KINETICS OF NITRIC-OXIDE LIBERATION BY 3,4-DIHYDRO-1,2-DIAZETE 1,2-DIOXIDES AND THEIR VASODILATORY PROPERTIES IN-VITRO AND IN-VIVO

Derivatives of 3,4-dihydro-1,2-diazete 1,2-dioxides (DD) have been inv estigated 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 molecule s of NO per one DD molecule. Rate constants of DD decomposition were f ound to be in the range from 10(-8) to 6.5x10(-7) c(-1) in water and b etween 3x10(-7) and 1.6x10(-5) c(-1) in dimethylsulfoxide. In vitro ex periments performed with perfused rat tail artery showed that some of DD derivatives are highly effective vasodilators in concentrations fro m 5 to 80 CIM while standard NO donor 3-(4-morpholino)-sydnonimine, SI N-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., wh ile 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.