Reversible inactivation of endothelial nitric oxide synthase by NG-nitro-L-arginine.

Abstract:

:NG-Methyl-L-arginine (L-NMA) and NG-nitro-L-arginine (L-NNA) inhibited NO-induced cGMP accumulation in porcine aortic endothelial cells with half-maximally effective concentrations of 15 and 3.4 microM, respectively. The effects of both compounds were reversible, but the L-NNA-induced inhibition was only reversed by wash-out in the presence of 1 mM L-arginine. In short-term incubations (45 s) of membrane fractions, L-NMA and L-NNA exhibited similar potencies to inhibit endothelial NO synthase, but L-NNA was markedly more potent than L-NMA after prolonged incubation periods (> or = 3 min) due to induction of a pronounced, reversible enzyme inactivation.

journal_name

FEBS Lett

journal_title

FEBS letters

authors

Mayer B,Schmid M,Klatt P,Schmidt K

doi

10.1016/0014-5793(93)80405-j

subject

Has Abstract

pub_date

1993-10-25 00:00:00

pages

203-6

issue

1-2

eissn

0014-5793

issn

1873-3468

pii

0014-5793(93)80405-J

journal_volume

333

pub_type

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