2002Zhongguo yaolixue yu dulixue zazhiRequires access

In vitro degradation of soman in blood of mouse, guinea pig, dog and human

Ying Xiang

Open publisher page 0 citations

Abstract

AIM To study the relationship between the capability of soman detoxification of blood and the detoxifying enzyme activities in blood of different species. METHODS By measuring residual levels of soman and activities of detoxifying enzymes. RESULTS The degradation of soman by plasma was more powerful than that by its own red blood cells, the rank order of soman degradation in plasma was mouseguinea pighumandog. The plasma carboxylesterase in rodents played a very significant role in inactivating soman due largely to its comparatively activity and large number of binding site. While, the plasma carboxylesterase in dog and human did not play an important role, as did in rodents. In contrast, the cholinesterase in blood of dog and human served as the major elimination pathways of soman. CONCLUSION The differences in the amount of esteratic site available for soman detoxification and the binding rate between soman and detoxifying enzymes might be responsible for the species variation of detoxification capability in blood.

About this research paper

What this paper is about

AIM To study the relationship between the capability of soman detoxification of blood and the detoxifying enzyme activities in blood of different species. METHODS By measuring residual levels of soman and activities of detoxifying enzymes. RESULTS The degradation of soman by plasma was more powerful than that by its own red blood cells, the rank order of soman degradation in plasma was mouseguinea pighumandog. The plasma carboxylesterase in rodents played a very significant role in inactivating soman due largely to its comparatively activity and large number of binding site. While, the plasma carboxylesterase in dog and human did not play an important role, as did in rodents. In contrast, the cholinesterase in blood of dog and human served as the major elimination pathways of soman. CONCLUSION The differences in the amount of esteratic site available for soman detoxification and the binding rate between soman and detoxifying enzymes might be responsible for the species variation of detoxification capability in blood.

Why it matters

A significance statement is not available in the OpenAlex record.

Key contribution

A contribution statement is not available in the OpenAlex record.

Method / approach

Method details are not available in the OpenAlex metadata.

Main findings

Findings are not separately available in the OpenAlex metadata.

Limitations

Limitations are not available in the OpenAlex metadata.

Applications

Application details are not available in the OpenAlex metadata.

Available abstract

AIM To study the relationship between the capability of soman detoxification of blood and the detoxifying enzyme activities in blood of different species. METHODS By measuring residual levels of soman and activities of detoxifying enzymes. RESULTS The degradation of soman by plasma was more powerful than that by its own red blood cells, the rank order of soman degradation in plasma was mouseguinea pighumandog. The plasma carboxylesterase in rodents played a very significant role in inactivating soman due largely to its comparatively activity and large number of binding site. While, the plasma carboxylesterase in dog and human did not play an important role, as did in rodents. In contrast, the cholinesterase in blood of dog and human served as the major elimination pathways of soman. CONCLUSION The differences in the amount of esteratic site available for soman detoxification and the binding rate between soman and detoxifying enzymes might be responsible for the species variation of detoxification capability in blood.

Key concepts: Soman, Carboxylesterase, Cholinesterase, Chemistry, Enzyme, Detoxification (alternative medicine), Blood plasma, Acetylcholinesterase

Related papers

Back to paper searchBrowse research topicsOriginal source
In vitro degradation of soman in blood of mouse, guinea pig, dog and human — Research Paper | ScholarLens