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犬体内被卡扎尔抑制剂或库尼茨抑制剂灭活的胰蛋白酶-α-巨球蛋白复合物的清除。

The elimination in dogs of trypsin-alpha-macroglobulin complexes inactivated by the Kazal or the Kunitz inhibitor.

作者信息

Eddeland A, Ohlsson K

出版信息

Hoppe Seylers Z Physiol Chem. 1978 Mar;359(3):379-84. doi: 10.1515/bchm.1978.359.1.379.

Abstract

The elimination of trypsin-alpha-macroglobulin complexes and similar complexes with the trypsin inactivated by low-molecular weight inhibitor was studied in anesthetized dogs. The complex was inactivated either by the Kazal (pancreatic secretory trypsin inhibitor, PSTI) or the Kunitz inhibitor (Trasylol BE). The inhibitors were labelled with 125I and in the case of the trypsin-alpha-macroglobulin complex the trypsin was labelled with 125I. All of the inactivated complexes exhibited a half-life of about 5 min in the dog. The elimination in plasma was exponential until 80 - 85% of the initial dose was cleared in 30 min and nearly negligible thereafter as seen by radioactivity measurements. Simultaneously increasing amounts of dialyzable radioactive substances with a lower molecular weight than the inhibitors were recovered in the urine. No significant differences in the elimination of trypsin-alpha-macroglobulin complexes were detected in plasma or in the urine before and after inactivation with the Kazal inhibitor (PSTI) or the Kunitz inhibitor (Trasylol BE).

摘要

在麻醉犬身上研究了胰蛋白酶-α-巨球蛋白复合物以及与被低分子量抑制剂灭活的胰蛋白酶形成的类似复合物的清除情况。该复合物可被卡扎尔抑制剂(胰腺分泌型胰蛋白酶抑制剂,PSTI)或库尼茨抑制剂(抑肽酶BE)灭活。抑制剂用125I标记,对于胰蛋白酶-α-巨球蛋白复合物,胰蛋白酶用125I标记。所有灭活的复合物在犬体内的半衰期约为5分钟。血浆中的清除呈指数形式,直到30分钟内清除了初始剂量的80 - 85%,此后通过放射性测量可见清除几乎可忽略不计。同时,尿液中回收了分子量低于抑制剂的可透析放射性物质,且其含量不断增加。在用卡扎尔抑制剂(PSTI)或库尼茨抑制剂(抑肽酶BE)灭活前后,血浆或尿液中胰蛋白酶-α-巨球蛋白复合物的清除未检测到显著差异。

相似文献

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Mechanism of proteinase complex formation with alpha 2-macroglobulin. Three modes of trypsin binding.
FEBS Lett. 1981 Jun 1;128(1):127-32. doi: 10.1016/0014-5793(81)81097-6.
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Trasylol prevents trypsin-induced shock in dogs.抑肽酶可预防犬胰蛋白酶诱导的休克。
Hoppe Seylers Z Physiol Chem. 1979 May;360(5):651-6. doi: 10.1515/bchm2.1979.360.1.651.

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