Evidence map›Paper›PMID 38835821›Full record

ArticleToxicology research2024

Identifying toxic effects and metabolic perturbations of

Fatima F Bebal, Akshay D Bagwe, Roshan C D'Souza, Bharatbhushan B Sharma

Abstract read
In one paragraph

Article in Toxicology research, 2024. 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. 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

4 authors.

Fatima F BebalDepartment of Zoology, KET's V. G. Vaze College of Arts, Science & Commerce (Autonomous), Mithagar Road, Mumbai - 400 081, Maharashtra, India.ORCID https://orcid.org/0009-0003-4014-7285
Akshay D BagweDepartment of Zoology, KET's V. G. Vaze College of Arts, Science & Commerce (Autonomous), Mithagar Road, Mumbai - 400 081, Maharashtra, India.ORCID https://orcid.org/0000-0003-2608-1251
Roshan C D'SouzaDepartment of Zoology, Sophia College for Women (Autonomous), Bhulabhai Desai Road, Mumbai - 400 026, Maharashtra, India.ORCID https://orcid.org/0000-0001-9432-4302
Bharatbhushan B SharmaDepartment of Zoology, KET's V. G. Vaze College of Arts, Science & Commerce (Autonomous), Mithagar Road, Mumbai - 400 081, Maharashtra, India.ORCID https://orcid.org/0009-0008-6120-461X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Skin secretions of toads are widely used in medicine all over the world for their antiviral, anti-infective, and cardiotonic properties. Because these secretions are mostly employed to combat blood parasite infection, it is important to understand their potential toxic effects on human erythrocytes. Therefore, the objective of the current investigation was to elucidate the effects of Methods: Toads captured from their natural habitat were separated into three groups according to their body size. Hydroalcoholic extracts of toad skin were prepared by reflux heating. These extracts were then evaluated for their hemolytic and hemoglobin denaturation potential. The effects of the extracts on cytosolic and membrane-bound enzymes of human erythrocytes were assessed. Results: The hemolysis and hemoglobin denaturation caused by these extracts correlated positively with the respective toad sizes. Extracts from medium and large toads led to increased osmotic fragility even at near iso-osmotic concentrations. Biochemical analysis of hemolysate showed that the treatment induced a shift of metabolic flux toward the glutathione pathway. Analysis of membrane-bound enzymes revealed a significant decrease in the activity of Na+/K+ ATPase and acetylcholinesterase. SDS-PAGE analysis of the erythrocyte membrane did not show the band of tropomodulin for the cells treated with 1000 𝜇g/ml extract from large toads. Conclusions: In conclusion, the present study demonstrates that the toxicity of toad skin secretions aggravates with the size of the animal and interferes with the physiology of human erythrocytes, leading to their membrane disruption and rapid lysis.

Indexed as

ATPaseglutathione pathwayHemotoxicitytoadstropomodulin

Identifiers

PMID38835821
PMCPMC11145735

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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.