6PPD and 6PPDQ embryonic exposure induced distinct developmental neurotoxicity in zebrafish

The ecological risks of tire antioxidant 6PPD and its transformed metabolite 6PPD-quinone (6PPDQ) have received high attention. The present study evaluated the developmental neurotoxicity and potential mechanisms under 6PPD or 6PPDQ embryonic exposures in zebrafish. Our findings revealed that embryo...

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Main Authors: Liang Yang, Xiangqi Lu, Dongliang Pan, Yusong Zhang, Yi Zheng, He Mei, Bo Yang, Da Sun, Qiong Li, Jian Lin, Jiangfei Chen
Format: Article
Language:English
Published: Elsevier 2025-07-01
Series:Ecotoxicology and Environmental Safety
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Online Access:http://www.sciencedirect.com/science/article/pii/S0147651325007961
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author Liang Yang
Xiangqi Lu
Dongliang Pan
Yusong Zhang
Yi Zheng
He Mei
Bo Yang
Da Sun
Qiong Li
Jian Lin
Jiangfei Chen
author_facet Liang Yang
Xiangqi Lu
Dongliang Pan
Yusong Zhang
Yi Zheng
He Mei
Bo Yang
Da Sun
Qiong Li
Jian Lin
Jiangfei Chen
author_sort Liang Yang
collection DOAJ
description The ecological risks of tire antioxidant 6PPD and its transformed metabolite 6PPD-quinone (6PPDQ) have received high attention. The present study evaluated the developmental neurotoxicity and potential mechanisms under 6PPD or 6PPDQ embryonic exposures in zebrafish. Our findings revealed that embryonic exposure to both compounds suppressed larval locomotion during dark periods, while only 6PPD significantly reduced the larval light stimulus sensitivity and phototactic response. Following recovery to juvenile stages, pretreated fish exhibited heightened anxiety and reduced sociability for both chemicals, aggression was exclusively occurred in 6PPDQ, shoaling pattern was tighter in 6PPDQ but looser in 6PPD. Both compounds elevated larval cell death and oxidative stress while inhibiting cranial development, with 6PPD increasing and 6PPDQ decreasing inter-ocular distance. Transgenic strain analyses demonstrated that 6PPD markedly activated Gfap and Olig2 expression in the eye-brain axis region, whereas 6PPDQ specifically enhanced Olig2 expression in brain region. Retinal müller cells (labeled by Gfap) and cone cell patterns were disrupted exclusively by 6PPD, as was the fan-like lens arrangement visualized via Cms1 mitochondrial labeling. Molecular analyses aligned with these observations that both compounds altered neural development genes (sox2, nrxn2a, rab33a), while 6PPD specifically dysregulated ocular development genes (cyp26a, rlbp1b, rdh5). Conversely, 6PPDQ exhibited stronger activation of xenobiotic metabolism and redox activity genes (cyp1a, gstp1, prdx1, p4ha1a) and uniquely upregulated intestinal immune (ccr9a) and potassium channel (kcnj1a.3) genes expression. In silico affinity analysis corroborated these distinctions, showing 6PPD’s preferential binding to CYP26A and 6PPDQ’s stronger interaction with CYP1A. These findings collectively suggest that 6PPD and 6PPDQ induce divergent neurotoxicity pathways of eye-brain axis disruption and gut-brain communication perturbation, respectively, which likely drive their compound-specific behavioral effects.
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spelling doaj-art-ee9b6bece0784d19a6ce76cf3e8b0c042025-08-20T02:07:39ZengElsevierEcotoxicology and Environmental Safety0147-65132025-07-0130011845610.1016/j.ecoenv.2025.1184566PPD and 6PPDQ embryonic exposure induced distinct developmental neurotoxicity in zebrafishLiang Yang0Xiangqi Lu1Dongliang Pan2Yusong Zhang3Yi Zheng4He Mei5Bo Yang6Da Sun7Qiong Li8Jian Lin9Jiangfei Chen10Wenzhou Municipal Key Laboratory of Neurodevelopmental Pathology and Physiology, the Second Affiliated Hospital of Wenzhou Medical University, Wenzhou 325035, China; School of Public health, Wenzhou Medical University, Wenzhou 325035, ChinaWenzhou Municipal Key Laboratory of Neurodevelopmental Pathology and Physiology, the Second Affiliated Hospital of Wenzhou Medical University, Wenzhou 325035, China; School of Public health, Wenzhou Medical University, Wenzhou 325035, ChinaWenzhou Municipal Key Laboratory of Neurodevelopmental Pathology and Physiology, the Second Affiliated Hospital of Wenzhou Medical University, Wenzhou 325035, China; School of Public health, Wenzhou Medical University, Wenzhou 325035, ChinaWenzhou Municipal Key Laboratory of Neurodevelopmental Pathology and Physiology, the Second Affiliated Hospital of Wenzhou Medical University, Wenzhou 325035, China; School of Public health, Wenzhou Medical University, Wenzhou 325035, ChinaWenzhou Municipal Key Laboratory of Neurodevelopmental Pathology and Physiology, the Second Affiliated Hospital of Wenzhou Medical University, Wenzhou 325035, China; School of Public health, Wenzhou Medical University, Wenzhou 325035, ChinaSchool of Public health, Wenzhou Medical University, Wenzhou 325035, ChinaSchool of Public health, Wenzhou Medical University, Wenzhou 325035, ChinaNational and Local Joint Engineering Research Center of Ecological Treatment Technology for Urban Water Pollution, College of Life and Environmental Science, Wenzhou University, Wenzhou 325035, ChinaKey Laboratory of Luminescence Analysis and Molecular Sensing, College of Pharmaceutical Sciences, Southwest University, Chongqing 400715, China; Corresponding author.Wenzhou Municipal Key Laboratory of Neurodevelopmental Pathology and Physiology, the Second Affiliated Hospital of Wenzhou Medical University, Wenzhou 325035, China; School of Public health, Wenzhou Medical University, Wenzhou 325035, China; Corresponding authors at: Wenzhou Municipal Key Laboratory of Neurodevelopmental Pathology and Physiology, The Second Affiliated Hospital of Wenzhou Medical University, Wenzhou 325035, China.Wenzhou Municipal Key Laboratory of Neurodevelopmental Pathology and Physiology, the Second Affiliated Hospital of Wenzhou Medical University, Wenzhou 325035, China; School of Public health, Wenzhou Medical University, Wenzhou 325035, China; South Zhejiang Institute of Radiation Medicine and Nuclear Technology, Wenzhou, China; Corresponding authors at: Wenzhou Municipal Key Laboratory of Neurodevelopmental Pathology and Physiology, The Second Affiliated Hospital of Wenzhou Medical University, Wenzhou 325035, China.The ecological risks of tire antioxidant 6PPD and its transformed metabolite 6PPD-quinone (6PPDQ) have received high attention. The present study evaluated the developmental neurotoxicity and potential mechanisms under 6PPD or 6PPDQ embryonic exposures in zebrafish. Our findings revealed that embryonic exposure to both compounds suppressed larval locomotion during dark periods, while only 6PPD significantly reduced the larval light stimulus sensitivity and phototactic response. Following recovery to juvenile stages, pretreated fish exhibited heightened anxiety and reduced sociability for both chemicals, aggression was exclusively occurred in 6PPDQ, shoaling pattern was tighter in 6PPDQ but looser in 6PPD. Both compounds elevated larval cell death and oxidative stress while inhibiting cranial development, with 6PPD increasing and 6PPDQ decreasing inter-ocular distance. Transgenic strain analyses demonstrated that 6PPD markedly activated Gfap and Olig2 expression in the eye-brain axis region, whereas 6PPDQ specifically enhanced Olig2 expression in brain region. Retinal müller cells (labeled by Gfap) and cone cell patterns were disrupted exclusively by 6PPD, as was the fan-like lens arrangement visualized via Cms1 mitochondrial labeling. Molecular analyses aligned with these observations that both compounds altered neural development genes (sox2, nrxn2a, rab33a), while 6PPD specifically dysregulated ocular development genes (cyp26a, rlbp1b, rdh5). Conversely, 6PPDQ exhibited stronger activation of xenobiotic metabolism and redox activity genes (cyp1a, gstp1, prdx1, p4ha1a) and uniquely upregulated intestinal immune (ccr9a) and potassium channel (kcnj1a.3) genes expression. In silico affinity analysis corroborated these distinctions, showing 6PPD’s preferential binding to CYP26A and 6PPDQ’s stronger interaction with CYP1A. These findings collectively suggest that 6PPD and 6PPDQ induce divergent neurotoxicity pathways of eye-brain axis disruption and gut-brain communication perturbation, respectively, which likely drive their compound-specific behavioral effects.http://www.sciencedirect.com/science/article/pii/S01476513250079616PPD6PPDQZebrafishNeurodevelopmental toxicityVisual impairmentIntestinal dysregulation
spellingShingle Liang Yang
Xiangqi Lu
Dongliang Pan
Yusong Zhang
Yi Zheng
He Mei
Bo Yang
Da Sun
Qiong Li
Jian Lin
Jiangfei Chen
6PPD and 6PPDQ embryonic exposure induced distinct developmental neurotoxicity in zebrafish
Ecotoxicology and Environmental Safety
6PPD
6PPDQ
Zebrafish
Neurodevelopmental toxicity
Visual impairment
Intestinal dysregulation
title 6PPD and 6PPDQ embryonic exposure induced distinct developmental neurotoxicity in zebrafish
title_full 6PPD and 6PPDQ embryonic exposure induced distinct developmental neurotoxicity in zebrafish
title_fullStr 6PPD and 6PPDQ embryonic exposure induced distinct developmental neurotoxicity in zebrafish
title_full_unstemmed 6PPD and 6PPDQ embryonic exposure induced distinct developmental neurotoxicity in zebrafish
title_short 6PPD and 6PPDQ embryonic exposure induced distinct developmental neurotoxicity in zebrafish
title_sort 6ppd and 6ppdq embryonic exposure induced distinct developmental neurotoxicity in zebrafish
topic 6PPD
6PPDQ
Zebrafish
Neurodevelopmental toxicity
Visual impairment
Intestinal dysregulation
url http://www.sciencedirect.com/science/article/pii/S0147651325007961
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