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Chronic, intermittent exposure to chlorpyrifos in rats: Protracted effects on axonal transport, neurotrophin receptors, cholinergic markers, and information processing

  • Alvin V. Terry(corresponding author)
    ,
  • Debra A. Gearhart
    ,
  • Wayne D. Beck
    ,
  • Jacob N. Truan
    ,
  • Mary Louise Middlemore
    ,
  • Leah N. Williamson
*Corresponding author for this work
Scholary Output:
Contribution to journal
Article
Peer-review

Abstract

Persistent behavioral abnormalities have been commonly associated with acute organophosphate (OP) pesticide poisoning; however, relatively little is known about the consequences of chronic OP exposures that are not associated with acute cholinergic symptoms. In this study, the behavioral and neurochemical effects of chronic, intermittent, and subthreshold exposures to the OP pesticide, chlorpyrifos (CPF), were investigated. Rats were injected with CPF s.c. (dose range, 2.5-18.0 mg/kg) every other day over the course of 30 days and then were given a 2-week CPF-free washout period. In behavioral experiments conducted during the washout period, dose-dependent decrements in a water-maze hidden platform task and a prepulse inhibition procedure were observed, without significant effects on open-field activity, Rotorod performance, grip strength, or a spontaneous novel object recognition task. After washout, levels of CPF and its metabolite 3,5,6-trichloro-2-pyridinol were minimal in plasma and brain; however, cholinesterase inhibition was still detectable. Furthermore, the 18.0 mg/kg dose of CPF was associated with (brain region-dependent) decreases in nerve growth factor receptors and cholinergic proteins including the vesicular acetylcholine transporter, the high-affinity choline transporter, and the α7-nicotinic acetylcholine receptor. These deficits were accompanied by decreases in anterograde and retrograde axonal transport measured in sciatic nerves ex vivo. Thus, low-level (intermittent) exposure to CPF has persistent effects on neurotrophin receptors and cholinergic proteins, possibly through inhibition of fast axonal transport. Such neurochemical changes may lead to deficits in information processing and cognitive function.

Publication Information

Output type

Scholary Output:
Contribution to journal
Article
Peer-review

Original language

English (US)

Pages from-to (Number of pages)

Pages 1117-1128 (12 pages)

Journal (Volume, Issue Number)

Journal of Pharmacology and Experimental Therapeutics (Volume 322, Issue 3)

Publication milestones

  • Published - 09/2007

Publication status

Published - 09/2007

ISSN

0022-3565

Publication IDs

  • Scopus: 34548098919
  • PubMed: 17548533
  • ORCID: /0000-0003-2071-4767/work/68251881

Publication metrics

Metrics

Scopus
citations
SciVal
citations
72
Fractional count
1
Fractional count
0.10
Fractional count
9
Fractional count
0.90
Fractional count
1
Fractional count
1
SciVal
FWCI
1.36
SciVal
Author count
10
SciVal
Paper percentile
92
SciVal
Top percentile
10

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Citation count
85
Captures
55

Funding Details

FunderFunding number
NIEHS
R01ES012241