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胆固醇和油酸在淋巴脂蛋白中的差异转运:嘌呤霉素敏感性的性别差异

Differential transport of cholesterol and oleic acid in lymph lipoproteins: sex differences in puromycin sensitivity.

作者信息

Vahouny G V, Blendermann E M, Gallo L L, Treadwell C R

出版信息

J Lipid Res. 1980 May;21(4):415-24.

PMID:7381333
Abstract

Adult rats of both sexes were prepared with indwelling drainage catheters in the left thoracic lymphatic duct, and with duodenal infusion catheters. Control and puromycin-treated animals were administered an aqueous test emulsion containing [7alpha-(3)H]cholesterol and [1-(14)C]oleic acid, followed two hours later, by a tracer dose of [1-(14)C]-leucine. Successive 2-hr lymph samples were subjected to ultracentrifugal separations of the major lipoprotein classes. These were specifically extracted for lipids, and for DNA- and lipid-free protein. In both sexes, oleic acid absorption was largely associated with the d < 1.006 g/ml chylomicron fraction throughout the 6-hr experimental period. Small but consistent levels of labeled fatty acid appeared in the 1.006 < d < 1.019 g/ml VLDL fraction. However, with both sexes 25-35% of the absorbed cholesterol appearing in lymph was recovered in the VLDL fraction. Furthermore, there were statistically greater levels of cholesterol in this lymph fraction in females than in males. Cumulative protein levels and leucine incorporation into chylomicron proteins was comparable in both sexes. However, VLDL protein in the female was significantly greater than in the male and this difference was mimicked by the greater incorporation of leucine into VLDL proteins in the female. In males, there were no significant effects of puromycin on cholesterol or oleic acid absorption, despite a marked inhibition in chylomicron protein levels and leucine incorporation into this fraction. There was also no effect of the inhibitor on VLDL protein levels or on leucine incorporation into VLDL peptides. Cholesterol but not oleic acid absorption in females was significantly depressed by administration of puromycin, and this was largely attributed to a decrease in VLDL transport of the sterol. Also, unlike males, leucine incorporation into VLDL peptides was inhibited by 75% by puromycin administration. These results emphasize the importance of non-chylomicron transport of cholesterol during absorption and suggest a hormonal influence on intestinal VLDL synthesis in female rats.-Vahouny, G. V., E. M. Blendermann, L. L. Gallo, and C. R. Treadwell. Differential transport of cholesterol and oleic acid in lymph lipoproteins: sex differences in puromycin sensitivity.

摘要

对成年雄性和雌性大鼠,在其左胸淋巴导管植入引流导管,并植入十二指肠输注导管。给对照组和嘌呤霉素处理组动物给予含有[7α-(3)H]胆固醇和[1-(14)C]油酸的水性测试乳剂,两小时后,给予示踪剂量的[1-(14)C]-亮氨酸。连续采集2小时的淋巴样本,对主要脂蛋白类别进行超速离心分离。对这些样本分别提取脂质、无DNA和脂质的蛋白质。在整个6小时的实验期内,两性的油酸吸收在很大程度上都与密度小于1.006 g/ml的乳糜微粒部分有关。在密度为1.006<d<1.019 g/ml的极低密度脂蛋白(VLDL)部分出现少量但稳定水平的标记脂肪酸。然而,两性吸收的胆固醇中,有25% - 35%出现在淋巴中的胆固醇在VLDL部分中被回收。此外,雌性大鼠该淋巴部分中的胆固醇水平在统计学上高于雄性。两性乳糜微粒蛋白质中的累积蛋白质水平和亮氨酸掺入量相当。然而,雌性大鼠的VLDL蛋白质显著高于雄性,雌性大鼠VLDL蛋白质中亮氨酸掺入量更高也体现了这种差异。在雄性大鼠中,尽管嘌呤霉素显著抑制了乳糜微粒蛋白质水平和亮氨酸掺入该部分,但对胆固醇或油酸吸收没有显著影响。该抑制剂对VLDL蛋白质水平或亮氨酸掺入VLDL肽也没有影响。在雌性大鼠中,给予嘌呤霉素会显著降低胆固醇而非油酸的吸收,这主要归因于固醇的VLDL转运减少。此外,与雄性不同,给予嘌呤霉素会使亮氨酸掺入VLDL肽的量减少75%。这些结果强调了胆固醇在吸收过程中非乳糜微粒转运的重要性,并表明激素对雌性大鼠肠道VLDL合成有影响。-瓦胡尼,G. V.,E. M. 布伦德曼,L. L. 加洛,和C. R. 特里德韦尔。淋巴脂蛋白中胆固醇和油酸的差异转运:嘌呤霉素敏感性的性别差异

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