Evidence map›Paper›PMID 33385490›Full record

ArticleNeuroscience2021

Chronic Ethanol Exposure Potentiates Cholinergic Neurotransmission in the Basolateral Amygdala.

Sarah E Sizer, Brian C Parrish, Brian A McCool

Open access · greenAbstract read
In one paragraph

Article in Neuroscience, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.7field-weighted citation impact, top 32% 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

7 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. 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

3 authors at 1 institution in 1 country.

Sarah E SizerDepartment of Physiology and Pharmacology, Piedmont Triad Community Research Center (PTCRC), Wake Forest School of Medicine, 115 S Chestnut Street, Winston-Salem, NC 27101, USA. Electronic address: ssizer@wakehealth.edu.
Brian C ParrishDepartment of Physiology and Pharmacology, Piedmont Triad Community Research Center (PTCRC), Wake Forest School of Medicine, 115 S Chestnut Street, Winston-Salem, NC 27101, USA. Electronic address: bparrish@wakehealth.edu.
Brian A McCoolDepartment of Physiology and Pharmacology, Piedmont Triad Community Research Center (PTCRC), Wake Forest School of Medicine, 115 S Chestnut Street, Winston-Salem, NC 27101, USA. Electronic address: bmccool@wakehealth.edu.
Wake Forest University · US

Funding

Wake Forest Translational Alcohol Research Center (WF-TARC)P50AA026117 · NIAAA · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI Colleen A Hanlon · 2018 to 2026
$16.2M
MULTI-DISCIPLINARY TRAINING IN THE BIOLOGY OF ALCOHOLISMT32AA007565 · NIAAA · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI BRIAN A MCCOOL · 1994 to 2026
$10.1M
The Ethanol - Anxiety Interaction: Cellular MechanismsR01AA014445 · NIAAA · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI MCCOOL, BRIAN A · 2004 to 2023
$5.2M
Ethanol Dependence Induced Changes in Dopamine Signaling in Basolateral AmygdalaR01AA023999 · NIAAA · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI JONES, SARA RAULERSON, MCCOOL, BRIAN A · 2015 to 2019
$1.8M
Ethanol Modulation of Presynaptic Vesicle Recycling: Role of Munc13 ProteinsR21AA026572 · NIAAA · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI MCCOOL, BRIAN A · 2018 to 2019
$404k
Dissecting the Role of Nucleus Basalis Magnocellularis Circuitry in Basolateral Amygdala Physiology and Regulation of Anxiety Following Chronic Ethanol Exposure and WithdrawalF31AA028722 · NIAAA · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI SIZER, SARAH ELIZABETH · 2021 to 2022
$72k
NIAAA NIH HHS F31 AA028722NIAAA NIH HHS P50 AA026117NIAAA NIH HHS R01 AA014445NIAAA NIH HHS R01 AA023999NIAAA NIH HHS R21 AA026572NIAAA NIH HHS T32 AA007565
6 · The paper itself

Abstract

Chronic intermittent ethanol (CIE) exposure dysregulates glutamatergic and GABAergic neurotransmission, facilitating basolateral amygdala (BLA) pyramidal neuron hyperexcitability and the expression of anxiety during withdrawal. It is unknown whether ethanol-induced alterations in nucleus basalis magnocellularis (NBM) cholinergic projections to the BLA mediate anxiety-related behaviors through direct modulation of GABA and glutamate afferents. Following 10 days of CIE exposure and 24 h of withdrawal, we recorded GABAergic and glutamatergic synaptic responses in BLA pyramidal neurons with electrophysiology, assessed total protein expression of cholinergic markers, and quantified acetylcholine and choline concentrations using a colorimetric assay. We measured α

Indexed as

AmygdalaBasolateral Nuclear ComplexEthanolAnimalsCholinergic AgentsExcitatory Postsynaptic PotentialsMaleRatsRats, Sprague-DawleySynapsesSynaptic TransmissionCholinergic AgentsEthanolacetylcholinebasolateral amygdalapatch-clamp electrophysiologypresynapticwithdrawal

Identifiers

PMID33385490
PMCPMC7856184
OpenAlexW3114961649

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.