Ito M, Connor W E, Blanchette E J, Treadwell C R, Vahouny G V
J Lipid Res. 1969 Nov;10(6):694-702.
The effect of cholestane-3,5alpha,6-triol (CT) on the intestinal absorption of cholesterol and oleic acid, as well as the absorption of labeled CT, was studied in lymph ductcannulated rats. Intragastric administration of 50 mg of CT in an emulsion with cholesterol-7alpha-(3)H and oleic acid-1-(14)C resulted in 50% inhibition of sterol transfer into lymph but only 8% depression of fatty acid absorption over an 8 hr period. The absorption of labeled CT into lymph was only 2-3% compared with 50% absorption of cholesterol when each was fed alone. 10% of the fed CT was recovered in the intestinal mucosa, and of this, one-half was associated with the brush border fraction. In rats fed CT 6 days prior to cholesterol and fatty acid administration, there was no effect on fatty acid absorption, while cholesterol absorption was reduced by almost 30%. When the intestinal mucosa from these animals were investigated by electron microscopy, it appeared that CT feeding resulted in numerous enlarged mitochondria and a marked increase in length of the microvilli. If animals were allowed to recover for 6 days from the CT prefeeding regime, the intestinal mucosa appeared normal, and the absorption of cholesterol approached that in controls. A possible mechanism for CT inhibition of cholesterol absorption was shown to be competition for the enzyme cholesterol esterase which esterifies cholesterol prior to entrance into the lymphatic system. CT itself is poorly esterified and poorly absorbed, but it is effective in inhibiting esterification of cholesterol in vitro.
在淋巴管插管的大鼠中研究了胆甾烷 - 3,5α,6 - 三醇(CT)对胆固醇和油酸肠道吸收以及标记CT吸收的影响。将50 mg CT与胆固醇 - 7α - (³H)和油酸 - 1 - (¹⁴C)制成乳剂进行胃内给药,在8小时内导致进入淋巴的固醇转移受到50%的抑制,但脂肪酸吸收仅降低8%。与单独喂食时胆固醇50%的吸收率相比,标记CT进入淋巴的吸收率仅为2 - 3%。喂食的CT中有10%在肠黏膜中回收,其中一半与刷状缘部分相关。在给予胆固醇和脂肪酸前6天喂食CT的大鼠中,对脂肪酸吸收没有影响,而胆固醇吸收降低了近30%。当通过电子显微镜检查这些动物的肠黏膜时,似乎喂食CT导致大量线粒体增大,微绒毛长度显著增加。如果动物从CT预喂食方案中恢复6天,肠黏膜看起来正常,胆固醇吸收接近对照组。CT抑制胆固醇吸收的一种可能机制被证明是与胆固醇酯酶竞争,该酶在胆固醇进入淋巴系统之前将其酯化。CT本身酯化程度低且吸收差,但它在体外有效抑制胆固醇的酯化。