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猪体内氚标记的二氢微囊藻毒素-LR的毒代动力学

Toxicokinetics of tritiated dihydromicrocystin-LR in swine.

作者信息

Stotts R R, Twardock A R, Koritz G D, Haschek W M, Manuel R K, Hollis W B, Beasley V R

机构信息

Department of Veterinary Biosciences, University of Illinois, Urbana 61801, USA.

出版信息

Toxicon. 1997 Mar;35(3):455-65. doi: 10.1016/s0041-0101(96)00120-1.

Abstract

The toxicokinetics of tritiated dihydromicrocystin-LR ([3H]2H-MCLR) were studied in anesthetized, specific-pathogen-free pigs. Pigs were dosed with radiolabeled plus non-labeled 2H-MCLR at 25 or 75 micrograms/kg i.v., or via an isolated ileal loop at 75 micrograms/kg. The i.v. doses were rapidly removed from the blood. At either i.v. dose, more than half the radiolabel from [3H]2H-MCLR present in the blood at 1 min postdosing was cleared by 6 min. The blood clearance at the 75 micrograms/kg dose was slower than at the 25 micrograms/kg dose. Accordingly, at the high dose, the concentrations of the toxin in blood were disproportionately higher from 10 min after dosing until the study ended 4 hr later. The decreased clearance is presumably due to decreased elimination from the blood as a consequence of the hepatic injury that was observed histologically. Following administration of [3H]2H-MCLR at 75 micrograms/kg via the ileum, the maximal toxin concentration in blood was achieved at 90 min after dosing. At that time the [3H]2H-MCLR concentration in portal venous blood was 3.6 times higher than in peripheral venous blood. Although bile production varied, following i.v. dosing radioactivity was detected in bile as early as 12 min postdosing in one animal. This study demonstrated that [3H]2H-MCLR is rapidly removed from the blood of anesthetized swine and that excretion of the radiolabel into bile may begin within 30 min of dosing.

摘要

在麻醉的、无特定病原体的猪身上研究了氚标记的二氢微囊藻毒素-LR([3H]2H-MCLR)的毒代动力学。给猪静脉注射放射性标记加未标记的2H-MCLR,剂量为25或75微克/千克,或通过分离的回肠袢给药,剂量为75微克/千克。静脉注射剂量的药物迅速从血液中清除。无论静脉注射哪种剂量,给药后1分钟血液中[3H]2H-MCLR的放射性标记,在6分钟内清除了一半以上。75微克/千克剂量的血液清除速度比25微克/千克剂量慢。因此,在高剂量时,给药后10分钟直至4小时后研究结束,血液中毒素浓度不成比例地更高。清除率降低可能是由于组织学观察到的肝损伤导致血液中消除减少。通过回肠给予75微克/千克的[3H]2H-MCLR后,给药后90分钟达到血液中毒素最大浓度。此时门静脉血中[3H]2H-MCLR浓度比外周静脉血高3.6倍。尽管胆汁生成有所不同,但静脉给药后,最早在给药后12分钟在一只动物的胆汁中检测到放射性。这项研究表明,[3H]2H-MCLR能迅速从麻醉猪的血液中清除,且放射性标记物在给药后30分钟内可能开始排入胆汁。

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