Johansson S R, Andersson R G
Acta Pharmacol Toxicol (Copenh). 1981 Oct;49(4):241-7. doi: 10.1111/j.1600-0773.1981.tb00901.x.
This study was performed in order to elucidate the mechanism behind the decreased responsiveness to beta-adrenergic stimulation occurring in uterine muscle after prolonged treatment with isoprenaline. Pretreatment of rats with isoprenaline, 20 nmol/kg, three times daily during four days, significantly decreased the myometrial relaxing effect of the beta-agonist. There was also a significant decrease of the beta-receptor binding capacity of the myometrial membranes measured by the (--)-(3H) DHA binding technique. In the animals pretreated with isoprenaline no significant increase of the adenylate cyclase activity could be observed after isoprenaline stimulation in vitro. The uterine cAMP level was diminished in the desensitized rats. The phosphodiesterase activity was increased. Thus both decreased production and increased degradation contribute to the lower level of uterine cAMP content. The activity of cAMP dependent protein kinase was also depressed. In this work, where low concentrations of isoprenaline have been administered in vivo, several biochemical parameters have been shown to contribute to the beta-adrenergic desensitization in myometrial tissue.
进行本研究是为了阐明长时间用异丙肾上腺素治疗后子宫肌对β-肾上腺素能刺激反应性降低背后的机制。用20 nmol/kg异丙肾上腺素对大鼠进行预处理,每天3次,持续4天,可显著降低β-激动剂对子宫肌的舒张作用。用(--)-(3H)DHA结合技术测定的子宫肌膜β-受体结合能力也显著降低。在用异丙肾上腺素预处理的动物中,体外给予异丙肾上腺素刺激后,未观察到腺苷酸环化酶活性有显著增加。脱敏大鼠的子宫cAMP水平降低。磷酸二酯酶活性增加。因此,生成减少和降解增加都导致子宫cAMP含量水平降低。cAMP依赖性蛋白激酶的活性也受到抑制。在本研究中,体内给予低浓度异丙肾上腺素后,已表明有几个生化参数导致子宫肌组织中的β-肾上腺素能脱敏。