Tsumura Research Laboratories, Tsumura & Co., 3586 Yoshiwara, Ami-machi, Inashiki-gun, Ibaraki, 300-1192, Japan.
Cell Mol Neurobiol. 2013 Jan;33(1):129-35. doi: 10.1007/s10571-012-9878-3. Epub 2012 Sep 12.
Effects of seven alkaloids, geissoschizine methyl ether (GM), hirsutine, hirsuteine, rhynchophylline, isorhynchophylline, corynoxeine and isocorynoxeine, in Uncaria hook, a constituent of the kampo medicine yokukansan, on serotonin(7) (5-HT(7)) receptor were investigated using Chinese hamster ovary (CHO) cell membranes and human embryonic kidney 293 (HEK293) cells stably expressing the human recombinant 5-HT(7) receptor. A competitive binding assay using CHO membranes showed that GM (IC(50) = 0.034 μM) more strongly inhibited the binding of the radioligand [(3)H] LSD to 5-HT(7) receptor than the other alkaloids, suggesting that GM is bound to 5-HT(7) receptor. Agonistic/antagonistic effects of GM (1-50 μM) on the receptor were evaluated by measuring intracellular cAMP levels in HEK239 cells. GM (IC(50) = 6.0 μM) inhibited 5-HT-induced cAMP production in a concentration-dependent manner, as well as the specific 5-HT(7) receptor antagonist SB-269970 (0.1-1 μM). However, GM did not induce intracellular cAMP production as 5-HT did. These results suggest that GM has an antagonistic effect on 5-HT(7) receptor.
钩藤中的七种生物碱,包括钩藤碱甲醚(GM)、育亨宾、育亨宾碱、钩藤碱、异钩藤碱、去氢钩藤碱和异去氢钩藤碱,作为汉方药物“和汉方稳心颗粒”的一种成分,对 5-羟色胺(7)(5-HT(7))受体的作用进行了研究。使用中国仓鼠卵巢(CHO)细胞膜和稳定表达人重组 5-HT(7)受体的人胚肾 293(HEK293)细胞进行了研究。使用 CHO 细胞膜的竞争性结合测定表明,GM(IC(50)= 0.034 μM)比其他生物碱更强烈地抑制放射性配体[(3)H] LSD 与 5-HT(7)受体的结合,表明 GM 与 5-HT(7)受体结合。通过测量 HEK239 细胞中的细胞内环磷酸腺苷(cAMP)水平,评估了 GM(1-50 μM)对受体的激动/拮抗作用。GM(IC(50)= 6.0 μM)以浓度依赖的方式抑制 5-HT 诱导的 cAMP 产生,以及 5-HT(7)受体拮抗剂 SB-269970(0.1-1 μM)。然而,GM 不像 5-HT 那样诱导细胞内 cAMP 产生。这些结果表明 GM 对 5-HT(7)受体具有拮抗作用。