Evidence map›Paper›PMID 25337378›Full record

ArticleBasic and clinical neuroscience2014

Microinfusion of bupropion inhibits putative GABAergic neuronal activity of the ventral tegmental area.

Sanaz Amirabadi, Firouz Ghaderi Pakdel, Parviz Shahabi, Somayyeh Naderi, Mostafa Ashrafi Osalou, Ulker Cankurt

Open access · greenAbstract read
In one paragraph

Article in Basic and clinical neuroscience, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
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

3 citing papers in PubMed, 6 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

6 authors at 2 institutions in 1 country.

Sanaz AmirabadiDepartment of Physiology, Faculty of Medicine, Urmia University of Medical Sciences, Urmia, Iran.
Firouz Ghaderi PakdelDepartment of Physiology, Faculty of Medicine, Urmia University of Medical Sciences, Urmia, Iran ; Neurophysiology Research Center, Urmia University of Medical Sciences, Urmia, Iran.
Parviz ShahabiNeuroscience Research Center, Department of Physiology, Tabriz University of Medical Sciences, Tabriz, Iran.
Somayyeh NaderiDanesh Pey Hadi Co., Faculty of Medicine, Urmia University of Medical Sciences, Urmia, Iran.
Mostafa Ashrafi OsalouDanesh Pey Hadi Co., Faculty of Medicine, Urmia University of Medical Sciences, Urmia, Iran ; Department of Histology & Embryology, School of Medicine, Dokuz Eylol University, Izmir, Turkey.
Ulker CankurtDepartment of Histology & Embryology, School of Medicine, Dokuz Eylol University, Izmir, Turkey.
Urmia University · IRUrmia University of Medical Sciences

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionThe most common interpretation for the mechanisms of antidepression is the increase of the brain monoamine levels such as dopamine (DA). The increase of DA can reduce depression but it can also decrease the monoamine release because of autoreceptor inhibition. Although bupropion can decrease the dopamine release, there is evidence about stimulatory effects of chronic application of bupropion on ventral tegmental area (VTA) neurons. In this study, the intra-VTA acute microinfusion of bupropion on putative VTA non-Dopaminergic (VTA-nonDA) neuronal firing rates was evaluated by a single neuron recording technique.

methodsAnimals were divided into 7 groups (sham, and 6 bupropion-microinfused groups with 1, 10(-1), 10(-2), 10(-3), 10(-4), and 10(-5) mol, 1 µl/3 min, intra-VTA). A single neuron recording technique was done according to the stereotaxic coordination. After 10 min baseline recording, ACSF or bupropion was microinfused. The recording continued to recovery period in the treated groups. The prestimulus time (PST) and interspike interval (ISI) histograms were calculated for every single unit. The assessment of the drug effect was carried out by one-way analysis of variance (ANOVA) and Post-hoc test.

results126 non-DA neurons were separated. Bupropion could inhibit 116 neurons and 11 neurons had no significant response. Maximum inhibition was 79.1% of baseline firing rate with 44.3 min duration. The inhibitory effect of bupropion was dose-dependent. DISCUSSION: The acute inhibitory effects of bupropion on VTA-nonDA neurons can explain the fast inhibitory effects of bupropion and other antidepressants on the VTA. These data can explain some side effects of antidepressants.

Indexed as

AntidepressantBupropionnon-DopaminergicPutative GABAergicRatVentral Tegmental Area

Identifiers

PMID25337378
PMCPMC4202543
OpenAlexW11861000

What OpenQuestion holds

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LicenceCC BY-NC
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Registered trials

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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.