Lin L H, Leonard S, Harris R A
Department of Pharmacology, University of Colorado Health Sciences Center, Denver.
Mol Pharmacol. 1993 Jun;43(6):941-8.
Modulation of the inositol 1,4,5-trisphosphate (IP3)-mediated signal transduction pathway by the inhalational anesthetic enflurane was studied in Xenopus oocytes expressing mouse and human cortical mRNA. We found that enflurane significantly inhibited ion currents activated by m1 muscarinic and 5-hydroxytryptamine (5-HT)1c receptors. This inhibition was dependent upon the concentration of acetylcholine or 5-HT, with large inhibition (80-89%) of low concentrations and small inhibition (8-44%) of high concentrations of acetylcholine and 5-HT. Similar effects were found with either mouse or human receptors. To investigate the mechanism of enflurane action, ion currents induced by intracellular injection of guanosine 5'-(3-O-thio)triphosphate and IP3 were examined. Enflurane strongly suppressed the guanosine 5'-(3-O-thio)triphosphate-activated current but not the IP3-activated current. These results suggest that an inhalational anesthetic can disrupt the function of mouse and human brain phosphatidylinositol-linked receptors by selectively inhibiting the guanine nucleotide-binding protein activity.
在表达小鼠和人类皮质mRNA的非洲爪蟾卵母细胞中,研究了吸入性麻醉药恩氟烷对肌醇1,4,5-三磷酸(IP3)介导的信号转导途径的调节作用。我们发现,恩氟烷显著抑制由毒蕈碱m1受体和5-羟色胺(5-HT)1c受体激活的离子电流。这种抑制作用取决于乙酰胆碱或5-HT的浓度,低浓度的乙酰胆碱和5-HT受到较大抑制(80-89%),高浓度的乙酰胆碱和5-HT受到较小抑制(8-44%)。在小鼠或人类受体中均发现了类似的效应。为了研究恩氟烷的作用机制,检测了通过细胞内注射鸟苷5'-(3-O-硫代)三磷酸和IP3诱导的离子电流。恩氟烷强烈抑制鸟苷5'-(3-O-硫代)三磷酸激活的电流,但不抑制IP3激活的电流。这些结果表明,吸入性麻醉药可通过选择性抑制鸟嘌呤核苷酸结合蛋白的活性来破坏小鼠和人类脑磷脂酰肌醇连接受体的功能。