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高血压大鼠离体心肌细胞中的自主受体相互作用

Autonomic receptor interactions in isolated cardiac myocytes from hypertensive rats.

作者信息

Grammas P, Dereski M O, Diglio C, Giacomelli F, Wiener J

机构信息

Department of Pathology, Wayne State University, School of Medicine, Detroit, MI 48201.

出版信息

J Mol Cell Cardiol. 1989 Aug;21(8):807-15. doi: 10.1016/0022-2828(89)90720-7.

Abstract

Isolated ventricular myocytes from adult (16 to 20 weeks) spontaneously hypertensive (SHR) and normotensive (WKY) rats were utilized to examine adrenergic and cholinergic receptor expression and interaction. Binding assays were performed using quinuclidinyl benzilate (QNB) and iodocyanopindolol (ICYP) for cholinergic and beta-adrenergic receptors, respectively. In addition, cAMP was measured as an index of adrenergic-cholinergic control of adenylate cyclase. Data from radioligand binding experiments indicated that muscarinic cholinergic receptors were depressed (22%) in SHR myocytes, while beta-adrenergic receptor density was comparable to that of WKY myocytes. Heterologous receptor modulation in isolated myocytes as assessed by displacement analysis with and without guanosine 5'-triphosphate (GTP), showed that carbachol displacement of QNB was shifted five fold to the right in the presence of GTP and that the beta-adrenergic agonist isoproterenol did not prevent the GTP-mediated binding alteration. In contrast, carbachol modulated the GTP-shift of ICYP displacement by isoproterenol and these effects were comparable in both WKY and SHR myocytes. Furthermore, the ability of carbachol to blunt the stimulation of adenylate cyclase by isoproterenol was also comparable in myocytes isolated from adult SHR and control animals. Thus, the observed decrement in muscarinic cholinergic receptor expression did not alter adrenergic-cholinergic interactions as assessed by displacement assays using guanine nucleotides, or the control of cAMP levels. In addition, isolated myocytes provide a useful system for analyzing receptor expression and regulation and how these parameters may be altered in the hypertensive heart.

摘要

利用成年(16至20周)自发性高血压(SHR)大鼠和正常血压(WKY)大鼠的离体心室肌细胞,研究肾上腺素能和胆碱能受体的表达及相互作用。分别使用喹核醇基苯甲酸酯(QNB)和碘氰吲哚洛尔(ICYP)进行胆碱能和β - 肾上腺素能受体的结合测定。此外,测定环磷酸腺苷(cAMP)作为肾上腺素能 - 胆碱能对腺苷酸环化酶控制的指标。放射性配体结合实验数据表明,SHR肌细胞中的毒蕈碱胆碱能受体减少(22%),而β - 肾上腺素能受体密度与WKY肌细胞相当。通过有无鸟苷5'-三磷酸(GTP)的置换分析评估离体肌细胞中的异源受体调节,结果显示,在存在GTP的情况下,卡巴胆碱对QNB的置换向右移动了五倍,并且β - 肾上腺素能激动剂异丙肾上腺素并未阻止GTP介导的结合改变。相反,卡巴胆碱调节了异丙肾上腺素对ICYP置换的GTP位移,并且这些效应在WKY和SHR肌细胞中相当。此外,卡巴胆碱抑制异丙肾上腺素对腺苷酸环化酶刺激的能力在成年SHR和对照动物分离的肌细胞中也相当。因此,观察到的毒蕈碱胆碱能受体表达的减少并未改变通过使用鸟嘌呤核苷酸的置换测定评估的肾上腺素能 - 胆碱能相互作用,也未改变cAMP水平的控制。此外,离体肌细胞为分析受体表达和调节以及这些参数在高血压心脏中如何改变提供了一个有用的系统。

相似文献

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