Takayanagi I, Satoh M, Koike K
Department of Chemical Pharmacology, Toho University School of Pharmaceutical Sciences, Chiba, Japan.
Nihon Yakurigaku Zasshi. 1993 Mar;101(3):111-22. doi: 10.1254/fpj.101.3_111.
Smooth muscle tissues were contracted by excitation of each muscle cell. Single cells prepared from guinea pig taenia caecum and trachea were contracted by extracellular application of acetylcholine and/or carbachol, whose concentrations were the same as those in the tissues. The concentration-response curve was shifted in a parallel fashion by competitive antagonists. The pA2-values of the antagonists were in good agreement with those estimated using the intact tissue. The apparent dissociation constants of cholinergic drugs estimated from inhibition of the specific binding of [3H]QNB (quinuclidinyl benzilate) to the single cells by the cholinergic drugs were also in agreement with the values in other membrane preparations. Similar findings were obtained in the single cells, microsomal fractions and isolated tissues from the guinea pig tracheal smooth muscles. In rabbit aortic single cells, the existence of two pharmacologically distinct alpha 1-adrenoceptor subtypes, alpha 1A and alpha 1B, in vascular smooth muscle cells was supported. Furthermore, the amount of prostaglandin F2 alpha released from guinea pig tracheal single cells was increased through activation by alpha 2-adrenoceptor agonists. The amount of prostaglandin F2 alpha released by norepinephrine decreased with age, while the total amount of alpha 2-adrenoceptors and the dissociation constants of the alpha 2-adrenergic drugs from the receptor did not change. The relaxation induced by beta-adrenoceptors did not alter with age. The total amount of beta-adrenoceptor and the dissociation constants of beta-adrenergic drugs from their receptor did not alter with age. An excellent relationship between the potency of isoprenaline and the maximum binding of [3H]dihydroalprenolol estimated in the single cells from 6- to 40-week-old guinea pigs was found, suggesting that the increase in the potency of isoprenaline is due to the increase in the maximum binding. The value in the single cells from 100-week-old guinea pigs deviated significantly from the regression line. This result suggests that the decrease in potency in the single cells from 100-week-old animals is due to a change in post beta-receptor processes in responsiveness. The smooth muscle single cells are useful for the study of drug-receptor interactions. Furthermore, post-receptor processes in responsiveness were discussed.
平滑肌组织通过每个肌细胞的兴奋而收缩。从豚鼠盲肠带和气管制备的单个细胞,在细胞外施加乙酰胆碱和/或卡巴胆碱时会收缩,其浓度与组织中的浓度相同。浓度-反应曲线因竞争性拮抗剂而呈平行移动。拮抗剂的pA2值与使用完整组织估计的值高度一致。从胆碱能药物对[3H]QNB(喹核醇苯甲酸酯)与单个细胞特异性结合的抑制作用估计的胆碱能药物的表观解离常数,也与其他膜制剂中的值一致。在豚鼠气管平滑肌的单个细胞、微粒体部分和分离组织中也获得了类似的结果。在兔主动脉单个细胞中,支持血管平滑肌细胞中存在两种药理学上不同的α1肾上腺素能受体亚型,即α1A和α1B。此外,豚鼠气管单个细胞释放的前列腺素F2α的量通过α2肾上腺素能受体激动剂的激活而增加。去甲肾上腺素释放的前列腺素F2α的量随年龄增长而减少,而α2肾上腺素能受体的总量以及α2肾上腺素能药物与受体的解离常数并未改变。β肾上腺素能受体诱导的舒张作用不随年龄而改变。β肾上腺素能受体的总量以及β肾上腺素能药物与受体的解离常数不随年龄而改变。在6至40周龄豚鼠的单个细胞中发现,异丙肾上腺素的效价与[3H]二氢阿普洛尔的最大结合之间存在良好的关系,这表明异丙肾上腺素效价的增加是由于最大结合的增加。100周龄豚鼠单个细胞中的值明显偏离回归线。该结果表明,100周龄动物单个细胞中效价的降低是由于β受体后反应过程的变化。平滑肌单个细胞对于药物-受体相互作用的研究很有用。此外,还讨论了反应性的受体后过程。