Syringol, a wildfire residual methoxyphenol causes cytotoxicity and teratogenicity in zebrafish model.


Journal

The Science of the total environment
ISSN: 1879-1026
Titre abrégé: Sci Total Environ
Pays: Netherlands
ID NLM: 0330500

Informations de publication

Date de publication:
15 Mar 2023
Historique:
received: 13 08 2022
revised: 12 12 2022
accepted: 12 12 2022
pubmed: 23 12 2022
medline: 27 1 2023
entrez: 22 12 2022
Statut: ppublish

Résumé

Natural toxicants, particularly methoxy phenols (MPs) generated by wildfire lignin, can accumulate in the environment, and cause serious health hazards in living organisms. Although the toxicity of MPs such as guaiacol and catechol has recently been described, there is minimal evidence of ecotoxicological effects of syringol. As a result, this study focuses on determining the toxicity by evaluating the cytotoxic and teratogenic effects of syringol in vitro and in vivo in human embryonic kidney (HEK-293) cells and zebrafish embryos, respectively. The ecotoxicity of syringol was predicted to be 63.8 mg/L using the ECOSAR (ECOlogical Structure Activity Relationship) prediction tool, and molecular docking analysis was used to determine the interaction and binding affinities of syringol with human apoptotic proteins in silico. In HEK-293 cells, exposure of syringol (0.5-2 mg/L) has induced cytotoxicity in a concentration-dependent manner. In zebrafish larvae, exposure of syringol (0.5-2 mg/L) has induced dose-dependent embryo toxic effects (or growth abnormalities such as yolk sac edema, pericardial edema, skeletal abnormality, and hyperemia), and changes in growth morphometrics (head height, eye, yolk sac, and pericardial area, heart rate) in particular, the heart rate of larvae was found to be significantly decreased (p<0.001). After a 4-day experimental trial, the accumulated concentration of syringol in zebrafish larvae was confirmed both qualitatively (HPLC-MS - High Performance Liquid Chromatography-Mass spectrometry) and quantitatively (LC-QTOF-HRMS - Liquid Chromatography-Quadrupolar Time of Flight-High Resolution Mass spectrometry). The craniofacial abnormalities induced by syringol exposure (0.5-2 mg/L) were detected as anomalies in cartilaginous development and locomotor deficits using alcian blue staining and locomotor analyses, respectively. Significant increase in oxidative stress parameters (including reactive oxygen species generation, lipid peroxidation, superoxide dismutase, catalase, lactate dehydrogenase and nitric oxide production) (p<0.001) and substantial decrease in glutathione levels were observed (p<0.05) in syringol exposed zebrafish larvae through enzymatic analysis. Additionally, through acridine orange staining and gene expression analyses, syringol (2 mg/L) was found to activate apoptosis in zebrafish larvae. Considering the cytotoxic, embryotoxic (teratogenicity), and oxidative stress-related apoptotic effects of syringol in the zebrafish model, syringol has the potential to emerge as a potent environmental toxicant posing serious health hazards in many living systems; however, further research on its toxicological effects on the actual ecosystem and in higher animal models is required to confirm its consequences.

Identifiants

pubmed: 36549541
pii: S0048-9697(22)08071-8
doi: 10.1016/j.scitotenv.2022.160968
pii:
doi:

Substances chimiques

pyrogallol 1,3-dimethyl ether 4UQT464H8K

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

160968

Informations de copyright

Copyright © 2022 Elsevier B.V. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

P Snega Priya (PS)

Department of Biotechnology, College of Science and Humanities, SRM Institute of Science and Technology, Kattankulatur, 603 203 Chennai, Tamil Nadu, India.

Ajay Guru (A)

Department of Conservative Dentistry and Endodontics, Saveetha Dental College and Hospitals, SIMATS, 600 077 Chennai, Tamil Nadu, India.

Ramu Meenatchi (R)

Department of Biotechnology, College of Science and Humanities, SRM Institute of Science and Technology, Kattankulatur, 603 203 Chennai, Tamil Nadu, India.

B Haridevamuthu (B)

Department of Biotechnology, College of Science and Humanities, SRM Institute of Science and Technology, Kattankulatur, 603 203 Chennai, Tamil Nadu, India.

Manikandan Velayutham (M)

Department of Medical Biotechnology and Integrative Physiology, Saveetha School of Engineering, SIMATS, 600 077, Chennai, Tamil Nadu, India.

Boopathi Seenivasan (B)

Department of Biotechnology, College of Science and Humanities, SRM Institute of Science and Technology, Kattankulatur, 603 203 Chennai, Tamil Nadu, India.

Raman Pachaiappan (R)

Department of Biotechnology, School of Bioengineering, College of Engineering and Technology, SRM Institute of Science and Technology, Kattankulathur, 603 203 Chennai, Tamil Nadu, India.

Rajakrishnan Rajagopal (R)

Department of Botany and Microbiology, College of Science, King Saud University, Riyadh, Saudi Arabia.

Palaniselvam Kuppusamy (P)

Department of Animal Biotechnology, Jeonbuk National University, Jeonju 54896, South Korea.

Annie Juliet (A)

Foundation for Aquaculture Innovations and Technology Transfer (FAITT), Thoraipakkam, Chennai 600 097, Tamil Nadu, India.

Jesu Arockiaraj (J)

Department of Biotechnology, College of Science and Humanities, SRM Institute of Science and Technology, Kattankulatur, 603 203 Chennai, Tamil Nadu, India. Electronic address: jesuaroa@srmist.edu.in.

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Classifications MeSH