Evidence map›Paper›PMID 30217435›Full record

ReviewAlcohol (Fayetteville, N.Y.)2018

CRF modulation of central monoaminergic function: Implications for sex differences in alcohol drinking and anxiety.

Kristen E Pleil, Mary Jane Skelly

Abstract readReview
In one paragraph

Review in Alcohol (Fayetteville, N.Y.), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.6field-weighted citation impact, top 20% 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

16 citing papers in PubMed, 30 citations in OpenAlex.

  1. Article
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  6. Sex differences in offspring risk and resilience following 11β-hydroxylase antagonism in a rodent model of maternal immune activation.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2024
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  16. Health anxiety in medical employees: A multicentre study.The Journal of international medical research · 2019
    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.

Kristen E PleilDepartment of Pharmacology, Weill Cornell Medicine, Cornell University, New York, NY 10065 United States. Electronic address: krp2013@med.cornell.edu.
Mary Jane SkellyDepartment of Pharmacology, Weill Cornell Medicine, Cornell University, New York, NY 10065 United States.
Cornell University · US

Funding

The role of excitatory inputs to BNST CRF neurons in alcohol drinking behaviorR00AA023559 · NIAAA · WEILL MEDICAL COLL OF CORNELL UNIV · PI PLEIL, KRISTEN ELIZABETH · 2017 to 2019
$887k
Alcoholism and Stress: A Framework for Future Treatment StrategiesR13AA017581 · NIAAA · SCRIPPS RESEARCH INSTITUTE, THE · PI ROBERTO, MARISA · 2008 to 2022
$285k
NIAAA NIH HHS R00 AA023559NIAAA NIH HHS R13 AA017581
6 · The paper itself

Abstract

Decades of research have described the importance of corticotropin-releasing factor (CRF) signaling in alcohol addiction, as well as in commonly co-expressed neuropsychiatric diseases, including anxiety and mood disorders. However, CRF signaling can also acutely regulate binge alcohol consumption, anxiety, and affect in non-dependent animals, possibly via modulation of central monoaminergic signaling. We hypothesize that basal CRF tone is particularly high in animals and humans with an inherent propensity for high anxiety and alcohol consumption, and thus these individuals are at increased risk for the development of alcohol use disorder and comorbid neuropsychiatric diseases. The current review focuses on extrahypothalamic CRF circuits, particularly those stemming from the bed nucleus of the stria terminalis (BNST), found to play a role in basal phenotypes, and examines whether the intrinsic hyperactivity of these circuits is sufficient to escalate the expression of these behaviors and steepen the trajectory of development of disease states. We focus our efforts on describing CRF modulation of biogenic amine neuron populations that have widespread projections to the forebrain to modulate behaviors, including alcohol and drug intake, stress reactivity, and anxiety. Further, we review the known sex differences and estradiol modulation of these neuron populations and CRF signaling at their synapses to address the question of whether females are more susceptible to the development of comorbid addiction and stress-related neuropsychiatric diseases because of hyperactive extrahypothalamic CRF circuits compared to males.

Indexed as

Alcohol DrinkingAlcohol-Related DisordersAnxietyAnxiety DisordersBinge DrinkingBiogenic MonoaminesCorticotropin-Releasing HormoneDopamineEstradiolFemaleHumansMaleNeural PathwaysNeuronsNorepinephrineSeptal NucleiBiogenic MonoaminesCorticotropin-Releasing HormoneDopamineEstradiolNorepinephrineSerotoninAlcoholAnxietyBed nucleus of the stria terminalis (BNST)Corticotropin releasing factor (CRF)Dopamine (DA)EstrogenNorepinephrine (NE)Serotonin (5-HT)

Identifiers

PMID30217435
PMCPMC6141347
OpenAlexW2793108325

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.