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Year:  2012        PMID: 22527353     DOI: 10.1007/s10787-012-0137-5

Source DB:  PubMed          Journal:  Inflammopharmacology        ISSN: 0925-4692            Impact factor:   4.473


  90 in total

1.  Relation between urinary kallikrein and renal function, hypertension, and excretion of sodium and water in man.

Authors:  A Adetuyibi; I H Mills
Journal:  Lancet       Date:  1972-07-29       Impact factor: 79.321

2.  Altered urinary kallikrein excretion in rats with hypertension.

Authors:  H S Margolius; R Geller; W De Jong; J J Pisano; A Sjoerdsma
Journal:  Circ Res       Date:  1972-03       Impact factor: 17.367

3.  Altered plasma kininogen in clinical hypertension.

Authors:  J N Sharma; I J Zeitlin
Journal:  Lancet       Date:  1981-06-06       Impact factor: 79.321

4.  Decreased exercise tolerance and hypertension in severe hereditary deficiency of plasma kininogens.

Authors:  F W James; V H Donaldson
Journal:  Lancet       Date:  1981-04-18       Impact factor: 79.321

5.  The renal kallikrein-kinin system and sodium excretion.

Authors:  I H Mills
Journal:  Q J Exp Physiol       Date:  1982-07

6.  Bradykinin stimulates the production of cyclic GMP via activation of B2 kinin receptors in cultured porcine aortic endothelial cells.

Authors:  V B Schini; C Boulanger; D Regoli; P M Vanhoutte
Journal:  J Pharmacol Exp Ther       Date:  1990-02       Impact factor: 4.030

7.  Effect of captopril on urinary kallikrein, blood pressure and myocardial hypertrophy in diabetic spontaneously hypertensive rats.

Authors:  Jagdish N Sharma; Uma Kesavarao
Journal:  Pharmacology       Date:  2002-04       Impact factor: 2.547

Review 8.  Pathogenic responses of bradykinin system in chronic inflammatory rheumatoid disease.

Authors:  J N Sharma; W W Buchanan
Journal:  Exp Toxicol Pathol       Date:  1994-12

9.  Cardiac kallikrein in hypertensive and normotensive rats with and without diabetes.

Authors:  J N Sharma; U Kesavarao
Journal:  Immunopharmacology       Date:  1996-06

10.  Cardiac regression and blood pressure control in the Dahl rat treated with either enalapril maleate (MK 421, an angiotensin converting enzyme inhibitor) or hydrochlorothiazide.

Authors:  J N Sharma; P G Fernandez; B K Kim; H Idikio; C R Triggle
Journal:  J Hypertens       Date:  1983-10       Impact factor: 4.844

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