Evidence map›Paper›PMID 42416494›Full record

ArticleThe journal of venomous animals and toxins including tropical diseases2026

Nephrotoxic acute kidney injury induced by

Narongsak Chaiyabutr, Sunutcha Suntrarachun, Suchitra Khunsap, Orawan Khow, Panithi Laoungbua, Taksa Vasaruchapong, Lawan Chanhome, Anudep Rungsipipat, Visith Sitprija

Abstract read
In one paragraph

Article in The journal of venomous animals and toxins including tropical diseases, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Review
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

9 authors.

Narongsak ChaiyabutrQueen Saovabha Memorial Institute, Thai Red Cross Society, Bangkok, Thailand.ORCID https://orcid.org/0000-0002-3207-0885
Sunutcha SuntrarachunDepartment of Research and Development, Queen Saovabha Memorial Institute, Thai Red Cross Society, Bangkok, Thailand.ORCID https://orcid.org/0000-0001-8358-8230
Suchitra KhunsapDepartment of Research and Development, Queen Saovabha Memorial Institute, Thai Red Cross Society, Bangkok, Thailand.ORCID https://orcid.org/0000-0003-2610-0627
Orawan KhowDepartment of Research and Development, Queen Saovabha Memorial Institute, Thai Red Cross Society, Bangkok, Thailand.ORCID https://orcid.org/0000-0002-0950-2045
Panithi LaoungbuaSnake Farm, Queen Saovabha Memorial Institute, Thai Red Cross Society, Bangkok, Thailand.ORCID https://orcid.org/0000-0002-2963-4811
Taksa VasaruchapongSnake Farm, Queen Saovabha Memorial Institute, Thai Red Cross Society, Bangkok, Thailand.ORCID https://orcid.org/0000-0001-8197-0356
Lawan ChanhomeSnake Farm, Queen Saovabha Memorial Institute, Thai Red Cross Society, Bangkok, Thailand.ORCID https://orcid.org/0000-0003-2425-5000
Anudep RungsipipatCenter of Excellence for Companion Animal Cancer, Department of Pathology, Faculty of Veterinary Science, Chulalongkorn University, Bangkok, Thailand.ORCID https://orcid.org/0000-0001-6137-969X
Visith SitprijaQueen Saovabha Memorial Institute, Thai Red Cross Society, Bangkok, Thailand.ORCID https://orcid.org/0000-0002-4885-0405

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Envenomation by Methods: Kidney tissue samples from intact rabbits ( Results: Following the administration of RVV and its venom fractions, histopathological analysis revealed extensive tubulonephrosis across all renal tubular segments in both intact kidneys and the IPK model. In contrast, renal tubular necrosis involving all tubular segments occurred in the IPK model after exposure to the RVV, PLA₂ and MP fractions. Immunohistochemical analysis revealed a trend toward increased Bax protein expression and decreased Bcl-2 expression in multiple tubular segments compared to controls in both models. RT-qPCR analysis demonstrated a 1.5-fold upregulation of Conclusions: Envenomation with RVV and its venom fractions induced nephrotoxic acute kidney injury by modulating Bax- and Bcl-2-mediated apoptosis in renal tubular epithelial cells, with greater susceptibility observed in intact kidneys and a reduced apoptotic response in the IPK model. These findings suggest that prolonged venom exposure may be partially reversible or may shift cell-death signaling from apoptosis toward necrosis.

Indexed as

Acute kidney injury (AKI)ApoptosisBcl-2 familyD. siamensis venomVenom fractions

Identifiers

PMID42416494
PMCPMC13341132

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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.