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罂粟碱增强腺苷对豚鼠心房的作用。

Papaverine enhances the effect of adenosine in guinea-pig atria.

作者信息

Moritoki H, Takei M, Fujita S, Ishida Y

出版信息

Naunyn Schmiedebergs Arch Pharmacol. 1984 Oct;327(4):326-31. doi: 10.1007/BF00506244.

Abstract

Papaverine, while enhancing the force of contraction of guinea-pig atria, remarkably and dose-dependently enhanced the negative inotropic response of the atria to adenosine. It also enhanced the actions of ATP and other adenine nucleotides, but not those of 2-chloroadenosine and ACh. At similar concentrations, papaverine inhibited the uptake of adenosine by the atrial tissue during incubation with adenosine. Adenosine in the medium was degraded to inactive inosine during incubation with the atrial tissue, and papaverine reduced its degradation. The enhancing effect of papaverine on the action of adenosine on guinea-pig atria was like those of dipyridamole, 6-(2-hydroxy-5-nitrobenzyl)thioguanosine and cinepazide. The effect seemed to be due mainly to inhibition of adenosine uptake into the tissue. Inhibition of adenosine degradation may also have contributed to the action of papaverine, but this action was probably much less important than inhibition of adenosine uptake.

摘要

罂粟碱在增强豚鼠心房收缩力的同时,显著且呈剂量依赖性地增强了心房对腺苷的负性肌力反应。它还增强了ATP和其他腺嘌呤核苷酸的作用,但对2-氯腺苷和乙酰胆碱的作用没有增强。在相似浓度下,罂粟碱在与腺苷共同孵育期间抑制了心房组织对腺苷的摄取。在与心房组织共同孵育期间,培养基中的腺苷被降解为无活性的肌苷,而罂粟碱减少了其降解。罂粟碱对腺苷作用于豚鼠心房的增强作用与双嘧达莫、6-(2-羟基-5-硝基苄基)硫代鸟苷和桂哌齐特的作用相似。这种作用似乎主要是由于抑制了腺苷摄取到组织中。抑制腺苷降解可能也对罂粟碱的作用有贡献,但这种作用可能远不如抑制腺苷摄取重要。

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