Evidence map›Paper›PMID 31587506›Full record

ArticlePhysiological reports2019

Synaptic GABAergic transmission in the central amygdala (CeA) of rats depends on slice preparation and recording conditions.

Elizabeth M Avegno, Jason W Middleton, Nicholas W Gilpin

Open access · goldAbstract read
In one paragraph

Article in Physiological reports, 2019. 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
0.6field-weighted citation impact, top 33% 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, 8 citations in OpenAlex.

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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.

Elizabeth M AvegnoDepartment of Physiology, Louisiana State University Health Science Center, New Orleans, Louisiana.ORCID 0000-0003-0833-1392
Jason W MiddletonDepartment of Cell Biology and Anatomy, Louisiana State University Health Science Center, New Orleans, Louisiana.
Nicholas W GilpinDepartment of Physiology, Louisiana State University Health Science Center, New Orleans, Louisiana.
Louisiana State University Health Sciences Center New Orleans · US

Funding

Role of Neuropeptides in Stress-Induced Escalation of Alcohol DrinkingR01AA023305 · NIAAA · LSU HEALTH SCIENCES CENTER · PI GILPIN, NICHOLAS WARREN · 2014 to 2024
$3.7M
Traumatic stress increases alcohol drinking via endocannabinoid disinhibition of basolateral amygdalaR01AA026531 · NIAAA · LSU HEALTH SCIENCES CENTER · PI GILPIN, NICHOLAS WARREN, TASKER, JEFFREY G · 2017 to 2021
$1.9M
Brain Reward and Stress System Interactions in Alcohol DependenceF32AA025831 · NIAAA · LSU HEALTH SCIENCES CENTER · PI AVEGNO, ELIZABETH MINOR · 2017 to 2020
$210k
NIAAA NIH HHS AA023305NIAAA NIH HHS AA025831NIAAA NIH HHS AA026531NIAAA NIH HHS F32 AA025831NIAAA NIH HHS R01 AA023305NIAAA NIH HHS R01 AA026531VA BX003451
6 · The paper itself

Abstract

The central nucleus of the amygdala (CeA) is a primarily GABAergic brain region implicated in stress and addictive disorders. Using in vitro slice electrophysiology, many studies measure GABAergic neurotransmission to evaluate the impact of experimental manipulations on inhibitory tone in the CeA, as a measure of alterations in CeA activity and function. In a recent study, we reported spontaneous inhibitory postsynaptic current (sIPSC) frequencies higher than those typically reported in CeA neurons in the literature, despite utilizing similar recording protocols and internal recording solutions. The purpose of this study was to systematically evaluate two common methods of slice preparation, an NMDG-based aCSF perfusion method and an ice-cold sucrose solution, as well as the use of an in-line heater to control recording temperature, on measures of intrinsic excitability and spontaneous inhibitory neurotransmission in CeA neurons. We report that both slice preparation and recording conditions significantly impact spontaneous GABAergic transmission in CeA neurons, and that recording temperature, but not slicing solution, alters measures of intrinsic excitability in CeA neurons. Bath application of corticotropin-releasing factor (CRF) increased sIPSC frequency under all conditions, but the magnitude of this effect was significantly different across recording conditions that elicited different baseline GABAergic transmission. Furthermore, CRF effects on synaptic transmission differed according to data reporting methods (i.e., raw vs. normalized data), which is important to consider in relation to baseline synaptic transmission values. These studies highlight the impact of experimental conditions and data reporting methods on neuronal excitability and synaptic transmission in the CeA.

Indexed as

AnimalsCentral Amygdaloid NucleusGABAergic NeuronsInhibitory Postsynaptic PotentialsMaleOrgan Culture TechniquesRatsRats, WistarSynaptic Transmissioncentral amygdalaCRFelectrophysiologyneurotransmissionNMDG

Identifiers

PMID31587506
PMCPMC6778595
OpenAlexW2978196640

What OpenQuestion holds

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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.