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与磷脂酰肌醇代谢偶联的α1肾上腺素能受体和内皮素-1受体的激动剂脱敏

Agonist desensitisation of alpha 1 adrenoceptors and endothelin-1 receptors coupled to phosphatidylinositol metabolism.

作者信息

Hamilton C A, Boyle J J, Huang Y T, McCulloch J, Nixon G F, Pryadarshi S

机构信息

Department of Medicine and Therapeutics, Gardiner Institute, Western Infirmary, Glasgow, UK.

出版信息

Fundam Clin Pharmacol. 1994;8(2):162-72. doi: 10.1111/j.1472-8206.1994.tb00793.x.

Abstract

Agonist desensitisation of responses coupled to phosphatidylinositol metabolism were studied. Responses mediated by two different agonists, endothelin-1 and noradrenaline were investigated. In vivo pressor responses were examined in conscious male New Zealand white rabbits, while effects on inositol phosphate formation were studied in rings of freshly isolated aorta and in cultured aortic vascular smooth muscle cells. No desensitisation of responses to noradrenaline were observed in vivo despite a 10-day infusion under conditions which cause desensitisation of alpha 2 and beta-adrenoceptor mediated responses. In contrast, responses to endothelin-1 were attenuated within 5 min of commencing endothelin-1 infusions. No reduction in noradrenaline stimulated inositol phosphate was observed in cultured vascular smooth muscle cells after pre-incubation with noradrenaline up to 10(-4) M, whereas with endothelin-1 pre-incubation a dose and time-related reduction in endothelin-1 stimulated inositol phosphate formation was observed. Thus, differences in the pattern of desensitisation of both pressor responses and phosphatidylinositol metabolism were observed for noradrenaline and endothelin-1 suggesting that the nature of the 2nd messenger involved in signal transduction is not the only determinant of agonist desensitisation. In addition, differences in the rate of desensitisation and sensitivity to endothelin-1, but not noradrenaline, were observed when responses in cultured cells were compared with in vivo responses or responses to freshly isolated tissues. These differences are discussed in relation to possible modifications of the endothelin receptor or its coupling to phosphatidylinositol metabolism during culture.

摘要

研究了与磷脂酰肌醇代谢偶联的反应的激动剂脱敏作用。研究了由两种不同激动剂内皮素-1和去甲肾上腺素介导的反应。在清醒的雄性新西兰白兔中检测体内升压反应,同时在新鲜分离的主动脉环和培养的主动脉血管平滑肌细胞中研究对肌醇磷酸形成的影响。尽管在导致α2和β肾上腺素能受体介导的反应脱敏的条件下进行了10天的输注,但在体内未观察到对去甲肾上腺素反应的脱敏。相反,在开始输注内皮素-1后5分钟内,对内皮素-1的反应减弱。在培养的血管平滑肌细胞中,用高达10(-4)M的去甲肾上腺素预孵育后,未观察到去甲肾上腺素刺激的肌醇磷酸减少,而用内皮素-1预孵育时,观察到内皮素-1刺激的肌醇磷酸形成呈剂量和时间依赖性减少。因此,观察到去甲肾上腺素和内皮素-1在升压反应和磷脂酰肌醇代谢的脱敏模式上存在差异,这表明参与信号转导的第二信使的性质不是激动剂脱敏的唯一决定因素。此外,当将培养细胞中的反应与体内反应或对新鲜分离组织的反应进行比较时,观察到对内皮素-1而非去甲肾上腺素的脱敏速率和敏感性存在差异。讨论了这些差异与培养过程中内皮素受体或其与磷脂酰肌醇代谢偶联的可能修饰的关系。

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