Literature DB >> 1714639

Comparison of in vivo cholinesterase inhibition in neonatal and adult rats by three organophosphorothioate insecticides.

C N Pope1, T K Chakraborti, M L Chapman, J D Farrar, D Arthun.   

Abstract

Developing mammals are more sensitive than adults to a variety of organophosphorothioate insecticides (OPs), compounds which act in vivo by inhibition of cholinesterase (ChE). Little is known, however, regarding age-related differences in biochemical responses to these toxicants. The time course of ChE inhibition and recovery in whole brain was compared in neonatal (7 days of age) and adult (80-100 days of age) rats after treatment with maximal tolerated doses (MTDs) of either methyl parathion (MPS), parathion (PS) or chlorpyrifos (CPF). Neonatal rats were more sensitive than adults in all cases (MTDs for MPS, PS and CPF; neonates = 7.8, 2.1 and 45 mg/kg, s.c.; adults = 18, 18, and 279 mg/kg, s.c., respectively). In general, maximal brain ChE inhibition was similar (greater than 78%) in both age groups but ChE activity recovered faster in neonates. Plasma and erythrocyte ChE activities correlated relatively well (r = 0.794-0.943) with brain ChE activity in neonatal rats at all time points between 4 h and 7 days after treatment but similar correlations between circulating and brain ChE activities in adults were more variable (r = 0.211-0.917). The results indicate that neonatal rats are more sensitive to acute lethality from these compounds and that MTD exposures produce extensive brain ChE inhibition in both age groups. Significant inhibitor-related and age-related differences in the duration of ChE inhibition can ensue, however, following such OP exposures.

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Year:  1991        PMID: 1714639     DOI: 10.1016/0300-483x(91)90061-5

Source DB:  PubMed          Journal:  Toxicology        ISSN: 0300-483X            Impact factor:   4.221


  40 in total

1.  Chlorpyrifos induced region specific vulnerability in rat CNS and modulation by age and cold stress: an interactive study.

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2.  Ontogenic expression of human carboxylesterase-2 and cytochrome P450 3A4 in liver and duodenum: postnatal surge and organ-dependent regulation.

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Journal:  Toxicology       Date:  2015-02-24       Impact factor: 4.221

3.  Pharmacokinetics and pharmacodynamics of chlorpyrifos in adult male Long-Evans rats following repeated subcutaneous exposure to chlorpyrifos.

Authors:  Corie A Ellison; Jordan Ned Smith; Pamela J Lein; James R Olson
Journal:  Toxicology       Date:  2011-06-17       Impact factor: 4.221

4.  A comparison of neurotoxicity in cerebellum produced by dermal application of chlorpyrifos in young and adult mice.

Authors:  K Krishnan; N K Mitra; L S Yee; H M Yang
Journal:  J Neural Transm (Vienna)       Date:  2011-09-16       Impact factor: 3.575

5.  Endocannabinoid signaling in neurotoxicity and neuroprotection.

Authors:  C Pope; R Mechoulam; L Parsons
Journal:  Neurotoxicology       Date:  2009-12-05       Impact factor: 4.294

6.  Human carboxylesterases HCE1 and HCE2: ontogenic expression, inter-individual variability and differential hydrolysis of oseltamivir, aspirin, deltamethrin and permethrin.

Authors:  Dongfang Yang; Robin E Pearce; Xiliang Wang; Roger Gaedigk; Yu-Jui Yvonne Wan; Bingfang Yan
Journal:  Biochem Pharmacol       Date:  2008-10-15       Impact factor: 5.858

7.  In vitro sensitivity of cholinesterases and [3H]oxotremorine-M binding in heart and brain of adult and aging rats to organophosphorus anticholinesterases.

Authors:  Nikita Mirajkar; Carey N Pope
Journal:  Biochem Pharmacol       Date:  2008-08-12       Impact factor: 5.858

8.  Effect of different administration paradigms on cholinesterase inhibition following repeated chlorpyrifos exposure in late preweanling rats.

Authors:  Russell L Carr; Carole A Nail
Journal:  Toxicol Sci       Date:  2008-08-14       Impact factor: 4.849

Review 9.  Pesticide exposure and neurodevelopmental outcomes: review of the epidemiologic and animal studies.

Authors:  Carol J Burns; Laura J McIntosh; Pamela J Mink; Anne M Jurek; Abby A Li
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10.  Chlorpyrifos and chlorpyrifos-oxon inhibit axonal growth by interfering with the morphogenic activity of acetylcholinesterase.

Authors:  Dongren Yang; Angela Howard; Donald Bruun; Mispa Ajua-Alemanj; Cecile Pickart; Pamela J Lein
Journal:  Toxicol Appl Pharmacol       Date:  2007-11-17       Impact factor: 4.219

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