Molecular mechanism underlying the temporal shift in androgen action in post-natal rat epididymis due to gestational-onset hypothyroidism

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Authors

  • Bungtown Road, Cold Spring Harbor Laboratories, Cold Spring Harbor, New York, 11724, USA ,IN
  • Department of Biomedical and Diagnostic Sciences, UT College of Veterinary Medicine,University of Tennessee, Knoxville, TN 37996-4550,USA ,US
  • Texas Tech University Health Sciences Centre, 5001 El Paso Dr, Texas, USA ,US
  • Department of Endocrinology, Dr.ALM Post Graduate Institute of Basic Medical Sciences,University of Madras- Taramani Campus, Chennai-600 113, India ,IN

Keywords:

Androgen Receptor, Dihydrotestosterone, 5α-Reductase, Testosterone, Thyroid Hormone

Abstract

Thyroid hormones are important regulators of male fertility and mammalian testis with has specific T3 receptors has emerged as its target. Men with history of congenital or juvenile onset hypothyroidism suffer infertility. The epididymis plays a pivotal role in post-testicular maturation of sperm. Recently we reported that transient gestational–onset hypothyroidism leads to infertility in the progeny of rats by affecting sperm maturation due to decreased androgen receptor (Ar) status in the epididymis. In the present study we tested the hypothesis "transient gestational exposure to antithyroid drugs during critical periods of differentiation of male reproductive tract organs may interfere with the functions of epididymis in F1 progeny by modifying the expression of Ar gene, and activity of its protein and the key steroidogenic enzyme, 5α-reductase”. To test the hypothesis, pregnant rats were exposed to the antithyroid drug methimazole (0.05% through drinking water) from embryonic day (ED)9 to 14/18/21covering specific periods of testicular and other male reproductive tract organs differentiation to induce hypothyroidism. Male pups with transient gestational hypothyroidism showed subnormal levels of serum testosterone, and estradiol, along with decreased expression of Ar, and 5α-reductase activity in the epididymis of pre-puberal rats at postnatal day (PND)29, whereas there was normal/boosted Ar expression, and 5α-reductase activity peripubertal rat epididymis at PND 49. Taken together, the present study and our previous report point out that gestational-onset hypothyroidism affect fertility of F1 progeny through an age-dependent divergent effect on 5α-reductase activity and AR gene expression in the epididymis.

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Published

2017-05-30

How to Cite

Jaganathan, A., Mary Sashi, A., Kannan, A., & Michael Aruldhas, M. (2017). Molecular mechanism underlying the temporal shift in androgen action in post-natal rat epididymis due to gestational-onset hypothyroidism. Journal of Endocrinology and Reproduction, 20(1), 66–75. Retrieved from https://informaticsjournals.co.in/index.php/jer/article/view/15745

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References

Anbalagan J. Transient gestational-onset hypothyroidism modifies the expression of androgen and estrogen receptors in the epididymis of post-natal rats [Ph.D. thesis]. University of Madras, Chennai, India; 2008.

Anbalagan J, Sashi AM, Vengatesh G, Stanley JA, Neelamohan R, Aruldhas MM. Mechanism underlying transient gestational-onset hypothyroidism-induced impairment of post-testicular sperm maturation in adult rats. Fertil Steril.2010; 8:2491–7. PMid:20303481. Retrieved from: https:// doi.org/10.1016/j.fertnstert.2010.02.005

Antony FF, Aruldhas MM, Udhayakumar RCR, Maran RRM, Govindarajulu P. Inhibition of Leydig cell activity in vivo and in vitro in hypothyroid rats. J Endocrinol. 1995; 144:293–300. PMid:7706982. Retrieved from: https://doi.org/10.1677/joe.0.1440293

Aruldhas MM, Valivullah HM, Govindarajulu P. Specific effect of thyroid hormone on testicular enzymes involved in carbohydrate metabolism II. Hyperthyroidism. Biochim Biophys Acta. 1982a; 715:121–5. Retrieved from: https:// doi.org/10.1016/0304-4165(82)90057-5

Aruldhas MM, Valivullah HM, Govindarajulu P. Specific effect of the thyroid on testicular enzymes involved in carbohydrate metabolism. Int J Androl. 1982b; 5:196–204.PMid:6213568. Retrieved from: https://doi.org/10.1111/j.1365-2605.1982.tb00248.x

Aruldhas MM, Valivullah HM, Govindarajulu P. Effect of thyroidectomy on testicular enzymes of the pyruvate/malate cycle involved in lipogenesis. Biochim Biophys Acta. 1983; 755:90–4. Retrieved from: https://doi.org/10.1016/03044165(83)90277-5

Aruldhas MM, Valivullah HM. Govindarajulu P. Effect of thyroxine-induced hyperthyroidism on some testicular enzymes of the pyruvate/malate cycle. Biochim BiophysActa.1984; 797:143–6. Retrieved from: https://doi.org/10.1016/0304-4165(84)90115-6

Aruldhas MM, Valivullah HM, Srinivasan N, Govindarajulu P. Role of thyroid on testicular lipids in prepubertal, pubertal and adult rats. I. Hyperthyroidism. Biochim Biophys Acta. 1986; 881:462–9. Retrieved from: https://doi.org/10.1016/0304-4165(86)90040-1

Bishop DW. Sex and Internal Secretion Young, W. C.2nd edition, London: Bailliere, Tindall and Cox Ltd; 1961. p.709.

Blandau RJ, Rumery RE. The relationship of swimming movements of epididymal spermatozoa to their fertilizing capacity. Fertil Steril. 1964; 15:571–57. Retrieved from: https://doi.org/10.1016/S0015-0282(16)35401-2

Blanchard Y, Robaire B. Le mode d' action androgens et ala 5alpha reductase. Med Sci. 1997; 13:467–73.

Blaquier JA, Burgos MH, Cameo MS. Role of androgens in maturation of epididymal spermatozoa in guinea-pig.Endocrinology. 1972; 90:839–42.PMid:5009352.Retrieved from: https://doi.org/10.1210/endo-90-3-839

Castro-Magana M, Angulo M, Canas A, Sharp A, Fuentes B. Hypothalamic-pituitary gonadal axis in boys with primary hypothyroidism and macroorchidism. J Pediatr. 1988; 112:397–402. Retrieved from: https://doi.org/10.1016/ S0022-3476(88)80319-6

Cooke PS, Kirby JD, Porcelli J. Increased testis growth and sperm production in adult rats following transient neonatal goitrogen treatment: optimization of the propyl-thiouracil dose and effects of methimazole. J Reprod Fertil. 1993; 97:493–9. PMid:8501721. Retrieved from: https://doi.org/10.1530/jrf.0.0970493

Cooper TG. In defense of a function for the human epididymis.Fertil Steril. 1990; 54:965–75. Retrieved from: https:// doi.org/10.1016/S0015-0282(16)53988-0

Dahia CL, Rao AJ. Demonstration of follicle-stimulating hormone receptor in cauda epididymis of rat. Biol Reprod.2006; 75:98–106. PMid:16598027. Retrieved from: https:// doi.org/10.1095/biolreprod.105.047704

Fisher D. The thyroid. In: Kaplan S, editor. Clinical pediatric endocrinology 2nd ed. USA. Philadelphia; 1990. p.87–126.

French FS, Ritzen EM. A high affinity androgen binding protein in rat testis: Evidence for secretion into efferent duct fluid and absorption by epididymis.Endocrinology.1973; 93:88–95. PMid:4712258. Retrieved from: https://doi.org/10.1210/endo-93-1-88

Griboff SI. Semen analysis in myxedema. Fertil and Steril.1962; 13:436–43. Retrieved from:https://doi.org/10.1016/ S0015-0282(16)34627-1

Hanna CE, LaFranchi SH. Adolescent thyroid disorders.Adolescent Medicine. 2002; 13:13–36.PMid:11841953.

Henderson NA, Robaire B. Effects of PNU157706, a dual 5alpha-reductase inhibitor, on rat epididymal sperm maturation and fertility. Biol Reprod. 2005; 72:36–43.PMid:15483222. Retrieved from: https://doi.org/10.1095/ biolreprod.104.033548

Holsberger DR, Cooke PS. Understanding the role of thyroid hormone in Sertoli cell development: a mechanistic hypothesis. Cell Tissue Res. 2005; 322:133–140.PMid:15856309. Retrieved from: https://doi.org/10.1007/ s00441-005-1082-z

Holsberger DR, Kiesewetter SE, Cooke PS. Regulation of neonatal Sertoli cell development by thyroid hormone receptor alpha1. Biol Reprod. 2005; 73:396–403.PMid:15858214. Retrieved from: https://doi.org/10.1095/ biolreprod.105.041426

Jannini EA, Ulisse S, D'Armiento M. Thyroid Hormone and Male Gonadal Function. Endocr Rev. 1995; 16:443–59.Retrieved from: https://doi.org/10.1210/er.16.4.443

Kala N, Ravisankar B, Govindarajulu P, Aruldhas MM.Impact of foetal-onset hypothyroidism on the epidid ymis of mature rats. Int J Androl. 2002; 25:139–48.PMid:12031041. Retrieved from: https://doi.org/10.1046/ j.1365-2605.2002.00338.x

Kumar BJ, Khurana ML, Ammini AC, Karmarkar MG, Ahuja MMS. Reproductive endocrine functions in men with primary hypothyroidism: effect of thyroxine replacement.Horm Res. 1990; 34:215–8. Retrieved from: https:// doi.org/10.1159/000181828

Longcope C. The male and female reproductive systems in hypothyroidism In: Lewis E, Braverman M, Robert D, Utiger, Ingbar SH, Werner MD, editors. Werner and Ingbar's the Thyroid, a Fundamental and Clinical Text.8th ed. Philadelphia: Lippincott Williams and Wilkins; 2000. p. 824–7.

Maran RR, Aruldhas MM. Adverse effects of neonatal hypothyroidism on Wistar rat spermatogenesis. Endocr Res.2002; 3:141–54. Retrieved from: https://doi.org/10.1081/ ERC-120015051

Maran RR, Ravisankar B and Ravichandran K and Aruldhas MM. Impact of neonatal onset hypothyroidism on Sertoli cell number, plasma and testicular interstitial fluid androgen binding protein concentration. Endocr Res.1999a; 25:307–22. PMid:10596725. Retrieved from: https://doi.org/10.1080/07435809909066150

Maran RRM, Sivakumar R, Arunakaran J, Ravisankar B, Ravichandran K, Siddharthan V, Jeyaraj DA, Aruldhas MM.Duration-dependent effect of transient neonatal hypothyroidism on Sertoli and germ cell number, and plasma and testicular interstitial fluid androgen binding protein concentration.Endo Res. 1999b; 25:323–40.PMid:10596726. Retrieved from: https://doi.org/10.1080/07435809909066151

Orgebin-Crist MC, Tichenor PL. Effect of testosterone on sperm maturation in vitro. Nature. 1973;245:328–9.PMid:4586442. Retrieved from: https://doi.org/10.1038/245328a0

Palmero S, Maggiani S, Fugassa E. Nuclear triiodothyronine receptors in rat Sertoli cells. Mol Cell Endocrinol. 1988; 58:253–6. Retrieved from: https://doi.org/10.1016/03037207(88)90161-X

Paris F, Weinbauer GF, Blüm V, Nieschlag E. The effect of androgens and antiandrogens on the immunohistochemical localization of the androgen receptor in accessory reproductive organs of male rats. J Steroid Biochem Mol Biol. 1994; 48:129–37. Retrieved from: https://doi.org/10.1016/0960-0760(94)90259-3

Pratis K, O'Donnell L, Ooi GT, Stanton PG, McLachlan RI, Robertson DM. Differential regulation of rat testicular 5alpha-reductase type 1 and 2 isoforms by testosterone and FSH. J Endocrinol. 2003; 176:393–403.PMid:12630924.Retrieved from: https://doi.org/10.1677/joe.0.1760393

Robaire B, Scheer H, Hachey C. Regulation of epididymal steroid metabolizing enzymes. In: Jagiello G and Vogel HJ, editors. Bioregulators of Reproduction. New York: Academic Press; 1981. p. 487–98. Retrieved from: https://doi.org/10.1016/b978-0-12-379980-7.50033-3

Robaire B, Hinton BT, Orgebin-Crist MC. The epididymis.In: Neil JD editor. KnobilAND Neil's Physiology of Reproduction.3rd ed. NewYork: Elsevier; 2006. p. 1071–148.Retrieved from: https://doi.org/10.1016/b978-0125154000/50027-0

Robaire B, Hermo L. Efferent ducts, epididymis, and vas deferens: structure, functions, and their regulation. In: Knobil and Neil J, editors. Knobil and Neil's Physiology of Reproduction, New York, USA: Raven Press. 1988. p. 999– 1080.

Robaire B, Henderson NA. Actions of 5alpha-reductase inhibitors on the epididymis. Mol Cell Endocrinol. 2006; 16:190–5. PMid:16476520. Retrieved from: https://doi.org/10.1016/j.mce.2005.12.044

Robaire B, Viger RS. Regulation of epididymal epithelial cell functions. Biol Reprod. 1995; 52:226–36.PMid:7711192.Retrieved from: https://doi.org/10.1095/biolreprod52.2.226

Sashi AMJ. Impact of gestational hypothyroidism on testicular development and differentiation in Wistar rats – An endocrine and histomorphometric study [Phd thesis].Chennai, India: University of Madras; 2007.

Sashi AMJ, Vengatesh G, Sekhar V, Anbalagan J, Kala N, Govindarajalu P, Akbarsha MA, Aruldhas MM. Transient hypothyroidism during the second week of gestation has a temporal and specific effect on the histo architecture of the epididymis at prepuberal, puberal and adult rats. Haldar C, editor. Proceedings of the XXI National Symposium of the Society for Reproductive Biology and Comparative Endocrinology.Varanasi, India: Banaras Hindu University.2002.p. 29.

Scheer H, Robaire B. Subcellular distribution of steroid Δ4 –5α-reductase and 3α-hydroxysteroid dehydrogenase in the rat epididymis during sexual maturation. Biol Reprod.1983; 29:1–10. PMid:6577916. Retrieved from: https://doi.org/10.1095/biolreprod29.1.1

Shan LX, Hardy MP. Developmental changes in levels of luteinizing hormone receptor and androgen receptor in rat Leydig cells. Endocrinology. 1992; 131:1107–14.PMid:1505454. Retrieved from: https://doi.org/10.1210/ endo.131.3.1505454

Tillmann C, Capel B. Mesonephric cell migration induces testis cord formation and Sertoli cell differentiation in the mammalian gonad. Development. 1999; 126:2883–90.

Toshimori K. Biology of spermatozoa maturation: an overview with an introduction to this issue. Micro Res Tech.2003; 61:1–6.

Turner TT. On the epididymis and its role in the development of the fertile ejaculate. J Androl. 1995; 16:292–8.PMid:8537245.

Venkatesh NS. Temporal shift in adult rat testicular steroidogenesis towards estradiol due to transient neonatal hypothyroidism [Phd thesis]. Chennai, India: University of Madras; 2004.

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