The Fungicide Ipconazole Can Activate Mediators of Cellular Damage in Rat Brain Regions

This study aimed to investigate the toxicity of the fungicide ipconazole on oxidative status, cell death and inflammasome complex activation in the hypothalamus, cerebral cortex, striatum and hippocampus of rats. Female albino rats were randomly divided into a control group and four groups treated with ipconazole at doses of 1, 5, 10 and 20 mg/kg b.w., administered for six days. Ipconazole significantly increased MDA and ROS levels in all brain regions studied, while reducing catalase enzyme activity. The molecular expression of cell death-related genes (AKT1, APAF1, BNIP3, CASP3 and BAX) and the inflammasome complex (CASP1, IL1β, IL6, NLRP3, NFĸB and TNFα) was also assessed, showing increased expression in at least one brain region. The findings demonstrate that ipconazole induces central nervous system toxicity in mammals, highlighting its potential role as a risk factor in the development of neurodegenerative disorders in individuals exposed to this contaminant.

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Publication Details

Journal
Toxics
Published
2024-08-31
DOI
https://doi.org/10.3390/toxics12090638
Citations
5
Primary Topic
Genomics, phytochemicals, and oxidative stress
Type
article
Field-Weighted Citation Impact
1.17
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article

The Fungicide Ipconazole Can Activate Mediators of Cellular Damage in Rat Brain Regions

Mariella Ramos-González, José-Luis Rodríguez, Alejandro Romero, Luis Alberto Inostroza-Ruiz et al.
5 citations
Toxics
Genomics, phytochemicals, and oxidative stress
1.17
article

The Fungicide Ipconazole Can Activate Mediators of Cellular Damage in Rat Brain Regions

Mariella Ramos-González, José-Luis Rodríguez, Alejandro Romero, Luis Alberto Inostroza-Ruiz, Olger Ramos-Coaguila, Luis Barrios-Arpi, Carlos Villaorduña, Boris Lira-Mejía
article en
5 citations

Abstract

This study aimed to investigate the toxicity of the fungicide ipconazole on oxidative status, cell death and inflammasome complex activation in the hypothalamus, cerebral cortex, striatum and hippocampus of rats. Female albino rats were randomly divided into a control group and four groups treated with ipconazole at doses of 1, 5, 10 and 20 mg/kg b.w., administered for six days. Ipconazole significantly increased MDA and ROS levels in all brain regions studied, while reducing catalase enzyme activity. The molecular expression of cell death-related genes (AKT1, APAF1, BNIP3, CASP3 and BAX) and the inflammasome complex (CASP1, IL1β, IL6, NLRP3, NFĸB and TNFα) was also assessed, showing increased expression in at least one brain region. The findings demonstrate that ipconazole induces central nervous system toxicity in mammals, highlighting its potential role as a risk factor in the development of neurodegenerative disorders in individuals exposed to this contaminant.

ToxicsVol. 12(9)
Universidad Complutense de Madrid (ES), National University of San Marcos (PE)
Good health and well-being
Openalex Percentile: Top 22%
Genomics, phytochemicals, and oxidative stress
1.17
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