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大鼠小肠乳糜微粒和极低密度脂蛋白组装及转运的不同途径的证据。

Evidence for separate pathways of chylomicron and very low-density lipoprotein assembly and transport by rat small intestine.

作者信息

Tso P, Drake D S, Black D D, Sabesin S M

出版信息

Am J Physiol. 1984 Dec;247(6 Pt 1):G599-610. doi: 10.1152/ajpgi.1984.247.6.G599.

Abstract

Previously, we demonstrated that the hydrophobic surfactant Pluronic L-81 (L-81) inhibits the intestinal formation and transport of chylomicrons (CM) but not of very low-density lipoprotein-sized (VLDL) particles. The present study was undertaken to determine whether infusion of egg lecithin results mainly in secretion of VLDL by the small intestine and whether L-81 has any effect on their formation and secretion. Intestinal fistula rats were infused intraduodenally at a rate of 3 ml/h with a lipid emulsion containing 20 mM egg lecithin and 19 mM sodium taurocholate for 8 h. This was then followed by another 8 h of infusion of a similar lipid emulsion but with 0.5 mg/h of L-81 added. Lymphatic lipid output was measured, and lymph lipoproteins were sized by use of electron microscopy. Whether L-81 was present or not, no significant difference was detected in the lymphatic triglyceride, phospholipid, or cholesterol outputs. Based on agarose gel electrophoresis, sizing of intestinal lymph lipoproteins, and also the determination of lipid in the intestinal lymph CM and VLDL as separated by ultracentrifugation, VLDL were the major lipoproteins present in lymph during the infusion of egg lecithin. Thus, intraduodenal infusion of egg lecithin in the rat results mainly in the transport of VLDL and is not affected by the administration of L-81. The results suggest that CM and VLDL are assembled separately by the enterocytes and indicate the usefulness of L-81 in further investigating the pathways and regulation of intestinal lipoprotein synthesis, assembly, and secretion.

摘要

此前,我们证明了疏水性表面活性剂普朗尼克L - 81(L - 81)可抑制乳糜微粒(CM)在肠道的形成和转运,但对极低密度脂蛋白大小(VLDL)的颗粒没有影响。本研究旨在确定输注卵磷脂是否主要导致小肠分泌VLDL,以及L - 81对其形成和分泌是否有任何影响。给肠瘘大鼠以3 ml/h的速率十二指肠内输注含20 mM卵磷脂和19 mM牛磺胆酸钠的脂质乳剂,持续8小时。随后再以同样的速率输注8小时类似的脂质乳剂,但添加了0.5 mg/h的L - 81。测量淋巴脂质输出,并通过电子显微镜对淋巴脂蛋白进行大小测定。无论是否存在L - 81,在淋巴甘油三酯、磷脂或胆固醇输出方面均未检测到显著差异。基于琼脂糖凝胶电泳、肠道淋巴脂蛋白大小测定以及通过超速离心分离的肠道淋巴CM和VLDL中的脂质测定,在输注卵磷脂期间,VLDL是淋巴中存在的主要脂蛋白。因此,大鼠十二指肠内输注卵磷脂主要导致VLDL的转运,且不受L - 81给药的影响。结果表明CM和VLDL是由肠细胞分别组装的,并表明L - 81在进一步研究肠道脂蛋白合成、组装和分泌的途径及调节方面具有实用性。

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