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      Carvedilol, a new β-adrenoceptor antagonist and vasodilator antihypertensive drug, inhibits superoxide release from human neutrophils

      , , ,
      European Journal of Pharmacology
      Elsevier BV

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          Abstract

          Carvedilol produced a dose-dependent inhibition of superoxide (O2-) release from human neutrophils (PMNs) (IC50 = 28 microM) and scavenged O2- generated during dihydroxyfumaric acid (DHF) autooxidation (IC50 = 41 microM). Other beta-blockers, such as celiprolol, labetalol and atenolol, or the antioxidant, 'lazaroid', U74500A had no effect on O2- either released from PMNs or generated during DHF autooxidation. Propranolol, at 0.3 mM, inhibited O2- release from PMNs (73%) but failed to scavenge O2- generated from DHF. The novel free radical-scavenging effect of carvedilol may contribute to the cardioprotective activity of the compound.

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          Author and article information

          Journal
          European Journal of Pharmacology
          European Journal of Pharmacology
          Elsevier BV
          00142999
          April 1992
          April 1992
          : 214
          : 2-3
          : 277-280
          Article
          10.1016/0014-2999(92)90130-V
          1355437
          5d7f0e5d-5607-4ea4-bef0-8695b777153d
          © 1992

          https://www.elsevier.com/tdm/userlicense/1.0/

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