Evidence map›Paper›PMID 41977394›Full record

ArticleInternational journal of molecular sciences2026

Antioxidant Astaxanthin Co-Treatment Protects Zebrafish from Dimethomorph-Induced Cardiovascular Toxicity.

Chia-Chen Wu, Ferry Saputra, Ross D Vasquez, Marri Jmelou M Roldan, Yu-Heng Lai, Chung-Der Hsiao, Chih-Hsin Hung

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

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.

Chia-Chen WuInstitute of Biotechnology and Chemical Engineering, I-Shou University, Kaohsiung 84001, Taiwan.ORCID 0000-0002-3392-4571
Ferry SaputraDepartment of Chemistry, Chung Yuan Christian University, Taoyuan 320314, Taiwan.ORCID 0000-0002-5715-9827
Ross D VasquezDepartment of Pharmacy, Faculty of Pharmacy, University of Santo Tomas, Manila 1015, Philippines.ORCID 0000-0002-5906-9710
Marri Jmelou M RoldanDepartment of Pharmacy, Faculty of Pharmacy, University of Santo Tomas, Manila 1015, Philippines.ORCID 0000-0001-6398-1828
Yu-Heng LaiDepartment of Chemistry, Chinese Culture University, Taipei 11114, Taiwan.
Chung-Der HsiaoDepartment of Chemistry, Chung Yuan Christian University, Taoyuan 320314, Taiwan.ORCID 0000-0002-6398-8672
Chih-Hsin HungInstitute of Biotechnology and Chemical Engineering, I-Shou University, Kaohsiung 84001, Taiwan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Dimethomorph (DIM) is a commonly applied morpholine fungicide, yet its potential toxicity to non-target organisms raises significant environmental concerns. This study aims to elucidate the toxicological effects of DIM on zebrafish, with a particular focus on its cardiovascular impacts. Zebrafish embryos were exposed to a range of DIM concentrations for 48 h, and their cardiac and vascular performance was meticulously assessed to determine the extent of cardiovascular toxicity. The findings revealed notable cardiac hypertrophy, evidenced by a substantial enlargement in heart size, alongside a dose-dependent reduction in heart rate. These observations suggest direct impairment of cardiac function following DIM exposure. To further investigate the molecular underpinnings of these effects, gene expression analysis was conducted using quantitative real-time PCR (qRT-PCR). The results demonstrated significant alterations in the expression of key genes associated with cardiovascular development and function, providing mechanistic insights into DIM's toxic effects. In addition to cardiac abnormalities, DIM exposure led to a significant increase in the metabolic rate of the zebrafish embryos, indicating a potential disruption in energy homeostasis. To explore possible protective measures, a rescue experiment was performed using Astaxanthin, a potent antioxidant. Notably, Astaxanthin treatment partially mitigated the observed cardiac and metabolic phenotypes, suggesting its potential as a therapeutic agent to counteract DIM-induced toxicity. In summary, this study provides compelling evidence of the cardiovascular toxicity of DIM in zebrafish, highlighting its potential to disrupt cardiac function and metabolic regulation. The observed effects underscore the importance of re-evaluating the environmental impact of DIM and emphasize the need for further research to fully understand its mechanisms of toxicity. The findings also suggest that Astaxanthin (AST) could serve as a protective agent against DIM-induced toxicity, opening avenues for future studies aimed at mitigating the adverse effects of this widely used fungicide. This research study contributes to the growing body of knowledge on the environmental and health risks associated with pesticide use, advocating for more stringent regulations and safer alternatives.

Indexed as

AntioxidantsCardiovascular SystemMorpholinesAnimalsEmbryo, NonmammalianFungicides, IndustrialHeartHeart RateXanthophyllsZebrafishAntioxidantsastaxanthineFungicides, IndustrialMorpholinesXanthophyllsantioxidantcardiovascular toxicitydimethomorphzebrafish

Identifiers

PMID41977394
PMCPMC13073923

What OpenQuestion holds

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LicenceCC BY
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Registered trials

None linked

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.