Perinatal development of the mammillothalamic tract and innervation of the anterior thalamic nuclei

Brain Research

Volumn 1248, Issue , 2009, Pages 1-13

  Alpeeva, E V ^a   Makarenko, I G ^a  

^a KOL TSOV INSTITUTE OF DEVELOPMENTAL BIOLOGY   (Russian Federation)

Author keywords

Anterior thalamus; Connection; DiI tracing; Mammillary body; Perinatal development; Synapsin I

Indexed keywords

CARBOCYANINE; SYNAPSIN I;

ARTICLE; BRAIN DEVELOPMENT; BRAIN REGION; CONTROLLED STUDY; MAMMILLARY BODY; NERVE FIBER; NONHUMAN; PERINATAL DEVELOPMENT; POSTNATAL DEVELOPMENT; PRIORITY JOURNAL; RAT; THALAMUS ANTERIOR NUCLEUS;

ANIMALS; ANTERIOR THALAMIC NUCLEI; AXONS; CARBOCYANINES; EFFERENT PATHWAYS; FETAL DEVELOPMENT; IMMUNOHISTOCHEMISTRY; LIMBIC SYSTEM; MAMILLARY BODIES; MICROSCOPY, FLUORESCENCE; NEURONS; RATS; RATS, WISTAR; SYNAPSINS;

RATTUS;

EID: 57649242613     PISSN: 00068993     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.brainres.2008.10.060     Document Type: Article

References (51)

1. Allen G.V., and Hopkins D.A. Mamillary body in the rat: a cytoarchitectonic, Golgi, and ultrastructural study. J. Comp. Neurol. 275 (1988) 39-64
2. Alpeeva E.V., and Makarenko I.G. Perinatal development of the mammillo-tegmental connections in rats. Russ. J. Dev. Biol. 38 (2007) 58-65 Translated from Ontogenez, 2007, 38, 86-93
3. Altman J., and Bayer S.A. Development of the rat thalamus: II. Time and site of origin and settling pattern of neurons derived from the anterior lobule of the thalamic neuroepithelium. J. Comp. Neurol. 275 (1988) 378-405
4. Alvarez-Bolado G., Zhou X., Voss A.K., Thomas T., and Gruss P. Winged helix transcription factor Foxb1 is essential for access of mammillothalamic axons to the thalamus. Development 127 (2000) 1029-1038
5. Anderson R.B., and Key B. Novel guidance cues during neuronal pathfinding in the early scaffold of axon tracts in the rostral brain. Development 126 (1999) 1859-1868
6. Balthazart J., Dupiereux V., Aste N., Viglietti-Panzica C., Barrese M., and Panzica G.C. Afferent and efferent connections of the sexually dimorphic medial preoptic nucleus of the male quail revealed by in vitro transport of DiI. Cell Tissue Res. 276 (1994) 455-475
7. Castejón O.J., Fuller L., and Dailey M.E. Localization of synapsin-I and PSD-95 in developing postnatal rat cerebellar cortex. Dev. Brain Res. 151 (2004) 25-32
8. Coggeshall R.E. A study of diencephalic development in the Albino rat. J. Comp. Neurol. 122 (1964) 241-270
9. Cruce J.A. An autoradiographic study of the projections of the mammillothalamic tract in the rat. Brain Res. 85 (1975) 211-219
10. Dai J., Swaab D.F., Van Der Vliet J., and Buijs R.M. Postmortem tracing reveals the organization of hypothalamic projections of the suprachiasmatic nucleus in the human brain. J. Comp. Neurol. 400 (1998) 87-102
11. Friedman D.I., Johnson J.K., Chorsky R.L., and Stopa E.G. Labeling of human retinohypothalamic tract with the carbocyanine dye, DiI. Brain Res. 560 (1991) 297-302
12. Godement P., Vanselow J., Thanos S., and Bonhoeffer F. A study in developing visual systems with a new method of staining neurons and their processes in fixed tissue. Development 101 (1987) 697-713
13. Gonzalo-Ruiz A., Morte L., and Sanz J.M. Glutamate/aspartate and leu-enkephalin immunoreactivity in mammillothalamic projection neurons of the rat. Brain Res. Bull. 47 (1998) 565-574
14. Guison N.G., Ahmed A.K., Dong K., Yamadori T., and Kobe D. Projections from the lateral mammillary nucleus to the anterodorsal thalamic nucleus in the rat. Kobe J. Med. Sci. 41 (1995) 213-220
15. Gurdjian E.S. The diencephalon of the albino rat. J. Comp. Neurol. 43 (1927) 1-114
16. Hamano K., Takeya T., Iwasaki N., Nakayama J., Ohto T., and Okada Y. A quantitative study of the progress of myelination in the rat central nervous system, using the immunohistochemical method for proteolipid protein. Brain Res. Dev. Brain Res. 108 (1998) 287-293
17. Hayakawa T., and Zyo K. Retrograde double-labeling study of the mammillothalamic and the mammillotegmental projections in the rat. J. Comp. Neurol. 284 (1989) 1-11
18. Hofmann M.H., and Bleckmann H. Effect of temperature and calcium on transneuronal diffusion of DiI in fixed brain preparations. J. Neurosci. Methods 88 (1999) 27-31
19. Jacobson J. Sequence of myelinization in the brain of the albino rat. A. Cerebral cortex, thalamus and related structures. J. Comp. Neurol. 121 (1963) 5-29
20. Kopelman M.D. The Korsakoff syndrome. Br. J. Psychiatry 166 (1995) 154-173
21. Lukas J.R., Aigner M., Denk M., Heinzl H., Burian M., and Mayr R. Carbocyanine postmortem neuronal tracing: influence of different parameters on tracing distance and combination with immunocytochemistry. J. Histochem. Cytochem. 46 (1998) 901-910
22. Makarenko I.G. Prenatal carbocyanine dye tracing of septo-hypothalamic connections. Brain Res., 1130 (2007) 38-47
23. Makarenko I.G. DiI tracing is a useful tool for studies of the hypothalamic connections during perinatal development. In: Pichler F.L. (Ed). Neural Pathways Research. Chapter II (2008), Nova Sci. Publishers, New-York 31-71
24. Makarenko I.G., Ugrumov M.V., and Calas A. Axonal projections from the hypothalamus to the pituitary intermediate lobe in rats during ontogenesis: DiI tracing study. Brain Res. Dev. Brain Res. 155 (2005) 117-126
25. Marion J.F., Yang C., Caqueret A., Boucher F., and Michaud J.L. Sim1 and Sim2 are required for the correct targeting of mammillary body axons. Development 132 (2005) 5527-5537
26. Mark L.P., Daniels D.L., Naidich T.P., and Hendrix L.E. Limbic connections. Am. J. Neuroradiol. 16 (1995) 1303-1306
27. Mastick G.S., and Easter S.S. Initial organization of neurons and tracts in the embryonic mouse fore- and midbrain. Dev. Biol. 173 (1996) 79-94
28. Melloni Jr. R.H., and DeGennaro L.J. Temporal onset of synapsin I gene expression coincides with neuronal differentiation during the development of the nervous system. J. Comp. Neurol. 342 (1994) 449-462
29. Papez J.W. A proposed mechanism of emotion. Arch. Neurol. Psych. 38 (1937) 725-743
30. Paxinos G., and Watson T. The Rat Brain in Stereotaxic Coordinates (1997), Acad. Press, New York
31. Paxinos, G., Törk, I., Tecott, L.H., Valentino, K.L., 1991, Atlas of the Developing Rat Brain. Academic Press Inc. Harcourt Brace Jovanovich, Publishers, San Diego, New York, Boston, London, Sydney, Tokyo, Toronto.
32. Polston E.K., and Simerly R.B. Ontogeny of the projections from the anteroventral periventricular nucleus of the hypothalamus in the female rat. J. Comp. Neurol. 495 (2006) 122-132
33. Ramón y Cajal S. Apuntes para el studio del bulbo raquídeo, cerebelo y orígen de los nervios encefálicos. Anales Soc. Española Historia Natural 24 (1895) 5-118
34. Ramón y Cajal S. Estudios talámicos. Trab. Lab. Investig. Biol. Univ. Madr. 2 (1903) 31-69
35. Seki M., and Zyo K. Anterior thalamic afferents from the mamillary body and the limbic cortex in the rat. J. Comp. Neurol. 229 (1984) 242-256
36. Shibata H. Topographic organization of subcortical projections to the anterior thalamic nuclei in the rat. J. Comp. Neurol. 323 (1992) 117-127
37. Sziklas V., and Petrides M. Memory and the region of the mammillary bodies. Prog. Neurobiol. 54 (1998) 55-70
38. Takeuchi Y., Allen G.V., and Hopkins D.A. Transnuclear transport and axon collateral projections of the mamillary nuclei in the rat. Brain Res. Bull. 14 (1985) 453-468
39. Tessier-Lavigne M., and Goodman C.S. The molecular biology of axon guidance. Science 274 (1996) 1123-1133
40. Trukhacheva A.A., and Aleksandrova M.A. The development of thalamocortical connections studied by using carbocyanine dyes in the early ontogeny of rats. Ontogenez 30 (1999) 210-219 [Article in Russian]
41. Valverde F. Golgi Atlas of the Postnatal Mouse Brain (1998), Springer, New York
42. Valverde F., Garcia C., Mascaraque L., and Carlos J. Development of the mammillothalamic tract in normal and Pax-6 mutant mice. J. Comp. Neurol. 419 (2000) 485-504
43. Van der Kooy D., Kuypers H.G., and Catsman-Berrevoets C.E. Single mammillary body cells with divergent axon collaterals. Demonstration by a simple, fluorescent retrograde double-labeling technique in the rat. Brain Res. 158 (1978) 189-196
44. Vann S.D., and Aggleton J.P. Evidence of a spatial encoding deficit in rats with lesions of the mammillary bodies or mammillothalamic tract. J. Neurosci. 23 (2003) 3506-3514
45. Vann S.D., and Aggleton J.P. The mammillary bodies: two memory systems in one?. Nat. Rev., Neurosci. 5 (2004) 35-44
46. Vann S.D., Saunders R.C., and Aggleton J.P. Distinct, parallel pathways link the medial mammillary bodies to the anterior thalamus in macaque monkeys. Eur. J. Neurosci. 26 (2007) 1575-1586
47. Vercelli A., Repici M., Garbossa D., and Grimaldi A. Recent techniques for tracing pathways in the central nervous system of developing and adult mammals. Brain Res. Bull. 51 (2000) 11-28
48. Vertes R.P., Albo Z., and Prisco G.V. Theta-rhythmically firing neurons in the anterior thalamus: implications for mnemonic functions of the Papez's circuit. Neurosci. 104 (2001) 619-625
49. Watanabe K., and Kawana E. A horseradish peroxidase study on the mammillothalamic tract in the rat. Acta Anat. (Basel) 108 (1980) 394-401
50. Wehr R., Mansouri A., de Maeyer T., and Gruss P. Fkh-5-deficient mice show dysgenesis in the caudal midbrain and hypothalamic mammillary body. Development 124 (1997) 4447-4456
51. Yoneoka Y., Takeda N., Inoue A., Ibuchi Y., Kumagai T., Sugai T., Takeda K., and Ueda K. Acute Korsakoff syndrome following mammillothalamic tract infarction. J. Neuroradiol. 25 (2004) 964-968