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S-丙基-巯基半胱氨酸对脂质代谢的影响(作者译)

[Effect of S-propyl-mercapto-cysteine on lipid metabolism (author's transl)].

作者信息

Nakamura H, Ishikawa M

出版信息

Hokkaido Igaku Zasshi. 1976 Nov;51(6):507-11.

PMID:1035573
Abstract

When intra tissue reduction of thiamine propyldisulfide (TPD) occurs the following changes take place : TPD+cysteine leads to thiamine+propyl-mercapto-cysteine (PMC). We have reports that PMC has an effect of blood cholesterol lowering or not. In the present paper experiments were conducted to determine whether the effect of TPD on blood cholesterol lowering lies in PMC or not. The following results were obtained. 1) It was shown that when PMC was added to liver homogenate, no change was seen in the biosynthesis of cholesterol where TPD inhibited the biosynthesis. 2) When administered to normal animals while PMC showed no change in the total blood cholesterol value, TPD produced a decrease. While no change in total liver cholesterol value was induced by both, total liver, fatty acid showed a decrease by both. The biosynthesis of liver cholesterol from acetate-1-14C showed a decrease by both PMC and TPD, while the uptake from mevalonic acid-2-14C showed no change by both. The uptake of total liver fatty acid from acetate-1-14C while showing no change by PMC, showed an increase by TPD. 3) In cholesterol fed animals, the increase of blood cholesterol and total liver cholesterol was inhibited by TPD but PMC showed no effect. The biosynthesis of liver cholesterol from acetate-1-14C, showed an inhibitory effect on the lowering of biosynthesis in cholesterol fed animals by both TPD and PMC. And it was shown that the effect of TPD was larger. The total fatty acid value and the lowering of the uptake of total liver fatty acid from acetate-1-14C was inhibited to a similar extent by both TPD and PMC. From the above results, it may be said that even when PMC, a degenerative product of TPD is administered, either no effect is seen on the cholesterol metabolism or even when there is an effect, it would be negligible. Therefore, it may be surmized that the total structure of TPD exerts its effect on cholesterol and while the effect on fatty acid metabolism shows the same degree as TPD no characteristic features are seen.

摘要

当组织内硫胺丙基二硫化物(TPD)发生降解时会发生以下变化:TPD + 半胱氨酸会生成硫胺 + 丙基 - 巯基 - 半胱氨酸(PMC)。我们有关于PMC是否具有降低血液胆固醇作用的报道。在本论文中,进行了实验以确定TPD降低血液胆固醇的作用是否在于PMC。得到了以下结果。1)结果表明,当将PMC添加到肝匀浆中时,胆固醇的生物合成未见变化,而TPD会抑制其生物合成。2)当给正常动物给药时,PMC对血液总胆固醇值无变化,而TPD会使其降低。两者均未引起肝脏总胆固醇值的变化,但两者均使肝脏总脂肪酸含量降低。由乙酸 - 1 - 14C合成肝脏胆固醇的过程,PMC和TPD均使其降低,而由甲羟戊酸 - 2 - 14C的摄取量两者均未使其改变。肝脏总脂肪酸从乙酸 - 1 - 14C的摄取量,PMC未使其改变,而TPD使其增加。3)在喂食胆固醇的动物中,TPD可抑制血液胆固醇和肝脏总胆固醇的升高,但PMC无作用。由乙酸 - 1 - 14C合成肝脏胆固醇的过程,TPD和PMC均对喂食胆固醇动物中胆固醇生物合成的降低有抑制作用,且表明TPD的作用更大。TPD和PMC对总脂肪酸值以及肝脏总脂肪酸从乙酸 - 1 - 14C摄取量降低的抑制程度相似。从上述结果可以看出,即使给予TPD的降解产物PMC,对胆固醇代谢要么无作用,要么即使有作用也可忽略不计。因此,可以推测TPD的整体结构对胆固醇发挥作用,而对脂肪酸代谢的作用与TPD相同,未见特征性差异。

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