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Time course of cholinesterase inhibition in adult rats treated acutely with carbaryl, carbofuran, formetanate, methomyl, methiocarb, oxamyl or propoxur.

Publication ,  Journal Article
Padilla, S; Marshall, RS; Hunter, DL; Lowit, A
Published in: Toxicology and applied pharmacology
March 2007

To compare the toxicity of seven N-methyl carbamates, time course profiles for brain and red blood cell (RBC) cholinesterase (ChE) inhibition were established for each. Adult, male, Long Evans rats (n=4-5 dose group) were dosed orally with either carbaryl (30 mg/kg in corn oil); carbofuran (0.5 mg/kg in corn oil); formetanate HCl (10 mg/kg in water); methomyl (3 mg/kg in water); methiocarb (25 mg/kg in corn oil); oxamyl (1 mg/kg in water); or propoxur (20 mg/kg in corn oil). This level of dosing produced at least 40% brain ChE inhibition. Brain and blood were taken from 0.5 to 24 h after dosing for analysis of ChE activity using two different methods: (1) a radiometric method which limits the amount of reactivation of ChE activity, and (2) a spectrophotometric method (Ellman method using traditional, unmodified conditions) which may encourage reactivation. The time of peak ChE inhibition was similar for all seven N-methyl carbamate pesticides: 0.5-1.0 h after dosing. By 24 h, brain and RBC ChE activity in all animals returned to normal. The spectrophotometric method underestimated ChE inhibition. Moreover, there was a strong, direct correlation between brain and RBC ChE activity (radiometric assay) for all seven compounds combined (r(2)=0.73, slope 1.1), while the spectrophotometric analysis of the same samples showed a poor correlation (r(2)=0.09). For formetanate, propoxur, methomyl, and methiocarb, brain and RBC ChE inhibitions were not different over time, but for carbaryl, carbofuran and oxamyl, the RBC ChE was slightly more inhibited than brain ChE. These data indicate (1) the radiometric method is superior for analyses of ChE activity in tissues from carbamate-treated animals (2) that animals treated with these N-methyl carbamate pesticides are affected rapidly, and recover rapidly, and (3) generally, assessment of RBC ChE is an accurate predictor of brain ChE inhibition for these seven pesticides.

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Published In

Toxicology and applied pharmacology

DOI

EISSN

1096-0333

ISSN

0041-008X

Publication Date

March 2007

Volume

219

Issue

2-3

Start / End Page

202 / 209

Related Subject Headings

  • Toxicology
  • Toxicity Tests, Acute
  • Time Factors
  • Rats, Long-Evans
  • Rats
  • Pesticides
  • Molecular Structure
  • Male
  • Cholinesterases
  • Cholinesterase Inhibitors
 

Citation

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Padilla, S., Marshall, R. S., Hunter, D. L., & Lowit, A. (2007). Time course of cholinesterase inhibition in adult rats treated acutely with carbaryl, carbofuran, formetanate, methomyl, methiocarb, oxamyl or propoxur. Toxicology and Applied Pharmacology, 219(2–3), 202–209. https://doi.org/10.1016/j.taap.2006.11.010
Padilla, S., R. S. Marshall, D. L. Hunter, and A. Lowit. “Time course of cholinesterase inhibition in adult rats treated acutely with carbaryl, carbofuran, formetanate, methomyl, methiocarb, oxamyl or propoxur.Toxicology and Applied Pharmacology 219, no. 2–3 (March 2007): 202–9. https://doi.org/10.1016/j.taap.2006.11.010.
Padilla S, Marshall RS, Hunter DL, Lowit A. Time course of cholinesterase inhibition in adult rats treated acutely with carbaryl, carbofuran, formetanate, methomyl, methiocarb, oxamyl or propoxur. Toxicology and applied pharmacology. 2007 Mar;219(2–3):202–9.
Padilla, S., et al. “Time course of cholinesterase inhibition in adult rats treated acutely with carbaryl, carbofuran, formetanate, methomyl, methiocarb, oxamyl or propoxur.Toxicology and Applied Pharmacology, vol. 219, no. 2–3, Mar. 2007, pp. 202–09. Epmc, doi:10.1016/j.taap.2006.11.010.
Padilla S, Marshall RS, Hunter DL, Lowit A. Time course of cholinesterase inhibition in adult rats treated acutely with carbaryl, carbofuran, formetanate, methomyl, methiocarb, oxamyl or propoxur. Toxicology and applied pharmacology. 2007 Mar;219(2–3):202–209.
Journal cover image

Published In

Toxicology and applied pharmacology

DOI

EISSN

1096-0333

ISSN

0041-008X

Publication Date

March 2007

Volume

219

Issue

2-3

Start / End Page

202 / 209

Related Subject Headings

  • Toxicology
  • Toxicity Tests, Acute
  • Time Factors
  • Rats, Long-Evans
  • Rats
  • Pesticides
  • Molecular Structure
  • Male
  • Cholinesterases
  • Cholinesterase Inhibitors