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大鼠和仓鼠组织中受体依赖性及非受体依赖性低密度脂蛋白转运的动力学常数。

Kinetic constants for receptor-dependent and receptor-independent low density lipoprotein transport in the tissues of the rat and hamster.

作者信息

Spady D K, Meddings J B, Dietschy J M

出版信息

J Clin Invest. 1986 May;77(5):1474-81. doi: 10.1172/JCI112460.

DOI:10.1172/JCI112460
PMID:3700649
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC424548/
Abstract

In this study, carried out in the rat and hamster, the receptor-dependent low density lipoprotein (LDL) transport process in each organ was characterized in terms of its maximal uptake rate (Jm) and Michaelis constant (Km), while the rate of receptor-independent uptake was defined in terms of its proportionality constant (P). The highest Jm values of 50-126 micrograms/h per g were found in the liver and endocrine glands in both species and receptor-dependent uptake also was detected in other organs like spleen, kidney, and intestine. The Km values were essentially the same in all of the organs and equaled approximately 90 mg/dl in both species. The receptor-independent uptake constants also were similar in the two species and were highest in the spleen, liver, and intestine. From these values for Jm, Km, and P, it was possible to construct theoretical curves that predict the plasma LDL-cholesterol concentration and fractional catabolic rate given any alteration in LDL-cholesterol production or the magnitude of receptor-dependent LDL transport in any organ of the rat or hamster.

摘要

在这项以大鼠和仓鼠为实验对象的研究中,各器官中受体依赖性低密度脂蛋白(LDL)转运过程的特征表现为其最大摄取率(Jm)和米氏常数(Km),而受体非依赖性摄取率则依据其比例常数(P)来定义。在这两个物种中,肝脏和内分泌腺的Jm值最高,为每克每小时50 - 126微克,并且在脾脏、肾脏和肠道等其他器官中也检测到了受体依赖性摄取。所有器官中的Km值基本相同,在这两个物种中均约为90毫克/分升。受体非依赖性摄取常数在这两个物种中也相似,在脾脏、肝脏和肠道中最高。根据这些Jm、Km和P值,可以构建理论曲线,以预测在大鼠或仓鼠的任何器官中,LDL - 胆固醇生成发生任何变化或受体依赖性LDL转运量发生任何改变时的血浆LDL - 胆固醇浓度和分数分解代谢率。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0e10/424548/3f6ecb10ea06/jcinvest00128-0076-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0e10/424548/3f6ecb10ea06/jcinvest00128-0076-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0e10/424548/3f6ecb10ea06/jcinvest00128-0076-a.jpg

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本文引用的文献

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2
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Med Clin North Am. 1982 Mar;66(2):519-35. doi: 10.1016/s0025-7125(16)31433-x.
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Sites of tissue binding and uptake in vivo of bacterial lipopolysaccharide-high density lipoprotein complexes: studies in the rat and squirrel monkey.细菌脂多糖-高密度脂蛋白复合物在体内的组织结合与摄取部位:大鼠和松鼠猴的研究
环糊精克服了 NPC1 小鼠几乎所有器官的转运缺陷,导致被隔离的胆固醇作为胆汁酸排出。
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Transport of maternal cholesterol to the fetus is affected by maternal plasma cholesterol concentrations in the golden Syrian hamster.在金黄地鼠中,母体胆固醇向胎儿的转运受母体血浆胆固醇浓度的影响。
J Lipid Res. 2009 Jun;50(6):1146-55. doi: 10.1194/jlr.M800538-JLR200. Epub 2009 Jan 3.
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Kinetic parameters for high density lipoprotein apoprotein AI and cholesteryl ester transport in the hamster.仓鼠中高密度脂蛋白载脂蛋白AI和胆固醇酯转运的动力学参数。
J Clin Invest. 1997 Apr 1;99(7):1704-13. doi: 10.1172/JCI119334.
6
Centripetal cholesterol flux from extrahepatic organs to the liver is independent of the concentration of high density lipoprotein-cholesterol in plasma.从肝外器官向肝脏的向心性胆固醇通量与血浆中高密度脂蛋白胆固醇的浓度无关。
Proc Natl Acad Sci U S A. 1996 Apr 30;93(9):4114-9. doi: 10.1073/pnas.93.9.4114.
7
Apolipoprotein E competitively inhibits receptor-dependent low density lipoprotein uptake by the liver but has no effect on cholesterol absorption or synthesis in the mouse.载脂蛋白E竞争性抑制肝脏中受体依赖性低密度脂蛋白的摄取,但对小鼠的胆固醇吸收或合成没有影响。
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Hypocholesterolaemic effect of beta beta'-methyl-substituted hexadecanedioic acid (MEDICA 16) in the male hamster.β,β'-甲基取代的十六烷二酸(MEDICA 16)对雄性仓鼠的降胆固醇作用
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