Evidence map›Paper›PMID 26157711›Full record

ArticleMedical journal of the Islamic Republic of Iran2015

Reduction in ischemic brain injury following the administration of pentoxifylline after transient global ischemia/ reperfusion in a rat model.

Zahra Nadia Sharifi, Shabnam Movassaghi, Farzaneh Mohamadzadeh, Sara Soleimani Asl, Bagher Pourheydar, Mehdi Mehdizadeh

Open access · greenAbstract read
In one paragraph

Article in Medical journal of the Islamic Republic of Iran, 2015. 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
1.3field-weighted citation impact, top 19% 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

3 citing papers in PubMed, 14 citations in OpenAlex.

  1. Trial
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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 4 institutions in 1 country.

Zahra Nadia SharifiPhD, Department of Anatomy, Islamic Azad University, Tehran Medical Branch, Tehran, Iran. nadiasharifi@yahoo.com.
Shabnam MovassaghiPhD, Department of Anatomy, Islamic Azad University, Tehran Medical Branch, Tehran, Iran. sm_movassaghi@yahoo.com.
Farzaneh MohamadzadehMSc, Department of Anatomy, Faculty of Medicine, Iran University of Medical Sciences, Tehran, Iran. farzaneh.mohammadzadeh@yahoo.com.
Sara Soleimani AslPhD, Department of Anatomy, School of Medicine, Hamadan University of Medical Sciences, Hamadan, Iran. S.soleimaniasl@umsha.ac.ir.
Bagher PourheydarPhD, Neurophysiology Research Center, Department of Anatomy, Urmia University of Medical Sciences, Urmia, Iran. bagher.pourheydar@gmail.com.
Mehdi MehdizadehPhD, Cellular and Molecular Research Center, Faculty of Advanced Technologies in Medicine, Department of Anatomy, Iran University of Medical Sciences, Tehran, Iran. mehdizadeh.m@iums.ac.ir.
Iran University of Medical Sciences · IRIslamic Azad University Medical Branch of Tehran · IRHamedan University of Medical Sciences · IRUrmia University · IR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIt is well known that the hippocampus, the CA1 Pyramidal cells in particular, is selectively vulnerable during global cerebral ischemia. Recently, it is observed that pentoxifylline has a neuroprotective effect. This study explored the pharmacological relationship between ischemiainduced cell death of the hippocampus and the efficacy of a vasodilator agent (pentoxifylline) in the prevention of delayed neuronal death.

methodsThis experimental study was performed on 4 groups: control, ischemia, experimental (200mg/kg pentoxifylline injection one hour prior to and one hour following ischemia) and vehicle (normal saline). Transient global ischemia was induced by bilateral common carotid arteries occlusion. To investigate the apoptotic bodies and caspase-3 activities as a central role in the execution phase of apoptosis, the brains were prepared for the TUNEL technique.

resultsPentoxifylline administration limited apoptosis and caspase-3 activities in rats' hippocampi. Our data showed no significant difference between the number of apoptotic bodies in the CA1 region of the hippocampus in the control and pentoxifylline -treated groups (p= 0.994). The results of one- way ANOVA revealed that that ischemia significantly increased caspase-3 levels in the hippocampus (p< 0.05); however, the level of caspase-3 in pentoxifylline -treated rats was less than the ischemic group.

conclusionThese results suggest that the neuroprotective effect of pentoxifylline (200mg/kg) may be accompanied by a reduction in ischemic damage within the CA1 region of the hippocampus in rats subjected to transient global cerebral ischemia.

Indexed as

Cerebral ischemiaHippocampusPentoxifyllineReperfusion

Identifiers

PMID26157711
PMCPMC4476215
OpenAlexW2289378878

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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.