Calbindin immunoreactivity delineates the circadian visual centers of the brain of the common marmoset (Callithrix jacchus)

Brain Research Bulletin

Volumn 43, Issue 4, 1997, Pages 369-373

  Costa, Miriam S M O ^a   Britto, Luiz R G ^b  

^a FEDERAL UNIVERSITY OF RIO GRANDE DO NORTE   (Brazil)

^b UNIVERSITY OF SÃO PAULO   (Brazil)

Author keywords

Calbindin D 28k; Circadian visual system; Intergeniculate leaflet; Marmoset; Pregeniculate nucleus; Suprachiasmatic nucleus

Indexed keywords

CALBINDIN; CHOLERA TOXIN B SUBUNIT;

ANIMAL EXPERIMENT; ANIMAL TISSUE; ARTICLE; CIRCADIAN RHYTHM; GENICULATE NUCLEUS; IMMUNOREACTIVITY; MALE; MARMOSET; NONHUMAN; PRIORITY JOURNAL; SUPRACHIASMATIC NUCLEUS; VISUAL CORTEX;

ANIMALS; BRAIN; CALCIUM-BINDING PROTEIN, VITAMIN D-DEPENDENT; CALLITHRIX; CIRCADIAN RHYTHM; IMMUNOHISTOCHEMISTRY; MALE; SUPRACHIASMATIC NUCLEUS; VISUAL CORTEX;

EID: 0030818819     PISSN: 03619230     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0361-9230(96)00378-4     Document Type: Article

References (44)

1. Albers H. E., Ferris C. F. Neuropeptide Y: Role in light-dark cycle entrainment of hamster circadian rhythms. Neurosci. Lett. 50:1984;163-168.
2. Andressen C., Blümcke I., Celio M. R. Calcium-binding proteins: Selective markers of nerve cells. Cell Tissue Res. 271:1993;181-208.
3. Baimbridge K. G., Celio M. R., Rogers J. H. Calcium-binding proteins in the nervous system. Trends Neurosci. 15:1992;303-308.
4. Britto L. R. G., Gobersztejn F., Karten H. J., Cox K. Depletion and recovery of the calcium-binding proteins calbindin and parvalbumin in the pigeon optic tectum following retinal lesions. Brain Res. 661:1994;289-292.
5. Card J. P., Moore R. Y. Ventral lateral geniculate nucleus efferents to the rat suprachiasmatic nucleus exhibit avian pancreatic polypeptide-like-immunoreactivity. J. Comp. Neurol. 206:1982;390-396.
6. Card J. P., Moore R. Y. The suprachiasmatic nucleus of the golden hamster: Immunohistochemical analysis of cell and fiber distribution. Neuroscience. 13:1984;415-431.
7. Card J. P., Moore R. Y. Organization of lateral geniculate-hypothalamic connections in the rat. J. Comp. Neurol. 284:1989;135-147.
8. Cassone V. M., Speh J. C., Card J. P., Moore R. Y. Comparative anatomy of mammalian suprachiasmatic nucleus. J. Biol. Rhythms. 3:1988;71-91.
9. Celio M. R. Calbindin D-28k and parvalbumin in the rat nervous system. Neuroscience. 35:1990;375-475.
10. Ericson H., Blomqvist A. Tracing of neuronal connections with cholera toxin subunit B: Light and electron microscopic immunohistochemistry using monoclonal antibodies. J. Neurosci. Methods. 24:1988;225-235.
11. Harrington M. E., Nance D. M., Rusak B. Neuropeptide Y immunoreactivity in the hamster geniculo-suprachiasmatic tract. Brain Res. Bull. 15:1985;465-472.
12. Harrington M. E., Nance D. M., Rusak B. Double-labeling of neuropeptide Y-immunoreactive neurons which project from the geniculate to the suprachiasmatic nuclei. Brain Res. 410:1987;275-282.
13. Harrington M. E., Rusak B. Ablation of the geniculo-hypothalamic tract alters circadian activity rhythms of hamsters housed under constant light. Physiol. Behav. 42:1988;183-189.
14. Hastings J. W., Rusak B., Boulos Z. Circadian rhythms: The physiology of biological timing. Prosser L. Annual physiology. 1991;435-546 Wiley-Liss, Inc, New York.
15. Hendrickson A. E., Wagoner N., Cowan W. N. An autoradiographic and electron microscopic study of retino-hypothalamic connections. Z. Zellforsch. 135:1972;1-26.
16. Hickey T. L., Spear P. D. Retinogeniculate projections in hooded and albino rats. Exp. Brain Res. 24:1976;523-529.
17. Huhman K. L., Albers H. E. Neuropeptide Y microinjected into the suprachiasmatic region phase shifts circadian rhythms in constant darkness. Peptides. 15:1994;1475-1478.
18. 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.
19. Johnson R. F., Smale L., Moore R. Y., Morin L. P. Lateral geniculate lesions block circadian phase-shift responses to a benzodiazepine. Proc. Natl. Acad. Sci. USA. 85:1988;5301-5304.
20. Jones E. G. The thalamus. 1985;723-733 Plenum Press, New York.
21. Mai J. K., Kedziora O., Teckhaus L., Sofroniew M. W. Evidence for subdivisions in the human suprahiasmatic nucleus. J. Comp. Neurol. 305:1991;508-525.
22. Mantyh P. W., Kemp J. A. The distribution of putative neurotransmitters in the lateral geniculate nucleus of the rat. Brain Res. 288:1983;344-348.
23. Meyer E. L., Harrington M. E., Rahmani T. A phase-response curve to the benzodiazepine chlordiazepoxide and the effect of geniculo-hypothalamic tract ablation. Physiol. Behav. 53:1993;237-243.
24. Moore R. Y. Retinohypothalamic projection in mammals: A comparative study. Brain Res. 49:1973;403-409.
25. Moore R. Y. The geniculohypothalamic tract in monkey and man. Brain Res. 486:1989;190-194.
26. Moore R. Y. The organization of the human circadian system. Swaab D. F., Hofman M. A., Mirmiran M., David R., Leewen F. W. Progress in brain research. 93:1992;101-117 Elsevier, Amsterdam.
27. Moore R. Y. Organization of the primate circadian system. J. Biol. Rhythms Suppl. 8:1993;s3-s9.
28. Moore R. Y. Functional organization of the suprachiasmatic nucleus. Guileminault C., et al. Fatal familial insomnia: Inherited prion diseases, sleep and the thalamus. 1994;191-201 Raven Press, New York.
29. Moore R. Y., Card J. P. Intergeniculate leaflet: An anatomically and functionally distinct subdivision of the lateral geniculate complex. J. Comp. Neurol. 344:1994;403-430.
30. Moore R. Y., Lenn N. J. A retinohypothalamic projection in the rat. J. Comp. Neurol. 146:1972;1-14.
31. Moore R. Y., Speh J. C. GABA is the principal neurotransmitter of the circadian system. Neurosci. Lett. 150:1993;112-116.
32. Morin L. P., Johnson R. F., Moore R. Y. Two brain nuclei regulating circadian rhythms are identified by GFAP immunoreactivity in hamsters and rats. Neurosci. Lett. 99:1989;55-60.
33. Pickard G. E. Entrainment of the circadian rhythm of wheel-running activity is phase shifted by ablation of the intergeniculate leaflet. Brain Res. 494:1989;151-154.
34. Pickard G. E. Intergeniculate leaflet ablation alters circadian rhythms in the mouse. Neuroreport. 5:1994;2186-2188.
35. Roger J. H., Résibois A. Calretinin and calbindin-D28k in rat brain: Patterns of partial co-localization. Neuroscience. 51:1992;843-865.
36. Rusak B., Meijer J. H., Harrington M. E. Hamster circadian rhythms are phase-shifted by electrical stimulation of the geniculo-hypothalamic tract. Brain Res. 493:1989;283-291.
37. Smale L., Blanchard J., Moore R. Y., Morin L. P. Immunocytochemical characterization of the suprachiasmatic nucleus and the intergeniculate leaflet in the diurnal ground squirrel, Spermophilus lateralis. Brain Res. 563:1991;77-86.
38. Sofroniew M. W., Weindl A. Identification of parvicellular vasopressin and neurophysin neurons in the suprachiasmatic nucleus of a variety of mammals including primates. J. Comp. Neurol. 193:1978;659-675.
39. Spatz W. B., Lohle E. Calcium-binding proteins in the spiral ganglion of the monkey, Callithrix jacchus. Hear. Res. 86:1995;89-99.
40. Takatsuji K., Tohyama M. The organization of the rat lateral geniculate body by immunohistochemical analysis of neuroactive substances. Brain Res. 480:1989;198-209.
41. Turek F. W. Circadian rhythms. Bardin C. W. Recent progress in hormone research. 49:1994;43-90 Academic Press, San Diego.
42. Ueda S., Kawata M., Sano Y. Identification of neuropeptide Y immunoreactivity in the suprachiasmatic nucleus and the lateral geniculate nucleus of some mammals. Neurosci. Lett. 68:1986;7-10.
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., Tsujimoto K. L. Neurotransmitters of the hypothalamic suprachiasmatic nucleus: Immunocytochemical analysis of 25 neuronal antigens. Neuroscience. 15:1985;1049-1086.