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体内磷脂耗尽的乳糜微粒的肝脏摄取。与乳糜微粒残粒摄取的比较。

Hepatic uptake of phospholipid-depleted chylomicrons in vivo. Comparison with the uptake of chylomicron remnants.

作者信息

Borensztajn J, Kotlar T J

出版信息

Biochem J. 1981 Dec 15;200(3):547-53. doi: 10.1042/bj2000547.

Abstract
  1. Rats pretreated with Triton WR-1339 to prevent the formation of remnants were injected with [3H]cholesterol-labelled remnants, intact chylomicrons or chylomicrons depleted of most of their surface phospholipids by treatment with phospholipase A2. Within 5 min about 80% of the injected label of remnants and phospholipid-depleted chylomicrons was incorporated into the livers compared with less than 10% of the injected radioactivity of intact chylomicrons. A similar rapid hepatic uptake of radioactivity occurred when rats not pretreated with Triton were injected with [3H]cholesterol-labelled phospholipid-depleted chylomicrons. This rapid hepatic uptake of phospholipid-depleted chylomicrons occurred apparently without any alteration in the apoprotein composition of the particles. 2. The participation of hepatocytes in the uptake of remnants and phospholipid-depleted chylomicrons was examined. Both types of particles were taken up by the hepatocytes. However, small chylomicrons (Sf less than 400) were taken up more efficiently than were large chylomicrons (Sf greater than 400), but neither was taken up as efficiently as the remnants. 3. The results of this study lend support to the hypothesis that phospholipid-depleted chylomicrons and chylomicron remnants are taken up by the liver by a similar mechanism, which depends on the loss of surface phospholipids.
摘要
  1. 用曲拉通WR - 1339预处理大鼠以防止残余物形成,然后给它们注射[³H]胆固醇标记的残余物、完整的乳糜微粒或经磷脂酶A2处理去除大部分表面磷脂的乳糜微粒。在5分钟内,与完整乳糜微粒注射放射性的不到10%相比,残余物和磷脂去除的乳糜微粒注射标记物的约80%被肝脏摄取。当未用曲拉通预处理的大鼠注射[³H]胆固醇标记的磷脂去除的乳糜微粒时,也发生了类似的肝脏对放射性的快速摄取。磷脂去除的乳糜微粒的这种快速肝脏摄取显然没有使颗粒的载脂蛋白组成发生任何改变。2. 研究了肝细胞在残余物和磷脂去除的乳糜微粒摄取中的参与情况。两种类型的颗粒都被肝细胞摄取。然而,小乳糜微粒(Sf小于400)比大乳糜微粒(Sf大于400)摄取效率更高,但两者的摄取效率都不如残余物。3. 本研究结果支持以下假说:磷脂去除的乳糜微粒和乳糜微粒残余物通过类似机制被肝脏摄取,该机制取决于表面磷脂的丧失。

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本文引用的文献

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Am J Physiol. 1957 Feb;188(2):399-402. doi: 10.1152/ajplegacy.1957.188.2.399.

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