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静脉注射透明质酸在兔体内的血浆清除率、组织分布及代谢

Plasma clearance, tissue distribution and metabolism of hyaluronic acid injected intravenously in the rabbit.

作者信息

Fraser J R, Laurent T C, Pertoft H, Baxter E

出版信息

Biochem J. 1981 Nov 15;200(2):415-24. doi: 10.1042/bj2000415.

Abstract

The plasma clearance, tissue distribution and metabolism of hyaluronic acid were studied with a high average molecular weight [3H]acetyl-labelled hyaluronic acid synthesized in synovial cell cultures. After intravenous injection in the rabbit the label disappeared from the plasma with a half-life of 2.5--4.5 min, which corresponds to a normal hyaluronic acid clearance of approx. 10 mg/day per kg body weight. Injection of unlabelled hyaluronic acid 15 min after the tracer failed to reverse its absorption. Clearance of labelled polymer was retarded by prior injection of excess unlabelled hyaluronic acid. The maximum clearance capacity was estimated in these circumstances to be about 30 mg/day per kg body wt. The injected material was concentrated in the liver and spleen. As much as 88% of the label was absorbed by the liver, where it was found almost entirely in non-parenchymal cells. Degradation was rapid and complete, since volatile material, presumably 3H2O, appeared in the plasma within 20 min. Undegraded [3H]hyaluronic acid, small labelled residues and 3H2O were detected in the liver, but there was little evidence of intermediate oligosaccharides. No metabolite except 3H2O was recognized in plasma or urine. Two-thirds of the radioactivity was retained in the body water 24 h later, and small amounts were found in liver lipids. Radioactivity did not decline in the spleen as rapidly as in the liver. The upper molecular weight limit for renal excretion was about 25 000. Renal excretion played a negligible part in clearance. It is concluded that hyaluronic acid is removed from the plasma and degraded quickly by an efficient extrarenal system with a high reserve capacity, sited mainly in the liver.

摘要

采用滑膜细胞培养合成的平均分子量较高的[³H]乙酰标记透明质酸,研究了透明质酸的血浆清除率、组织分布及代谢情况。给家兔静脉注射后,标记物从血浆中消失的半衰期为2.5 - 4.5分钟,这相当于正常情况下透明质酸的清除率约为每千克体重每天10毫克。在注射示踪剂15分钟后注射未标记的透明质酸,未能逆转其吸收。预先注射过量未标记的透明质酸会延缓标记聚合物的清除。在这些情况下,最大清除能力估计约为每千克体重每天30毫克。注射的物质集中在肝脏和脾脏。多达88%的标记物被肝脏吸收,几乎全部存在于非实质细胞中。降解迅速且完全,因为在20分钟内血浆中出现了挥发性物质,推测为³H₂O。在肝脏中检测到未降解的[³H]透明质酸、少量标记残留物和³H₂O,但几乎没有中间寡糖的证据。在血浆或尿液中未识别出除³H₂O以外的代谢产物。24小时后,三分之二的放射性保留在体内水分中,在肝脏脂质中发现少量放射性。脾脏中的放射性下降速度不如肝脏快。肾脏排泄的分子量上限约为25000。肾脏排泄在清除过程中起的作用可忽略不计。结论是,透明质酸通过一个主要位于肝脏的高效肾外系统从血浆中被清除并迅速降解,该系统具有高储备能力。

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