Evidence map›Paper›PMID 17622340›Full record

ArticlePloS one2007

The circadian system is a target and modulator of prenatal cocaine effects.

Eva H Shang, Irina V Zhdanova

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
0.7field-weighted citation impact, top 39% 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

12 citing papers in PubMed, 39 citations in OpenAlex.

  1. Article
  2. Maternal developmental history alters transfer of circadian clock genes to offspring in Japanese quail (Coturnix japonica).Journal of comparative physiology. A, Neuroethology, sensory, neural, and behavioral physiology · 2024
    Article
  3. Article
  4. Article
  5. Article
  6. Dopaminergic control of anxiety in young and aged zebrafish.Pharmacology, biochemistry, and behavior · 2017
    Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Cocainomics: new insights into the molecular basis of cocaine addiction.Journal of neuroimmune pharmacology : the official journal of the Society on NeuroImmune Pharmacology · 2010
    Review
  12. 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

2 authors at 1 institution in 1 country.

Eva H ShangDepartment of Anatomy and Neurobiology, Boston University School of Medicine, Boston, Massachusetts, United States of America.
Irina V Zhdanova
Boston University · US

Funding

Cocaine-induced behaviors in larval zebrafishR01DA015418 · NIDA · BOSTON UNIVERSITY MEDICAL CAMPUS · PI ZHDANOVA, IRINA V. · 2003 to 2013
$2.3M
Melatonin, behavior and neuronal activity in zebrafishR01MH065528 · NIMH · BOSTON UNIVERSITY MEDICAL CAMPUS · PI ZHDANOVA, IRINA V. · 2003 to 2006
$1.1M
NIDA NIH HHS DA 1541801NIDA NIH HHS DA-4-7733NIMH NIH HHS MH 065528NIMH NIH HHS R01 MH065528
6 · The paper itself

Abstract

backgroundPrenatal exposure to cocaine can be deleterious to embryonic brain development, but the results in humans remain controversial, the mechanisms involved are not well understood and effective therapies are yet to be designed. We hypothesize that some of the prenatal effects of cocaine might be related to dysregulation of physiological rhythms due to alterations in the integrating circadian clock function. METHODOLOGY AND PRINCIPLE

findingsHere we introduce a new high-throughput genetically well-characterized diurnal vertebrate model for studying the mechanisms of prenatal cocaine effects by demonstrating reduced viability and alterations in the pattern of neuronal development following repeated cocaine exposure in zebrafish embryos. This effect is associated with acute cocaine-induced changes in the expression of genes affecting growth (growth hormone, zGH) and neurotransmission (dopamine transporter, zDAT). Analysis of circadian gene expression, using quantitative real-time RT-PCR (QPCR), demonstrates that cocaine acutely and dose-dependently changes the expression of the circadian genes (zPer-3, zBmal-1) and genes encoding melatonin receptors (zMelR) that mediate the circadian message to the entire organism. Moreover, the effects of prenatal cocaine depend on the time of treatment, being more robust during the day, independent of whether the embryos are raised under the light-dark cycle or in constant light. The latter suggests involvement of the inherited circadian factors. The principal circadian hormone, melatonin, counteracts the effects of cocaine on neuronal development and gene expression, acting via specific melatonin receptors. CONCLUSIONS/SIGNIFICANCE: These findings demonstrate that, in a diurnal vertebrate, prenatal cocaine can acutely dysregulate the expression of circadian genes and those affecting melatonin signaling, growth and neurotransmission, while repeated cocaine exposure can alter neuronal development. Daily variation in these effects of cocaine and their attenuation by melatonin suggest a potential prophylactic or therapeutic role for circadian factors in prenatal cocaine exposure.

Indexed as

AnimalsAnimals, Genetically ModifiedCircadian RhythmCocaineCocaine-Related DisordersEmbryo, NonmammalianFemaleFetal DeathGenes, ReporterGreen Fluorescent ProteinsHumansMelatoninModels, AnimalPregnancyPrenatal Exposure Delayed EffectsSynaptic TransmissionCocaineGreen Fluorescent ProteinsMelatonin

Identifiers

PMID17622340
PMCPMC1899232
OpenAlexW1967342025

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.