删除或更新信息,请邮件至freekaoyan#163.com(#换成@)

双酚A对哺乳类实验动物雄性生殖系统发育的影响

本站小编 Free考研考试/2021-12-30

熊忆茗1,2,
李红梅1,2,
秦占芬1,2,,
1. 中国科学院生态环境研究中心, 环境化学与生态毒理学国家重点实验室, 北京 100085;
2. 中国科学院大学, 北京 100049
作者简介: 熊忆茗(1998-),女,硕士研究生,研究方向为环境毒理学,E-mail:xiongym70680@163.com.
通讯作者: 秦占芬,qinzhanfen@rcees.ac.cn
基金项目: 国家自然科学基金面上项目(21876196);国家重点研发计划资助项目(2018YFA0901103)


中图分类号: X171.5


Effects of Bisphenol A on Development of Male Reproductive System in Mammal Laboratory Animals

Xiong Yiming1,2,
Li Hongmei1,2,
Qin Zhanfen1,2,,
1. State Key Laboratory of Environmental Chemistry and Ecotoxicology, Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, Beijing 100085, China;
2. University of Chinese Academy of Sciences, Beijing 100049, China
Corresponding author: Qin Zhanfen,qinzhanfen@rcees.ac.cn

CLC number: X171.5

-->

摘要
HTML全文
(0)(0)
参考文献(60)
相关文章
施引文献
资源附件(0)
访问统计

摘要:内分泌干扰物双酚A(bisphenol A,BPA)对生殖系统尤其是雄性生殖系统的影响一直受到关注,然而目前相关研究中存在诸多不一致的结果。本文系统分析了低剂量BPA对哺乳类实验动物大鼠和小鼠雄性生殖系统发育影响的文献,重点关注睾丸和附睾的质量、睾丸组织学结构、附属腺和外生殖器参数、肛殖距、精子参数和性激素水平等指标的变化,并探讨了实验结果与实验设计某些因素的相关性。经分析发现,妊娠期BPA暴露对实验鼠雄性生殖系统的影响呈现比较一致的阳性结果,但是哺乳期暴露和妊娠至哺乳期的暴露存在很多矛盾的结果;而动物品系、给药方式等因素与实验结果之间没有明确的关系,即便相似甚至相同的实验设计下也出现了不同的结果。进一步分析发现,有些研究在实验质量控制方面存在一定的缺陷,这可能是造成矛盾结果的主要原因。综合来看,BPA在器官水平和组织病理学水平对雄性生殖系统发育的影响较弱,基于此类指标的效应判断容易受到实验设计因素和质量控制的影响,最终可能导致不一致的结果。由此建议,今后相关研究在加强质量控制的同时,应重点关注BPA对细胞和分子层面的损伤。
关键词: 双酚A/
雄性生殖系统/
内分泌干扰物/
质量控制

Abstract:The effects of bisphenol A (BPA), a known endocrine disrupting chemical (EDC), on the reproductive system, especially the male reproductive system, have received much attention. However, some contradictory results are confusing. This review systematically analyzed the literatures concerning on the effects of low doses of BPA on the development of the male reproductive system in mammal laboratory animals, with focus on changes in testis mass, epididymis mass, testis histology, development of accessory glands and external genitals, anogenital distance, sperm parameters and sex hormone levels, and explored the possible correlations between the results and certain experimental factors. As a result, it was concluded that gestational exposure to BPA generally produced consistent adverse effects, while contradictory results appeared when animals were treated during lactation or from gestation to lactation, even under similar or the same experimental design. The data show no clear correlation between experimental results and experimental factors. Further analysis revealed certain defects of quality control in some literatures, which could be responsible for inconsistent results among experimental results. Taken together, BPA could lack strong influences on the development of the male reproductive system at the organ and histopathological levels, thereby resulting in the experimental results being easily interfered by experimental factors or quality control. Therefore, future relevant research should focus on cellular and molecular damages of BPA to the male reproductive system while strengthening experimental quality control.
Key words:bisphenol A/
male reproductive system/
endocrine disrupting chemical/
quality control.

加载中
Rochester J R. Bisphenol A and human health:A review of the literature[J]. Reproductive Toxicology, 2013, 42:132-155
Inoue K, Kato K, Yoshimura Y, et al. Determination of bisphenol A in human serum by high-performance liquid chromatography with multi-electrode electrochemical detection[J]. Journal of Chromatography B:Biomedical Sciences and Applications, 2000, 749(1):17-23
Takeuchi T, Tsutsumi O. Serum bisphenol A concentrations showed gender differences, possibly linked to androgen levels[J]. Biochemical and Biophysical Research Communications, 2002, 291(1):76-78
Rubin B S. Bisphenol A:An endocrine disruptor with widespread exposure and multiple effects[J]. The Journal of Steroid Biochemistry and Molecular Biology, 2011, 127(1-2):27-34
Matuszczak E, Komarowska M D, Debek W, et al. The impact of bisphenol A on fertility, reproductive system, and development:A review of the literature[J]. International Journal of Endocrinology, 2019, 2019:4068717
Mínguez-Alarcón L, Hauser R, Gaskins A J. Effects of bisphenol A on male and couple reproductive health:A review[J]. Fertility and Sterility, 2016, 106(4):864-870
United States Food and Drug Administration (US FDA). Update on bisphenol A for use in food contact applications[R]. Rockville:United States Food and Drug Administration, 2010
Tyl R W, Myers C B, Marr M C, et al. Three-generation reproductive toxicity study of dietary bisphenol A in CD Sprague-Dawley rats[J]. Toxicological Sciences, 2002, 68(1):121-146
Piprek R P. Molecular Mechanisms of Cell Differentiation in Gonad Development[M]. Cham:Springer International Publishing, 2016:v-ix
Pask A. The reproductive system[J]. Advances in Experimental Medicine and Biology, 2016, 886:1-12
Hong J, Chen F, Wang X L, et al. Exposure of preimplantation embryos to low-dose bisphenol A impairs testes development and suppresses histone acetylation of StAR promoter to reduce production of testosterone in mice[J]. Molecular and Cellular Endocrinology, 2016, 427:101-111
Rahman M S, Kwon W S, Karmakar P C, et al. Gestational exposure to bisphenol A affects the function and proteome profile of F1 spermatozoa in adult mice[J]. Environmental Health Perspectives, 2017, 125(2):238-245
LaRocca J, Boyajian A, Brown C, et al. Effects of in utero exposure to bisphenol A or diethylstilbestrol on the adult male reproductive system[J]. Birth Defects Research Part B, Developmental and Reproductive Toxicology, 2011, 92(6):526-533
Quan C, Wang C, Duan P, et al. Prenatal bisphenol A exposure leads to reproductive hazards on male offspring via the Akt/mTOR and mitochondrial apoptosis pathways[J]. Environmental Toxicology, 2017, 32(3):1007-1023
Lv Y, Li L L, Fang Y H, et al. In utero exposure to bisphenol A disrupts fetal testis development in rats[J]. Environmental Pollution, 2019, 246:217-224
Abdel-Maksoud F M, Ali F A Z, Akingbemi B T. Prenatal exposures to bisphenol A and di (2-ethylhexyl) phthalate disrupted seminiferous tubular development in growing male rats[J]. Reproductive Toxicology, 2019, 88:85-90
Timms B G, Howdeshell K L, Barton L, et al. Estrogenic chemicals in plastic and oral contraceptives disrupt development of the fetal mouse prostate and urethra[J]. PNAS, 2005, 102(19):7014-7019
Gupta C. Reproductive malformation of the male offspring following maternal exposure to estrogenic chemicals[J]. Proceedings of the Society for Experimental Biology and Medicine Society for Experimental Biology and Medicine, 2000, 224(2):61-68
Schwartz C L, Christiansen S, Vinggaard A M, et al. Anogenital distance as a toxicological or clinical marker for fetal androgen action and risk for reproductive disorders[J]. Archives of Toxicology, 2019, 93(2):253-272
Ullah A, Pirzada M, Jahan S, et al. Prenatal BPA and its analogs BPB, BPF, and BPS exposure and reproductive axis function in the male offspring of Sprague Dawley rats[J]. Human & Experimental Toxicology, 2019, 38(12):1344-1365
Yang Q T, Sui X X, Cao J J, et al. Effects of exposure to bisphenol A during pregnancy on the pup testis function[J]. International Journal of Endocrinology, 2019, 2019:1-8
Tanaka M, Nakaya S, Katayama M, et al. Effect of prenatal exposure to bisphenol A on the serum testosterone concentration of rats at birth[J]. Human & Experimental Toxicology, 2006, 25(7):369-373
Henafy H M A, Ibrahim M A, Abd El Aziz S A, et al. Oxidative stress and DNA methylation in male rat pups provoked by the transplacental and translactational exposure to bisphenol A[J]. Environmental Science and Pollution Research, 2020, 27(4):4513-4519
Ma L, Yu H Y, Wang X, et al. The effects of maternal exposure to BPA during pregnancy on the male reproductive system and the testicular microRNA expression profile[J]. Environmental Science and Pollution Research, 2020, 27(14):17290-17302
Vilela J, Hartmann A, Silva E F, et al. Sperm impairments in adult vesper mice (Calomys laucha) caused by in utero exposure to bisphenol A[J]. Andrologia, 2014, 46(9):971-978
Olukole S G, Lanipekun D O, Ola-Davies E O, et al. Maternal exposure to environmentally relevant doses of bisphenol A causes reproductive dysfunction in F1 adult male rats:Protective role of melatonin[J]. Environmental Science and Pollution Research, 2019, 26(28):28940-28950
Uchtmann K S, Taylor J A, Timms B G, et al. Fetal bisphenol A and ethinylestradiol exposure alters male rat urogenital tract morphology at birth:Confirmation of prior low-dose findings in CLARITY-BPA[J]. Reproductive Toxicology, 2020, 91:131-141
Wistuba J, Brinkworth M H, Schlatt S, et al. Intrauterine bisphenol A exposure leads to stimulatory effects on Sertoli cell number in rats[J]. Environmental Research, 2003, 91(2):95-103
Shi M X, Sekulovski N, MacLean J A, et al. Prenatal exposure to bisphenol A analogues on female reproductive functions in mice[J]. Toxicological Sciences, 2019, 168(2):561-571
Wei Y Y, Han C, Geng Y M, et al. Maternal exposure to bisphenol A during pregnancy interferes testis development of F1 male mice[J]. Environmental Science and Pollution Research, 2019, 26(23):23491-23504
Kalb A C, Kalb A L, Cardoso T F, et al. Maternal transfer of bisphenol A during nursing causes sperm impairment in male offspring[J]. Archives of Environmental Contamination and Toxicology, 2016, 70(4):793-801
解美娜, 李锋杰. 哺乳期接触双酚A对子代小鼠睾丸线粒体的影响[J]. 卫生研究, 2014, 43(6):962-966Xie M N, Li F J. Effects of bisphenol A exposure during lactation on testicular mitochondria in male mouse offspring[J]. Journal of Hygiene Research, 2014, 43(6):962-966(in Chinese)
Xie M N, Bu P L, Li F J, et al. Neonatal bisphenol A exposure induces meiotic arrest and apoptosis of spermatogenic cells[J]. Oncotarget, 2016, 7(9):10606-10615
Aikawa H, Koyama S, Matsuda M, et al. Relief effect of vitamin A on the decreased motility of sperm and the increased incidence of malformed sperm in mice exposed neonatally to bisphenol A[J]. Cell and Tissue Research, 2004, 315(1):119-124
Salian S, Doshi T, Vanage G. Neonatal exposure of male rats to bisphenol A impairs fertility and expression of Sertoli cell junctional proteins in the testis[J]. Toxicology, 2009, 265(1-2):56-67
Toyama Y, Yuasa S. Effects of neonatal administration of 17β-estradiol, β-estradiol 3-benzoate, or bisphenol A on mouse and rat spermatogenesis[J]. Reproductive Toxicology, 2004, 19(2):181-188
Nagao T, Saito Y, Usumi K, et al. Reproductive function in rats exposed neonatally to bisphenol A and estradiol benzoate[J]. Reproductive Toxicology, 1999, 13(4):303-311
Kato H, Furuhashi T, Tanaka M, et al. Effects of bisphenol A given neonatally on reproductive functions of male rats[J]. Reproductive Toxicology, 2006, 22(1):20-29
Brouard V, Guénon I, Bouraima-Lelong H, et al. Differential effects of bisphenol A and estradiol on rat spermatogenesis' establishment[J]. Reproductive Toxicology, 2016, 63:49-61
Zhang G L, Zhang X F, Feng Y M, et al. Exposure to bisphenol A results in a decline in mouse spermatogenesis[J]. Reproduction, Fertility, and Development, 2013, 25(6):847-859
Liu X L, Chen X Y, Wang Z C, et al. Effects of exposure to bisphenol A during pregnancy and lactation on the testicular morphology and caspase-3 protein expression of ICR pups[J]. Biomedical Reports, 2013, 1(3):420-424
Cardoso N, Pandolfi M, Lavalle J, et al. Probable gamma-aminobutyric acid involvement in bisphenol A effect at the hypothalamic level in adult male rats[J]. Journal of Physiology and Biochemistry, 2011, 67(4):559-567
Gámez J M, Penalba R, Cardoso N, et al. Low dose of bisphenol A impairs the reproductive axis of prepuberal male rats[J]. Journal of Physiology and Biochemistry, 2014, 70(1):239-246
Okada A, Kai O. Effects of estradiol-17beta and bisphenol A administered chronically to mice throughout pregnancy and lactation on the male pups' reproductive system[J]. Asian Journal of Andrology, 2008, 10(2):271-276
Sadowski R N, Park P, Neese S L, et al. Effects of perinatal bisphenol A exposure during early development on radial arm maze behavior in adult male and female rats[J]. Neurotoxicology and Teratology, 2014, 42:17-24
Spörndly-Nees E, Boberg J, Ekstedt E, et al. Low-dose exposure to bisphenol A during development has limited effects on male reproduction in midpubertal and aging Fischer 344 rats[J]. Reproductive Toxicology, 2018, 81:196-206
Meng Y, Lin R, Wu F J, et al. Decreased capacity for sperm production induced by perinatal bisphenol A exposure is associated with an increased inflammatory response in the offspring of C57BL/6 male mice[J]. International Journal of Environmental Research and Public Health, 2018, 15(10):2158
Kobayashi K, Kubota H, Ohtani K, et al. Lack of effects for dietary exposure of bisphenol A during in utero and lactational periods on reproductive development in rat offspring[J]. The Journal of Toxicological Sciences, 2012, 37(3):565-573
Untied States Department of Health and Human Services (NIEHS). National Toxicology Program research report on the CLARITY-BPA core study:A perinatal and chronic extended-dose-range study of bisphenol A in rats[R]. Morrisville:NIEHS, 2018
Delclos K B, Camacho L, Lewis S M, et al. Toxicity evaluation of bisphenol A administered by gavage to Sprague Dawley rats from gestation day 6 through postnatal day 90[J]. Toxicological Sciences, 2014, 139(1):174-197
Christiansen S, Axelstad M, Boberg J, et al. Low-dose effects of bisphenol A on early sexual development in male and female rats[J]. Reproduction, 2014, 147(4):477-487
Hass U, Christiansen S, Boberg J, et al. Low-dose effect of developmental bisphenol A exposure on sperm count and behaviour in rats[J]. Andrology, 2016, 4(4):594-607
Watanabe S, Wang R S, Miyagawa M, et al. Imbalance of testosterone level in male offspring of rats perinatally exposed to bisphenol A[J]. Industrial Health, 2003, 41(4):338-341
Salian S, Doshi T, Vanage G. Perinatal exposure of rats to bisphenol A affects the fertility of male offspring[J]. Life Sciences, 2009, 85(21-22):742-752
Nanjappa M K, Simon L, Akingbemi B T. The industrial chemical bisphenol A (BPA) interferes with proliferative activity and development of steroidogenic capacity in rat leydig cells[J]. Biology of Reproduction, 2012, 86(5):135-146
Oliveira I M, Romano R M, de Campos P, et al. Delayed onset of puberty in male offspring from bisphenol A-treated dams is followed by the modulation of gene expression in the hypothalamic-pituitary-testis axis in adulthood[J]. Reproduction, Fertility, and Development, 2017, 29(12):2496-2505
Campos P D, Oliveira I M, Sena de Souza J, et al. Maternal bisphenol A exposure disrupts spermatogenesis in adult rat offspring[J]. Journal of Toxicology and Environmental Health, Part A, 2019, 82(3):163-175
Goodman J E, Witorsch R J, McConnell E E, et al. Weight-of-evidence evaluation of reproductive and developmental effects of low doses of bisphenol A[J]. Critical Reviews in Toxicology, 2009, 39(1):1-75
Goodman J E, McConnell E E, Sipes I G, et al. An updated weight of the evidence evaluation of reproductive and developmental effects of low doses of bisphenol A[J]. Critical Reviews in Toxicology, 2006, 36(5):387-457
Upmeier A, Degen G H, Diel P, et al. Toxicokinetics of bisphenol A in female DA/Han rats after a single i.v. and oral administration[J]. Archives of Toxicology, 2000, 74(8):431-436

相关话题/实验 干扰 设计 环境 北京