Mechanisms of beta-adrenergic desensitization in rat myometrium.

S R Johansson, R G Andersson
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引用次数: 1

Abstract

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.

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大鼠肌层β -肾上腺素能脱敏的机制。
本研究是为了阐明长期异丙肾上腺素治疗后子宫肌对-肾上腺素能刺激反应性降低的机制。用异丙肾上腺素20 nmol/kg预处理大鼠,每天3次,连续4天,显著降低β激动剂的肌层舒张作用。用(——)-(3H) DHA结合技术测定的肌膜β受体结合能力也明显下降。经异丙肾上腺素预处理的动物,体外刺激后腺苷酸环化酶活性未见明显升高。脱敏大鼠子宫cAMP水平降低。磷酸二酯酶活性升高。因此,减少生产和增加降解有助于降低子宫cAMP含量水平。cAMP依赖性蛋白激酶的活性也受到抑制。在这项工作中,低浓度异丙肾上腺素在体内被施用,几个生化参数已被证明有助于肌组织的β -肾上腺素能脱敏。
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