Excessive testosterone treatment and castration induce reactive astrocytes and fos immunoreactivity in suprachiasmatic nucleus of mice

Brain Research

Volumn 1020, Issue 1-2, 2004, Pages 130-139

  Satriotomo, Irawan ^a   Miki, Takanori ^a   Gonzalez, Daniel ^a   Matsumoto, Yoshiki ^a   Li, Hong Peng ^a   Gu, He ^a   Takeuchi, Yoshiki ^a  

^a KAGAWA UNIVERSITY   (Japan)

Author keywords

Biological rhythms and sleep; Calbindin D28k; Castration; Fos; Glial fibrillary acidic protein; Neural basis of behavior; Suprachiasmatic nucleus; Testosterone

Indexed keywords

PROTEIN FOS; TESTOSTERONE;

ANIMAL EXPERIMENT; ARTICLE; ASTROCYTE; CASTRATION; CIRCADIAN RHYTHM; CONTROLLED STUDY; GENE; HORMONAL REGULATION; HYPOTHALAMUS; IMMUNOHISTOCHEMISTRY; IMMUNOREACTIVITY; MALE; MOUSE; NEUROSECRETORY CELL; NONHUMAN; PRIORITY JOURNAL; STIMULUS RESPONSE; SUPRACHIASMATIC NUCLEUS;

ANIMALS; ASTROCYTES; BRAIN MAPPING; CALCIUM-BINDING PROTEIN, VITAMIN D-DEPENDENT; CASTRATION; CIRCADIAN RHYTHM; GLIAL FIBRILLARY ACIDIC PROTEIN; IMMUNOHISTOCHEMISTRY; MALE; MICE; MICE, INBRED ICR; NEURONS; NEUROSECRETORY SYSTEMS; ONCOGENE PROTEINS V-FOS; SUPRACHIASMATIC NUCLEUS; TESTOSTERONE;

EID: 4143049088     PISSN: 00068993     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.brainres.2004.06.020     Document Type: Article

References (50)

1. Altman J., Bayer S.A. The development of the rat hypothalamus. Adv. Anat. Embryol. Cell Biol. 100:1986;1-178
2. Aronin N., Sagar S.M., Sharp F.R., Schwartz W.J. Light regulates expression of a Fos-related protein in rat suprachiasmatic nuclei. Proc. Natl. Acad. Sci. U. S. A. 87:1990;5959-5962
3. Arvanitogiannis A., Robinson B., Bealue C., Amir S. Calbindin-D28k immunoreactivity in the suprachiasmatic nucleus and the circadian response to constant light in the rat. Neuroscience. 99:2000;397-401
4. Buijs R.M., Kalsbeek A., van der Woude T.P., van Heerikhuize J.J., Shinn S. Suprachiasmatic nucleus lesion increases corticosterone secretion. Am. J. Physiol. 264:1993;1186-1192
5. Butler J.A., Sjöberg M., Coen C.W. Evidence for estrogen receptor α-immunoreactivity in gonadotropin-releasing hormone-expressing neurones. J. Neuroendocrinol. 11:1999;331-335
6. Celotti F., Melcangi R.C., Negri-Cesi P., Poletti A. Testosterone metabolism in brain cells and membranes. J. Steroid Biochem. Mol. Biol. 40:1991;673-678
7. Challet E., Pévet P., Malan A. Lesion of the serotonergic terminals in the suprachiasmatic nuclei limits the phase advance of body temperature rhythm in food-restricted rats fed during daytime. J. Biol. Rhythms. 12:1997;235-244
8. Chowen J.A., Argente J., Busiguina S., Garcia-Segura L.M. The role of glia in the neuroendocrine hypothalamus: possible implications in hormone secretion. Horm. Res. 45:1996;15-18
9. Day J.R., Laping N.J., Lampert-Etchells M., Brown S.A., O'Callaghan J.P., McNeill T.H., Finch C.E. Gonadal steroids regulate the expression of glial fibrillary acidic protein in the adult male rat hippocampus. Neuroscience. 55:1993;435-443
10. Dluzen D.E., Ramirez V.D. In vivo activity of the LHRH pulse generator as determined with push-pull perfusion of the anterior pituitary gland of unrestrained intact and castrate male rats. Neuroendocrinology. 45:1987;328-332
11. Earnest D.J., Iadarola M., Yeh H.H., Olschowka J.A. Photic regulation of c-fos expression in neural components governing the entrainment of circadian rhythms. Exp. Neurol. 109:1990;353-361
12. Edelstein K., Amir S. The role of the intergeniculate leaflet in entrainment of circadian rhythms to a skeleton photoperiod. J. Neurosci. 19:1999;372-380
13. Fernandez-Galaz M.C., Munoz R.M., Villanua M.A., Garcia-Segura L.M. Diurnal oscillation in glial fibrillary acidic protein in a perisuprachiasmatic area and its relationship to the luteinizing hormone surge in the female rat. Neuroendocrinology. 70:1999;368-376
14. Franklin K.B.J., Paxinos G. The Mouse Brain in Stereotaxic Coordinates. 1997;Academic Press, San Diego, CA, USA
15. Garcia A., Schiff M., Marshall J.C. Regulation of pituitary gonadotropin-releasing hormone receptors by pulsatile gonadotropin-releasing hormone injections in male rats. Modulation by testosterone. J. Clin. Invest. 74:1984;920-928
16. Garcia-Segura L.M., Chowen J.A., Naftolin F. Endocrine glia: roles of glia cells in the brain actions of steroids and thyroid hormones and in hormone secretion. Front. Neuroendocrinol. 17:1996;180-211
17. Itoh M., Miyamoto K., Satriotomo I., Takeuchi Y. Spermatic granulomata are experimentally induced in epididymis of mice receiving high-dose testosterone implants: I. Light-microscopical study. J. Androl. 20:1999;551-558
18. Johnson R.F., Morin L.P., Moore R.Y. Retinohypothalamic projections in the hamster and rat demonstrated using cholera toxin. Brain Res. 462:1988;301-312
19. Johnson R.F., Moore R.Y., Morin L.P. Lateral geniculate lesions alter circadian activity rhythms in the hamster. Brain Res. Bull. 22:1989;411-422
20. Jung-Testas I., Baulieu E.E. Steroid hormone receptors and steroid action in rat glial cells of the central and peripheral nervous system. J. Steroid Biochem. Mol. Biol. 65:1998;243-251
21. Kornhauser J.M., Nelson D.E., Mayo K.E., Takahashi J.S. Photic and circadian regulation of c-fos gene expression in the hamster suprachiasmatic nucleus. Neuron. 5:1990;127-134
22. Langub M.C., Watson R.E. Estrogen receptor-immunoreactive glia, endothelia, and ependyma in guinea pig preoptic area and median eminence: electron microscopy. Endocrinology. 130:1992;364-372
23. Leak R.K., Card J.P., Moore R.Y. Suprachiasmatic pacemaker organization analyzed by viral transynaptic transport. Brain Res. 819:1999;23-32
24. Levine J.E., Duffy M.T. Simultaneous measurement of luteinizing hormone (LH)-releasing hormone, LH, and follicle-stimulating hormone release in intact and short-term castrate rats. Endocrinology. 122:1988;2211-2221
25. Mattson M.P., Rychlik B., Chu C., Christakos S. Evidence for calcium-reducing and excito-protective roles for the calcium binding protein calbindin D28k in cultured hippocampal neurons. Neuron. 6:1991;41-51
26. Moga M.M., Moore R.Y. Organization of neural inputs to the suprachiasmatic nucleus in the rat. J. Comp. Neurol. 389:1997;508-534
27. Mong J.A., Glaser E., McCarthy M.M. Gonadal steroids promote glial differentiation and alter neuronal morphology in the developing hypothalamus in a regionally specific manner. J. Neurosci. 19:1999;1464-1472
28. Moore R.Y., Eichler V.B. Loss of a circadian adrenal corticosterone rhythm following suprachiasmatic lesions in the rat. Brain Res. 42:1972;201-206
29. Morin L.P. The circadian visual system. Brains Res. Rev. 19:1994;102-127
30. Mouret J., Coindet J., Debilly G., Chouvet G. Suprachiasmatic nuclei lesions in the rat: alterations in sleep circadian rhythms. Electroencephalogr. Clin. Neurophysiol. 45:1978;402-408
31. Pieper D.R., Gala R.R., Schiff M.A., Regiani S.R., Marshall J.C. Pituitary gonadotropin-releasing hormone (GnRH) receptor responses to GnRH in hypothalamus-lesioned rats: inhibition of responses by hyperprolactinemia and evidence that testosterone and estradiol modulate gonadotropin secretion at postreceptor sites. Endocrinology. 115:1984;1190-1196
32. Prosser R.A., Edgar D.M., Heller H.C., Miller J.D. A Possible glial role in the mammalian circadian clock. Brain Res. 643:1994;296-301
33. Rea M.A. Light increases Fos-related protein immunoreactivity in the rat suprachiasmatic nuclei. Brain Res. Bull. 23:1989;577-581
34. Roselli C.E., Kelly M.J., Ronnekleiv O.K. Testosterone regulates progonadotropin-releasing hormone levels in the preoptic area and basal hypothalamus of the male rat. Endocrinology. 126:1990;1080-1086
35. Rusak A., Robertson H.A., Wisden W., Hunt S.P. Light pulses that shift rhythms induce gene expression in the suprachiasmatic nucleus. Science. 248:1990;1237-1240
36. Sar M., Lubahn D.B., French F.S., Wilson E.M. Immunohistochemical localization of the androgen receptor in rat and human tissues. Endocrinology. 127:1990;3180-3186
37. Satriotomo I., Miki T., Itoh M., Xie Q., Ameno K., Takeuchi Y. Effect of short-term ethanol exposure on the suprachiasmatic nucleus of hypothalamus: immunohistochemical study in mice. Brain Res. 847:1999;124-129
38. Shibata S., Oomura Y., Liou S.Y., Ueki S. Electrophysiological studies of the development of suprachiasmatic neuronal activity in hypothalamic slice preparations. Brain Res. 315:1984;29-35
39. Shughrue P.J., Bushnell C.D., Dorsa D.M. Estrogen receptor messenger ribonucleic acid in female rat brain during the estrous cycle: a comparison with ovariectomized females and intact males. Endocrinology. 131:1992;381-388
40. Shughrue P.J., Komm B., Merchenthaler I. The distribution of estrogen receptor-β mRNA in the rat hypothalamus. Steroids. 61:1996;678-681
41. Silver R., Romero M.T., Besmer H.R., Leak R., Nunez J.M., LeSauter J. Calbindin-D28K cells in the hamster SCN express light-induced Fos. NeuroReport. 7:1996;1224-1228
42. Spratt D.P., Herbison A.E. Regulation of preoptic area gonadotropin-releasing hormone (GnRH) mRNA expression by gonadal steroids in the long-term gonadectomized male rat. Mol. Brain Res. 47:1997;125-133
43. van den Pol A.N. The hypothalamic suprachiasmatic nucleus of rat: intrinsic anatomy. J. Comp. Neurol. 191:1980;661-702
44. van den Pol A.N., Finkbeiner S.M., Cornell-Bell A.H. Calcium excitability and oscillations in suprachiasmatic nucleus neurons and glial in vitro. J. Neurosci. 12:1992;2648-2664
45. van der Beek E.M., Horvath T.L, Wiegant V.M., van den Hurk R., Buijs R.M. Evidence for a direct neuronal pathway from the suprachiasmatic nucleus to the gonadotropin-releasing hormone system: combined tracing and light and electron microscopic immunocytochemical studies. J. Comp. Neurol. 384:1997;569-579
46. van der Beek E.M., Wiegant V.M., van Oudheusden H.J., van der Donk H.A., van den Hurk R., Buijis R.M. Synaptic contacts between gonadotropin-releasing hormone-containing fibers and neurons in the suprachiasmatic nucleus and perichiasmatic area: an anatomical substrate for feedback regulation? Brain Res. 755:1997;101-111
47. van Esseveldt K.E., Lehman M.N., Boer G.J. The suprachiasmatic nucleus and the circadian time-keeping system revisited. Brains Res. Rev. 33:2000;34-77
48. Verjans J.L., Cooke B.A., De Jong F.H., De Jong C.C.M., van der Molen H.J. Evaluation of a radioimmunoassay for testosterone estimation. J. Steroid Biochem. 4:1973;665-676
49. Waleszczyk W.J., Wang C., Burke W., Dreher B. Velocity response profiles of collicular neurons: parallel and convergent visual information channels. Neuroscience. 93:1999;1063-1076
50. Zwart A.D., Iranmanesh A., Veldhuis J.D. Disparate serum free testosterone concentrations and degrees of hypothalamo-pituitary-luteinizing hormone suppression are achieved by continuous versus pulsatile intravenous androgen replacement in men: a clinical experimental model of ketoconazole-induced reversible hypoandrogenemia with controlled testosterone add-back. J. Clin. Endocrinol. Metab. 82:1997;2062-2069