Field F J, Mathur S N
J Lipid Res. 1983 Apr;24(4):409-17.
Rabbits were fed either 10% coconut oil, 10% coconut oil and 1% beta-sitosterol, 10% coconut oil and 1% cholesterol, or 10% coconut oil and 1% beta-sitosterol plus 1% cholesterol for 4 weeks. Microsomal membranes from intestines of animals fed the 1% beta-sitosterol diet had 48% less cholesterol and were enriched twofold in beta-sitosterol compared to membranes from animals fed the coconut oil diet alone. Acylcoenzyme A:cholesterol acyltransferase (ACAT) activity in jejunum and ileum was decreased significantly in animals fed the plant sterol alone. In membranes from animals fed 1% beta-sitosterol and 1% cholesterol, beta-sitosterol content increased 50% whereas cholesterol was modestly decreased compared to their controls fed only cholesterol. Intestinal ACAT was unchanged in the animals fed both sterols when compared to their controls. beta-Sitosterol esterification was determined by incubating intestinal microsomal membranes with either [(14)C]beta-sitosterol-albumin emulsion or [(14)C]beta-sitosterol:dipalmitoyl phosphatidylcholine (DPPC) liposomes to radiolabel the endogenous sterol pool. Oleoyl-CoA was then added. The CoA-dependent esterification rate of beta-sitosterol was very slow compared to that of cholesterol using both techniques. An increased amount of endogenous microsomal beta-sitosterol, which occurs in animals fed 1% beta-sitosterol, did not interfere with the stimulation of ACAT activity secondary to cholesterol enrichment of the membranes. Enriching microsomal membranes three- to five-fold with beta-sitosterol did not affect ACAT activity. Freshly isolated intestinal cells were incubated for 1 hour with [(3)H]oleic acid and beta-sitosterol:DPPC or 25-hydroxycholesterol:DPPC. Incorporation of oleic acid into cholesteryl esters did not change in the presence of beta-sitosterol but increased fourfold after the addition of 25-hydroxycholesterol. We conclude that the CoA-dependent esterification rate of cholesterol is at least 60 times greater than that of beta-sitosterol. Membrane beta-sitosterol does not interfere with nor compete with cholesterol esterification. Inadequate esterification of this plant sterol may play a role in the poor absorption of beta-sitosterol by the gut.-Field, F. J., and S. N. Mathur. beta-Sitosterol: esterification by intestinal acylcoenzyme A:cholesterol acyltransferase (ACAT) and its effect on cholesterol esterification.
给兔子喂食10%的椰子油、10%的椰子油加1%的β-谷甾醇、10%的椰子油加1%的胆固醇,或10%的椰子油加1%的β-谷甾醇再加1%的胆固醇,持续4周。与仅喂食椰子油的动物的肠微体膜相比,喂食含1%β-谷甾醇饮食的动物的肠微体膜胆固醇含量降低了48%,β-谷甾醇含量增加了两倍。单独喂食植物甾醇的动物空肠和回肠中的酰基辅酶A:胆固醇酰基转移酶(ACAT)活性显著降低。在喂食1%β-谷甾醇和1%胆固醇的动物的膜中,与仅喂食胆固醇的对照动物相比,β-谷甾醇含量增加了50%,而胆固醇略有降低。与对照动物相比,同时喂食两种甾醇的动物的肠ACAT没有变化。通过将肠微体膜与[(14)C]β-谷甾醇-白蛋白乳剂或[(14)C]β-谷甾醇:二棕榈酰磷脂酰胆碱(DPPC)脂质体孵育以放射性标记内源性甾醇池来测定β-谷甾醇的酯化。然后加入油酰辅酶A。与使用两种技术的胆固醇相比,β-谷甾醇的辅酶A依赖性酯化速率非常慢。在喂食1%β-谷甾醇的动物中出现的内源性微体β-谷甾醇量的增加,并不干扰膜胆固醇富集继发的ACAT活性的刺激。用β-谷甾醇将微体膜富集三到五倍并不影响ACAT活性。将新鲜分离的肠细胞与[(3)H]油酸和β-谷甾醇:DPPC或25-羟基胆固醇:DPPC一起孵育1小时。在β-谷甾醇存在下,油酸掺入胆固醇酯的情况没有变化,但在加入25-羟基胆固醇后增加了四倍。我们得出结论,胆固醇的辅酶A依赖性酯化速率至少比β-谷甾醇的酯化速率大60倍。膜β-谷甾醇不干扰也不与胆固醇酯化竞争。这种植物甾醇的酯化不足可能在肠道对β-谷甾醇吸收不良中起作用。-菲尔德,F.J.,和S.N.马图尔。β-谷甾醇:肠酰基辅酶A:胆固醇酰基转移酶(ACAT)的酯化及其对胆固醇酯化的影响