Evidence map›Paper›PMID 39123263›Full record

ArticleBMC pharmacology & toxicology2024

Echis ocellatus venom-induced sperm functional deficits, pro-apoptotic and inflammatory activities in male reproductive organs in rats: antagonistic role of kaempferol.

Babafemi Siji Ajisebiola, Adesola Abigeal Toromade, Johnson Olaleye Oladele, Abdur-Rahman Kolawole Mustapha, Olukunle Silas Fagbenro, Akindele Oluwatosin Adeyi

Abstract read
In one paragraph

Article in BMC pharmacology & toxicology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed, 1 pooled it
–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, 1 synthesis or guideline pooled it.

  1. Pooled it
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  3. Article
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.

Babafemi Siji AjisebiolaDepartment of Animal and Environmental Biology, Osun State University, Osogbo, Nigeria. dbabslinks@yahoo.com.
Adesola Abigeal ToromadeDepartment of Animal and Environmental Biology, Osun State University, Osogbo, Nigeria.
Johnson Olaleye OladeleBiochemistry Unit, Department of Chemical Sciences, Kings University, Ode-Omu, Nigeria.
Abdur-Rahman Kolawole MustaphaDepartment of Animal and Environmental Biology, Osun State University, Osogbo, Nigeria.
Olukunle Silas FagbenroCell Biology and Genetics Unit, Department of Zoology, University of Ibadan, Ibadan, Nigeria.
Akindele Oluwatosin AdeyiCell Biology and Genetics Unit, Department of Zoology, University of Ibadan, Ibadan, Nigeria.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundEchis ocellatus envenoming is potentially toxic initiating clinical damages on male reproductive system. Kaempferol is a therapeutic agent with neutralizing potentials on snake venom toxins. This study investigated the antagonistic effect of kaempferol on E. ocellatus venom (EoV)-induced reproductive toxicities.

methodsFifty adult male rats were sorted at random into five groups of ten rats for this study. The control rats were allotted to group 1, while rats in groups 2-5 were injected with 0.22 mg/kg bw (LD

resultsEoV actuated reproductive toxicity, significantly decreased sperm parameters, and enhanced inflammatory, oxidative stress, and apoptotic biomarkers in reproductive organs of untreated envenomed rats. However, treatment with kaempferol alleviated the venom-induced reproductive disorders with a dose dependent effect. Kaempferol significantly increased the testicular weight, organo-somatic index, sperm parameters, and normalized the levels of serum luteinizing hormone, testosterone, and follicle stimulating hormone. Kaempferol ameliorated testicular and epididymal oxidative stress as evidenced by significant decrease in malondialdehyde (MDA) levels, enhancement of reduced glutathione (GSH) levels, superoxide dismutase (SOD) and glutathione peroxidase (GPX) activities. The inflammatory biomarkers; nitric oxide (NO) levels and myeloperoxidase activity (MPO), and apoptotic biomarkers; caspase 3 and caspase 9 activities were substantially suppressed in the testis and epididymis of envenomed rats treated with kaempferol.

conclusionResults revealed kaempferol as a potential remedial agent against reproductive toxicity that could manifest post-viper envenoming.

Indexed as

ApoptosisKaempferolsSpermatozoaTestisAnimalsEchisInflammationMaleOxidative StressRatsRats, WistarViper VenomskaempferolKaempferolsViper VenomsApoptosisEchis ocellatusInflammationKaempferolReproductive toxicitySnakebite

Identifiers

PMID39123263
PMCPMC11311923

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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.