Evidence map›Paper›PMID 42460024›Full record

ArticleFrontiers in pharmacology2026

Sperm-disrupting activity of a root bark fraction of

Kehongo M Nyanguru, Caroline Maina, Mutiat Ibrahim, James Kuria, Ephantus Ndirangu, Sospeter Ngoci Njeru, Abdullahi Abdulraheem, Edwin Murungi, Moses Obimbo, Adeyemi O Aremu and 5 more

Abstract read
In one paragraph

Article in Frontiers in pharmacology, 2026. 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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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

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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

15 authors.

Kehongo M NyanguruDepartment of Mathematics and Physical Sciences, Maasai Mara University, Narok, Kenya.
Caroline MainaCenter for Community Driven Research (CCDR), Kenya Medical Research Institute (KEMRI), Nairobi, Kenya.
Mutiat IbrahimDepartment of Pharmacognosy, Faculty of Pharmacy, University of Lagos, Lagos, Nigeria.
James KuriaCenter for Community Driven Research (CCDR), Kenya Medical Research Institute (KEMRI), Nairobi, Kenya.
Ephantus NdiranguCenter for Community Driven Research (CCDR), Kenya Medical Research Institute (KEMRI), Nairobi, Kenya.
Sospeter Ngoci NjeruCenter for Community Driven Research (CCDR), Kenya Medical Research Institute (KEMRI), Nairobi, Kenya.
Abdullahi AbdulraheemDepartment of Pharmacognosy, Faculty of Pharmacy, University of Lagos, Lagos, Nigeria.
Edwin MurungiDepartment of Medical Biochemistry, Kisii University, Kisii, Kenya.
Moses ObimboDepartment of Human Anatomy and Physiology, University of Nairobi, Nairobi, Kenya.
Adeyemi O AremuIndigenous Knowledge Systems (IKS) Centre, Faculty of Natural and Agricultural Sciences, North-West University, Potchefstroom, South Africa.
Aloys Mosima OsanoDepartment of Mathematics and Physical Sciences, Maasai Mara University, Narok, Kenya.
Samwel CheruiyotDepartment of Mathematics and Physical Sciences, Maasai Mara University, Narok, Kenya.
Margaret O IlomuanyaDepartment of Pharmaceutics and Pharmaceutical Technology, Faculty of Pharmacy, University of Lagos, Lagos, Nigeria.
Peter Waweru MwangiDepartment of Human Anatomy and Medical Physiology, University of Nairobi, Nairobi, Kenya.
Elizabeth KigonduCenter for Community Driven Research (CCDR), Kenya Medical Research Institute (KEMRI), Nairobi, Kenya.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: While Methods: Following extraction and fractionation of authenticated root bark, the resulting extracts were evaluated for cytotoxicity in Vero cells and for disruption of human sperm functions by ascertaining immobilization, revival, viability, cervical mucus penetration and acrosin-related activity. Thereafter, chemical profiling of the most active fraction was performed using liquid chromatography-tandem mass spectrometry (LC-MS/MS) for descriptive annotation. Moreover, Results: The methanolic fraction (KBLM) demonstrated the strongest activity, completely immobilizing sperm, abolishing sperm revival after washing, markedly reducing sperm viability, strongly inhibiting cervical mucus penetration and suppressing acrosin-related activity at 1.62 mg/mL. In a rabbit proof-of-concept experiment, a single intravaginal dose prevented pregnancy at all tested concentrations (3.9, 7.8, and 15.6 mg/mL). Besides, repeated intravaginal exposure for 10 days revealed absent-to-mild cervicovaginal changes. Chemical fingerprinting putatively annotated flavonoid-, tannin-, and phenolic-related features, including catechin, quercetin derivatives, rutin, corilagin, and kaempferol glycosides, as prominent features of KBLM. Conclusion: Our findings have demonstrated the sperm disruption activity of the methanolic fraction of

Indexed as

Acrosin-related activityFlueggea virosaintravaginal contraceptionLC-MS/MS profilingrabbit modelsperm immobilization

Identifiers

PMID42460024
PMCPMC13369495

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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.