Differential effects of glutamatergic blockade on circadian and photic regulation of gene expression in the hamster suprachiasmatic nucleus

Molecular Brain Research

Volumn 67, Issue 2, 1999, Pages 247-257

  Guido, Mario E ^a,b   De Guido, Liliana ^a,b   Goguen, Donna ^a   Robertson, Harold A ^a,b   Rusak, Benjamin ^a,b  

^a DALHOUSIE UNIVERSITY   (Canada)

^b DALHOUSIE UNIVERSITY   (Canada)

Author keywords

Circadian rhythm; Dizocilpine (MK 801, (+) 5 methyl 10,11 dihydro 5H dibenzo a,d cyclohepten 5,10 imine maleate); Entrainment; Excitatory amino acid; Gene expression; Immediate early gene; JunB, fosB; Light; NGFI A (zif 268; Krox24); NMDA (N methyl D aspartate) receptor; Spontaneous expression; Suprachiasmatic nucleus; Transcription regulation

Indexed keywords

GLUTAMATE RECEPTOR; MESSENGER RNA; N METHYL DEXTRO ASPARTIC ACID RECEPTOR;

ANIMAL TISSUE; ARTICLE; CIRCADIAN RHYTHM; CONTROLLED STUDY; GENE EXPRESSION REGULATION; IN SITU HYBRIDIZATION; MALE; NONHUMAN; PHOTOSTIMULATION; PRIORITY JOURNAL; SUPRACHIASMATIC NUCLEUS; SYRIAN HAMSTER;

ANIMALS; CIRCADIAN RHYTHM; CRICETINAE; DIZOCILPINE MALEATE; EXCITATORY AMINO ACID ANTAGONISTS; GENE EXPRESSION; GENES, IMMEDIATE-EARLY; GLUTAMIC ACID; MALE; MESOCRICETUS; PHOTIC STIMULATION; PROTO-ONCOGENE PROTEINS C-FOS; PROTO-ONCOGENE PROTEINS C-JUN; RECEPTORS, N-METHYL-D-ASPARTATE; RNA, MESSENGER; SUPRACHIASMATIC NUCLEUS;

ANIMALIA; CRICETINAE; MAMMALIA; MESOCRICETUS AURATUS;

EID: 0033586653     PISSN: 0169328X     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0169-328X(99)00074-1     Document Type: Article

References (48)

1. Abe H., Rusak B., Robertson H.A. Photic induction of Fos protein in the suprachiasmatic nucleus is inhibited by the NMDA receptor antagonist MK-801. Neurosci. Lett. 127:1991;9-12.
2. Abe H., Rusak B., Robertson H.A. NMDA and non-NMDA receptor antagonists inhibit photic induction of Fos protein in the hamster suprachiasmatic nucleus. Brain Res. Bull. 28:1992;831-835.
3. Abe H., Rusak B. Physiological mechanisms regulating photic induction of Fos-like protein in hamster suprachiasmatic nucleus. Neurosci. Biobehav. Rev. 18:1994;531-536.
4. Aronin N., Sagar S., Sharp F., Schwartz W. Light regulates expression of a Fos-related protein in rat suprachiasmatic nucleus. Proc. Natl. Acad. Sci. U.S.A. 87:1990;5959-5962.
5. Cahill G.M., Ralph M.R., Menaker M. Effects of excitatory amino acid receptor antagonists and agonists on suprachiasmatic nucleus responses to retinohypothalamic volleys. Brain Res. 479:1989;76-82.
6. Colwell C.S., Ralph M.R., Menaker M. Do NMDA receptors mediate the effects of light on circadian behavior? Brain Res. 523:1990;117-120.
7. Daan S., Pittendrigh C.S. A functional analysis of circadian pacemakers in nocturnal rodents: II. The variability of phase response curves. J. Comp. Physiol. 106:1976;253-266.
8. Ebling F.J.P. The role of glutamate in the photic regulation of the suprachiasmatic nucleus. Prog. Neurobiol. 50:1996;109-132.
9. Galligan J.J., North R.A. MK-801 blocks nicotinic depolarization of guinea pig myenteric neurons. Neurosci Lett. 108:1990;105-109.
10. Guido M.E., Rusak B., Robertson H.A. Light-induced and circadian expression of fosB, c-fos, junB and c-jun in the hamster suprachiasmatic nucleus. Soc. Neurosci. Abstr. 21:1995;658.14.
11. Guido M.E., Rusak B., Robertson H.A. Spontaneous circadian and light-induced expression of junB mRNA in the hamster suprachiasmatic nucleus. Brain Res. 732:1996;215-222.
12. Guido M.E., Rusak B., Robertson H.A. Expression of fosB mRNA in the hamster suprachiasmatic nucleus is induced at only selected circadian phases. Brain Res. 739:1996;132-138.
13. Guido M.E., Goguen D., Robertson H.A., Rusak B. Spontaneous and light-evoked expression of JunB-like protein in the hamster suprachiasmatic nucleus near subjective dawn. Neurosci Lett. 217:1996;9-12.
14. M.E. Guido, D.M. Goguen, L. de Guido, H.A. Robertson, B. Rusak, Circadian and photic regulation of immediate-early gene expression in the hamster suprachiasmatic nucleus, Neuroscience (1998) in press.
15. Hartgraves M.D., Fuchs J.L. NMDA receptor binding in rodent suprachiasmatic nucleus. Brain Res. 640:1994;113-118.
16. J. Hastings, B. Rusak, Z, Boulos, Circadian rhythms: the physiology of biological timing, in: C.L. Prosser (Ed.), Neural and Integrative Animal Physiology, Wiley-Liss, New York, 1991, pp. 435-546.
17. Hughes P., Dragunow M. Induction of Immediate-early genes and the control of neurotransmitter-regulated gene expression within the nervous system. Pharmacol. Rev. 47:1995;133-178.
18. Kim Y.I., Dudek F.E. Intracellular electrophysiological study of suprachiasmatic nucleus neurons in rodents: excitatory synaptic mechanisms. J. Physiol. 444:1991;268-287.
19. 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.
20. Kornhauser J.M., Nelson D.E., Mayo K.E., Takahashi J.S. Regulation of junB messenger RNA and AP-1 activity by light and a circadian clock. Science. 255:1992;1581-1584.
21. Li X., Hallqvist A., Jacobson I., Orwar O., Sandberg M. Studies on the identity of the rat optic nerve transmitter. Brain Res. 706:1996;89-96.
22. Lin J.T., Kornhauser J.M., Singh N.P., Mayo K.E., Takahashi J.S. Visual sensitivities of nur77 (NGFI-B) and zif268 (NGFI-A) induction in the suprachiasmatic nucleus are dissociated from c-fos induction and behavioral phase-shifting responses. Mol. Brain Res. 46:1997;303-310.
23. Mason R., Rusak B. NMDA-evoked responses in the Syrian hamster suprachiasmatic nucleus in vitro. J. Physiol. 435:1991;39.
24. Meijer J.H., Rietveld W.J. Neurophysiology of the suprachiasmatic circadian pacemaker in rodents. Physiol. Rev. 69:1989;671-707.
25. Mikkelsen J.D., Larsen P.J., Mick G., Vrang N., Ebling F.J.P., Maywood E.S., Hasting M.H., Møller M. Gating of retinal inputs through the suprachiaasmatic nucleus: role of excitatory neurotransmission. Neurochem. Int. 27:1995;263-272.
26. Milbrandt J. A nerve growth factor-induced gene encodes a possible transcriptional regulatory factor. Science. 238:1987;797-799.
27. Moore R.Y., Lenn N.J.A. A retinohypothalamic projection in the rat. J. Comp. Neurol. 146:1972;1-14.
28. Moore R.Y. Retinohypothalamic projection in mammals: a comparative study. Brain Res. 183:1973;458-463.
29. Morgan J., Curran T. Stimulus-transcription coupling in the nervous system: involvement of the inducible proto-oncogenes fos and jun. Annu. Rev. Neurosci. 14:1991;421-451.
30. Morin L.P. The circadian visual system. Brain Res. Rev. 19:1994;102-127.
31. Peters R.V., Aronin N., Schwartz W.J. Circadian regulation of FosB is different from c-Fos in the rat suprachiasmatic nucleus. Mol. Brain Res. 27:1994;243-248.
32. Pickard G.E. The afferent connections of the suprachiasmatic nucleus of the golden hamster with emphasis on the retinohypothalamic projection. J. Comp. Neurol. 211:1982;65-83.
33. Rea M. Light increases Fos-related protein immunoreactivity in the rat suprachiasmatic nucleus. Brain Res. Bull. 23:1989;577-581.
34. Rea M. Different populations of cells in the suprachiasmatic nuclei express c-fos in association with light-induced phase delays and advances of the free-running activity rhythm in hamsters. Brain Res. 579:1992;107-112.
35. Robertson H.A. Immediate-early genes, neuronal plasticity and memory. Biochem. Cell Biol. 70:1992;729-737.
36. Rusak B., Zucker I. Neural regulation of circadian rhythms. Physiol. Rev. 59:1979;449-527.
37. Rusak B., 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.
38. Rusak B., Bina K.G. Neurotransmitters in the mammalian circadian system. Annu. Rev. Neurosci. 13:1990;387-401.
39. Rusak B., McNaughton L., Robertson H.A., Hunt S.P. Circadian variation in photic regulation of immediate-early gene mRNAs in rat suprachiasmatic nucleus cells. Mol. Brain Res. 14:1992;124-130.
40. Ryder K., Lau L.F., Nathans D. A gene activated by growth factors is related to the oncogene v-jun. Proc. Natl. Acad. Sci. U.S.A. 85:1988;1487-1491.
41. Schwartz W.J., Takeuchi J., Shannon W., Davis E.M., Aronin N. Temporal regulation of light-induced Fos and Fos-like protein expression in the ventrolateral subdivision of the rat suprachiasmatic nucleus. Neuroscience. 58:1994;573-583.
42. Shibata S., Watanabe A., Hamada T., Ono M., Watanabe S. N-methyl-D-aspartate induces phase shifts in circadian rhythm of neuronal activity of rat SCN in vitro. Am. J. Physiol. 267:1994;R360-R364.
43. Shiegeshoyi Y., Taguchi K., Yamamoto S., Takekida S., Yan L., Tei H., Moriya T., Shibata S., Loros J.J., Dunlap J.C., Okamura H. Light-induced resetting of a mammalian circadian clock is associated with rapid induction of the mPer1 transcript. Cell. 91:1997;1043-1053.
44. Sun Z.S., Albrecht U., Zhuchenko O., Bailey J., Eichele G., Lee C.C. RIGUI, a putative mammalian ortholog of the Drosophila period gene. Cell. 90:1997;1003-1011.
45. Tei H., Okamura H., Shigeyoshi Y., Fukuhara C., Ozawa R., Hirose M., Sakaki Y. Circadian oscillation of a mammalian homologue of the Drosophila period gene. Nature. 389:1997;512-516.
46. Wollnik F., Brysh W., Uhlmann E., Gillardon F., Bravo R., Zimmermann M., Schlingensiepen K.H., Herdegen T. Block of c-Fos and JunB expression by antisense oligonucleotides inhibits light-induced phase shifts of the mammalian circadian clock. Eur. J. Neurosci. 7:1995;388-393.
47. Zerial M., Toschi L., Ryseck R.P., Schuermann M., Muller R., Bravo R. The product of a novel growth factor activated gene, fosB, interacts with Jun proteins enhancing their DNA binding activity. EMBO J. 8:1989;805-813.
48. Ikeda H., Dawes E., Hankins M. Spontaneous firing level distinguishes the effects of NMDA and non-NMDA receptor antagonists on the ganglion cells in the cat retina. Eur. J. Pharmacol. 210:1992;53-59.