Mayer B, Brunner F, Schmidt K
Institute für Pharmakologie und Toxikologie Karl-Franzens-Universität Graz, Austria.
Eur Heart J. 1993 Nov;14 Suppl I:22-6.
Methylene blue has been frequently used as an inhibitor of soluble guanylyl cyclase. We found that endothelium-dependent relaxations of isolated blood vessels were considerably more sensitive to inhibition by methylene blue than relaxation induced by direct activators of soluble guanylyl cyclase. Similar data were obtained in the presence of superoxide dismutase, indicating that the diverse potencies of methylene blue were not due to superoxide-induced inactivation of nitric oxide (NO). Subsequent experiments revealed that methylene blue is an inhibitor of purified NO synthase. Conversion of L-arginine to L-citrulline was inhibited by the dye in a concentration-dependent fashion with half-maximal effects observed at 5.3 microM and 9.2 microM in the absence and presence of superoxide dismutase, respectively. Purified soluble guanylyl cyclase, however, was far less sensitive to methylene blue. When the enzyme was maximally stimulated with S-nitroso-glutathione, cyclic guanosine monophosphate, (cGMP) formation was reduced by 50% at approximately 60 microM methylene blue; 1 mM produced maximal inhibitions of about 70%. Our data indicate that methylene blue is only a poor inhibitor of soluble guanylyl cyclase. The dye seems to act primarily via inhibition of NO synthase, with enzyme-bound heme being a possible target in its inhibitory action.
亚甲蓝一直被频繁用作可溶性鸟苷酸环化酶的抑制剂。我们发现,与可溶性鸟苷酸环化酶直接激活剂所诱导的舒张相比,亚甲蓝对离体血管内皮依赖性舒张的抑制作用更为显著。在超氧化物歧化酶存在的情况下也获得了类似的数据,这表明亚甲蓝的不同效力并非源于超氧化物诱导的一氧化氮(NO)失活。后续实验表明,亚甲蓝是纯化的一氧化氮合酶的抑制剂。该染料以浓度依赖性方式抑制L-精氨酸向L-瓜氨酸的转化,在不存在和存在超氧化物歧化酶的情况下,半最大效应分别在5.3 microM和9.2 microM时观察到。然而,纯化的可溶性鸟苷酸环化酶对亚甲蓝的敏感性要低得多。当用S-亚硝基谷胱甘肽最大程度刺激该酶时,在约60 microM亚甲蓝时,环磷酸鸟苷(cGMP)生成减少50%;1 mM时产生约70%的最大抑制作用。我们的数据表明,亚甲蓝只是可溶性鸟苷酸环化酶的一种低效抑制剂。该染料似乎主要通过抑制一氧化氮合酶起作用,酶结合的血红素可能是其抑制作用的靶点。