Oximes-induced reactivation of rat brain acetylcholinesterase inhibited by VX agent

Author:

Kuča Kamil1,Kassa Jiří1

Affiliation:

1. Purkyně Military Medical Academy, Department of Toxicology, PO Box 35/T, 500 01 Hradec Krá lové, Czech Republic

Abstract

A comparison of one mono- and seven bisquaternary acetylcholinesterase (AChE) reactivators of acetylcholinesterase inhibited by VX agent was performed. As a source of the acetylcholinesterase, a rat brain homogenate was taken. There were significant differences in reactivation potency of all tested oximes. The oxime TO205 seems to be the most efficacious followed by TO046, HI-6, HS-6, K027, obidoxime, MMC and 2-PAM. In addition, the results of this study showed that the reactivation potency of the tested reactivators depends on many factors-such as the number of pyridinium rings, the number of oxime groups and their position, as well as the length and the shape of linkage bridge between two pyridinium rings.

Publisher

SAGE Publications

Subject

Health, Toxicology and Mutagenesis,Toxicology,General Medicine

Reference25 articles.

1. Zajtchuk R , Bellamy RF . Medical aspects of chemical and biological warfare. Office of the Surgeon General; Department of the Army, United states of America , 1997: 721-721.

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