吡哆醇和吡哆醇-5′-磷酸存在下肝动脉条带对肾上腺素力学反应的比较研究。

Acta vitaminologica et enzymologica Pub Date : 1985-01-01
V Bettini, R Martino, L Munari, F Mayellaro, P Ton
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引用次数: 0

摘要

由于已知PLP在“体外”抑制COMT的作用比吡哆醇大得多;吡哆醇对AD分离肝动脉反应的影响已与PLP对同一动脉的影响进行了比较。就增加的百分比而言,结果是PLP比吡哆醇对AD的应答更大。当邻苯三酚(一种强大的COMT抑制剂)存在时,这种效果就没有了。以此为基础,推断吡哆醇和PLP的作用机制是代谢性的,基于COMT的抑制作用,甚至对肝动脉也有抑制作用。我们还推断,与吡哆醇相比,PLP的效率更高是由于其抑制COMT的能力更强。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Comparative study of mechanical responses of hepatic arteries strips to adrenalin in presence of pyridoxine and pyridoxal-5'-phosphate.

Since it is known that PLP inhibits "in vitro" the COMT much more than pyridoxine; the influence of pyridoxine to the response of hepatic arteries isolated to AD has been compared to the influence of PLP to the same arteries. As for as the increase in percent is concerned, the result is that PLP gives rise to a greater answer to AD than pyridoxine. Such effects lacked when pyrogallol, a powerful COMT inhibitor, was present. Taking such results as a basis, it has been concluded that the mechanism of action of pyridoxine and of PLP was metabolic and that it was based on the COMT inhibition, even for the hepatic arteries. It was been also deduced that the higher efficiency of PLP compared to the pyridoxine's was due to its greater capacity to inhibit the COMT.

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