» Articles » PMID: 7935859

Contribution by Bradykinin to the Natriuretic Response to the Angiotensin Converting Enzyme Inhibitor Ramiprilat in Spontaneously Hypertensive Rats

Overview
Specialty Pharmacology
Date 1994 Jul 1
PMID 7935859
Citations 2
Authors
Affiliations
Soon will be listed here.
Abstract

It is well documented that angiotensin converting enzyme inhibitors decrease blood pressure, which is associated with natriuresis in humans and certain animal models of hypertension. However, it is not clear whether these beneficial effects are due solely to blockade of angiotensin-II production and/or also involves any contribution by kinins. The present study was performed in Inactin (5-ethyl-5-(1-methylpropyl)-2-thio-barbiturate sodium)-anesthetized spontaneously hypertensive rats aged 10-13 wks to examine the relative influence of the angiotensin receptor antagonist losartan (2-n-butyl-4-chloro-5-hydroxymethyl-1- [(2'-(1H-tetrazol-5-yl)biphenyl-4-yl)methyl] imidazole potassium salt) and the bradykinin receptor 2 antagonist HOE 140 (D-Arg-[Hyp3, Thi5, D-Tic7, Oic8] bradykinin) on renal and hemodynamic responses to the angiotensin converting enzyme inhibitor ramiprilat. We found that ramiprilat (1 mg/kg, i.v.) caused sustained reduction in mean blood pressure, marked increases in urine output and urinary sodium excretion without alteration in glomerular filtration rate. In a separate group of animals, it was found that losartan (1 mg/kg, i.v.) decreased blood pressure to a similar degree as ramiprilat and the magnitude of blood pressure fall seen following the combined administration of ramiprilat and losartan was similar to that caused by either compound alone. However, the increase in urinary sodium excretion seen following losartan administration was significantly smaller than that following ramiprilat or ramiprilat plus losartan.(ABSTRACT TRUNCATED AT 250 WORDS)

Citing Articles

Ramipril-induced decrease in renal lithium excretion in the rat.

Barthelmebs M, Grima M, IMBS J Br J Pharmacol. 1995; 116(4):2161-5.

PMID: 8564243 PMC: 1908975. DOI: 10.1111/j.1476-5381.1995.tb15048.x.


Potentiation by enalaprilat of fenoldopam-evoked natriuresis is due to blockade of intrarenal production of angiotensin-II in rats.

Chen C, Lokhandwala M Naunyn Schmiedebergs Arch Pharmacol. 1995; 352(2):194-200.

PMID: 7477443 DOI: 10.1007/BF00176774.

References
1.
Wong P, PRICE Jr W, Chiu A, Carini D, Duncia J, Johnson A . Nonpeptide angiotensin II receptor antagonists. Studies with EXP9270 and DuP 753. Hypertension. 1990; 15(6 Pt 2):823-34. DOI: 10.1161/01.hyp.15.6.823. View

2.
Clappison B, Anderson W, Johnston C . Role of the kallikrein-kinin system in the renal effects of angiotensin-converting enzyme inhibition in anaesthetized dogs. Clin Exp Pharmacol Physiol. 1981; 8(5):509-13. DOI: 10.1111/j.1440-1681.1981.tb00758.x. View

3.
Levens N, Peach M, Carey R . Role of the intrarenal renin-angiotensin system in the control of renal function. Circ Res. 1981; 48(2):157-67. DOI: 10.1161/01.res.48.2.157. View

4.
Fenoy F, Scicli G, Carretero O, Roman R . Effect of an angiotensin II and a kinin receptor antagonist on the renal hemodynamic response to captopril. Hypertension. 1991; 17(6 Pt 2):1038-44. DOI: 10.1161/01.hyp.17.6.1038. View

5.
Tomita K, Pisano J . Binding of [3H]bradykinin in isolated nephron segments of the rabbit. Am J Physiol. 1984; 246(5 Pt 2):F732-7. DOI: 10.1152/ajprenal.1984.246.5.F732. View