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鸡胚心脏中一个胚胎期的钙动员毒蕈碱系统。

An embryonic Ca++ mobilizing muscarinic system in the chick embryo heart.

作者信息

Oettling G, Schmidt H, Drews U

机构信息

Institute of Anatomy, University of Tübingen, Federal Republic of Germany.

出版信息

J Dev Physiol. 1989 Aug;12(2):85-94.

PMID:2576029
Abstract

In the embryonic and in the adult heart muscarinic stimulation reduces the heart rate. Here we demonstrate that in the embryonic heart an additional muscarinic system is present, which is characterized by Ca++ mobilization and corresponds to the embryonic muscarinic system in other organ anlagen. In suspensions of embryonic chick heart cells we measured release of Ca++ from intracellular stores and influx of extracellular Ca++ with fura-2 and chlorotetracycline after muscarinic stimulation and determined the [3H]quinuclidinylbenzilate binding sites. We observed intense Ca++ mobilization at day 4, weaker reactions between day 4.5 and 11, and no Ca++ response at day 13. The pharmacological profile was identical to the profile of Ca++ mobilization in cells from other embryonic tissues in which the general embryonic muscarinic system is expressed. In parallel, we studied the effect of muscarinic agonists and antagonists on the heart rate of isolated embryonic hearts at day 4 and 5 in a perfusion chamber. Oxotremorine and bethanechol being antagonists or weak partial agonists in Ca++ mobilization, behaved as full agonists in frequency regulation. Thus, the pharmacological profile of the transient embryonic muscarinic system was different from that of the definitive adult form.

摘要

在胚胎期和成体心脏中,毒蕈碱刺激可降低心率。在此我们证明,胚胎心脏中存在一种额外的毒蕈碱系统,其特征为钙离子动员,且与其他器官原基中的胚胎毒蕈碱系统相对应。在胚胎鸡心脏细胞悬液中,我们在毒蕈碱刺激后,用fura - 2和氯四环素测量了细胞内储存钙离子的释放以及细胞外钙离子的内流,并测定了[3H]喹核酯苄酯结合位点。我们观察到在第4天有强烈的钙离子动员,在第4.5天至第11天反应较弱,而在第13天没有钙离子反应。药理学特征与表达一般胚胎毒蕈碱系统的其他胚胎组织细胞中的钙离子动员特征相同。同时,我们在灌注室中研究了毒蕈碱激动剂和拮抗剂对第4天和第5天分离的胚胎心脏心率的影响。氧震颤素和氨甲酰甲胆碱在钙离子动员中为拮抗剂或弱部分激动剂,但在频率调节中表现为完全激动剂。因此,短暂的胚胎毒蕈碱系统的药理学特征与确定的成体形式不同。

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