Van Renterghem C, Renit-Soria J, Stinnakre J
Proc R Soc Lond B Biol Sci. 1985 Jan 22;223(1232):389-402. doi: 10.1098/rspb.1985.0008.
The K+ current induced by isoprenaline acting on beta-adrenergic receptors in Xenopus laevis has been studied in oocytes still surrounded by their follicular cells and inner ovarian epithelium. Forskolin, an adenylate cyclase activator, induced a similar K+ current and when used at subliminal concentration it potentiated the current induced by isoprenaline. Inhibition of phosphodiesterase by methylisobutylxanthine also enhanced the response to isoprenaline. 8-Br-cAMP, a permeant analogue of cAMP also produced a K+ current. Acetylcholine produced a long lasting inhibition of the isoprenaline current. This inhibition was not seen in the presence of atropine. It is concluded that the K+ current induced by the activation of beta-adrenergic receptors in the oocyte is mediated by an intracellular rise of cAMP.
在仍被滤泡细胞和卵巢内层上皮包围的非洲爪蟾卵母细胞中,研究了异丙肾上腺素作用于β - 肾上腺素能受体所诱导的钾离子电流。腺苷酸环化酶激活剂福斯高林可诱导出类似的钾离子电流,当以阈下浓度使用时,它可增强异丙肾上腺素所诱导的电流。甲基异丁基黄嘌呤对磷酸二酯酶的抑制作用也增强了对异丙肾上腺素的反应。环磷酸腺苷(cAMP)的渗透性类似物8 - 溴 - cAMP也可产生钾离子电流。乙酰胆碱对异丙肾上腺素电流产生了持久的抑制作用。在阿托品存在的情况下未观察到这种抑制作用。得出的结论是,卵母细胞中β - 肾上腺素能受体激活所诱导的钾离子电流是由细胞内cAMP升高介导的。