Evidence map›Paper›PMID 39393811›Full record

ArticleInternational journal of immunopathology and pharmacology

The effect of

Ali Tavakoli Pirzaman, Ghazaleh Sadeghnezhad, Zahra Azmoun, Amirreza Eslami, Razieh Mansoori, Sohrab Kazemi, Seyed Mohammad Hosseini

Abstract read
In one paragraph

Article in International journal of immunopathology and pharmacology. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

7 authors.

Ali Tavakoli PirzamanStudent Research Committee, Babol University of Medical Sciences, Babol, Iran.ORCID 0000-0002-9426-7034
Ghazaleh SadeghnezhadDepartment of Veterinary Pathology, Babol-Branch, Islamic Azad University, Babol, Iran.
Zahra AzmounDepartment of Veterinary Pathology, Babol-Branch, Islamic Azad University, Babol, Iran.
Amirreza EslamiDepartment of Veterinary Pathology, Babol-Branch, Islamic Azad University, Babol, Iran.
Razieh MansooriCellular and Molecular Biology Research Center, Health Research Institute, Babol University of Medical Sciences, Babol, Iran.
Sohrab KazemiCellular and Molecular Biology Research Center, Health Research Institute, Babol University of Medical Sciences, Babol, Iran.ORCID 0000-0002-8068-5745
Seyed Mohammad HosseiniDepartment of Veterinary Pathology, Babol-Branch, Islamic Azad University, Babol, Iran.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundNickel (Ni), commonly-used heavy metals in industrial activities, can lead to embryo and organ toxicity, especially cardiovascular damage. Geraniol (GER) has various beneficial effects such as anti-oxidant, anti-inflammatory, anti-tumor, anti-ulcer, anti-microbial, and neuroprotective activities.

objectiveThe objective of this study was to investigate the effect of GER on Ni-induced embryotoxicity and cardiotoxicity in rats.

methods40 mother Wistar rats were randomly divided into five groups: Control, GER 250, Ni, Ni + GER 100, and Ni + GER 250. On the 20

resultsMorphological assessments revealed GER's capacity to mitigate the incomplete ossification of fetal skeletons, indicating a potential safeguarding against the impact of Ni-induced embryotoxicity. Serological and biochemical analyses further affirm GER's role, with noteworthy reductions in cardiac injury markers, such as CRP, CKMB, CPK, LDH, and troponin, in response to GER administration, thereby suggesting its cardioprotective potential. Moreover, treatment with GER 250 could significantly reduce the level of MDA and increase the level of TAC compared to the Ni group. Histopathological examinations corroborated these findings, underscoring GER's ability to counteract cardiac injury and diminish structural damage in affected tissue.

conclusionsThese multidimensional analyses indicate the protective prowess of GER against Ni-induced embryotoxic and cardiotoxic effects, shedding light on its potential therapeutic significance in combating adverse impacts stemming from Ni exposure.

Indexed as

Acyclic MonoterpenesCardiotoxicityNickelRats, WistarAnimalsAntioxidantsFemaleHeartOxidative StressPregnancyRatsAcyclic MonoterpenesAntioxidantsgeraniolNickelcardiotoxicityembryotoxicitygeraniolnickeloxidative stress

Identifiers

PMID39393811
PMCPMC11483796

What OpenQuestion holds

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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.