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Developmental, behavioral and endocrine alterations in male rats at early and late postnatal life following in utero exposure to low dose di-n-butylphthalate

  • Reznikov, Alexander (Department of Endocrinology of Reproduction and Adaptation, VP Komisarenko Institute of Endocrinology and Metabolism, National Academy of Medical Sciences of Ukraine) ;
  • Sachynska, Olga (Department of Endocrinology of Reproduction and Adaptation, VP Komisarenko Institute of Endocrinology and Metabolism, National Academy of Medical Sciences of Ukraine) ;
  • Lymareva, Anna (Department of Endocrinology of Reproduction and Adaptation, VP Komisarenko Institute of Endocrinology and Metabolism, National Academy of Medical Sciences of Ukraine) ;
  • Faliush, Oksana (Department of Endocrinology of Reproduction and Adaptation, VP Komisarenko Institute of Endocrinology and Metabolism, National Academy of Medical Sciences of Ukraine)
  • Received : 2020.01.28
  • Accepted : 2020.05.25
  • Published : 2021.04.15

Abstract

Environmental chemical pollutants that interfere with hormonal homeostasis or hormone signaling are the relevant agents inducing congenital or postnatally developed reproductive abnormalities in human beings, wild and domestic animals. In this study, we are examining reproductive effects of prenatal exposure of male rats to a low dose di-n-butylphthalate (DBP). Wistar female rats were given intragastrically DBP at a daily dose of 100 mg/kg b.w. during 15th-21st days of pregnancy. Anogenital distance (AGD) in male offspring decreased on postnatal day (PND) 2 followed by its normalization on PND 7 and 10. There were no other visible teratogenic lesions in the newborns. The testicle descent into scrotum of control males occurred on PND 38.5±0.1, while in DBP group it accelerated by 5.3 days on the average. At the age of 6 months, DBP-exposed animals exhibited double increase of blood plasma testosterone level as compared to controls, and hyperactive male sexual behavior in the presence of receptive female. The duration of latent periods of the first mount and the first intromission, as well as post-ejaculatory refractory period, have been shortened; the number of mounts with intromission and the number of ejaculations increased significantly. Histological examination of the testes indicated activation of Leydig cells. The female-type sexual behavior as evaluated by appearance of lordosis of orchidectomized and primed with estradiol and progesterone 10-month-old males in response to mount or approach of sexually active normal male was enhanced in DBP-group. Both 10-month-old and aging males (18 months), castrated and hormone-primed, displayed homosexual type of behavior. Prenatal low dose DBP caused in 18-month-old males premature atrophy of the testes and accessory sexual glands, increased number of Leydig cell adenomas, a twice decrease of plasma testosterone level and exhausting of sexual potency. We concluded that prenatal exposition of male rats to low dose DBP determines epigenetic alterations of programming of sex brain differentiation and regulation of testicular steroidogenesis that leads to reproductive disorders and accelerated aging of reproductive system.

Keywords

Acknowledgement

This study was supported by the National Academy of Medical Sciences of Ukraine (Grant no. 523/2017-2019).

References

  1. Boivin J, Bunting L, Collins JA, Nygren KG (2007) International estimates of infertility prevalence and treatment-seeking: potential need and demand for infertility medical care. Hum Reprod 22:1506-1512 https://doi.org/10.1093/humrep/dem046
  2. Perera F, Herbstman J (2011) Prenatal environmental exposures, epigenetics, and disease. Reprod Toxicol 31:363-373 https://doi.org/10.1016/j.reprotox.2010.12.055
  3. Andersson AM, Frederiksen H, Grigor KM, Toppari J, Skakkebaek NE (2014) Special issue on the impact of endocrine disrupters on reproductive health. Reproduction 147:E1 https://doi.org/10.1530/REP-14-0060
  4. Reznikov AG (2014) Reproductive targets of endocrine disruptors. Reprod Endocrinol 17:18-25 (Russian)
  5. Vaiserman A (2014) Early-life exposure to endocrine disrupting chemicals and later-life health outcomes: an epigenetic bridge. Aging Dis 5:419-429
  6. Rattan S, Zhou C, Chiang C, Mahalingam S, Brehm E, Flaws JA (2017) Exposure to endocrine disruptors during adulthood: consequences for female fertility. J Endocrinol 233:R109-R129 https://doi.org/10.1530/JOE-17-0023
  7. Axelstad M, Hass U, Scholze M, Christiansen S, Kortenkamp A, Boberg J (2018) EDC IMPACT: reduced sperm counts in rats exposed to human relevant mixtures of endocrine disrupters. Endocr Connect 7:139-148 https://doi.org/10.1530/EC-17-0307
  8. Darbre PD (2018) Overview of air pollution and endocrine disorders. Int J Gen Med 11:191-207 https://doi.org/10.2147/IJGM.S102230
  9. Hernandez-Diaz S, Mitchell AA, Kelley KE, Calafat AM, Hauser R (2009) Medications as a potential source of exposure to phthalates in the U.S. population. Environ Health Perspect 117:185-189 https://doi.org/10.1289/ehp.11766
  10. Barlow NJ, McIntyre BS, Foster PM (2004) Male reproductive tract lesions at 6, 12, and 18 months of age following in utero exposure to di(n-butyl) phthalate. Toxicol Pathol 32:79-90 https://doi.org/10.1080/01926230490265894
  11. Zhang Y, Jiang X, Chen B (2004) Reproductive and developmental toxicity in F1 Sprague-Dawley male rats exposed to di-n-butyl phthalate in utero and during lactation and determination of its NOAEL. Reprod Toxicol 18:669-676 https://doi.org/10.1016/j.reprotox.2004.04.009
  12. Foster PM, Cattley RC, Mylchreest E (2000) Effects of di-n-butyl phthalate (DBP) on male reproductive development in the rat: implications for human risk assessment. Food Chem Toxicol 38:S97-S99 https://doi.org/10.1016/S0278-6915(99)00128-3
  13. Ge RS, Chen GR, Tanrikut C, Hardy MP (2007) Phthalate ester toxicity in Leydig cells: developmental timing and dosage considerations. Reprod Toxicol 23:366-373 https://doi.org/10.1016/j.reprotox.2006.12.006
  14. Wittassek M, Koch HM, Angerer J, Bruning T (2011) Assessing exposure to phthalates-the human biomonitoring approach. Mol Nutr Food Res 55:7-31 https://doi.org/10.1002/mnfr.201000121
  15. Martinez-Arguelles DB, Campioli E, Culty M, Zirkin BR, Papadopoulos V (2013) Fetal origin of endocrine dysfunction in the adult: the phthalate model. J Steroid Biochem Mol Biol 137:5-17 https://doi.org/10.1016/j.jsbmb.2013.01.007
  16. Pinto A, Carvalho D (2013) Human infertility: are endocrine disruptors to blame? Endocr Connect 2:R15-R29 https://doi.org/10.1530/EC-13-0036
  17. Hannon PR, Flaws JA (2015) The effects of phthalates on the ovary. Front Endocrinol 6:8 https://doi.org/10.3389/fendo.2015.00008
  18. Moore RW, Rudy TA, Lin TM, Ko K, Peterson RE (2001) Abnormalities of sexual development in male rats with in utero and lactational exposure to the antiandrogenic plasticizer Di(2-ethylhexyl) phthalate. Environ Health Perspect 109:229-237 https://doi.org/10.1289/ehp.01109229
  19. Reznikov AG, Sachynska OV, Limareva AA, Falyush OA, Perchik IG (2017) Hypersexual behavior and hyperandrogenism in F1 male rats caused by dibutylphtalate treatment of pregnant. Fiziol Zh 63:13-20 (Ukrainian) https://doi.org/10.15407/fz63.05.013
  20. Reznikov AG (1994) Hormone-neurotransmitter imprinting in the neuroendocrine control of reproduction. Harwood Acad Publ, Harwood
  21. Holson RR, Gough B, Sullivan P, Badger T, Sheehan DM (1995) Prenatal dexamethasone or stress but not ACTH or corticosterone alter sexual behavior in male rats. Neurotoxicol Teratol 17:393-401 https://doi.org/10.1016/0892-0362(94)00074-N
  22. Hull EM, Dominguez JM (2007) Sexual behavior in male rodents. Horm Behav 52:45-55 https://doi.org/10.1016/j.yhbeh.2007.03.030
  23. Kropotov AV, Lisakovskaia OV, Khotimchenko IS (2001) Seasonal features of the effect of adaptogens on sex behavior of experimental animals. Eksp Klin Farmakol 64:60-62 (Russian)
  24. Foster PM (2006) Disruption of reproductive development in male rat offspring following in utero exposure to phthalate esters. Int J Androl 29:140-147 https://doi.org/10.1111/j.1365-2605.2005.00563.x
  25. Ivell R, Heng K, Nicholson H, Anand-Ivell R (2013) Brief maternal exposure of rats to the xenobiotics dibutyl phthalate or diethylstilbestrol alters adult-type Leydig cell development in male offspring. Asian J Androl 15:261-268 https://doi.org/10.1038/aja.2012.138
  26. Scarano WR, Toledo FC, Guerra MT, Pinheiro PF, Domeniconi RF, Felisbino SL, Campos SG, Taboga SR, Kempinas WG (2010) Functional and morphological reproductive aspects in male rats exposed to di-n-butyl phthalate (DBP) in utero and during lactation. J Toxicol Environ Health A 73:972-984 https://doi.org/10.1080/15287391003751760
  27. Motohashi M, Wempe MF, Mutou T, Okayama Y, Kansaku N, Takahashi H, Ikegami M, Asari M, Wakui S (2016) In utero-exposed di(n-butyl) phthalate induce dose dependent, age-related changes of morphology and testosterone-biosynthesis enzymes/associated proteins of Leydig cell mitochondria in rats. J Toxicol Sci 41:195-206 https://doi.org/10.2131/jts.41.195
  28. Drake AJ, van den Driesche S, Scott HM, Hutchison GR, Seckl JR, Sharpe RM (2009) Glucocorticoids amplify dibutyl phthalate-induced disruption of testosterone production and male reproductive development. Endocrinol 150:5055-5064 https://doi.org/10.1210/en.2009-0700
  29. Gladkova AI (1999) The regulation of male sexual behavior by the sex hormones. Usp Fiziol Nauk 30:97-105 (Russian)
  30. Chen X, Zhou QH, Leng L, Chen X, Sun ZR, Tang NJ (2013) Effects of di(n-butyl) and monobutyl phthalate on steroidogenesis pathways in the murine Leydig tumor cell line MLTC-1. Environ Toxicol Pharmacol 6:332-338
  31. Wang Y, Song L, Hong X, Cui L, Zhang Z, Xiao H, Zhou J, Wang X (2006) Low concentrations mono-butyl phthalate stimulates steroidogenesis by facilitating steroidogenic acute regulatory protein expression in mouse Leydig tumor cells (MLTC-1). Chem Biol Interact 164:15-24 https://doi.org/10.1016/j.cbi.2006.08.022
  32. Shultz VD, Phillips S, Sar M, Foster PM, Gaido KW (2001) Altered gene profiles in fetal rat testes after in utero exposure to di(n-butyl) phthalate. Toxicol Sci 64:233-242 https://doi.org/10.1093/toxsci/64.2.233
  33. Lehmann KP, Phillips S, Sar M, Foster PM, Gaido KW (2004) Dose-dependent alterations in gene expression and testosterone synthesis in the fetal testes of male rats exposed to di (n-butyl) phthalate. Toxicol Sci 8:60-68
  34. Struve MF, Gaido KW, Hensley JB, Lehmann KP, Ross SM, Sochaski MA, Willson GA, Dorman DC (2009) Reproductive toxicity and pharmacokinetics of di-n-butyl phthalate (DBP) following dietary exposure of pregnant rats. Birth Defects Res B Dev Reprod Toxicol 86:345-354 https://doi.org/10.1002/bdrb.20199
  35. Johnson KJ, McDowell EN, Viereck MP, Xia JQ (2011) Species-specific dibutyl phthalate fetal testis endocrine disruption correlates with inhibition of SREBP2-dependent gene expression pathways. Toxicol Sci 120:460-474 https://doi.org/10.1093/toxsci/kfr020
  36. Clewell RA, Kremer JJ, Williams CC, Campbell JL, Sochaski MA, Andersen ME, Borghoff SJ (2009) Kinetics of selected di-n-butyl phthalate metabolites and fetal testosterone following repeated and single administration in pregnant rats. Toxicology 8:80-90
  37. Lee BM, Koo HJ (2007) Hershberger assay for antiandrogenic effects of phthalates. J Toxicol Environ Health A 70:1365-1370 https://doi.org/10.1080/15287390701432285
  38. Ema M, Miyawaki E (2001) Adverse effects on development of the reproductive system in male offspring of rats given monobutyl phthalate, a metabolite of dibutyl phthalate, during late pregnancy. Reprod Toxicol 15:189-194 https://doi.org/10.1016/S0890-6238(01)00111-3
  39. Wang Y, Chen F, Ye L, Zirkin B, Chen H (2017) Steroidogenesis in Leydig cells: effects of aging and environmental factors. Reproduction 154:R111-R122 https://doi.org/10.1530/REP-17-0064
  40. Aly HA, Hassan MH, El-Beshbishy HA, Alahdal AM, Osman AM (2016) Dibutyl phthalate induces oxidative stress and impairs spermatogenesis in adult rats. Toxicol Ind Health 32:1467-1477 https://doi.org/10.1177/0748233714566877
  41. Sidorkiewicz I, Zareba K, Wolczynski S, Czerniecki J (2017) Endocrine-disrupting chemicals-mechanisms of action on male reproductive system. Toxicol Ind Health 33:601-609 https://doi.org/10.1177/0748233717695160