ACETYLCHOLINESTERASE AND ATPASE ACTIVITIES IN ERYTHROCYTE-GHOSTS ARE NOT AFFECTED BY 1,2,4-TRICHLOROBENZENE - IMPLICATIONS FOR TOXICITY BY NARCOTIC CHEMICALS

Citation
Ap. Vanwezel et al., ACETYLCHOLINESTERASE AND ATPASE ACTIVITIES IN ERYTHROCYTE-GHOSTS ARE NOT AFFECTED BY 1,2,4-TRICHLOROBENZENE - IMPLICATIONS FOR TOXICITY BY NARCOTIC CHEMICALS, Environmental toxicology and chemistry, 16(11), 1997, pp. 2347-2352
Citations number
36
Categorie Soggetti
Toxicology,"Environmental Sciences",Chemistry
ISSN journal
07307268
Volume
16
Issue
11
Year of publication
1997
Pages
2347 - 2352
Database
ISI
SICI code
0730-7268(1997)16:11<2347:AAAAIE>2.0.ZU;2-A
Abstract
The membrane concentration at which 1,2,4-trichlorobenzene (1,2,4-triC Bz) affects the functioning of diverse membrane proteins and the parti tion coefficient of 1,2,4-triCBz between ghosts and water were studied . Earlier studies showed that the fluidity of phospholipids is increas ed at concentrations of 20 to 60 mmol/kg lipid and that lethality by n arcosis in an organism occurs at concentrations of 40 to 160 mmol/kg l ipid, irrespective of the physicochemical properties of the nonpolar n arcotic chemical. Concentrations in a horse erythrocyte membrane of 11 0 to 1,100 mmol/kg lipid did not affect the activity of the Na+/K+ ATP ase and Mg2+ ATPase. Acetylcholinesterase functioning was not disturbe d at membrane concentrations of 33 to 330 mmol/kg lipid. Therefore, di sturbance of the membrane proteins studied is not the mechanism by whi ch narcotic chemicals act. The functioning of these membrane proteins is not affected by the change in phospholipid fluidity that is known t o occur in organisms that die due to exposure to narcotic chemicals. I n vitro bioassays often contain a high concentration of lipids in the system. With hydrophobic test compounds, the concentration of the test compound in the exposure medium at the start of the experiment is muc h higher than the exposure concentration at equilibrium. Therefore, ef fects in in vitro bioassays should not be expressed in terms of the ex posure concentration at the start of the experiment.