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双酚B对斑马鱼性别分化的影响及作用机制

本站小编 Free考研考试/2021-12-30

杨倩1,
刘建梅2,
丁洁2,
陈丽红3,,
1. 南京财经大学食品科学与工程学院, 南京 210023;
2. 江苏雅信昆成检测科技有限公司, 南京 210034;
3. 南京中医药大学药学院, 南京 210023
作者简介: 杨倩(1986-),女,博士,研究方向为生态毒理学,E-mail:jsyqhappy@126.com.
通讯作者: 陈丽红,clh_helen@njucm.edu.cn
基金项目: 国家重点研发计划(2018YFC1801501,2018YFC1706500)


中图分类号: X171.5


Effects and Mechanism of Bisphenol B on Sexual Differentiation of Zebrafish

Yang Qian1,
Liu Jianmei2,
Ding Jie2,
Chen Lihong3,,
1. College of Food Science and Engineering, Nanjing University of Finance and Economics, Nanjing 210023, China;
2. Jiangsu Yaxin Tech. Co. Ltd., Nanjing 210034, China;
3. School of Pharmacy, Nanjing University of Chinese Medicine, Nanjing 210023, China
Corresponding author: Chen Lihong,clh_helen@njucm.edu.cn

CLC number: X171.5

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摘要:双酚A(bisphenol A,BPA)是一种典型的内分泌干扰物,双酚B(bisphenol B,BPA)作为其替代物,使用量逐渐增多。一些研究表明,BPB也具有内分泌干扰效应,但是其对鱼类性别分化的影响尚无报道。本文将斑马鱼胚胎暴露于不同浓度的BPB中至受精后60 d(days post fertilization,dpf),研究BPB对斑马鱼性别分化的影响及可能的分子机制。结果表明,10、100和1 000 μg·L-1的BPB暴露导致斑马鱼性别比例向雌鱼偏离,雄鱼的精巢中发育出初级卵母细胞,并导致斑马鱼体内17β-雌二醇(17β-estradiol,E2)水平升高,睾酮(testosterone,T)水平降低,表明BPB对斑马鱼具有雌激素效应。从基因水平探讨这2种物质导致斑马鱼雌性化的原因,发现BPB使卵巢分化相关基因foxl2的表达水平上升,精巢分化相关基因dmrt1amhsox9a表达水平降低,并进一步提高了芳香化酶基因cyp19a1a的转录水平,促进E2的合成,导致斑马鱼的性别分化过程发生异常。
关键词: 双酚B/
斑马鱼/
内分泌干扰效应/
性别分化/
性腺发育

Abstract:Bisphenol B (BPB) has been increasingly used as an alternative to bisphenol A (BPA) owing to BPA’s endocrine disrupting effects. Some researches indicate that BPB exhibits similar adverse effects, while data of toxicity on sexual differentiation and sex determination are still limited. In the present study, zebrafish embryos were exposed to BPB from 2 hours post fertilization (hpf) to 60 days post fertilization (dpf) to investigate the effects of BPB on sex differentiation of zebrafish. The results indicated that 10, 100 and 1 000μ g·L-1 BPB exposure during sex differentiation tended to result in a female sex ratio bias. Histological analyses at 60 dpf indicated that the development of ovo-testes and immature ovaries were induced. The concentration of testosterone (T) decreased while concentration of 17β-estradiol (E2) increased in a concentration-dependent manner, indicating BPB has estrogen activity. BPB exposure induced expression of foxl2, which is crucial for the ovarian development, and suppressed gene expression of dmrt1, amh and sox9a, which are crucial for the testicular development. Variation of these genes leaded to increased expression of cyp19a1a, which promoted production of estrogens, and further caused phenotypic feminization.
Key words:bisphenol B/
zebrafish/
endocrine disrupting effects/
sex determination/
gonad development.

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den Braver-Sewradj S P, van Spronsen R, Hessel E V S. Substitution of bisphenol A:A review of the carcinogenicity, reproductive toxicity, and endocrine disruption potential of alternative substances[J]. Critical Reviews in Toxicology, 2020, 50(2):128-147
Yan Z Y, Liu Y H, Yan K, et al. Bisphenol analogues in surface water and sediment from the shallow Chinese freshwater lakes:Occurrence, distribution, source apportionment, and ecological and human health risk[J]. Chemosphere, 2017, 184:318-328
Liu Y H, Zhang S H, Song N H, et al. Occurrence, distribution and sources of bisphenol analogues in a shallow Chinese freshwater lake (Taihu Lake):Implications for ecological and human health risk[J]. Science of the Total Environment, 2017, 599-600:1090-1098
Liao C Y, Kannan K. Concentrations and profiles of bisphenol A and other bisphenol analogues in foodstuffs from the United States and their implications for human exposure[J]. Journal of Agricultural and Food Chemistry, 2013, 61(19):4655-4662
Cunha S C, Almeida C, Mendes E, et al. Simultaneous determination of bisphenol A and bisphenol B in beverages and powdered infant formula by dispersive liquid-liquid micro-extraction and heart-cutting multidimensional gas chromatography-mass spectrometry[J]. Food Additives & Contaminants:Part A, 2011, 28(4):513-526
Fattore M, Russo G, Barbato F, et al. Monitoring of bisphenols in canned tuna from Italian markets[J]. Food and Chemical Toxicology, 2015, 83:68-75
Liao C Y, Kannan K. A survey of alkylphenols, bisphenols, and triclosan in personal care products from China and the United States[J]. Archives of Environmental Contamination and Toxicology, 2014, 67(1):50-59
Cunha S C, Fernandes J O. Quantification of free and total bisphenol A and bisphenol B in human urine by dispersive liquid-liquid microextraction (DLLME) and heart-cutting multidimensional gas chromatography-mass spectrometry (MD-GC/MS)[J]. Talanta, 2010, 83(1):117-125
Cobellis L, Colacurci N, Trabucco E, et al. Measurement of bisphenol A and bisphenol B levels in human blood sera from healthy and endometriotic women[J]. Biomedical Chromatography:BMC, 2009, 23(11):1186-1190
Chang B V, Liu J H, Liao C S. Aerobic degradation of bisphenol-A and its derivatives in river sediment[J]. Environmental Technology, 2014, 35(4):416-424
Ike M, Chen M Y, Danzl E, et al. Biodegradation of a variety of bisphenols under aerobic and anaerobic conditions[J]. Water Science and Technology, 2006, 53(6):153-159
Kitamura S, Suzuki T, Sanoh S, et al. Comparative study of the endocrine-disrupting activity of bisphenol A and 19 related compounds[J]. Toxicological Sciences:an Official Journal of the Society of Toxicology, 2005, 84(2):249-259
Yang X H, Liu H H, Yang Q, et al. Predicting anti-androgenic activity of bisphenols using molecular docking and quantitative structure-activity relationships[J]. Chemosphere, 2016, 163:373-381
Ullah A, Pirzada M, Jahan S, et al. Impact of low-dose chronic exposure to bisphenol A and its analogue bisphenol B, bisphenol F and bisphenol S on hypothalamo-pituitary-testicular activities in adult rats:A focus on the possible hormonal mode of action[J]. Food and Chemical Toxicology, 2018, 121:24-36
Yang Q, Yang X H, Liu J N, et al. Exposure to bisphenol B disrupts steroid hormone homeostasis and gene expression in the hypothalamic-pituitary-gonadal axis of zebrafish[J]. Water, Air, & Soil Pollution, 2017, 228(3):1-12
Scholz S, Klüver N. Effects of endocrine disrupters on sexual, gonadal development in fish[J]. Sexual Development, 2009, 3(2-3):136-151
Crain D A, Eriksen M, Iguchi T, et al. An ecological assessment of bisphenol-A:Evidence from comparative biology[J]. Reproductive Toxicology, 2007, 24(2):225-239
Metcalfe C D, Metcalfe T L, Kiparissis Y, et al. Estrogenic potency of chemicals detected in sewage treatment plant effluents as determined by in vivo assays with Japanese medaka (Oryzias latipes)[J]. Environmental Toxicology and Chemistry, 2001, 20(2):297-308
Naderi M, Wong M Y, Gholami F. Developmental exposure of zebrafish (Danio rerio) to bisphenol-S impairs subsequent reproduction potential and hormonal balance in adults[J]. Aquatic Toxicology, 2014, 148:195-203
Hill R L Jr, Janz D M. Developmental estrogenic exposure in zebrafish (Danio rerio):Ⅰ. Effects on sex ratio and breeding success[J]. Aquatic Toxicology, 2003, 63(4):417-429
陈玫宏, 郭敏, 徐怀洲, 等. 太湖表层水体及沉积物中双酚A类似物的分布特征及潜在风险[J]. 环境科学, 2017, 38(7):2793-2800Chen M H, Guo M, Xu H Z, et al. Distribution characteristics and potential risk of bisphenol analogues in surface water and sediments of Lake Taihu[J]. Environmental Science, 2017, 38(7):2793-2800(in Chinese)
Ji K, Hong S, Kho Y, et al. Effects of bisphenol S exposure on endocrine functions and reproduction of zebrafish[J]. Environmental Science & Technology, 2013, 47(15):8793-8800
Yang Q, Yang X H, Liu J N, et al. Effects of exposure to BPF on development and sexual differentiation during early life stages of zebrafish (Danio rerio)[J]. Comparative Biochemistry and Physiology Toxicology & Pharmacology:CBP, 2018, 210:44-56
Scholz S, Klüver N. Effects of endocrine disrupters on sexual, gonadal development in fish[J]. Sexual Development, 2009, 3(2-3):136-151
Guiguen Y, Fostier A, Piferrer F, et al. Ovarian aromatase and estrogens:A pivotal role for gonadal sex differentiation and sex change in fish[J]. General and Comparative Endocrinology, 2010, 165(3):352-366
von Hofsten J, Olsson P E. Zebrafish sex determination and differentiation:Involvement of FTZ-F1 genes[J]. Reproductive Biology and Endocrinology, 2005, 3:63
Webster K A, Schach U, Ordaz A, et al. Dmrt1 is necessary for male sexual development in zebrafish[J]. Developmental Biology, 2017, 422(1):33-46
Rodríguez-Marí A, Yan Y L, Bremiller R A, et al. Characterization and expression pattern of zebrafish Anti-Müllerian hormone (Amh) relative to sox9a, sox9b, and cyp19a1a, during gonad development[J]. Gene Expression Patterns:GEP, 2005, 5(5):655-667
Leet J K, Gall H E, Sepúlveda M S. A review of studies on androgen and estrogen exposure in fish early life stages:Effects on gene and hormonal control of sexual differentiation[J]. Journal of Applied Toxicology, 2011, 31(5):379-398
Schulz R W, Bogerd J, Male R, et al. Estrogen-induced alterations in amh and dmrt1 expression signal for disruption in male sexual development in the zebrafish[J]. Environmental Science & Technology, 2007, 41(17):6305-6310
Wang D S, Zhou L Y, Kobayashi T, et al. Doublesex- and Mab-3-related transcription factor-1 repression of aromatase transcription, a possible mechanism favoring the male pathway in tilapia[J]. Endocrinology, 2010, 151(3):1331-1340
Chai C, Chan W K. Developmental expression of a novel Ftz-F1 homologue, ff1b (NR5A4), in the zebrafish Danio rerio[J]. Mechanisms of Development, 2000, 91(1-2):421-426
Siegfried K R. In search of determinants:Gene expression during gonadal sex differentiation[J]. Journal of Fish Biology, 2010, 76(8):1879-1902
Cluzet V, Devillers M M, Petit F, et al. Aberrant granulosa cell-fate related to inactivated p53/Rb signaling contributes to granulosa cell tumors and to FOXL2 downregulation in the mouse ovary[J]. Oncogene, 2020, 39(9):1875-1890
Zhang X, Gao L, Yang K, et al. Monocrotophos pesticide modulates the expression of sexual differentiation genes and causes phenotypic feminization in zebrafish (Danio rerio)[J]. Comparative Biochemistry & Physiology Part C Toxicology & Pharmacology, 2013, 157(1):33-40

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