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PRECLINICAL PUBLICATION · 2020

Crotoxin-Induced Mice Lung Impairment: Role of Nicotinic Acetylcholine Receptors and COX-Derived Prostanoids.

Mouse / Chemical/toxin

Evidence by therapy association

Study details and outcomes are extracted in the context of a specific intervention. Separate associations are retained rather than silently merged.

PMID 32443924 ↗2020Mixed findings

Crotoxin-Induced Mice Lung Impairment: Role of Nicotinic Acetylcholine Receptors and COX-Derived Prostanoids.

MouseChemical/toxinSwissMaleIndomethacin intraperitoneal; hexamethonium intravenous by tail vein; the other agents intraperitonealIndomethacin 3 mg/kg; hexamethonium bromide 10 mg/kg; MK-59…All drugs given as pre-treatment before crotoxin: indomethacin 4.5 h before, he…

Model: Acute lung impairment and respiratory failure induced by subcutaneous crotoxin, the phospholipase A2 complex of Crotalus durissus terrificus venom, at 300 microgram/kg, being 1.3 times the measured LD50 of 229.6 microgram/kg, with a parallel dorsal air pouch model

Indomethacin and hexamethonium each increased survival, whereas MK-591, neostigmine, methyl-atropine and propranolol did not. Indomethacin, but not hexamethonium, blocked the early rise in vascular permeability and lung PGE2. Hexamethonium, but not indomethacin, blocked the late rise in myeloperoxi…

Extraction: extract · Supplied extraction confidence: 0.85. Machine-extracted fields require source verification.