Umeki S, Nozawa Y
Biol Chem Hoppe Seyler. 1986 Jan;367(1):61-5. doi: 10.1515/bchm3.1986.367.1.61.
The effect of local anesthetics on the stearoyl-CoA desaturase activity was studied using Tetrahymena microsomal preparation. Dibucaine, tetracaine, and propranolol, a beta-blocking agent, nonspecifically inhibited the activities of NADPH-ferrihemoprotein reductase as well as of stearoyl-CoA desaturase and the terminal component, but lidocaine and procaine had no effect on these activities. The inhibitory potency was decreased in the order of dibucaine greater than propranolol greater than tetracaine much greater than lidocaine = procaine. According to the double-reciprocal plots of stearoyl-CoA desaturase, the inhibition by dibucaine appeared to be noncompetitive with respect to stearoyl-CoA as substrate. However, the activity of NADH-ferricyanide reductase was not significantly affected by concentrations of propranolol and tetracaine lower than 10mM, but by dibucaine. The terminal component, cyanide-sensitive factor, was most sensitive to local anesthetics among the microsomal electron transport components, suggesting a rate-limiting enzyme.
使用四膜虫微粒体制剂研究了局部麻醉药对硬脂酰辅酶A去饱和酶活性的影响。丁卡因、丁哌卡因和β受体阻滞剂普萘洛尔非特异性地抑制了NADPH-高铁血红蛋白还原酶以及硬脂酰辅酶A去饱和酶和末端成分的活性,但利多卡因和普鲁卡因对这些活性没有影响。抑制效力的降低顺序为:丁卡因>普萘洛尔>丁哌卡因>利多卡因 = 普鲁卡因。根据硬脂酰辅酶A去饱和酶的双倒数图,丁卡因对作为底物的硬脂酰辅酶A的抑制作用似乎是非竞争性的。然而,低于10mM的普萘洛尔和丁哌卡因浓度对NADH-铁氰化物还原酶的活性没有显著影响,但丁卡因有影响。末端成分,即氰化物敏感因子,在微粒体电子传递成分中对局部麻醉药最为敏感,提示它是一种限速酶。