Cargando…

Effects of long‐term exposure to TDCPP in zebrafish (Danio rerio) – Alternations of hormone balance and gene transcriptions along hypothalamus‐pituitary axes

BACKGROUND: TDCPP is one of the major chemical of organophosphate flame retardants (OPFRs) that has been detected ubiquitously in both the environment and biota. Previously we observed that it influenced the concentrations of sex and thyroid hormones in a sex‐dependent pattern, leading to reproducti...

Descripción completa

Detalles Bibliográficos
Autores principales: Liu, Xiaoshan, Lu, Xiaoxun, Hong, Jiabin, Zhang, Jing, Lin, Juntong, Jiang, Mengzhu, Liu, Qian, Choi, Kyungho, Zhang, Jingjing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9240729/
https://www.ncbi.nlm.nih.gov/pubmed/35234363
http://dx.doi.org/10.1002/ame2.12215
_version_ 1784737631852036096
author Liu, Xiaoshan
Lu, Xiaoxun
Hong, Jiabin
Zhang, Jing
Lin, Juntong
Jiang, Mengzhu
Liu, Qian
Choi, Kyungho
Zhang, Jingjing
author_facet Liu, Xiaoshan
Lu, Xiaoxun
Hong, Jiabin
Zhang, Jing
Lin, Juntong
Jiang, Mengzhu
Liu, Qian
Choi, Kyungho
Zhang, Jingjing
author_sort Liu, Xiaoshan
collection PubMed
description BACKGROUND: TDCPP is one of the major chemical of organophosphate flame retardants (OPFRs) that has been detected ubiquitously in both the environment and biota. Previously we observed that it influenced the concentrations of sex and thyroid hormones in a sex‐dependent pattern, leading to reproductive impairments after short‐term exposure in zebrafish. Here we investigate the consequences of longer‐term exposure to TDCPP on the hypothalamic‐pituitary‐gonad (HPG), hypothalamic‐pituitary‐interrenal (HPI), and hypothalamic‐pituitary‐thyroid (HPT) axes of zebrafish (Danio rerio). METHODS: A 120‐day exposure test to 0.005, 0.05 and 0.5 mg/L TDCPP was initiated with fertilized eggs. Sex steroid hormones in the treated fishes were measured and transcriptional changes were analyzed. RESULTS: In female fish, exposure to TDCPP resulted in increases in plasma cortisol, follicle stimulating hormone (FSH), luteinizing hormone (LH), 17β‐estradiol (E2), cortisol, thyroxine (T4), and triiodothyronine (T3). Transcription of most target genes along HPG, HPI and HPT axes were increased by the exposure. While in male fish the exposure led to decreases in cortisol, FSH, LH, T4, T3, testosterone (T), and 11‐ketotestosterone (11‐KT). Transcription of genes along HPG, HPI and HPT axes, especially steroidogenic genes, were inhibited in male zebrafish. While, E2/T or E2/11‐KT ratio was increased in both female and females. The sex‐dependent changes in hormones might be due to differential responses to TDCPP induced stresses. An increase in cortisol level coincided with increases in E2 and THs in female fish, while in males decreases in cortisol as well as T, 11‐KT and THs were observed. Long‐term exposure to TDCPP at very low (μg/L) concentrations could disrupt hormone balances in a sex dependent way. CONCLUSION: This study revealed that TDCPP could affect endocrine axes – HPG, HPI and HPT – in zebrafish, and impair zebrafish development.
format Online
Article
Text
id pubmed-9240729
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher John Wiley and Sons Inc.
record_format MEDLINE/PubMed
spelling pubmed-92407292022-07-01 Effects of long‐term exposure to TDCPP in zebrafish (Danio rerio) – Alternations of hormone balance and gene transcriptions along hypothalamus‐pituitary axes Liu, Xiaoshan Lu, Xiaoxun Hong, Jiabin Zhang, Jing Lin, Juntong Jiang, Mengzhu Liu, Qian Choi, Kyungho Zhang, Jingjing Animal Model Exp Med Regular Articles BACKGROUND: TDCPP is one of the major chemical of organophosphate flame retardants (OPFRs) that has been detected ubiquitously in both the environment and biota. Previously we observed that it influenced the concentrations of sex and thyroid hormones in a sex‐dependent pattern, leading to reproductive impairments after short‐term exposure in zebrafish. Here we investigate the consequences of longer‐term exposure to TDCPP on the hypothalamic‐pituitary‐gonad (HPG), hypothalamic‐pituitary‐interrenal (HPI), and hypothalamic‐pituitary‐thyroid (HPT) axes of zebrafish (Danio rerio). METHODS: A 120‐day exposure test to 0.005, 0.05 and 0.5 mg/L TDCPP was initiated with fertilized eggs. Sex steroid hormones in the treated fishes were measured and transcriptional changes were analyzed. RESULTS: In female fish, exposure to TDCPP resulted in increases in plasma cortisol, follicle stimulating hormone (FSH), luteinizing hormone (LH), 17β‐estradiol (E2), cortisol, thyroxine (T4), and triiodothyronine (T3). Transcription of most target genes along HPG, HPI and HPT axes were increased by the exposure. While in male fish the exposure led to decreases in cortisol, FSH, LH, T4, T3, testosterone (T), and 11‐ketotestosterone (11‐KT). Transcription of genes along HPG, HPI and HPT axes, especially steroidogenic genes, were inhibited in male zebrafish. While, E2/T or E2/11‐KT ratio was increased in both female and females. The sex‐dependent changes in hormones might be due to differential responses to TDCPP induced stresses. An increase in cortisol level coincided with increases in E2 and THs in female fish, while in males decreases in cortisol as well as T, 11‐KT and THs were observed. Long‐term exposure to TDCPP at very low (μg/L) concentrations could disrupt hormone balances in a sex dependent way. CONCLUSION: This study revealed that TDCPP could affect endocrine axes – HPG, HPI and HPT – in zebrafish, and impair zebrafish development. John Wiley and Sons Inc. 2022-02-16 /pmc/articles/PMC9240729/ /pubmed/35234363 http://dx.doi.org/10.1002/ame2.12215 Text en © 2022 The Authors. Animal Models and Experimental Medicine published by John Wiley & Sons Australia, Ltd on behalf of The Chinese Association for Laboratory Animal Sciences. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Regular Articles
Liu, Xiaoshan
Lu, Xiaoxun
Hong, Jiabin
Zhang, Jing
Lin, Juntong
Jiang, Mengzhu
Liu, Qian
Choi, Kyungho
Zhang, Jingjing
Effects of long‐term exposure to TDCPP in zebrafish (Danio rerio) – Alternations of hormone balance and gene transcriptions along hypothalamus‐pituitary axes
title Effects of long‐term exposure to TDCPP in zebrafish (Danio rerio) – Alternations of hormone balance and gene transcriptions along hypothalamus‐pituitary axes
title_full Effects of long‐term exposure to TDCPP in zebrafish (Danio rerio) – Alternations of hormone balance and gene transcriptions along hypothalamus‐pituitary axes
title_fullStr Effects of long‐term exposure to TDCPP in zebrafish (Danio rerio) – Alternations of hormone balance and gene transcriptions along hypothalamus‐pituitary axes
title_full_unstemmed Effects of long‐term exposure to TDCPP in zebrafish (Danio rerio) – Alternations of hormone balance and gene transcriptions along hypothalamus‐pituitary axes
title_short Effects of long‐term exposure to TDCPP in zebrafish (Danio rerio) – Alternations of hormone balance and gene transcriptions along hypothalamus‐pituitary axes
title_sort effects of long‐term exposure to tdcpp in zebrafish (danio rerio) – alternations of hormone balance and gene transcriptions along hypothalamus‐pituitary axes
topic Regular Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9240729/
https://www.ncbi.nlm.nih.gov/pubmed/35234363
http://dx.doi.org/10.1002/ame2.12215
work_keys_str_mv AT liuxiaoshan effectsoflongtermexposuretotdcppinzebrafishdaniorerioalternationsofhormonebalanceandgenetranscriptionsalonghypothalamuspituitaryaxes
AT luxiaoxun effectsoflongtermexposuretotdcppinzebrafishdaniorerioalternationsofhormonebalanceandgenetranscriptionsalonghypothalamuspituitaryaxes
AT hongjiabin effectsoflongtermexposuretotdcppinzebrafishdaniorerioalternationsofhormonebalanceandgenetranscriptionsalonghypothalamuspituitaryaxes
AT zhangjing effectsoflongtermexposuretotdcppinzebrafishdaniorerioalternationsofhormonebalanceandgenetranscriptionsalonghypothalamuspituitaryaxes
AT linjuntong effectsoflongtermexposuretotdcppinzebrafishdaniorerioalternationsofhormonebalanceandgenetranscriptionsalonghypothalamuspituitaryaxes
AT jiangmengzhu effectsoflongtermexposuretotdcppinzebrafishdaniorerioalternationsofhormonebalanceandgenetranscriptionsalonghypothalamuspituitaryaxes
AT liuqian effectsoflongtermexposuretotdcppinzebrafishdaniorerioalternationsofhormonebalanceandgenetranscriptionsalonghypothalamuspituitaryaxes
AT choikyungho effectsoflongtermexposuretotdcppinzebrafishdaniorerioalternationsofhormonebalanceandgenetranscriptionsalonghypothalamuspituitaryaxes
AT zhangjingjing effectsoflongtermexposuretotdcppinzebrafishdaniorerioalternationsofhormonebalanceandgenetranscriptionsalonghypothalamuspituitaryaxes