Evidence map›Paper›PMID 39063550›Full record

ArticleLife (Basel, Switzerland)2024

Zonisamide Ameliorated the Apoptosis and Inflammation in Cerebellar Tissue of Induced Alcohol Addiction Animal Model.

Fırat Aşır, Fikri Erdemci, Zuhal Çankırı, Tuğcan Korak, Süreyya Özdemir Başaran, Özge Kaplan, Özkan Yükselmiş, Nilüfer Dönmezdil, Hayat Ayaz, Şehmus Kaplan and 1 more

Abstract read
In one paragraph

Article in Life (Basel, Switzerland), 2024. 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
–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

7 citing papers in PubMed.

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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

11 authors.

Fırat AşırDepartment of Histology and Embryology, Medical Faculty, Dicle University, 21280 Diyarbakır, Turkey.ORCID 0000-0002-6384-9146
Fikri ErdemciDepartment of Histology and Embryology, Medical Faculty, Dicle University, 21280 Diyarbakır, Turkey.
Zuhal ÇankırıDepartment of Histology and Embryology, Medical Faculty, Dicle University, 21280 Diyarbakır, Turkey.
Tuğcan KorakDepartment of Medical Biology, Medical Faculty, Kocaeli University, 41001 Kocaeli, Turkey.
Süreyya Özdemir BaşaranDepartment of Andrology, Gazi Yasargil Education and Research Hospital, Health Sciences University, 21090 Diyarbakir, Turkey.
Özge KaplanDepartment of Andrology, Gazi Yasargil Education and Research Hospital, Health Sciences University, 21090 Diyarbakir, Turkey.
Özkan YükselmişDivision of Physical Medicine and Rehabilitation, Diyarbakır Dağ Kapı State Hospital, 21100 Diyarbakır, Turkey.
Nilüfer DönmezdilDepartment of Audiology, Faculty of Health Sciences, Mardin Artuklu University, 47200 Mardin, Turkey.
Hayat AyazDepartment of Histology and Embryology, Medical Faculty, Dicle University, 21280 Diyarbakır, Turkey.
Şehmus KaplanDepartment of Histology and Embryology, Medical Faculty, Dicle University, 21280 Diyarbakır, Turkey.
Selçuk TunikDepartment of Histology and Embryology, Medical Faculty, Dicle University, 21280 Diyarbakır, Turkey.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This study investigated the effects of zonisamide treatment on cerebellar tissues in an experimental alcohol addiction (AA) model and its potential mechanisms of action, particularly regarding apoptotic protease activating factor-1 (APAF-1) and tumor necrosis factor-alpha (TNF-α) expression. Thirty rats were divided into three groups: sham, ethanol (EtOH), and EtOH + zonisamide. AA was induced by administering 6 cc of EtOH orally every 8 h for 4 days. Zonisamide (100 mg/kg) was given to rats once daily before EtOH administration. Motor defects were evaluated using an open field maze. Serum TNF-α levels were measured from blood samples. Cerebellar sections were processed for histological examination and immunostained for APAF-1 and TNF-α. Protein interaction networks were constructed using Cytoscape, and functional annotations were performed with ShinyGO (version 0.80) software. The traveled area in the EtOH group was significantly reduced compared to the sham group (

Indexed as

apoptosiscerebelluminflammationneuroinflammationzonisamide

Identifiers

PMID39063550
PMCPMC11278003

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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.