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[S-腺苷-L-高半胱氨酸对多巴胺分解代谢的影响]

[Effect of S-adenosyl-L-homocysteine of dopamine catabolism].

作者信息

Bidard J N, Sokoloff P, Cronenberger L, Pacheco H

出版信息

Arch Int Physiol Biochim. 1979 May;87(2):253-64. doi: 10.3109/13813457909070498.

Abstract

1.--The administration of SAH to rats, at physiologically active dose on the sleep, does not change the urinary level of MD and NM. On the other hand, the excretion of DA and NA decreases. 2.--In the brain, SAH does not modify neither the concentration of NA and NM in hypothalamus and thalamus, nor the concentration of DA and MD in corpus striatum. 3.--After intracisternally injection of [14C]DA or [3H]NA, SAH increases the level of [14C]MD and [3H]NM. 4.--Contrary to the studies in vitro, where SAH is an inhibitor of COMT, on the rat it does not seem prevent the methylation of DA and NA.

摘要
  1. 以对睡眠具有生理活性剂量给大鼠施用SAH,不会改变MD和NM的尿液水平。另一方面,DA和NA的排泄减少。2. 在大脑中,SAH既不改变下丘脑和丘脑中NA和NM的浓度,也不改变纹状体中DA和MD的浓度。3. 脑池内注射[14C]DA或[3H]NA后,SAH会增加[14C]MD和[3H]NM的水平。4. 与体外研究不同,在体外研究中SAH是COMT的抑制剂,但在大鼠体内它似乎不会阻止DA和NA的甲基化。

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