4
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: not found
      • Article: not found

      Losartan: First of a New Class of Angiotensin Antagonists for the Management of Hypertension

      ,
      The Journal of Clinical Pharmacology
      Wiley

      Read this article at

      ScienceOpenPublisher
      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Related collections

          Most cited references21

          • Record: found
          • Abstract: not found
          • Article: not found

          Niere und Kreislauf1

            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            Drug concentration response relationships in normal volunteers after oral administration of losartan, an angiotensin II receptor antagonist.

            The aim of this study was to investigate the relationships between plasma concentrations of losartan, an orally active angiotensin II inhibitor, its active metabolite EXP3174, and angiotensin II blockade. Six healthy subjects received single oral doses of 40, 80, or 120 mg losartan and placebo at 1-week intervals in a crossover study. Angiotensin II blockade was assessed by the blood pressure response to exogenous angiotensin II before and after losartan administration. EXP3174 reached higher plasma concentrations and was eliminated more slowly than its parent compound; its levels paralleled the profile of angiotensin II blockade closer than losartan. Inhibition of the pressure response was dose dependent. The Hill-shaped relationship between response and EXP3174 concentration (or time-integrated variables) approached a plateau with 80 mg. The dose-dependent increase in plasma renin and angiotensin II exhibited a considerable individual scatter. We conclude that losartan produces a dose-dependent, effective angiotensin II blockade that is largely determined by the active metabolite EXP3174.
              Bookmark
              • Record: found
              • Abstract: found
              • Article: not found

              Oral administration of DuP 753, a specific angiotensin II receptor antagonist, to normal male volunteers. Inhibition of pressor response to exogenous angiotensin I and II.

              The purpose of the present study was to assess the inhibitory effect of DuP 753, an orally active angiotensin II receptor antagonist, on the pressor action of exogenous angiotensin I and II in healthy male volunteers.
                Bookmark

                Author and article information

                Journal
                The Journal of Clinical Pharmacology
                Wiley
                00912700
                January 1996
                January 1996
                March 08 2013
                : 36
                : 1
                : 3-12
                Article
                10.1002/j.1552-4604.1996.tb04146.x
                528979eb-97e2-44b5-9e15-5f94f5f2fa9a
                © 2013

                http://doi.wiley.com/10.1002/tdm_license_1.1

                History

                Comments

                Comment on this article