ROLE OF NITRIC OXIDE METABOLITES WITHIN THE IMPACT OF THE SUB-TOXIC SUCCINAMIDES DOSES ON STATE OF HEMOSTASIS.

I A Palagina, M Y Kudria, O S Lalymenko
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引用次数: 2

Abstract

We investigated the role of changes in the endogenous nitric oxide (NO) metabolism during the influence of succinic acid amides as biotransformation products of an anti-diabetic drug on the state of hemostasis. In experiment with rats, synthetic succinamides were applied in quanti- ties equimolar to the sub-toxic dose of the pharmaceutical substance. We investigated the indicators characterizing the state of platelet and coagulation hemostasis in the blood plasma, the content of the stable NO metabolites and the activity of nitrogen oxide synthase (NOS) in the liver homogenate, blood plasma and urine of rats. We found that sub-chronic succinamides introduction reduced the nitrite and nitrate anions concentration in the blood plasma (by 30-50 and 20-35% resp.), liver (by 16-19 and 14-18%) and urine (by 50-70 and 38-55%). These changes were essentially dependent on the reduction in the NOS activity (by 33%). The studied compounds showed a 1.5 fold increase in the coagulation potential of the blood plasma and cause a 20% boost in the aggregation of thrombocytes. Analysis of the pair correlation coefficients showed positive association of the changes in indicators of the NO metabolism and hemostasis. The obtained results suggest that the registered manifestation of the pro-coagulation and thrombogenic action of succinamides applied in the sub-toxic doses is partially determined by a drop of the vasoactive NO pool that in turn, occurs due to a decline of the NOS activity.

一氧化氮代谢物在亚毒性琥珀胺剂量对止血状态影响中的作用。
我们研究了内源性一氧化氮(NO)代谢变化在琥珀酸酰胺作为一种降糖药的生物转化产物对止血状态的影响过程中的作用。在大鼠实验中,将合成琥珀胺按亚毒性剂量等量施用。研究了大鼠肝脏匀浆、血浆和尿液中表征血小板和凝血止血状态的指标、稳定NO代谢产物的含量和一氧化氮合酶(NOS)的活性。我们发现亚慢性琥珀酰胺的引入降低了血浆(分别降低30- 50%和20-35%)、肝脏(分别降低16- 19%和14-18%)和尿液(分别降低50- 70%和38-55%)中的亚硝酸盐和硝酸盐阴离子浓度。这些变化主要取决于NOS活性的降低(33%)。所研究的化合物表明,血浆的凝血电位增加1.5倍,并导致血栓细胞聚集增加20%。对相关系数的分析显示NO代谢指标的变化与止血呈正相关。所得结果表明,亚毒性剂量琥珀胺的促凝和血栓形成作用的记录表现部分是由血管活性NO池的下降决定的,而这反过来又由于NOS活性的下降而发生。
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