JPET Introducing ALZET?ew Model 2006 Pump

Home Help [Feedback] [For Subscribers] [Archive] [Search] [Contents]
 QUICK SEARCH:   [advanced]


     


This Article
Right arrow Full Text (PDF)
Right arrow Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when eLetters are posted
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Broomfield, C. A.
Right arrow Articles by Lenz, D. E.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Broomfield, C. A.
Right arrow Articles by Lenz, D. E.

Protection by butyrylcholinesterase against organophosphorus poisoning in nonhuman primates

CA Broomfield, DM Maxwell, RP Solana, CA Castro, AV Finger and DE Lenz

U.S. Army Medical Research Institute of Chemical Defense, Aberdeen Proving Ground, Maryland.

Butyrylcholinesterase (BuChE) was examined as an in vivo exogenous scavenger for highly toxic organophosphorus (OP) poisons. Protection studies with equine BuChE were carried out in rhesus monkeys trained to perform a Serial Probe Recognition task. The pharmacokinetics of equine BuChE administered i.v. in rhesus monkeys revealed an elimination T1/2 of approximately 620 hr. Animals given 503 nmol of BuChE i.v. and then challenged with 220 to 260 nmol of soman (two LD50; a lethal dose in untreated animals) all survived with no clinical signs of OP poisoning. Serial Probe Recognition performance was depressed after enzyme administration and at 1 hr postsoman. However, all monkeys performed the task at base-line levels at 8 hr after soman and throughout the remainder of the experimental period. Two different monkeys each were given two doses of sarin, 183 nmol/dose (one LD50) after 460 nmol of BuChE. No signs were observed. A third group of monkeys given 253 or 340 nmol (three and four LD50, respectively) of soman after 460 nmol of BuChE required 1 mg/kg of atropine i.v. 10 min postsoman, but recovered completely within 24 hr. Our results indicate that BuChE has the required properties to function as a biological scavenger to protect against the pharmacological and behavioral toxicity of OP poisons.

Volume 259, Issue 2, pp. 633-638, 11/01/1991
Copyright © 1991 by American Society for Pharmacology and Experimental Therapeutics




This article has been cited by other articles:


Home page
Hum Exp ToxicolHome page
M. Guven, M. Sungur, and B. Eser
The effect of plasmapheresis on plasma cholinesterase levels in a patient with organophosphate poisoning
Human and Experimental Toxicology, July 1, 2004; 23(7): 365 - 368.
[Abstract] [PDF]


Home page
J. Biol. Chem.Home page
Y. Nicolet, O. Lockridge, P. Masson, J. C. Fontecilla-Camps, and F. Nachon
Crystal Structure of Human Butyrylcholinesterase and of Its Complexes with Substrate and Products
J. Biol. Chem., October 17, 2003; 278(42): 41141 - 41147.
[Abstract] [Full Text] [PDF]


Home page
J. Pharmacol. Exp. Ther.Home page
E. G. Duysen, C. F. Bartels, and O. Lockridge
Wild-Type and A328W Mutant Human Butyrylcholinesterase Tetramers Expressed in Chinese Hamster Ovary Cells Have a 16-Hour Half-Life in the Circulation and Protect Mice from Cocaine Toxicity
J. Pharmacol. Exp. Ther., August 1, 2002; 302(2): 751 - 758.
[Abstract] [Full Text] [PDF]


Home page
Drug Metab. Dispos.Home page
G. N. Carmona, R. A. Jufer, S. R. Goldberg, D. A. Gorelick, N. H. Greig, Q.-S. Yu, E. J. Cone, and C. W. Schindler
Butyrylcholinesterase Accelerates Cocaine Metabolism: In Vitro and In Vivo Effects in Nonhuman Primates and Humans
Drug Metab. Dispos., March 1, 2000; 28(3): 367 - 371.
[Abstract] [Full Text] [PDF]


Home page
Mol. Pharmacol.Home page
A. Saxena, Y. Ashani, L. Raveh, D. Stevenson, T. Patel, and B. P. Doctor
Role of Oligosaccharides in the Pharmacokinetics of Tissue-Derived and Genetically Engineered Cholinesterases
Mol. Pharmacol., January 1, 1998; 53(1): 112 - 122.
[Abstract] [Full Text]




Home Help [Feedback] [For Subscribers] [Archive] [Search] [Contents]
All ASPET Journals Molecular Pharmacology Pharmacological Reviews
 Molecular Interventions Drug Metabolism and Disposition

Copyright © 1991 by the American Society for Pharmacology and Experimental Therapeutics.