Yeates R A, Schmid M, Leitold M
Department of Pharmacology, Pfizer/Mack Ltd, Illertissen, Federal Republic of Germany.
Biochem Pharmacol. 1989 Jun 1;38(11):1749-53. doi: 10.1016/0006-2952(89)90408-5.
The in vitro spasmolytic activity of glycerol trinitrate was measured on the KCl-contraction of aorta strips from the rabbit. In the presence of sulphobromophthalein, a known inhibitor of glutathione S-transferase, the dose-activity curve for the nitrate was displaced to the right. Much smaller displacements were obtained with the control spasmolytic substances--papaverine and S-nitroso-N-acetylpenicillamine. It was confirmed that sulphobromophthalein inhibits glutathione S-transferase activity in aorta homogenates. Aorta extracts did not detectably catalyze the reaction between glutathione and sulphobromophthalein and the glutathione level was not decreased by treating the intact aorta with sulphobromophthalein. It is concluded that sulphobromophthalein acts as a specific antagonist of the spasmolytic activity of glycerol trinitrate, probably as a result of its inhibition of glutathione S-transferase. It thus seems probable that glutathione and glutathione S-transferase are involved in the pharmacological activation of the organic nitrates.
在兔主动脉条氯化钾收缩实验中测定了硝酸甘油的体外解痉活性。在存在已知的谷胱甘肽S-转移酶抑制剂磺溴酞的情况下,硝酸盐的剂量-活性曲线向右移动。对照解痉物质罂粟碱和S-亚硝基-N-乙酰青霉胺的位移则小得多。已证实磺溴酞可抑制主动脉匀浆中的谷胱甘肽S-转移酶活性。主动脉提取物未检测到对谷胱甘肽和磺溴酞之间反应的催化作用,且用磺溴酞处理完整主动脉后谷胱甘肽水平未降低。得出的结论是,磺溴酞作为硝酸甘油解痉活性的特异性拮抗剂起作用,可能是由于其对谷胱甘肽S-转移酶的抑制作用。因此,谷胱甘肽和谷胱甘肽S-转移酶似乎参与了有机硝酸盐的药理活化过程。