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组胺受体的纯化(VI)。一种改进的“双重保护”双标记方法。

Purification of histamine receptor (VI). An improved double labeling method with "double protection".

作者信息

Uchida M

出版信息

Jpn J Pharmacol. 1977 Dec;27(6):781-9. doi: 10.1254/jjp.27.781.

Abstract

Studies were done on the specific labeling of the histaminergic H1-receptor of the longitudinal smooth muscle of cat small intestine. A procedure involving 'double protection' combined with the double labeling technique was developed. The first protection was the usual with a protective antihistamine, promethazine, and the second was cross protection of non-specific sites with non-hitaminergic drugs, thioriazine and atropine. Muscle tissue protected with promethazine against non-radioactive dibenamine was treated with 3H-dibenamine in the presence of these second protectors. The second protectors covered non-receptor sites which had been protected from non-radioactive dibenamine with promethazine. The dose-response curves were carefully checked in each experiment to confirm that the second protectors did not interfere with the specific coverage provided by the first protector. Finally 14C-dibenamine was applied to measure non-specific binding after which the labeled muscles were fractionated and the radioactivity was counted. The specificity of labeling achieved in the receptor-rich fraction by this method is discussed.

摘要

对猫小肠纵行平滑肌组胺能H1受体的特异性标记进行了研究。开发了一种结合“双重保护”与双重标记技术的方法。第一种保护是使用常用的保护性抗组胺药异丙嗪,第二种保护是用非组胺能药物硫利达嗪和阿托品对非特异性位点进行交叉保护。用异丙嗪保护的肌肉组织免受非放射性地布卡因的影响,在这些第二种保护剂存在的情况下用3H-地布卡因处理。第二种保护剂覆盖了已用异丙嗪保护免受非放射性地布卡因影响的非受体位点。在每个实验中仔细检查剂量反应曲线,以确认第二种保护剂不会干扰第一种保护剂提供的特异性覆盖。最后应用14C-地布卡因测量非特异性结合,之后将标记的肌肉分级并计数放射性。讨论了通过该方法在富含受体的部分中实现的标记特异性。

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