학술논문

YC-1-like potentiation of NO-dependent activation of soluble guanylate cyclase by derivatives of protoporphyrin IX.
Document Type
Article
Source
Biochemistry (00062979). Mar2006, Vol. 71 Issue 3, p340-344. 5p. 1 Diagram, 2 Charts.
Subject
*PORPHYRINS
*MACROCYCLIC compounds
*BIOLOGICAL pigments
*NITROUS oxide
*GUANYLATE cyclase
*BLOOD platelets
Language
ISSN
0006-2979
Abstract
The influence of protoporphyrin IX derivatives—2,4-di(1-methoxyethyl)-deuteroporphyrin IX disodium salt (dimegin) and hematoporphyrin IX (HP)—on the activation of human platelet soluble guanylate cyclase by sodium nitroprusside was investigated. Dimegin and HP, like 1-benzyl-3-(hydroxymethyl-2-furyl)indazole (YC-1), produce synergistic effects on the activation of soluble guanylate cyclase by sodium nitroprusside. The synergistic activation of the enzyme by the combination of 10 µM sodium nitroprusside and 5 µM dimegin (or 5 µM HP) was 190 ± 19 and 134 ± 10%, respectively. The synergistic activation of guanylate cyclase by 3 µM YC-1 and 10 µM sodium nitroprusside was 255 ± 19%. Dimegin and HP had no effect on the activation of guanylate cyclase by YC-1; they did not change the synergistic effect of YC-1 (3 µM) and sodium nitroprusside (10 µM) on guanylate cyclase activity. The synergistic activation of NO-stimulated guanylate cyclase activity by dimegin and HP represents a new biochemical effect of these compounds that may have important pharmacotherapeutic and physiological significance. [ABSTRACT FROM AUTHOR]