Evidence map›Paper›PMID 31206717›Full record

ArticleAlcoholism, clinical and experimental research2019

Embryonic Ethanol Exposure Affects the Early Development, Migration, and Location of Hypocretin/Orexin Neurons in Zebrafish.

Adam D Collier, Viktoriya Halkina, Soe S Min, Mia Y Roberts, Samantha D Campbell, Kaylin Camidge, Sarah F Leibowitz

Open access · greenAbstract read
In one paragraph

Article in Alcoholism, clinical and experimental research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
1.9field-weighted citation impact, top 15% 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

23 citing papers in PubMed, 30 citations in OpenAlex.

  1. Review
  2. Varanid Teeth Asymmetry and Correlation to Body Size.Journal of developmental biology · 2025
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  17. Sleep dysregulation in binge eating disorder and "food addiction": the orexin (hypocretin) system as a potential neurobiological link.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2021
    Review
  18. Zebrafish models of fetal alcohol spectrum disorders.Genesis (New York, N.Y. : 2000) · 2021
    Review
  19. Article
  20. 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

7 authors at 1 institution in 1 country.

Adam D CollierLaboratory of Behavioral Neurobiology, The Rockefeller University, New York, New York.ORCID 0000-0001-5104-8889
Viktoriya HalkinaLaboratory of Behavioral Neurobiology, The Rockefeller University, New York, New York.
Soe S MinLaboratory of Behavioral Neurobiology, The Rockefeller University, New York, New York.
Mia Y RobertsLaboratory of Behavioral Neurobiology, The Rockefeller University, New York, New York.
Samantha D CampbellLaboratory of Behavioral Neurobiology, The Rockefeller University, New York, New York.
Kaylin CamidgeLaboratory of Behavioral Neurobiology, The Rockefeller University, New York, New York.
Sarah F LeibowitzLaboratory of Behavioral Neurobiology, The Rockefeller University, New York, New York.
Rockefeller University · US

Funding

Excess ethanol drinking after prenatal exposure to ethanol: chemokine signaling and orexigenic neuropeptidesR01AA024798 · NIAAA · ROCKEFELLER UNIVERSITY · PI LEIBOWITZ, SARAH F. · 2016 to 2020
$1.9M
NIAAA NIH HHS R01 AA024798
6 · The paper itself

Abstract

backgroundEmbryonic ethanol (EtOH) exposure is known to increase alcohol drinking later in life and have long-term effects on neurochemical systems in the brain. With zebrafish having marked advantages for elucidating neural mechanisms underlying brain disorders, we recently tested and showed in these fish, similar to rodents, that low-dose embryonic EtOH stimulates voluntary consumption of EtOH while increasing expression of hypocretin/orexin (hcrt) neurons, a neuropeptide that promotes consummatory and reward-related behaviors. The goal of the present study was to characterize how embryonic EtOH affects early development of the hcrt system and produces persistent changes at older ages that may contribute to this increase in EtOH consumption.

methodsWe utilized live imaging and Imaris software to investigate how low-dose embryonic EtOH (0.5%), administered from 22 to 24 hours postfertilization, affects specific properties of hcrt neurons in hcrt:EGFP transgenic zebrafish at different ages.

resultsTime-lapse imaging from 24 to 28 hpf showed that embryonic EtOH increased the number of hcrt neurons, reduced the speed, straightness, and displacement of their migratory paths, and altered their direction early in development. At older ages up to 6 dpf, the embryonic EtOH-induced increase in hcrt neurons was persistent, and the neurons became more widely dispersed. These effects of embryonic EtOH were found to be asymmetric, occurring predominantly on the left side of the brain, and at 6 dpf, they resulted in marked changes in the anatomical location of the hcrt neurons, with some detected outside their normal position in the anterior hypothalamus again primarily on the left side.

conclusionsOur findings demonstrate that low-dose embryonic EtOH has diverse, persistent, and asymmetric effects on the early development of hypothalamic hcrt neurons, which lead to abnormalities in their ultimate location that may contribute to behavioral disturbances, including an increase in EtOH consumption.

Indexed as

AgingAlcohol DrinkingAnimalsAnimals, Genetically ModifiedCell CountCell MovementDominance, CerebralEmbryo, NonmammalianEthanolHypothalamus, AnteriorNeuronsOrexinsZebrafishEthanolOrexinsFetal Alcohol SyndromeHypocretinOrexinPrenatal EtOH ExposureZebrafish

Identifiers

PMID31206717
PMCPMC6677602
OpenAlexW2951547619

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.