Abstract: Derivatives of 3,4-dihydro-1,2-diazete 1,2-dioxides (DD) have been investigated as NO donors in vitro and in vivo. Using nitronylnitroxides as spin traps for NO, these compounds were shown to decompose in water solutions al physiological pH and temperature, producing two molecules of NO per one DD molecule. Rate constants of DD decomposition were found to be in the range from 10(-8) to 6.5x10(-7) c(-1) in water and between 3x10(-7) and 1.6x10(-5) c(-1) in dimethylsulfoxide. In vitro experiments performed with perfused rat tail artery showed that some of DD derivatives are highly effective vasodilators in concentrations from 5 to 80 CIM while standard NO donor 3-(4-morpholino)-sydnonimine, SIN-1, does not lead to arterial vasodilatation in these concentrations. Significant (up to 30%) decrease of systolic arterial blood pressure was observed in hereditary hypertensive rats (ISIAH-strain) when some of DD were injected intraperitoneally in doses 40-200 mu g/kg b.w., while the same effect of trinitroglycerin, TNG, was found at much higher dose equal to 900 mu g/kg b.w. (C) 1995 Academic Press. Inc.

Cite: Utepbergenov D.I. , Khramtsov V.V. , Vlassenko L.P. , Markel A.L. , Mazhukin D.G. , Tikhonov A.Y. , Volodarsky L.B.
KINETICS OF NITRIC-OXIDE LIBERATION BY 3,4-DIHYDRO-1,2-DIAZETE 1,2-DIOXIDES AND THEIR VASODILATORY PROPERTIES IN-VITRO AND IN-VIVO
Biochemical and Biophysical Research Communications. 1995. V.214. N3. P.1023-1032. DOI: 10.1006/bbrc.1995.2388 WOS Scopus РИНЦ

Dates:

Published print:

Sep 1, 1995

Identifiers:

Web of science	WOS:A1995RW55600039
Scopus	2-s2.0-0028860517
Elibrary	31176916
OpenAlex	W2002469686

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