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Effect on atrial natriuretic peptides of chronic treatment with alpha-methyldopa and hydralazine in spontaneously hypertensive rats.

Abstract
The present study was designed to examine the effect of antihypertensive therapy on plasma and atrial concentration of atrial natriuretic peptides (ANP) in spontaneously hypertensive rats (SHR) by using alpha-methyldopa and hydralazine. Methyldopa and hydralazine treatment reduced blood pressure (P less than .05, P less than .05, respectively); however, ventricular weight was reduced by methyldopa (P less than .05) but not by hydralazine. Plasma ANP concentration in untreated SHR was higher than that observed in Wistar-Kyoto rats (WKY). Methyldopa treatment decreased plasma ANP concentration, but hydralazine treatment did not. Moreover, plasma ANP concentration and ventricular weight were positively correlated in untreated and treated SHR. The left atrial ANP concentration in untreated SHR was lower than that observed in WKY. Methyldopa treatment increased left atrial ANP concentration, but hydralazine treatment did not. These results suggest that the ANP release from the left atrium is chronically stimulated in adult SHR, and that a decrease in plasma ANP concentration by methyldopa treatment is, in part, associated with the decline of ANP release from the heart due to the reductions of blood pressure and cardiac hypertrophy.
AuthorsM Kohno, K Yasunari, K Murakawa, K Yokokawa, T Horio, N Kurihara, T Takeda
JournalAmerican journal of hypertension (Am J Hypertens) Vol. 3 Issue 2 Pg. 111-6 (Feb 1990) ISSN: 0895-7061 [Print] United States
PMID2137701 (Publication Type: Comparative Study, Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Hydralazine
  • Methyldopa
  • Atrial Natriuretic Factor
Topics
  • Animals
  • Atrial Natriuretic Factor (blood, metabolism)
  • Blood Pressure (drug effects)
  • Cardiomegaly (drug therapy, pathology)
  • Heart Atria (drug effects, metabolism)
  • Heart Ventricles (drug effects, pathology)
  • Hydralazine (administration & dosage, therapeutic use)
  • Hypertension (drug therapy, metabolism, physiopathology)
  • Male
  • Methyldopa (administration & dosage, therapeutic use)
  • Organ Size (drug effects)
  • Rats
  • Rats, Inbred SHR
  • Rats, Inbred WKY
  • Time Factors

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