Single-dose and 13-week repeated-dose neurotoxicity screening studies of chlorpyrifos insecticide

• Published in: Food and chemical toxicology Vol. 34; no. 4; pp. 393 - 405
• Main Authors: Mattsson, J.L., Wilmer, J.W., Shankar, M.R., Berdasco, N.M., Crissman, J.W., Maurissen, J.P., Bond, D.M.
• Format: Journal Article
• Language: English
• Published: Oxford Elsevier Ltd 01.04.1996; New York, NY Elsevier Science
• Subjects: Administration, Oral; Animals; Behavior, Animal - drug effects; Biological and medical sciences; Body Weight - drug effects; Central Nervous System - drug effects; Central Nervous System - pathology; Chlorpyrifos - administration & dosage; Chlorpyrifos - toxicity; Dose-Response Relationship, Drug; Drug Administration Schedule; Drug Evaluation, Preclinical; Eliminative Behavior, Animal - drug effects; Female; Hindlimb - physiology; Intubation, Gastrointestinal; Male; Medical sciences; Motor Activity - drug effects; Pesticides, fertilizers and other agrochemicals toxicology; Rats; Rats, Inbred F344; Toxicology; AChE; ChE; OP; Rep-ANOVA; ANOVA; CPF; FOB; US EPA; OPIDN; CPF-oxon; NTE; Chlorpyrifos; Nervous system diseases; Insecticide; Rat; Toxicity; Rodentia; Single dose; Pesticides; Neuropsychological test; Oral administration; Administration schedule; Multiple dose; Vertebrata; Mammalia; Histopathology; Animal; Organophosphorus compounds; Anticholinesterase agent; Behavior
• ISSN: 0278-6915; 1873-6351
• DOI: 10.1016/0278-6915(96)00121-4

Chlorpyrifos (CPF), a widely used organophosphate insecticide, was screened for neurotoxic effects in Fischer 344 rats using United States Environmental Protection Agency 1991 guidelines for single-dose and 13-wk repeated dose studies. The studies emphasized a functional observational battery (which included grip performance and hindlimb splay tests), automated motor activity testing and comprehensive neurohistopathology of perfused tissues. Doses of up to 100 mg/kg body weight in corn oil by gavage in the single-dose study and up to 15 mg/kg body weight/day in diet for 13 wk in the repeated dose study were administered. It is known that CPF and other phosphorothionates can be activated to the oxon in local (extrahepatic) tissues. Local activation could possibly cause different effects in different tissues with cholinergic innervation, and thereby create syndromes unique to each phosphorothionate according to their structure. Consequently, the conduct of CPF neurotoxicity screening studies by contemporary guidelines offered an opportunity to characterize the CPF over-exposure syndrome in rats. Single-dose Zhigh levels of oral exposure to CPF caused a range of clinical signs characteristic of cholinergic overstimulation. Although there was no clinical evidence of wide differences in sensitivity of one cholinergic response versus another, motor dysfunction (inco-ordination etc.) was more prominent than other signs, for example soiling. Effects were much more apparent in females and regressed over several days. Effects were minimal in the 13-wk study, and there was no evidence of accumulation of toxicity during the 13 wk of daily dietary exposure. Motor activity was decreased at the high dose in males and females at wk 4, but was not significantly different from controls in subsequent weeks. The ‘normalization’ of motor activity later in the study was interpreted as tolerance to repeated administration of CPF. Comprehensive neuropathological examination revealed no treatment-related lesions in either study