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异构反式-18:1酸对大鼠肝脏微粒体使棕榈酸、亚油酸和二十碳-8,11,14-三烯酸去饱和作用的影响。

The effect of isomeric trans-18:1 acids on the desaturation of palmitic, linoleic and eicosa-8,11,14-trienoic acids by rat liver microsomes.

作者信息

Mahfouz M M, Johnson S, Holman R T

出版信息

Lipids. 1980 Feb;15(2):100-7. doi: 10.1007/BF02533884.

Abstract

The inhibitory effects of the positional isomers of trans-18:1 acids on the desaturation of palmitic acid to palmitoleic (delta 9-desaturase), linoleic to gamma-linolenic (delta 6-desaturase) and eicosa-8,11,14-trienoic to arachidonic acid (delta 5-desaturase) were investigated. These trans-18:1 acids were found to be inhibitory for the microsomal delta 6-, delta 9- and delta 5-desaturases of rat liver. The position of the double bond in the trans-18:1 acids seems to be important in determining the degree of inhibition. At inhibitor/substrate ratio of 3:1, the delta 6-desaturase was most strongly inhibited by trans-delta 3, -delta 4, -delta 7 and -delta 15-18:1 isomers, whereas the delta 9-desaturase was most strongly inhibited by trans-delta3, -delta 5, -delta 7, -delta 10, -delta 12, -delta 13 and -delta 16 isomers. At inhibitor/substrate ratio of 6:1, the delta 5-desaturase was most strongly inhibited by delta 3-, delta 9-, delta 13- and delta 15-isomers. When 18:0 was added to the incubations of 16:0, 18:2 and 20:3 at the same I/S ratios used for the trans-18:1 acids, weak inhibition for delta 9- desaturase and no inhibition for delta 5- and delta 6-desaturases was observed.

摘要

研究了反式-18:1酸的位置异构体对棕榈酸去饱和生成棕榈油酸(Δ9-去饱和酶)、亚油酸去饱和生成γ-亚麻酸(Δ6-去饱和酶)以及二十碳-8,11,14-三烯酸去饱和生成花生四烯酸(Δ5-去饱和酶)的抑制作用。发现这些反式-18:1酸对大鼠肝脏微粒体的Δ6-、Δ9-和Δ5-去饱和酶具有抑制作用。反式-18:1酸中双键的位置在决定抑制程度方面似乎很重要。在抑制剂/底物比例为3:1时,Δ6-去饱和酶受反式Δ3-、Δ4-、Δ7-和Δ15-18:1异构体的抑制作用最强,而Δ9-去饱和酶受反式Δ3-、Δ5-、Δ7-、Δ10-、Δ12-、Δ13-和Δ16-异构体的抑制作用最强。在抑制剂/底物比例为6:1时,Δ5-去饱和酶受Δ3-、Δ9-、Δ13-和Δ15-异构体的抑制作用最强。当以与反式-18:1酸相同的抑制剂/底物比例将18:0添加到16:0、18:2和20:3的孵育体系中时,观察到对Δ9-去饱和酶有微弱抑制作用,而对Δ5-和Δ6-去饱和酶无抑制作用。

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