Kamitani T
Eur J Pharmacol. 1984 Apr 20;100(2):145-54. doi: 10.1016/0014-2999(84)90216-4.
The mechanism of nitroglycerin-induced vasodilation was examined in isolated arteries. Nitroglycerin relaxed the large coronary artery preferentially whereas nitroprusside and the so-called non-specific vasodilators showed the same activities on both the large and small coronary arteries. Nitroglycerin-induced vasodilation but not the vasodilation induced by the other agents was antagonized markedly by pretreatment with CuSO4. Other metal ions except Fe2+ had no antagonizing effect. The Cu2+-induced antagonism was restored by treatment with sulfhydryl reagents. Nitroglycerin formed inorganic nitrite by non-enzymatic reaction with the tissue sulfhydryl groups; the reaction was also inhibited by Cu2+ . Cu2+ suppressed the membrane stabilizing effect of Ca2+. It seems that nitroglycerin reacts with the sulfhydryl groups on the inner surface of the cell membrane, which may take part in the selectivity of this drug, and subsequently the intermediate(s) formed may activate guanylate cyclase.
在离体动脉中研究了硝酸甘油诱导血管舒张的机制。硝酸甘油优先使大冠状动脉舒张,而硝普钠和所谓的非特异性血管舒张剂对大、小冠状动脉表现出相同的活性。硫酸铜预处理可显著拮抗硝酸甘油诱导的血管舒张,但不拮抗其他药物诱导的血管舒张。除Fe2+外,其他金属离子无拮抗作用。用巯基试剂处理可恢复Cu2+诱导的拮抗作用。硝酸甘油通过与组织巯基的非酶反应形成无机亚硝酸盐;该反应也受Cu2+抑制。Cu2+抑制Ca2+的膜稳定作用。似乎硝酸甘油与细胞膜内表面的巯基反应,这可能参与了该药物的选择性,随后形成的中间体可能激活鸟苷酸环化酶。