Evidence map›Paper›PMID 25530353›Full record

ArticleNeurotoxicology2015

Drug-dependent behaviors and nicotinic acetylcholine receptor expressions in Caenorhabditis elegans following chronic nicotine exposure.

Joseph R Polli, Dorothy L Dobbins, Robert A Kobet, Mary A Farwell, Baohong Zhang, Myon-Hee Lee, Xiaoping Pan

Open access · bronzeAbstract read
In one paragraph

Article in Neurotoxicology, 2015. 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
0.3field-weighted citation impact, top 46% 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, 22 citations in OpenAlex.

  1. Advances in drug addiction research usingFrontiers in cell and developmental biology · 2026
    Review
  2. Behavioral Changes inJournal of clinical medicine · 2025
    Article
  3. Article
  4. Article
  5. Nicotine Motivated Behavior inInternational journal of molecular sciences · 2024
    Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
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

7 authors at 1 institution in 1 country.

Joseph R PolliDepartment of Biology, East Carolina University, Greenville, NC 27858, USA.
Dorothy L DobbinsDepartment of Biology, East Carolina University, Greenville, NC 27858, USA.
Robert A KobetDepartment of Biology, East Carolina University, Greenville, NC 27858, USA.
Mary A FarwellDepartment of Biology, East Carolina University, Greenville, NC 27858, USA.
Baohong ZhangDepartment of Biology, East Carolina University, Greenville, NC 27858, USA.
Myon-Hee LeeDepartment of Medicine, East Carolina University, Greenville, NC 27858, USA.
Xiaoping PanDepartment of Biology, East Carolina University, Greenville, NC 27858, USA. Electronic address: Panx@ecu.edu.
East Carolina University · US

Funding

Identification of microRNAs responsive to nicotine exposureR03DA032515 · NIDA · EAST CAROLINA UNIVERSITY · PI ZHANG, BAOHONG · 2011 to 2013
$80k
NIDA NIH HHS R03 DA032515NIDA NIH HHS R03DA032515
6 · The paper itself

Abstract

Nicotine, the major psychoactive compound in tobacco, targets nicotinic acetylcholine receptors (nAChRs) and results in drug dependence. The nematode Caenorhabditis elegans' (C. elegans) genome encodes conserved and extensive nicotinic receptor subunits, representing a useful system to investigate nicotine-induced nAChR expressions in the context of drug dependence. However, the in vivo expression pattern of nAChR genes under chronic nicotine exposure has not been fully investigated. To define the role of nAChR genes involved in nicotine-induced locomotion changes and the development of tolerance to these effects, we characterized the locomotion behavior combining the use of two systems: the Worm Tracker hardware and the WormLab software. Our results indicate that the combined system is an advantageous alternative to define drug-dependent locomotion behavior in C. elegans. Chronic (24-h dosing) nicotine exposure at 6.17 and 61.7μM induced nicotine-dependent behaviors, including drug stimulation, tolerance/adaption, and withdrawal responses. Specifically, the movement speed of naïve worms on nicotine-containing environments was significantly higher than on nicotine-free environments, suggesting locomotion stimulation by nicotine. In contrast, the 24-h 6.17μM nicotine-treated worms exhibited significantly higher speeds on nicotine-free plates than on nicotine-containing plates. Furthermore significantly increased locomotion behavior during nicotine cessation was observed in worms treated with a higher nicotine concentration of 61.7μM. The relatively low locomotion speed of nicotine-treated worms on nicotine-containing environments also indicates adaption/tolerance of worms to nicotine following chronic nicotine exposure. In addition, this study provides useful information regarding the comprehensive in vivo expression profile of the 28 "core" nAChRs following different dosages of chronic nicotine treatments. Eleven genes (lev-1, acr-6, acr-7, acr-11, lev-8, acr-14, acr-16, acr-20, acr-21, ric-3, and unc-29) were significantly up-regulated following 61.7μM nicotine treatment, in which worms showed significantly increased locomotion behavior. This study provides insights into the linkage between nicotine-induced locomotion behavior and the regulation of nicotinic acetylcholine receptors.

Indexed as

AnimalsCaenorhabditis elegansMotor ActivityNicotineNicotinic AgonistsReceptors, NicotinicTobacco Use DisorderNicotineNicotinic AgonistsReceptors, NicotinicC. elegansDrug-dependent behaviorsGene expressionnAChRsNicotine

Identifiers

PMID25530353
PMCPMC4385460
OpenAlexW2031803302

What OpenQuestion holds

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Registered trials

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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.