环境内分泌干扰物影响垂体促性腺激素的研究进展
Influences of Endocrine-disrupting Chemicals on Pituitary Gonadotropins: A Review
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摘要: 通过工业和农业生产活动排入环境的多种农药、阻燃剂、多氯联苯、塑料包装成分、防腐剂、工业副产物和重金属等化学物质,已被证明是内分泌干扰物(endocrine-disrupting chemicals, EDCs),通过各种途径干扰内分泌系统,例如作用下丘脑-垂体-性腺(hypothalamic-pituitary-gonad, HPG)轴。垂体是HPG轴中联系下丘脑与性腺的重要内分泌器官,合成和分泌2种促性腺激素,即黄体生成素(luteinizing hormone, LH)和卵泡刺激素(follicle-stimulating hormone, FSH),在调控性成熟与生殖发育过程中起到不可或缺的作用。如果垂体促性腺细胞作为EDCs作用的靶标,LH和FSH的合成、分泌、转运或者代谢受到干扰,可能会引起生殖系统的内分泌紊乱,影响性成熟和生殖功能,甚至增加生殖障碍等相关疾病风险。已有一些环境流行病学调查和动物实验报道EDCs暴露与人体及哺乳动物体内LH和FSH水平改变相关,但影响促性腺激素的作用机制研究却相对有限。本文对近年来EDCs影响促性腺激素的环境流行病学调查、动物实验以及毒理学机制研究的进展进行综述,并探讨未来的研究方向。Abstract: A variety of pesticides, flame retardants, polychlorinated biphenyls, chemical in plastic articles, preservatives, industrial by-products, heavy metals and other pollutants, which are discharged into the environment through industrial and agricultural activities, have been proven to be endocrine-disrupting chemicals (EDCs). Disruption of endocrine system by EDCs can occur in various ways, such as acting on the hypothalamic-pituitary-gonad (HPG) axis. The pituitary is an important endocrine organ in the HPG axis that connects the hypothalamus and the gonads. The gonadotropic cells in pituitary synthesize and secrete two gonadotropins, i.e. luteinizing hormone (LH) and follicle-stimulating hormone (FSH), which play an essential role in sexual maturation and reproduction. When the gonadotropin cells act as the targets of EDCs, the synthesis, secretion, transportation or metabolism of LH and FSH may be disturbed, resulting in hormone imbalance, altering sexual maturity, impairing reproduction and even increasing the risk of endocrine and reproductive diseases. Some environmental epidemiological investigations and animal experiments have reported that EDCs exposure was associated with the changes in the serum levels of LH and FSH in humans and mammals. However, the studies on the toxicological mechanisms of EDCs affecting the synthesis and secretion of these two gonadotropins are relatively limited. This review aims to summarize the environmental epidemiological investigations, animal studies, and toxicological mechanisms regarding the effects of EDCs on gonadotropins, as well as discuss future research directions.
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Kumar M, Sarma D K, Shubham S, et al. Environmental endocrine-disrupting chemical exposure: Role in non-communicable diseases [J]. Frontiers in Public Health, 2020, 8: 553850 Zoeller R T, Brown T R, Doan L L, et al. Endocrine-disrupting chemicals and public health protection: A statement of principles from The Endocrine Society [J]. Endocrinology, 2012, 153(9): 4097-4110 Maqbool F, Mostafalou S, Bahadar H, et al. Review of endocrine disorders associated with environmental toxicants and possible involved mechanisms [J]. Life Sciences, 2016, 145: 265-273 Oyola M G, Handa R J. Hypothalamic-pituitary-adrenal and hypothalamic-pituitary-gonadal axes: Sex differences in regulation of stress responsivity [J]. Stress, 2017, 20(5): 476-494 Melgarejo M, Mendiola J, Koch H M, et al. Associations between urinary organophosphate pesticide metabolite levels and reproductive parameters in men from an infertility clinic [J]. Environmental Research, 2015, 137: 292-298 Ye X Q, Pan W Y, Zhao S L, et al. Relationships of pyrethroid exposure with gonadotropin levels and pubertal development in Chinese boys [J]. Environmental Science & Technology, 2017, 51(11): 6379-6386 Kaprara A, Huhtaniemi I T. The hypothalamus-pituitary-gonad axis: Tales of mice and men [J]. Metabolism, 2018, 86: 3-17 Stamatiades G A, Kaiser U B. Gonadotropin regulation by pulsatile GnRH: Signaling and gene expression [J]. Molecular and Cellular Endocrinology, 2018, 463: 131-141 Plunk E C, Richards S M. Endocrine-disrupting air pollutants and their effects on the hypothalamus-pituitary-gonadal axis [J]. International Journal of Molecular Sciences, 2020, 21(23): 9191 Dwyer A A, Chavan N R, Lewkowitz-Shpuntoff H, et al. Functional hypogonadotropic hypogonadism in men: Underlying neuroendocrine mechanisms and natural history [J]. The Journal of Clinical Endocrinology & Metabolism, 2019, 104(8): 3403-3414 Goodarzi M O, Dumesic D A, Chazenbalk G, et al. Polycystic ovary syndrome: Etiology, pathogenesis and diagnosis [J]. Nature Reviews Endocrinology, 2011(7): 219-231 Saadia Z. Follicle stimulating hormone (LH: FSH) ratio in polycystic ovary syndrome (PCOS)-obese vs. non-obese women [J]. Medical Archives, 2020, 74(4): 289 McKinlay R, Plant J A, Bell J N B, et al. Endocrine disrupting pesticides: Implications for risk assessment [J]. Environment International, 2008, 34(2): 168-183 Bornman M, Delport R, Farías P, et al. Alterations in male reproductive hormones in relation to environmental DDT exposure [J]. Environment International, 2018, 113: 281-289 Freire C, Koifman R J, Sarcinelli P N, et al. Association between serum levels of organochlorine pesticides and sex hormones in adults living in a heavily contaminated area in Brazil [J]. International Journal of Hygiene and Environmental Health, 2014, 217(2-3): 370-378 Eskenazi B, Rauch S A, Tenerelli R, et al. In utero and childhood DDT, DDE, PBDE and PCBs exposure and sex hormones in adolescent boys: The CHAMACOS study [J]. International Journal of Hygiene and Environmental Health, 2017, 220(2): 364-372 Aguilar-Garduño C, Lacasaña M, Blanco-Muñoz J, et al. Changes in male hormone profile after occupational organophosphate exposure. A longitudinal study [J]. Toxicology, 2013, 307: 55-65 Qin K L, Zhang Y, Wang Y W, et al. Prenatal organophosphate pesticide exposure and reproductive hormones in cord blood in Shandong, China [J]. International Journal of Hygiene and Environmental Health, 2020, 225: 113479 Li C M, Cao M F, Ma L J, et al. Pyrethroid pesticide exposure and risk of primary ovarian insufficiency in Chinese women [J]. Environmental Science & Technology, 2018, 52(5): 3240-3248 Jurewicz J, Radwan P, Wielgomas B, et al. Exposure to pyrethroid pesticides and ovarian reserve [J]. Environment International, 2020, 144: 106028 Hoh E, Zhu L Y, Hites R A. Dechlorane plus, a chlorinated flame retardant, in the Great Lakes [J]. Environmental Science & Technology, 2006, 40(4): 1184-1189 Zhu J P, Feng Y L, Shoeib M. Detection of dechlorane plus in residential indoor dust in the city of Ottawa, Canada [J]. Environmental Science & Technology, 2007, 41(22): 7694-7698 Siddique S, Xian Q M, Abdelouahab N, et al. Levels of dechlorane plus and polybrominated diphenylethers in human milk in two Canadian cities [J]. Environment International, 2012, 39(1): 50-55 Ren G F, Yu Z Q, Ma S T, et al. Determination of dechlorane plus in serum from electronics dismantling workers in South China [J]. Environmental Science & Technology, 2009, 43(24): 9453-9457 Johnson P I, Stapleton H M, Mukherjee B, et al. Associations between brominated flame retardants in house dust and hormone levels in men [J]. Science of the Total Environment, 2013, 445-446: 177-184 Makey C M, McClean M D, Braverman L E, et al. Polybrominated diphenyl ether exposure and reproductive hormones in North American men [J]. Reproductive Toxicology, 2016, 62: 46-52 Gao Y, Chen L M, Wang C F, et al. Exposure to polybrominated diphenyl ethers and female reproductive function: A study in the production area of Shandong, China [J]. Science of the Total Environment, 2016, 572: 9-15 Gravel S, Lavoué J, Bakhiyi B, et al. Multi-exposures to suspected endocrine disruptors in electronic waste recycling workers: Associations with thyroid and reproductive hormones [J]. International Journal of Hygiene and Environmental Health, 2020, 225: 113445 Pan W Y, Ye X Q, Yin S S, et al. Selected persistent organic pollutants associated with the risk of primary ovarian insufficiency in women [J]. Environment International, 2019, 129: 51-58 Tang M L, Yin S S, Zhang J Y, et al. Prenatal exposure to polychlorinated biphenyl and umbilical cord hormones and birth outcomes in an island population [J]. Environmental Pollution, 2018, 237: 581-591 Miyashita C, Araki A, Mitsui T, et al. Sex-related differences in the associations between maternal dioxin-like compounds and reproductive and steroid hormones in cord blood: The Hokkaido study [J]. Environment International, 2018, 117: 175-185 Casals-Casas C, Desvergne B. Endocrine disruptors: From endocrine to metabolic disruption [J]. Annual Review of Physiology, 2011, 73: 135-162 Adoamnei E, Mendiola J, Vela-Soria F, et al. Urinary bisphenol A concentrations are associated with reproductive parameters in young men [J]. Environmental Research, 2018, 161: 122-128 Gao C Z, He H H, Qiu W H, et al. Oxidative stress, endocrine disturbance, and immune interference in humans showed relationships to serum bisphenol concentrations in a dense industrial area [J]. Environmental Science & Technology, 2021, 55(3): 1953-1963 Lassen T H, Frederiksen H, Jensen T K, et al. Urinary bisphenol A levels in young men: Association with reproductive hormones and semen quality [J]. Environmental Health Perspectives, 2014, 122(5): 478-484 Liang H, Xu W P, Chen J P, et al. The association between exposure to environmental bisphenol A and gonadotropic hormone levels among men [J]. PLoS One, 2017, 12(1): e0169217 Meeker J D, Calafat A M, Hauser R. Urinary bisphenol A concentrations in relation to serum thyroid and reproductive hormone levels in men from an infertility clinic [J]. Environmental Science & Technology, 2010, 44(4): 1458-1463 Chen Y, Wang Y C, Ding G D, et al. Association between bisphenol A exposure and idiopathic central precocious puberty (ICPP) among school-aged girls in Shanghai, China [J]. Environment International, 2018, 115: 410-416 Hyun Kim D, Min Choi S, Soo Lim D, et al. Risk assessment of endocrine disrupting phthalates and hormonal alterations in children and adolescents [J]. Journal of Toxicology and Environmental Health, Part A, 2018, 81(21): 1150-1164 Wang B, Qin X L, Xiao N, et al. Phthalate exposure and semen quality in infertile male population from Tianjin, China: Associations and potential mediation by reproductive hormones [J]. Science of the Total Environment, 2020, 744: 140673 Chen Q, Yang H, Zhou N Y, et al. Phthalate exposure, even below US EPA reference doses, was associated with semen quality and reproductive hormones: Prospective MARHCS study in general population [J]. Environment International, 2017, 104: 58-68 Muerköster A P, Frederiksen H, Juul A, et al. Maternal phthalate exposure associated with decreased testosterone/LH ratio in male offspring during mini-puberty. Odense Child Cohort [J]. Environment International, 2020, 144: 106025 Cao M F, Pan W Y, Shen X Y, et al. Urinary levels of phthalate metabolites in women associated with risk of premature ovarian failure and reproductive hormones [J]. Chemosphere, 2020, 242: 125206 Guth M, Pollock T, Fisher M, et al. Concentrations of urinary parabens and reproductive hormones in girls 6-17 years living in Canada [J]. International Journal of Hygiene and Environmental Health, 2021, 231: 113633 Jensen T K, Andersson A M, Main K M, et al. Prenatal paraben exposure and anogenital distance and reproductive hormones during mini-puberty: A study from the Odense Child Cohort [J]. Science of the Total Environment, 2021, 769: 145119 Janjua N R, Mortensen G K, Andersson A M, et al. Systemic uptake of diethyl phthalate, dibutyl phthalate, and butyl paraben following whole-body topical application and reproductive and thyroid hormone levels in humans [J]. Environmental Science & Technology, 2007, 41(15): 5564-5570 Smith K W, Souter I, Dimitriadis I, et al. Urinary paraben concentrations and ovarian aging among women from a fertility center [J]. Environmental Health Perspectives, 2013, 121(11-12): 1299-1305 Jurewicz J, Radwan M, Wielgomas B, et al. Parameters of ovarian reserve in relation to urinary concentrations of parabens [J]. Environmental Health, 2020, 19(1): 26 Liang Y S, Tang Z, Jiang Y S, et al. Serum metabolic changes associated with dioxin exposure in a Chinese male cohort [J]. Environment International, 2020, 143: 105984 Patrizi B, Siciliani de Cumis M. TCDD toxicity mediated by epigenetic mechanisms [J]. International Journal of Molecular Sciences, 2018, 19(12): 4101 Mocarelli P, Gerthoux P M, Needham L L, et al. Perinatal exposure to low doses of dioxin can permanently impair human semen quality [J]. Environmental Health Perspectives, 2011, 119(5): 713-718 Lambertino A, Persky V, Freels S, et al. Associations of PCBS, dioxins and furans with follicle-stimulating hormone and luteinizing hormone in postmenopausal women: National Health and Nutrition Examination Survey 1999-2002 [J]. Chemosphere, 2021, 262: 128309 Ye X Q, Pan W Y, Li C M, et al. Exposure to polycyclic aromatic hydrocarbons and risk for premature ovarian failure and reproductive hormones imbalance [J]. Journal of Environmental Sciences, 2020, 91: 1-9 Yin S S, Tang M L, Chen F F, et al. Environmental exposure to polycyclic aromatic hydrocarbons (PAHs): The correlation with and impact on reproductive hormones in umbilical cord serum [J]. Environmental Pollution, 2017, 220: 1429-1437 Chen Q, Wang F R, Yang H, et al. Exposure to fine particulate matter-bound polycyclic aromatic hydrocarbons, male semen quality, and reproductive hormones: The MARCHS study [J]. Environmental Pollution, 2021, 280: 116883 Interdonato M, Pizzino G, Bitto A, et al. Cadmium delays puberty onset and testis growth in adolescents [J]. Clinical Endocrinology, 2015, 83(3): 357-362 Ciarrocca M, Capozzella A, Tomei F, et al. Exposure to cadmium in male urban and rural workers and effects on FSH, LH and testosterone [J]. Chemosphere, 2013, 90(7): 2077-2084 Jackson L W, Howards P P, Wactawski-Wende J, et al. The association between cadmium, lead and mercury blood levels and reproductive hormones among healthy, premenopausal women [J]. Human Reproduction, 2011, 26(10): 2887-2895 Pollack A Z, Schisterman E F, Goldman L R, et al. Cadmium, lead, and mercury in relation to reproductive hormones and anovulation in premenopausal women [J]. Environmental Health Perspectives, 2011, 119(8): 1156-1161 Pan W Y, Ye X Q, Zhu Z Y, et al. Urinary cadmium concentrations and risk of primary ovarian insufficiency in women: A case-control study [J]. Environmental Geochemistry and Health, 2021, 43(5): 2025-2035 Lee T W, Kim D H, Ryu J Y. The effects of exposure to lead, cadmium and mercury on follicle-stimulating hormone levels in men and postmenopausal women: Data from the Second Korean National Environmental Health Survey (2012-2014) [J]. Annals of Occupational and Environmental Medicine, 2019, 31: e21 Dehghan S F, Mehrifar Y, Ardalan A. The relationship between exposure to lead-containing welding fumes and the levels of reproductive hormones [J]. Annals of Global Health, 2019, 85(1): 125 Ben Rhouma K, Tébourbi O, Krichah R, et al. Reproductive toxicity of DDT in adult male rats [J]. Human & Experimental Toxicology, 2001, 20(8): 393-397 Rasier G, Parent A S, Gérard A, et al. Early maturation of gonadotropin-releasing hormone secretion and sexual precocity after exposure of infant female rats to estradiol or dichlorodiphenyltrichloroethane [J]. Biology of Reproduction, 2007, 77(4): 734-742 Alaa-Eldin E A, El-Shafei D A, Abouhashem N S. Individual and combined effect of chlorpyrifos and cypermethrin on reproductive system of adult male albino rats [J]. Environmental Science and Pollution Research International, 2017, 24(2): 1532-1543 Ye X Q, Li F X, Zhang J Y, et al. Pyrethroid insecticide cypermethrin accelerates pubertal onset in male mice via disrupting hypothalamic-pituitary-gonadal axis [J]. Environmental Science & Technology, 2017, 51(17): 10212-10221 Zhang S Y, Ito Y, Yamanoshita O, et al. Permethrin may disrupt testosterone biosynthesis via mitochondrial membrane damage of leydig cells in adult male mouse [J]. Endocrinology, 2007, 148(8): 3941-3949 Zhou Y J, Wang X D, Xiao S, et al. Exposure to beta-cypermethrin impairs the reproductive function of female mice [J]. Regulatory Toxicology and Pharmacology, 2018, 95: 385-394 Li Y F, Pan C, Hu J X, et al. Effects of cypermethrin on male reproductive system in adult rats [J]. Biomedical and Environmental Sciences, 2013, 26(3): 201-208 Simon-Delso N, Amaral-Rogers V, Belzunces L P, et al. Systemic insecticides (neonicotinoids and fipronil): Trends, uses, mode of action and metabolites [J]. Environmental Science and Pollution Research International, 2015, 22(1): 5-34 Bass C, Field L M. Neonicotinoids [J]. Current Biology, 2018, 28(14): R772-R773 Kapoor U, Srivastava M K, Srivastava L P. Toxicological impact of technical imidacloprid on ovarian morphology, hormones and antioxidant enzymes in female rats [J]. Food and Chemical Toxicology, 2011, 49(12): 3086-3089 Abdel-Razik R K, Mosallam E M, Hamed N A, et al. Testicular deficiency associated with exposure to cypermethrin, imidacloprid, and chlorpyrifos in adult rats [J]. Environmental Toxicology and Pharmacology, 2021, 87: 103724 Arıcan E Y, Gökçeoğlu Kayalı D, Ulus Karaca B, et al. Reproductive effects of subchronic exposure to acetamiprid in male rats [J]. Scientific Reports, 2020, 10(1): 8985 Li Z Q, Li H T, Li C C, et al. Low dose of fire retardant, 2,2’,4,4’-tetrabromodiphenyl ether (BDE47), stimulates the proliferation and differentiation of progenitor Leydig cells of male rats during prepuberty [J]. Toxicology Letters, 2021, 342: 6-19 Lefèvre P L C, Berger R G, Ernest S R, et al. Exposure of female rats to an environmentally relevant mixture of brominated flame retardants targets the ovary, affecting folliculogenesis and steroidogenesis [J]. Biology of Reproduction, 2016, 94(1): 9, 1-11 Steinberg R M, Walker D M, Juenger T E, et al. Effects of perinatal polychlorinated biphenyls on adult female rat reproduction: Development, reproductive physiology, and second generational effects [J]. Biology of Reproduction, 2008, 78(6): 1091-1101 Yamamoto M, Narita A, Kagohata M, et al. Effects of maternal exposure to 3,3’,4,4’,5-pentachlorobiphenyl (PCB126) or 3,3’,4,4’,5,5’-hexachlorobiphenyl (PCB169) on testicular steroidogenesis and spermatogenesis in male offspring rats [J]. Journal of Andrology, 2005, 26(2): 205-214 Fiandanese N, Borromeo V, Berrini A, et al. Maternal exposure to a mixture of di(2-ethylhexyl) phthalate (DEHP) and polychlorinated biphenyls (PCBs) causes reproductive dysfunction in adult male mouse offspring [J]. Reproductive Toxicology, 2016, 65: 123-132 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 Yuan M, Zhao Y N, Lin R, et al. Adverse reproductive function induced by maternal BPA exposure is associated with abnormal autophagy and activating inflamation via mTOR and TLR4/NF-κB signaling pathways in female offspring rats [J]. Reproductive Toxicology, 2020, 96: 185-194 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 Nourian A, Soleimanzadeh A, Shalizar Jalali A, et al. Bisphenol-A analogue (bisphenol-S) exposure alters female reproductive tract and apoptosis/oxidative gene expression in blastocyst-derived cells [J]. Iranian Journal of Basic Medical Sciences, 2020, 23(5): 576-585 Giribabu N, Reddy P S. Protection of male reproductive toxicity in rats exposed to di-n-butyl phthalate during embryonic development by testosterone [J]. Biomedicine & Pharmacotherapy, 2017, 87: 355-365 于淼, 张林媛, 乔佩环, 等. 邻苯二甲酸二丁酯诱导氧化应激及抑制CYP17a1干扰睾酮合成[J]. 卫生研究, 2015, 44(3): 364-370 Yu M, Zhang L Y, Qiao P H, et al. Testicular oxidative stress and downregulation of CYP17a1 induced by di(n-butyl) phthalate inhibit synthesis of testosterone [J]. Journal of Hygiene Research, 2015, 44(3): 364-370 (in Chinese)
Nelli G, Pamanji S R. Di-n-butyl phthalate prompts interruption of spermatogenesis, steroidogenesis, and fertility associated with increased testicular oxidative stress in adult male rats [J]. Environmental Science and Pollution Research International, 2017, 24(22): 18563-18574 Ha M, Guan X, Wei L, et al. Di-(2-ethylhexyl) phthalate inhibits testosterone level through disturbed hypothalamic-pituitary-testis axis and ERK-mediated 5α-Reductase 2 [J]. Science of the Total Environment, 2016, 563-564: 566-575 Yue M, Ma R S, Zhang R Z, et al. Effects of dimethyl phthalate (DMP) on serum sex hormone levels and apoptosis in C57 female mice [J]. International Journal of Endocrinology and Metabolism, 2019, 17(2): e82882 Guerra M T, Sanabria M, Leite G A A, et al. Maternal exposure to butyl paraben impairs testicular structure and sperm quality on male rats [J]. Environmental Toxicology, 2017, 32(4): 1273-1289 Zhang L Y, Dong L, Ding S J, et al. Effects of n-butylparaben on steroidogenesis and spermatogenesis through changed E2 levels in male rat offspring [J]. Environmental Toxicology and Pharmacology, 2014, 37(2): 705-717 Maske P, Dighe V, Mote C, et al. n-butylparaben exposure through gestation and lactation impairs spermatogenesis and steroidogenesis causing reduced fertility in the F1 generation male rats [J]. Environmental Pollution, 2020, 256: 112957 Takeda T, Matsumoto Y, Koga T, et al. Maternal exposure to dioxin disrupts gonadotropin production in fetal rats and imprints defects in sexual behavior [J]. The Journal of Pharmacology and Experimental Therapeutics, 2009, 329(3): 1091-1099 Yu K L, Zhang X L, Tan X M, et al. Transgenerational impairment of ovarian induced by 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) associated with Igf2 and H19 in adult female rat [J]. Toxicology, 2019, 428: 152311 Li X S, Guo J T, Jiang X W, et al. Cyanidin-3-O-glucoside protects against cadmium-induced dysfunction of sex hormone secretion via the regulation of hypothalamus-pituitary-gonadal axis in male pubertal mice [J]. Food and Chemical Toxicology, 2019, 129: 13-21 da Costa C S, Oliveira T F, Freitas-Lima L C, et al. Subacute cadmium exposure disrupts the hypothalamic-pituitary-gonadal axis, leading to polycystic ovarian syndrome and premature ovarian failure features in female rats [J]. Environmental Pollution, 2021, 269: 116154 Madboli A E N A, Seif M M. Immunohistochemical, histopathological, and biochemical studies of the NF-B P65 marker in rat ovaries experimentally intoxicated by cadmium and the protective effect of the purslane plant extract [J]. Environmental Science and Pollution Research International, 2021, 28(14): 17613-17626 Wang J C, Zhu H L, Lin S, et al. Protective effect of naringenin against cadmium-induced testicular toxicity in male SD rats [J]. Journal of Inorganic Biochemistry, 2021, 214: 111310 Alotaibi M F, Al-Joufi F, Abou Seif H S, et al. Umbelliferone inhibits spermatogenic defects and testicular injury in lead-intoxicated rats by suppressing oxidative stress and inflammation, and improving Nrf2/HO-1 signaling [J]. Drug Design, Development and Therapy, 2020, 14: 4003-4019 Svechnikova I, Svechnikov K, Söder O. The influence of di-(2-ethylhexyl) phthalate on steroidogenesis by the ovarian granulosa cells of immature female rats [J]. The Journal of Endocrinology, 2007, 194(3): 603-609 Zhou J H, Yang Y, Xiong K, et al. Endocrine disrupting effects of dichlorodiphenyltrichloroethane analogues on gonadotropin hormones in pituitary gonadotrope cells [J]. Environmental Toxicology and Pharmacology, 2014, 37(3): 1194-1201 Li F X, Ma H H, Liu J. Pyrethroid insecticide cypermethrin modulates gonadotropin synthesis via calcium homeostasis and ERK1/2 signaling in LβT2 mouse pituitary cells [J]. Toxicological Sciences, 2017, 162(1): 43-52 Xin F, Susiarjo M, Bartolomei M S. Multigenerational and transgenerational effects of endocrine disrupting chemicals: A role for altered epigenetic regulation? [J]. Seminars in Cell & Developmental Biology, 2015, 43: 66-75 Latchney S E, Fields A M, Susiarjo M. Linking inter-individual variability to endocrine disruptors: Insights for epigenetic inheritance [J]. Mammalian Genome, 2018, 29(1-2): 141-152 Takeda T, Fujii M, Taura J, et al. Dioxin silences gonadotropin expression in perinatal pups by inducing histone deacetylases: A new insight into the mechanism for the imprinting of sexual immaturity by dioxin [J]. Journal of Biological Chemistry, 2012, 287(22): 18440-18450
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