Title : Characterization of an inhibitor of nitric oxide synthase in human-hand veins.

Pub. Date : 1994 Feb

PMID : 7515369






7 Functional Relationships(s)
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1 We characterized the potency, efficacy and time course of NG-monomethyl-l-arginine (l-NMMA) as an inhibitor of bradykinin-mediated, endothelium-dependent dilation using the human hand-vein compliance technique. omega-N-Methylarginine kininogen 1 Homo sapiens
2 We characterized the potency, efficacy and time course of NG-monomethyl-l-arginine (l-NMMA) as an inhibitor of bradykinin-mediated, endothelium-dependent dilation using the human hand-vein compliance technique. omega-N-Methylarginine kininogen 1 Homo sapiens
3 We also compared the efficacy of l-NMMA with methylene blue, an inhibitor of guanylate cyclase, in blocking bradykinin-mediated vasodilation. omega-N-Methylarginine kininogen 1 Homo sapiens
4 l-NMMA potently inhibited bradykinin-induced venodilation with a log ED50 of 3.74 +/- 0.52 (geometric mean of 5.5 micrograms/min). omega-N-Methylarginine kininogen 1 Homo sapiens
5 l-NMMA (25 micrograms/min) decreased bradykinin"s maximal venodilatory response from 90 +/- 22% to 39 +/- 15% (p < 0.05). omega-N-Methylarginine kininogen 1 Homo sapiens
6 Complete recovery of bradykinin venodilation was obtained within 155 minutes after stopping l-NMMA infusion, indicating that its effects were reversible. omega-N-Methylarginine kininogen 1 Homo sapiens
7 In another set of experiments we compared the efficacy of methylene blue to l-NMMA; methylene blue decreased bradykinin-mediated venodilatory response to 53 +/- 17%; when l-NMMA was added, the response was further decreased to 32 +/- 9% (p < 0.002). omega-N-Methylarginine kininogen 1 Homo sapiens