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在有和没有双嘧达莫存在的情况下,腺嘌呤核苷酸和腺苷对豚鼠结肠带的抑制作用比较。

Comparison of the inhibitory effects on the guinea-pig taenia coli of adenine nucleotides and adenosine in the presence and absence of dipyridamole.

作者信息

Satchell D G, Burnstock G

出版信息

Eur J Pharmacol. 1975 Jun-Jul;32(02):324-8. doi: 10.1016/0014-2999(75)90299-x.

Abstract

Dipyridamole potentiated the inhibitory responses to ATP and ADP and in particular responses to AMP and adenosine. The results are discussed in relation to the known actions of dipyridamole and suggest that adenine nucleotides are metabolized to adenosine during contact with the preparation; and that previous observations of the relative potencies of adenine nucleotides and nucleosides do not represent the actual receptor agonist potencies because of rapid uptake of adenosine into the tissues.

摘要

双嘧达莫增强了对ATP和ADP的抑制反应,尤其是对AMP和腺苷的反应。结合双嘧达莫的已知作用对结果进行了讨论,结果表明腺嘌呤核苷酸在与制剂接触过程中代谢为腺苷;并且由于腺苷迅速被组织摄取,先前关于腺嘌呤核苷酸和核苷相对效力的观察结果并不代表实际的受体激动剂效力。

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