Evidence map›Paper›PMID 29935250›Full record

ArticleFood and chemical toxicology : an international journal published for the British Industrial Biological Research Association2018

Inhibition of cholinergic and non-cholinergic targets following subacute exposure to chlorpyrifos in normal and high fat fed male C57BL/6J mice.

George E Howell, Sandeep Kondakala, Julie Holdridge, Jung Hwa Lee, Matthew K Ross

Abstract read
In one paragraph

Article in Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
4.4field-weighted citation impact, top 6% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

10 citing papers in PubMed, 26 citations in OpenAlex.

  1. Article
  2. Endocannabinoid System and Metabolism: The Influences of Sex.International journal of molecular sciences · 2024
    Review
  3. Article
  4. Cnr1Chemico-biological interactions · 2023
    Article
  5. Article
  6. Concentration-dependent effects of chlorpyrifos oxon on peroxisome proliferator-activated receptor signaling in MCF-7 cells.Toxicology in vitro : an international journal published in association with BIBRA · 2022
    Article
  7. Article
  8. Article
  9. Effects ofFrontiers in nutrition · 2021
    Article
  10. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors at 1 institution in 1 country.

George E HowellMississippi State University College of Veterinary Medicine, 240 Wise Center, Drive P.O. Box 6100, Mississippi State, MS, 39762, USA. Electronic address: geh3@msstate.edu.
Sandeep KondakalaMississippi State University College of Veterinary Medicine, 240 Wise Center, Drive P.O. Box 6100, Mississippi State, MS, 39762, USA.
Julie HoldridgeMississippi State University College of Veterinary Medicine, 240 Wise Center, Drive P.O. Box 6100, Mississippi State, MS, 39762, USA.
Jung Hwa LeeMississippi State University College of Veterinary Medicine, 240 Wise Center, Drive P.O. Box 6100, Mississippi State, MS, 39762, USA.
Matthew K RossMississippi State University College of Veterinary Medicine, 240 Wise Center, Drive P.O. Box 6100, Mississippi State, MS, 39762, USA.
Mississippi State University · US

Funding

Summer Research Experience for Veterinary StudentsT35OD010432 · OD · MISSISSIPPI STATE UNIVERSITY · PI Barbara Lee-Faubert Kaplan, Temesgen Samuel · 2012 to 2026
$1.3M
NIH HHS T35 OD010432
6 · The paper itself

Abstract

The effects of obesity on organophosphate pesticide-mediated toxicities, including both cholinergic and non-cholinergic targets, have not been fully elucidated. Therefore, the present study was designed to determine if high fat diet intake alters the effects of repeated exposure to chlorpyrifos (CPS) on the activities of both cholinergic and noncholinergic serine hydrolase targets. Male C57BL/6J mice were placed on either standard rodent chow or high fat diet for four weeks with CPS exposure (2.0 mg/kg) for the last 10 days of diet intake. Exposure to CPS did not alter acetylcholinesterase in the central nervous system, but it did significantly inhibit circulating cholinesterase activities in both diet groups. CPS significantly inhibited hepatic carboxylesterase and fatty acid amide hydrolase and this inhibition was significantly greater in high fat fed animals. Additionally, CPS exposure and high fat diet intake downregulated genes involved in hepatic de novo lipogenesis as well as cytochrome P450 enzymes involved in hepatic xenobiotic metabolism. In summary, the present study demonstrates that high fat diet intake potentiates CPS mediated inhibition of both carboxylesterase and fatty acid amide hydrolase in the liver of obese animals following subacute exposure and suggests obesity may be a risk factor for increased non-cholinergic hepatic CPS toxicity.

Indexed as

Diet, High-FatAmidohydrolasesAnimalsChlorpyrifosCholinesterase InhibitorsCholinesterasesEndocannabinoidsErythrocytesFatty Acid Amide HydrolasesInsecticidesLiverMaleMice, Inbred C57BLMonoacylglycerol LipasesToxicity Tests, SubacuteAmidohydrolasesChlorpyrifosCholinesterase InhibitorsCholinesterasesEndocannabinoidsFatty Acid Amide HydrolasesInsecticidesMonoacylglycerol LipasesAcetylcholinesteraseCarboxylesteraseChlorpyrifosEndocannabinoidHigh fat dietOrganophosphate

Identifiers

PMID29935250
PMCPMC6534279
OpenAlexW2809346128

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.