Suppression of bisphenol A‐induced oxidative stress by taurine promotes neuroprotection and restores altered neurobehavioral response in zebrafish (Danio rerio)

Bisphenol A (BPA) has been documented as a mediator for a number of health effects, including inflammation, oxidative stress, carcinogenicity, and mood dysfunction. The literature on the role of BPA in inducing altered neurobehavioral response and brain morphology and plausible neuroprotective role...

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Veröffentlicht in:Environmental toxicology 2021-11, Vol.36 (11), p.2342-2353
Hauptverfasser: Pradhan, Lilesh Kumar, Sahoo, Pradyumna Kumar, Aparna, Sai, Sargam, Meghana, Biswal, Amit Kumar, Polai, Omkar, Chauhan, Nishant Ranjan, Das, Saroj Kumar
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container_end_page 2353
container_issue 11
container_start_page 2342
container_title Environmental toxicology
container_volume 36
creator Pradhan, Lilesh Kumar
Sahoo, Pradyumna Kumar
Aparna, Sai
Sargam, Meghana
Biswal, Amit Kumar
Polai, Omkar
Chauhan, Nishant Ranjan
Das, Saroj Kumar
description Bisphenol A (BPA) has been documented as a mediator for a number of health effects, including inflammation, oxidative stress, carcinogenicity, and mood dysfunction. The literature on the role of BPA in inducing altered neurobehavioral response and brain morphology and plausible neuroprotective role of taurine against BPA induced oxidative stress mediated neurotoxicity is limited. Therefore, the present experimental paradigm was set for 21 days to expound the neuroprotective efficacy of taurine against BPA‐induced neurotoxicity in zebrafish (Danio rerio) following waterborne exposure. Neurobehavioral studies were conducted by light–dark preference test (LDPT) and novel tank diving test (NTDT). To validate that the neuroprotective efficacy of taurine against BPA‐induced neurotoxicity is associated with the modulation of the antioxidant defense system, we have conducted biochemical studies in zebrafish brain. Changes in brain morphology leading to neurobehavioral variations following co‐supplementation of BPA and taurine were evaluated by Hoechst staining and cresyl violet staining (CVS) in periventricular gray zone (PGZ) of zebrafish brain. Our findings show that taurine co‐supplementation significantly improved the BPA‐induced altered scototaxis and explorative behavior of zebrafish. Further, BPA‐induced augmented oxidative stress was considerably ameliorated by taurine co‐supplementation. Subsequently, our observation also points toward the neuroprotective role of taurine against BPA‐induced neuronal pyknosis and chromatin condensation in PGZ of zebrafish brain. In a nutshell, the findings of the current study show the neuroprotective efficacy of taurine against BPA‐induced oxidative stress‐mediated neurotoxicity. Elucidation of the underlying signaling mechanism of taurine‐mediated neuroprotection would provide novel strategies for the prevention/treatment of BPA‐persuaded serious neurological consequences.
doi_str_mv 10.1002/tox.23348
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The literature on the role of BPA in inducing altered neurobehavioral response and brain morphology and plausible neuroprotective role of taurine against BPA induced oxidative stress mediated neurotoxicity is limited. Therefore, the present experimental paradigm was set for 21 days to expound the neuroprotective efficacy of taurine against BPA‐induced neurotoxicity in zebrafish (Danio rerio) following waterborne exposure. Neurobehavioral studies were conducted by light–dark preference test (LDPT) and novel tank diving test (NTDT). To validate that the neuroprotective efficacy of taurine against BPA‐induced neurotoxicity is associated with the modulation of the antioxidant defense system, we have conducted biochemical studies in zebrafish brain. Changes in brain morphology leading to neurobehavioral variations following co‐supplementation of BPA and taurine were evaluated by Hoechst staining and cresyl violet staining (CVS) in periventricular gray zone (PGZ) of zebrafish brain. Our findings show that taurine co‐supplementation significantly improved the BPA‐induced altered scototaxis and explorative behavior of zebrafish. Further, BPA‐induced augmented oxidative stress was considerably ameliorated by taurine co‐supplementation. Subsequently, our observation also points toward the neuroprotective role of taurine against BPA‐induced neuronal pyknosis and chromatin condensation in PGZ of zebrafish brain. In a nutshell, the findings of the current study show the neuroprotective efficacy of taurine against BPA‐induced oxidative stress‐mediated neurotoxicity. 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subjects Antioxidants
Bisphenol A
Brain
Carcinogenicity
Carcinogens
Chromatin
Danio rerio
Exploratory behavior
Freshwater fishes
Morphology
Neuroprotection
Neurotoxicity
Oxidative stress
Scototaxis
Staining
Supplements
Taurine
Zebrafish
title Suppression of bisphenol A‐induced oxidative stress by taurine promotes neuroprotection and restores altered neurobehavioral response in zebrafish (Danio rerio)
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