Effect of short-term ethanol exposure on the suprachiasmatic nucleus of hypothalamus: Immunohystochemical study in mice

Brain Research

Volumn 847, Issue 1, 1999, Pages 124-129

  Satriotomo, Irawan ^a   Miki, Takanori ^a   Itoh, Masahiro ^a   Xie, Qiang ^a   Ameno, Kiyoshi ^a   Takeuchi, Yoshiki ^a  

^a KAGAWA UNIVERSITY   (Japan)

Author keywords

Acute ethanol treatment; Calbindin D28k; Glial fibrillary acidic protein; Intoxication sign; Suprachiasmatic nucleus

Indexed keywords

ALCOHOL; CALBINDIN; GLIAL FIBRILLARY ACIDIC PROTEIN;

ALCOHOL BLOOD LEVEL; ALCOHOL INTOXICATION; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; CONTROLLED STUDY; GLIA CELL; IMMUNOHISTOCHEMISTRY; MALE; MOUSE; NONHUMAN; PRIORITY JOURNAL; SUPRACHIASMATIC NUCLEUS;

ANIMALS; ASTROCYTES; CALCIUM-BINDING PROTEIN, VITAMIN D-DEPENDENT; ETHANOL; GLIAL FIBRILLARY ACIDIC PROTEIN; IMMUNOHISTOCHEMISTRY; MALE; MICE; MICE, INBRED BALB C; NEURONS; SUPRACHIASMATIC NUCLEUS; TIME FACTORS;

EID: 0032745118     PISSN: 00068993     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0006-8993(99)01980-0     Document Type: Article

References (36)

1. Airaksinen M.S., Eilers J., Garaschuk O., Thoenen H., Konnerth A., Meyer M. Ataxia and altered dendritic calcium signaling in mice carryng a targeted null mutations of calbindin D28k gene. Proc. Natl. Acad. Sci. U. S. A. 94:1997;1488-1493.
2. Batini C., Palestini M., Thomasset M., Vigot R. Cytoplasmic calcium buffer, calbindin D28k, is regulated by excitatory amino acids. NeuroReport. 4:1993;927-930.
3. Buijs R.M., Kalsbeek A., van der Woude T.P., van Heeikhuize J.J., Shinn S. Suprachiasmatic nucleus lesion increase corticosterone secretion. Am. J. Physiol. 264:1993;R1186-R1192.
4. D'Amelio F.E., Smith M.E., Eng L.F. Sequence of tissue responses in the early stages of experimental allergic encephalomyelitis (EAE): immunohistochemical, light microscopic and ultrastructural observations in the spinal cord. Glia. 3:1990;229-240.
5. Davies D.L., Cox W.E. Delayed growth and maturation of astrocytes cultures following exposure to ethanol: electron microscopic observation. Brain Res. 547:1991;53-61.
6. Eng L.F., D'Amelio F.E., Smith M.E. Dissociation of the GFAP intermediate filaments in the EAE: observations in the spinal cord. Glia. 2:1989;308-317.
7. Franke H. Influence of chronic alcohol treatment on the GFAP-immunoreactivity in astrocytes of the hippocampus in rats. Acta Histochem. 97:1995;263-271.
8. Freund G. Alcohol withdrawal syndrome in mice. Arch. Neurol. 21:1969;315-320.
9. German D.C., Ng M.C., Liang C.L., McMahon A., Iacopino A.M. Calbindin-D28k in nerve cell nuclei. Neuroscience. 81:1997;735-743.
10. Gruol D.L., Curry J.G. Calcium signals elicited by quisqualate in cultured Purkinje neurons show developmental changes in sensitivity to acute alcohol. Brain Res. 673:1995;1-12.
11. Hall L.L., Borke R.C., Anders J.J. Transection or electrical stimulation of the hypoglossal nerve increases glial fibrillary acidic protein immunoreactivity in the hypoglossal nucleus. Brain Res. 490:1989;157-161.
12. Johnsons 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.
13. Renau-Piqueras J., Zaragoza R., De vaz P., Cervellera R.B., Megias L., Guerri C. Effects of prolonged ethanol exposure on the glial fibrillary acidic protein containing intermediate filaments of astrocytes in primary culture: a quantitative immunofluorescense and immunogold electron microscopic study. J. Histochem. Cytochem. 37:1989;229-240.
14. Kalsbeek A., van Heerikhuize J.J., Wortel J., Buijs R.M. Restricted daytime feeding modifies suprachiasmatic nucleus vasopressin release in rats. J. Biol. Rhythms. 13:1998;18-29.
15. Kelly T.H., Cherek D.R., Steinberg J.L., Robinson D. Effects of provocation and alcohol on human aggressive behaviour. Drug Alcohol Depend. 21:1988;105-112.
16. Kennaway D.J. Light, neurotransmitter and the suprachiasmatic nucleus control of pineal melatonin production in the rat. Biol. Signals. 6:1997;247-254.
17. Kimelberg H.K. Astrocytic edema in CNS trauma. J. Neurotrauma. 9:1992;S71-S81.
18. H.K. Kimelberg, M. Aschner, Astrocytes and their functions, past and present, in: F.E. Lancaster (Ed.), Alcohol and Glial Cells, Res. Monogr. 27, NIH, NIAAA, MD (1994) 1-40.
19. Kraig R.P., Dong L., Thisted R., Jaeger C.B. Spreading depression increases immunohistochemical staining of glial fibrillary acidic protein. J. Neurosci. 11:1991;2187-2198.
20. Lavialle M., Servire J. Developmental study in the circadian clock of the golden hamster: a putative role of astrocytes. Dev. Brain Res. 86:1995;275-282.
21. Lawrence N.W., Herbert M., Jeffcoate W.J. Circadian variation in effects of ethanol in man. Pharmacol. Biochem. Behav. Suppl. 1(18):1983;555-558.
22. Lukoyanov N.V., Madeira M.D., Paula-Barbosa M.M. Behavioral and neuroanatomical consequence of chronic ethanol intake and withdrawal. Physiol. Behav. 66:1999;337-346.
23. Lundqvist C., Alling C., Knoth R., Volk B. Intermittent ethanol exposure of adult rats: hippocampal cell loss after one month of treatment. Alcohol Alcoholism. 30:1995;737-748.
24. Madeira M.D., Andrade J.P., Lieberman A.R., Sousa N., Almeida O.F.X., Paula-Barbosa M.M. Chronic alcohol consumption and withdrawal do not induce cell death in the suprachiasmatic nucleus, but lead to irreversible depression of peptide immuno-reactivity and mRNA levels. J. Neurosci. 17:1997;1302-1319.
25. M. Manthorpe, J.S Rudge, S. Varon, Astroglial cell contribution to neuronal survival and neuritic growth, in: S. Fedoroff, Vernadakis, A. (Eds.), Astrocytes, Academic Press, New York (1986) 315-376.
26. Martin P.M., O'Callaghan J.P. A direct comparison of GFAP immunocytochemistry and GFAP concentration in various regions of ethanol fixed rat and mouse brain. J. Neurosci. Methods. 58:1995;181-192.
27. Mattson M.P., Rychlick 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.
28. Orzi F., Zoli M., Passarelli F., Ferrguti F., Fieschi C., Agnati L.F. Repeated electroconvulsive shock increases glial fibrillary acidic protein, ornithine decarboxylase, somatostatin and cholecystokinin immunoreactivity in the hippocampal formation of the rat. Brain Res. 533:1990;223-231.
29. Pierce D.R., West J.R. Alcohol-induced microcephaly during the third trimester equivalent: relationship to dose and blood alcohol concentration. Alcohol. 3:1986;185-191.
30. Pierce D.R., West J.R. Blood alcohol concentration: a critical factor for producing fetal alcohol effects. Alcohol. 3:1986;269-272.
31. Reinberg A. Circadian changes in psychologic effects of ethanol. Neuropsychopharmacology. 7:1992;149-156.
32. Valles S., Pitarch J., Renau-Piqueras J., Guerri C. Ethanol exposure affects glial fibrillary acidic protein gene expression and transcription during rat brain development. J. Neurochem. 69:1997;2484-2493.
33. van den Pol A.N. The hypothalamic suprachiasmatic nucleus of rat: intrinsic anatomy. J. Comp. Neurol. 191:1980;661-702.
34. van den Pol A.N., Finkbeiner S.M., Cornell-Bell A.H. Calcium excitability and oscillations in suprachiasmatic nucleus neurons and glia in vitro. J. Neurosci. 12:1992;2648-2664.
35. Vijayan V.K., Lee Y.L., Eng L.F. Increase in glial fibrillary acidic protein following neural trauma. Mol. Chem. Neuropathol. 13:1990;107-118.
36. Walker D.W., Barnes D.E., Zornetzer S.F., Steven F., Hunter B.E., Kubanis P. Neuronal loss in hippocampus induced by prolonged ethanol consumption in rats. Science. 209:1980;711-713.