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Protection from lethality and behavioral incapacitation resulting from intoxication by soman (pinacolyl methylphosphonofluoridate) and treatment with atropine sulfate and 2-PAM chloride in the guinea pig, cavia porcellus.
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- Additional Information
- Source:
Publisher: Taylor & Francis Group Country of Publication: United States NLM ID: 7801723 Publication Model: Print Cited Medium: Print ISSN: 0148-0545 (Print) Linking ISSN: 01480545 NLM ISO Abbreviation: Drug Chem Toxicol Subsets: MEDLINE
- Publication Information:
Publication: [Philadelphia, PA] : Taylor & Francis Group
Original Publication: New York, Dekker.
- Subject Terms:
- Abstract:
The lethal and incapacitating effects of the toxic organophosphorus (OP) agent, soman were evaluated in guinea pigs. The protective effects of the standard therapies atropine sulfate (ATR) and pralidoxime chloride (2-PAM) in minimizing or reducing soman-produced lethality and incapacitation (evaluated using a modification of the rat conditioned avoidance procedure) were also studied. At 0.75 and 1.5 LD50 soman was extremely toxic and fast-acting; its effects appeared within five minutes, and its lethal effects occurred within the first three hours. Therapeutic combinations of ATR (64 or 128 mg/kg) and 2-PAM (25 or 100 mg/kg) protected animals from the lethality of soman, but not from its incapacitating effects. However, therapeutic treatment with ATR and 2-PAM also produced a behavioral toxicity in its own right, an effect which lasted for at least three hours in the guinea pig. This behavioral toxicity was lessened by reducing ATR dosage from 128 to 64 mg/kg, but 2-PAM dosage did not influence the behavioral toxicity of the treatment combinations within the range of dosages studied.
- Accession Number:
0 (Cholinesterase Reactivators)
0 (Pralidoxime Compounds)
7C0697DR9I (Atropine)
96-64-0 (Soman)
P7MU9UTP52 (pralidoxime)
- Publication Date:
Date Created: 19910111 Date Completed: 19911015 Latest Revision: 20190116
- Publication Date:
20231215
- Accession Number:
10.3109/01480549109017867
- Accession Number:
1889376
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