Suppr超能文献

使用选择性激动剂对豚鼠左心房对组胺的张力反应进行进一步表征。

Further characterization of the guinea pig left atrial tension response to histamine by use of selective agonists.

作者信息

Wilson C, Broadley K J

出版信息

Agents Actions. 1981 May;11(3):215-22. doi: 10.1007/BF01967617.

Abstract
  1. The responses of guinea pig left atrial tension and right atrial rate to histamine receptor agonists and histamine were compared. 2. Single doses of histamine and another non-selective agonist, N,N-dimethylhistamine, produced biophasic inotropic responses, with an initial increase in tension and a secondary sustained tension increase separated by a negative inotropic component. 3. Selective H1-receptor agonists -- 2-methylhistamine, 3-methylhistamine and 2-pyridylethylamine (2-PEA) -- also exhibited biphasic inotropic responses. 2-PEA did so only after blockade with propranolol or in atria from reserpine-pretreated animals, indicating an additional release of endogenous catecholamines which masked the biophasic response. 4. Selective H2-receptor agonists -- 4-methylhistamine and dimaprit -- failed to produce biphasic responses except at high concentrations only in the case of 4-methylhistamine. 5. The biophasic responses were converted to monophasic responses by mepyramine. This was a result of antagonism of the initial positive component and the secondary negative component which were therefore mediated via H1-receptors. The production of a biphasic inotropic response therefore depends upon these two components which were exhibited preferentially by the H1-receptor-selective agonists.
摘要
  1. 比较了组胺受体激动剂和组胺对豚鼠左心房张力和右心房心率的反应。2. 组胺单剂量以及另一种非选择性激动剂N,N-二甲基组胺产生双相变力反应,初始张力增加,随后是由负性变力成分分隔的继发性持续张力增加。3. 选择性H1受体激动剂——2-甲基组胺、3-甲基组胺和2-吡啶乙胺(2-PEA)——也表现出双相变力反应。2-PEA仅在普萘洛尔阻断后或在利血平预处理动物的心房中才表现出双相变力反应,表明内源性儿茶酚胺的额外释放掩盖了双相反应。4. 选择性H2受体激动剂——4-甲基组胺和二甲双咪——除了在高浓度时(仅4-甲基组胺的情况)未能产生双相反应。5. 美吡拉敏将双相反应转变为单相反应。这是拮抗初始阳性成分和继发性阴性成分的结果,因此这两种成分是通过H1受体介导的。因此,双相变力反应的产生取决于这两个成分,而这两个成分优先由H1受体选择性激动剂表现出来。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验