Literature DB >> 19934164

Time-course, dose-response, and age comparative sensitivity of N-methyl carbamates in rats.

Virginia C Moser1, Katherine L McDaniel, Pamela M Phillips, Anna B Lowit.   

Abstract

N-Methyl carbamate insecticides are reversible inhibitors of central and peripheral acetylcholinesterase (ChE). Despite their widespread use, there are few studies of neurotoxicity in young animals. To study potential age-related differences, we evaluated seven carbamates (carbaryl, carbofuran, formetanate, methiocarb, methomyl, oxamyl, and propoxur) in preweanling (17 days old or postnatal day [PND] 17) male rats. Motor activity was monitored, and ChE inhibition was measured in brain and red blood cells (RBCs) using a radiometric assay that minimized reactivation of ChE. First, we conducted time-course studies in PND17 Long-Evans male rats, using a single oral dose of each carbamate. Almost all carbamates showed maximal ChE inhibition at a 45-min time point; only methomyl showed an earlier peak effect (15 min). At 24 h, most inhibition had recovered. Next, dose-response data were collected for each carbamate, using four doses and control, with motor activity testing beginning 15 min after dosing and tissue collection at 40-45 min. RBC ChE was generally inhibited to a greater degree than brain. Motor activity was not as sensitive a measure for some of the carbamates, with some differences across carbamates in the shapes of the dose-response curves. Additional studies documented age-related differences by comparing ChE inhibition in PND11, PND17, and adult rats following administration of carbaryl or carbofuran. Only the youngest (PND11) rats were more sensitive than adults to carbaryl, but both younger ages showed more effects than adults with carbofuran. Comparisons of the other carbamates to previous studies in adult rats suggest similar age-related sensitivity. Thus, these data show the time-course and dose-response characteristics for each carbamate and document greater sensitivity of the young for carbofuran and carbaryl.

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Year:  2009        PMID: 19934164     DOI: 10.1093/toxsci/kfp286

Source DB:  PubMed          Journal:  Toxicol Sci        ISSN: 1096-0929            Impact factor:   4.849


  6 in total

1.  Inhibition of the transforming growth factor-β/SMAD cascade mitigates the anti-neurogenic effects of the carbamate pesticide carbofuran.

Authors:  Brashket Seth; Anuradha Yadav; Swati Agarwal; Shashi Kant Tiwari; Rajnish Kumar Chaturvedi
Journal:  J Biol Chem       Date:  2017-10-05       Impact factor: 5.157

Review 2.  Developmental neurotoxicity of succeeding generations of insecticides.

Authors:  Yael Abreu-Villaça; Edward D Levin
Journal:  Environ Int       Date:  2016-11-28       Impact factor: 9.621

Review 3.  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
Journal:  J Toxicol Environ Health B Crit Rev       Date:  2013       Impact factor: 6.393

4.  Carbofuran occupational dermal toxicity, exposure and risk assessment.

Authors:  Derek W Gammon; Zhiwei Liu; John M Becker
Journal:  Pest Manag Sci       Date:  2011-08-10       Impact factor: 4.845

5.  Analysis of biomarker utility using a PBPK/PD model for carbaryl.

Authors:  Martin B Phillips; Miyoung Yoon; Bruce Young; Yu-Mei Tan
Journal:  Front Pharmacol       Date:  2014-11-18       Impact factor: 5.810

6.  Zinc Ameliorate Oxidative Stress and Hormonal Disturbance Induced by Methomyl, Abamectin, and Their Mixture in Male Rats.

Authors:  Sameeh A Mansour; Mostafa A Abbassy; Hassan A Shaldam
Journal:  Toxics       Date:  2017-12-03
  6 in total

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