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豚鼠单次亚致死吸入暴露后沙林(GB)的动力学。

Kinetics of sarin (GB) following a single sublethal inhalation exposure in the guinea pig.

作者信息

Whalley Christopher E, McGuire Jeffrey M, Miller Dennis B, Jakubowski Edward M, Mioduszewski Robert J, Thomson Sandra A, Lumley Lucille A, McDonough John H, Shih Tsung-Ming A

机构信息

U.S. Army Edgewood Chemical Biological Center, Aberdeen Proving Ground, Maryland 21010-5424, USA.

出版信息

Inhal Toxicol. 2007 Jun;19(8):667-81. doi: 10.1080/08958370701353296.

Abstract

To improve toxicity estimates from sublethal exposures to chemical warfare nerve agents (CWNA), it is necessary to generate mathematical models of the absorption, distribution, and elimination of nerve agents. However, current models are based on representative data sets generated with different routes of exposure and in different species and are designed to interpolate between limited laboratory data sets to predict a wide range of possible human exposure scenarios. This study was performed to integrate CWNA sublethal toxicity data in male Duncan Hartley guinea pigs. Specific goal was to compare uptake and clearance kinetics of different sublethal doses of sarin (either 0.1 x or 0.4 x LC50) in blood and tissues of guinea pigs exposed to agent by acute whole-body inhalation exposure after the 60-min LC50 was determined. Arterial catheterization allowed repeated blood sampling from the same animal at various time periods. Blood and tissue levels of acetylcholinesterase, butyrylcholinesterase, and regenerated sarin (rGB) were determined at various time points during and following sarin exposure. The following pharmacokinetic parameters were calculated from the graph of plasma or RBC rGB concentration versus time: time to reach the maximal concentration; maximal concentration; mean residence time; clearance; volume of distribution at steady state; terminal elimination-phase rate constant; and area under plasma concentration time curve extrapolated to infinity using the WinNonlin analysis program 5.0. Plasma and RBC t(1/2) for rGB was also calculated. Data will be used to develop mathematical model of absorption and distribution of sublethal sarin doses into susceptible tissues.

摘要

为了改进从化学战神经毒剂(CWNA)亚致死暴露得出的毒性估计,有必要建立神经毒剂吸收、分布和消除的数学模型。然而,当前的模型基于通过不同暴露途径和在不同物种中生成的代表性数据集,并且旨在在有限的实验室数据集之间进行插值,以预测广泛的可能的人类暴露情景。本研究旨在整合雄性邓肯·哈特利豚鼠的CWNA亚致死毒性数据。具体目标是在确定60分钟半数致死浓度(LC50)后,比较经急性全身吸入暴露染毒的豚鼠,不同亚致死剂量沙林(0.1倍或0.4倍LC50)在血液和组织中的摄取和清除动力学。动脉插管允许在不同时间段从同一只动物重复采集血液样本。在沙林暴露期间及之后的不同时间点,测定血液和组织中乙酰胆碱酯酶、丁酰胆碱酯酶和再生沙林(rGB)的水平。根据血浆或红细胞rGB浓度随时间变化的曲线计算以下药代动力学参数:达到最大浓度的时间;最大浓度;平均驻留时间;清除率;稳态分布容积;终末消除相速率常数;以及使用WinNonlin分析程序5.0外推至无穷大的血浆浓度-时间曲线下面积。还计算了rGB的血浆和红细胞半衰期(t(1/2))。这些数据将用于建立亚致死剂量沙林进入易感组织的吸收和分布数学模型。

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