Hisayama T, Takayanagi I
Jpn J Pharmacol. 1986 Jan;40(1):69-82. doi: 10.1254/jjp.40.69.
The properties and mechanisms of Ca release induced by thymol from the intracellular Ca-store in the guinea-pig taenia caecum were investigated and compared with those by carbachol, using an intact muscle and a microsomal fraction. In Ca, Na-free, EGTA-containing K-solution, a transient contraction was evoked by each drug, and carbachol produced the contraction following treatment with thymol; however, a reversed sequence did not. The efflux of preloaded 45Ca in the presence and absence of ATP from taenia microsomes was accelerated by increasing concentrations of Ca ions outside. The minimal concentration to stimulate 45Ca-efflux was below 0.2 microM in both cases, and the Km values for Ca ions in the presence and absence of ATP were estimated to be 0.65 microM and 2.0 microM Ca ions, respectively. Thymol, which has been reported to be one of the most potent stimulators of the Ca-induced Ca release in the sarcoplasmic reticulum of skeletal muscle, enhanced the 45Ca-efflux from the taenia microsomes in the presence of ATP dose-dependently, and its mode of action seemed bimodal. That is, at 0.5 mM, thymol lowered the concentration of Ca ions which are needed to induce stimulation of 45Ca-efflux, whereas, at 1 mM, the stimulative effect of thymol on 45Ca-efflux was to augment the maximum rate of 45Ca-efflux, independent of concentrations of Ca ions. Carbachol (1 mM) did not have an effect on 45Ca-efflux with or without 0.1 mM GTP. In conclusion, the possibility has been suggested that in the guinea-pig taenia caecum, carbachol might release stored Ca ions via unknown pathway(s), whereas thymol directly releases Ca ions in a ATP-regulated fashion. Further, carbachol would be more efficacious for releasing stored Ca ions. Notwithstanding, the Ca-stores and/or the Ca-releasing mechanisms, which are utilized by both thymol and carbachol, seemed to share a common part(s) to some degree.
利用完整肌肉和微粒体部分,研究了百里香酚从豚鼠盲肠带细胞内钙库诱导钙释放的特性和机制,并与卡巴胆碱的相关特性和机制进行了比较。在不含钙、钠且含有乙二醇双(2-氨基乙基醚)四乙酸(EGTA)的钾溶液中,每种药物均引发短暂收缩,且卡巴胆碱在百里香酚处理后产生收缩;然而,顺序相反的情况则不会发生。通过增加微粒体外钙离子浓度,可加速豚鼠盲肠带微粒体在有或无三磷酸腺苷(ATP)存在时预加载的45钙的流出。两种情况下,刺激45钙流出的最小浓度均低于0.2微摩尔,且在有和无ATP存在时钙离子的米氏常数(Km值)分别估计为0.65微摩尔和2.0微摩尔钙离子。据报道,百里香酚是骨骼肌肌浆网中钙诱导钙释放最有效的刺激剂之一,在有ATP存在时,它剂量依赖性地增强了豚鼠盲肠带微粒体的45钙流出,其作用方式似乎是双峰的。也就是说,在0.5毫摩尔时,百里香酚降低了诱导刺激45钙流出所需的钙离子浓度,而在1毫摩尔时,百里香酚对45钙流出的刺激作用是增加45钙流出的最大速率,与钙离子浓度无关。卡巴胆碱(1毫摩尔)在有或无0.1毫摩尔鸟苷三磷酸(GTP)时对45钙流出均无影响。总之,有人提出,在豚鼠盲肠带中,卡巴胆碱可能通过未知途径释放储存的钙离子,而百里香酚则以ATP调节的方式直接释放钙离子。此外,卡巴胆碱在释放储存的钙离子方面可能更有效。尽管如此,百里香酚和卡巴胆碱所利用的钙库和/或钙释放机制似乎在一定程度上有共同之处。