Negrescu E V, Sazonova L N, Baldenkov G N, Mukharliamov N M, Mazaev A V, Tkachuk V A
Cardiology Research Center, Moscow, U.S.S.R.
Int J Cardiol. 1990 Feb;26(2):175-84. doi: 10.1016/0167-5273(90)90031-y.
Nitroglycerin, isosorbide dinitrate and sodium nitroprusside, like nifedipine, were found to inhibit the receptor-provoked increase of cytosolic free calcium concentration in human platelets loaded with 2-[(2-amino-5-methylphenoxy)methyl]-6-methoxy-8-aminoquinoline-N,N,N',N' - tetraacetate. Sodium nitroprusside and nitroglycerin induced elevation of cyclic guanosine 3',5'-monophosphate content in platelets which correlated with their calcium-blocking activity. Methylene blue and epinephrine decreased the calcium-blocking effect and the influence of nitroglycerin on cyclic guanosine 3'-5'-monophosphate content, but failed to suppress the inhibitory effect of sodium nitroprusside. Ascorbic acid increased the calcium blocking effect of sodium nitroprusside and its influence on cyclic guanosine 3'-5'-monophosphate content, but did not alter the inhibitory effect of nitroglycerin. In order to evaluate the relationship between the mode of action of nitrates at cellular level and their vasodilatory effectiveness, we studied the circulatory response of the forearm to isosorbide dinitrate and the influence of nitroglycerin on free calcium concentration in the platelets in 10 patients with chronic heart failure. We established a significant positive correlation between the basal values for venous tone and its peak decrease after administration of the 10-mg dose of isosorbide dinitrate. A correlation was also found between the deviation of maximal decrease of venous tone by this dose of isosorbide dinitrate from the regression line (the relationship between the basal venous tone and its lowering by the drug) and mean inhibitory concentration values for nitroglycerin in blocking that proportion of the rise of calcium ion concentration in platelets due to blocking of the platelet-activating factor. Thus, nitrates, like calcium antagonists, inhibit the receptor-provoked calcium supply to the contractile system of the cells so neutralizing the effects of increased concentrations of vasoconstrictors. This suggests that the effectiveness of nitrates appears to be positively related to the contribution of receptor-induced increase of cytosolic free calcium concentration in vasoconstriction together with their capacity to raise cyclic guanosine 3',5'-monophosphate.
硝酸甘油、二硝酸异山梨酯和硝普钠,与硝苯地平一样,被发现可抑制用2-[(2-氨基-5-甲基苯氧基)甲基]-6-甲氧基-8-氨基喹啉-N,N,N',N'-四乙酸负载的人血小板中受体引发的细胞内游离钙浓度升高。硝普钠和硝酸甘油可诱导血小板中环鸟苷酸3',5'-单磷酸含量升高,这与其钙阻断活性相关。亚甲蓝和肾上腺素可降低钙阻断作用以及硝酸甘油对环鸟苷酸3'-5'-单磷酸含量的影响,但未能抑制硝普钠的抑制作用。抗坏血酸可增强硝普钠的钙阻断作用及其对环鸟苷酸3'-5'-单磷酸含量的影响,但未改变硝酸甘油的抑制作用。为了评估硝酸盐在细胞水平的作用方式与其血管舒张效果之间的关系,我们研究了10例慢性心力衰竭患者前臂对二硝酸异山梨酯的循环反应以及硝酸甘油对血小板中游离钙浓度的影响。我们发现静脉张力的基础值与其在给予10 mg剂量二硝酸异山梨酯后的峰值下降之间存在显著正相关。还发现该剂量二硝酸异山梨酯引起的静脉张力最大下降值与回归线(基础静脉张力与其药物降低值之间的关系)的偏差与硝酸甘油在阻断血小板活化因子引起的血小板钙离子浓度升高比例方面的平均抑制浓度值之间存在相关性。因此,硝酸盐与钙拮抗剂一样,抑制受体引发的钙向细胞收缩系统的供应,从而抵消血管收缩剂浓度升高的影响。这表明硝酸盐的有效性似乎与受体诱导的细胞内游离钙浓度升高在血管收缩中的作用以及它们提高环鸟苷酸3',5'-单磷酸的能力呈正相关。