Literature DB >> 11561228

Angiotensin II type 1 receptor blockade with 80 and 160 mg valsartan in healthy, normotensive subjects.

F Latif1, S Tandon, R Obeleniene, S R Hankins, M S Berlowitz, P V Ennezat, T H Le Jemtel.   

Abstract

BACKGROUND: An 80-mg dose once or twice daily is the dose of valsartan frequently administered for treatment of hypertension. The target dose selected for the Val-HeFT trial in patients with chronic heart failure is 160 mg twice daily. The level and time course of angiotensin II type 1 (AT(1))-receptor blockade achieved by 160 mg valsartan have not been reported. METHODS AND
RESULTS: Seven normotensive healthy subjects were assigned in random order to receive a single dose of placebo, 80 mg valsartan, and 160 mg valsartan at 7- to 10-day intervals. AT(1)-receptor blockade level (%) was determined by the pressure response to administration of exogenous angiotensin II. The pressure response to angiotensin II was measured at baseline and 2, 6, 12, and 24 hours after oral administration of placebo, 80 mg valsartan, and 160 mg valsartan. Eighty and 160 mg valsartan resulted in a significant and similar level of AT(1)-receptor blockade at 2 and 6 hours compared with placebo. The 160-mg dose resulted in a significantly greater level of AT(1)-receptor blockade than 80 mg at 12 and 24 hours.
CONCLUSIONS: During the first 6 hours after oral administration of 80 and 160 mg valsartan the level of AT(1)-receptor blockade is similar. However, only 160 mg valsartan provides sustained AT(1)-receptor blockade over 24 hours.

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Year:  2001        PMID: 11561228     DOI: 10.1054/jcaf.2001.26242

Source DB:  PubMed          Journal:  J Card Fail        ISSN: 1071-9164            Impact factor:   5.712


  6 in total

1.  Comparison of once-daily versus twice-daily dosing of valsartan in patients with chronic stable heart failure.

Authors:  Inder S Anand; Anita Deswal; Dean J Kereiakes; Das Purkayastha; Dion H Zappe
Journal:  Vasc Health Risk Manag       Date:  2010-08-09

Review 2.  Valsartan/hydrochlorothiazide: a review of its pharmacology, therapeutic efficacy and place in the management of hypertension.

Authors:  Keri Wellington; Diana M Faulds
Journal:  Drugs       Date:  2002       Impact factor: 9.546

Review 3.  Clinical impact of renin-angiotensin system blockade: angiotensin-converting enzyme inhibitors vs. angiotensin receptor antagonists.

Authors:  Joseph L Izzo; Marvin Moser
Journal:  J Clin Hypertens (Greenwich)       Date:  2002 Nov-Dec       Impact factor: 3.738

4.  Non-equilibrium atmospheric pressure plasma assisted degradation of the pharmaceutical drug valsartan: influence of catalyst and degradation environment.

Authors:  A Raji; K Navaneetha Pandiyaraj; D Vasu; M C Ramkumar; R R Deshmukh; V Kandavelu
Journal:  RSC Adv       Date:  2020-09-29       Impact factor: 4.036

5.  Valsartan Dosage on Ventriculo-Vascular Coupling Index Dose-Dependency in Heart Failure Patients.

Authors:  Kyung Jin Ahn; Jongwook Yu; Albert Youngwoo Jang; Dae Hyeok Kim; Jun Kwan; Wook Jin Chung
Journal:  Yonsei Med J       Date:  2021-05       Impact factor: 2.759

6.  Randomized study to compare valsartan +/- HCTZ versus amlodipine +/- HCTZ strategies to maximize blood pressure control.

Authors:  Dion Zappe; Cheraz Cherif Papst; Philippe Ferber
Journal:  Vasc Health Risk Manag       Date:  2009-11-02
  6 in total

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