Central amygdaloid axon terminals are in contact with retrorubral field neurons that project to the parvicellular reticular formation of the medulla oblongata in the rat

Brain Research

Volumn 1306, Issue , 2010, Pages 18-28

  Tsumori, Toshiko ^a   Qin, Yi ^b   Yokota, Shigefumi ^a   Niu, Jian guo ^a,b   Yasui, Yukihiko ^a  

^a SHIMANE UNIVERSITY FACULTY OF MEDICINE   (Japan)

^b NINGXIA MEDICAL UNIVERSITY   (China)

Author keywords

Amygdala; GABAergic; Orofacial movement; Parvicellular reticular formation; Rat; Retrorubral field

Indexed keywords

GLUTAMATE DECARBOXYLASE; TYROSINE 3 MONOOXYGENASE;

AMYGDALOID NUCLEUS; ARTICLE; CONTROLLED STUDY; GABAERGIC SYSTEM; MALE; MEDULLA OBLONGATA; NERVE FIBER; NONHUMAN; PRIORITY JOURNAL; RAT; RETICULAR FORMATION; SIGNAL TRANSDUCTION;

RATTUS;

EID: 71549118912     PISSN: 00068993     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.brainres.2009.09.118     Document Type: Article

References (59)

1. Alheid G.F., and Heimer L. Theories of basal forebrain organization and the "emotional motor system". In: Holstege R., Bandler R., and Saper C.B. (Eds). The Emotional Motor System. Prog. Brain Res. Vol. 107 (1996), Elsevier, Amsterdam 461-484
2. Arts M.P.M., Bemelmans F.F.J., and Cools A.R. Role of the retrorubral nucleus in striatally elicited orofacial dyskinesia in cats: effects of muscimol and bicuculline. Psychopharmacol. 140 (1998) 150-156
3. Batten T.F.C., Gamboa-Esteves F.O., and Saha S. Evidence for peptide co-transmission in retrograde- and anterograde-labelled central nucleus of amygdala neurones projecting to NTS. Auton. Neurosci. Basic Clin. 98 (2002) 28-32
4. Cassell M.D., Gray T.S., and Kiss J.Z. Neuronal architecture in the rat central nucleus of the amygdala: a cytological, hodological, and immunocytochemical study. J. Comp. Neurol. 246 (1986) 478-499
5. Chan J., Aoki C., and Pickel V.M. Optimization of differential immunogold-silver and peroxidase labeling with maintenance of ultrastructure in brain sections before plastic embedding. J. Neurosci. Methods 33 (1990) 113-127
6. Cohen R.S., Blomberg F., Bertins B., and Siekevitz P. Structure of post synaptic densities isolated from dog cerebral cortex. I. Overall morphology and protein composition. J. Cell Biol. 74 (1977) 181-203
7. Dahlström A., and Fuxe K. Evidence for the existence of monoamine-containing neurons in the central nervous system. I. Demonstration of monoamines in the cell bodies of brain stem neurons. Acta Physiol. Scand. 62 Suppl. 232 (1964) 1-55
8. Deutch A.Y., Goldstein M., Baldino F., and Roth R.H. Telencephalic projections of the A8 dopamine cell group. Ann. N.Y. Acad. Sci. 537 (1988) 27-50
9. Fallon J.H., and Loughlin S.E. Substantia nigra. In: Paxinos G. (Ed). The Rat Central Nervous System. 2nd ed. (1995), Academic Press, Sydney 215-237
10. François C., Yelnik J., Tandé D., Agid Y., and Hirsch E.C. Dopaminergic cell group A8 in the monkey: anatomical organization and projections to the striatum. J. Comp. Neurol. 414 (1999) 334-347
11. Gasbarri A., Packard M.G., Sulli A., Pacitti C., Innocenzi R., and Perciavalle V. The projections of the retrorubral field A8 to the hippocampal formation in the rat. Exp. Brain Res. 112 (1996) 244-252
12. Gasbarri A., Sulli A., and Packard M.G. The dopaminergic mesencephalic projections to the hippocampal formation in the rat. Prog. Neuropsychopharmacol. Biol. Psychiatry 21 (1997) 1-22
13. Gonzales C., and Chesselet M.-F. Amygdalonigral pathway: an anterograde study in the rat with Phaseolus vulgaris Leucoagglutinin (PHA-L). J. Comp. Neurol. 297 (1990) 182-200
14. Gray T.S., and Magnuson D.J. Galanin-like immunoreactivity within amygdaloid and hypothalamic neurons that project to the midbrain central grey in rat. Neurosci. Lett. 83 (1987) 264-268
15. Gray T.S., and Magnuson D.J. Peptide immunoreactive neurons in the amygdala and the bed nucleus of the stria terminalis project to the midbrain central gray in the rat. Peptides 13 (1992) 451-460
16. Hasue R.H., and Shammah-Lagnado S.J. Origin of the dopaminergic innervation of the central extended amygdala and accumbens shell: a combined retrograde tracing and immunohistochemical study in the rat. J. Comp. Neurol. 454 (2002) 15-33
17. Holstege G. Descending motor pathways and the spinal motor system: limbic and non-limbic components. In: Holstege G. (Ed). Role of the Forebrain in Sensation and Behavior, Progress in Brain Research vol. 87 (1991), Elsevier, Amsterdam 307-421
18. Jia H.-G., Rao Z.-R., and Shi J.-W. Evidence of gamma-aminobutyric acidergic control over the catecholaminergic projection from the medulla oblongata to the central nucleus of the amygdala. J. Comp. Neurol. 381 (1997) 262-281
19. Jia H.-G., Zhang G.-Y., and Wan Q. A GABAergic projection from the central nucleus of the amygdala to the parabrachial nucleus: an ultrastructural study of anterograde tracing in combination with post-embedding immunocytochemistry in the rat. Neurosci. Lett. 382 (2005) 153-157
20. Kolta A., Westberg K.-G., and Lund J.P. Identification of brainstem interneurons projecting to the trigeminal motor nucleus and adjacent structures in the rabbit. J. Chem. Neuroanat. 19 (2000) 175-195
21. LeDoux J. The amygdala. Curr. Biol. 17 (2007) R868-R874
22. Li Y.-Q., Takada M., Kaneko T., and Mizuno N. Premotor neurons for trigeminal motor nucleus neurons innervating the jaw-closing and jaw-opening muscles: differential distribution in the lower brainstem of the rat. J. Comp. Neurol. 356 (1995) 563-579
23. Mishima K., Sasamoto K., and Ohta M. Amygdaloid or cortical facilitation of antidromic activity of trigeminal motoneurons in the rat. Comp. Biochem. Physiol. 73A (1982) 355-359
24. Mogoseanu D., Smith A.D., and Bolam J.P. Monosynaptic innervation of trigeminal motor neurones involved in mastication by neurones of the parvicellular reticular formation. J. Comp. Neurol. 336 (1993) 53-65
25. Mogoseanu D., Smith A.D., and Bolam J.P. Monosynaptic innervation of facial motoneurones by neurones of the parvicellular reticular formation. Exp. Brain Res. 101 (1994) 427-438
26. Mugnaini E., and Oertel W.H. Atlas of the distribution of GABAergic neurons and terminals in the rat as revealed by GAD immunoreactivity. In: Björklund A., and Hökfelt T. (Eds). Handbook of Chemical Neuroanatomy: GABA and Neuropeptides in the CNS, Part 1 Vol. 4 (1985), Elsevier, Amsterdam 436-595
27. Nakamura S., Tsumori T., Yokota S., Oka T., and Yasui Y. Amygdaloid axons innervate melanin-concentrating hormone- and orexin-containing neurons in the mouse lateral hypothalamus. Brain Res. 1278 (2009) 66-74
28. Nitecka L., and Ben-Ari Y. Distribution of GABA-like immunoreactivity in the rat amygdaloid complex. J. Comp. Neurol. 266 (1987) 45-55
29. Notsu K., Tsumori T., Yokota S., Sekine J., and Yasui Y. Posterior lateral hypothalamic axon terminals are in contact with trigeminal premotor neurons in the parvicellular reticular formation of the rat medulla oblongata. Brain Res. 1244 (2008) 71-81
30. Oertel W.H., Riethmüller G., Mugnaini E., Schmechel D.E., Weindl A., Gramsch C., and Herz A. Opioid peptide-like immunoreactivity localized in GABAergic neurons of rat neostriatum and central amygdaloid nucleus. Life Sci. 33 (1983) 73-76
31. Ohta M., and Moriyama Y. Supratrigeminal neurons mediate shortest, disynaptic pathway from the central amygdaloid nucleus to the contralateral trigeminal motoneurons in the rat. Comp. Biochem. Physiol. 83A (1986) 633-641
32. Oka T., Tsumori T., Yokota S., and Yasui Y. Neuroanatomical and neurochemical organization of projections from the central amygadaloid nucleus to the nucleus retroambiguus via the periaqueductal gray in the rat. Neurosci. Res. 62 (2008) 286-298
33. Paxinos G., and Watson C. The rat brain in stereotaxic coordinates. 5th. ed (2005), Elsevier Academic Press, Amsterdam
34. Peters A., and Palay S.L. The morphology of synapses. J. Neurocytol. 25 (1996) 687-700
35. Peters A., Palay S.L., and Webster H. The fine structure of the nervous system: neurons and their supporting cells. 3rd ed (1991), Oxford University Press, New York
36. Pickel V.M., and Chan J. Electron microscopic immunocytochemical labeling of endogeneous and/or transported antigens in rat brain using silver-intensified one-nanometre colloidal gold. In: Cuello A.C. (Ed). Immunohistochemistry II (1993), John Wiley and Sons, New York 265-280
37. Pickel V.M., Van Bockstaele E.J., Chan J., and Cestari D.M. Amygdala efferents form inhibitory-type synapses with a subpopulation of catecholaminergic neurons in the rat nucleus tractus solitarius. J. Comp. Neurol. 362 (1995) 510-523
38. Pohl K., and Stierhof Y.-D. Action of gold chloride ("gold toning") on silver-enhanced 1 nm gold markers. Microsc. Res. Tech. 42 (1998) 59-65
39. Poulin J.F., Castonguay-Lebel Z., Laforest S., and Drolet G. Enkephalin co-expression with classic neurotransmitters in the amygdaloid complex of the rat. J. Comp. Neurol. 506 (2008) 943-959
40. Rye D.B., Lee H.J., Saper C.B., and Wainer B.H. Medullary and spinal efferents of the pedunculopontine tegmental nucleus and adjacent mesopontine tegmentum in the rat. J. Comp. Neurol. 269 (1988) 315-341
41. Saha S., Batten T.F.C., and Henderson Z. A GABAergic projection from the central nucleus of the amygdala to the nucleus of the solitary tract: a combined anterograde tracing and electron microscopic immunohistochemical study. Neuroscience 99 (2000) 613-626
42. Sasamoto K., and Ohta M. Amygdaloid-induced jaw opening and facilitation or inhibition of the trigeminal motoneurons in the rat. Comp. Biochem. Physiol. 73A (1982) 349-354
43. Shammah-Lagnado S.J., Costa M.S., and Ricardo J.A. Afferent connections of the parvocellular reticular formation: a horseradish peroxidase study in the rat. Neuroscience 50 (1992) 403-425
44. Ter Horst G.J., Copray J.C.V.M., Liem R.S.B., and Van Willigen J.D. Projections from the rostral parvicellular reticular formation to pontine and medullary nuclei in the rat: involvement in autonomic regulation and orofacial motor control. Neuroscience 40 (1991) 735-758
45. Travers J.B., and Norgren R. Afferent projections to the oral motor nuclei in the rat. J. Comp. Neurol. 220 (1983) 280-298
46. Tsubouchi K., Tsumori T., Yokota S., Okunishi H., and Yasui Y. A disynaptic pathway from the central amygdaloid nucleus to the paraventricular hypothalamic nucleus via the parastrial nucleus in the rat. Neurosci. Res. 59 (2007) 390-398
47. Tsumori T., Yokota S., Qin Y., Oka T., and Yasui Y. A light and electron microscopic analysis of the convergent insular cortical and amygdaloid projections to the posterior lateral hypothalamus in the rat, with special reference to cardiovascular function. Neurosci. Res. 56 (2006) 261-269
48. Areceptors in the retrorubral filed and ventral pallidum in rat jaw movements elicited by dopaminergic stimulation of the nucleus accumbens shell. Eur. J. Pharmacol. 510 (2005) 39-47
49. Veening J.G., Swanson L.W., and Sawchenko P.E. The organization of projections from the central nucleus of the amygdala to brainstem sites involved in central autonomic regulation: a combined retrograde transport-immunohistochemical study. Brain Res. 303 (1984) 337-357
50. Veinante P., Stoeckel M.-E., and Freund-Mercier M.-J. GABA- and peptide-immunoreactivities co-localize in the rat central extended amygdala. NeuroReport 8 (1997) 2985-2989
51. Viollet C., Lepousez G., Loudes C., Videau C., Simon A., and Epelbaum J. Somatostatinergic systems in brain: networks and functions. Mol. Cell. Endocrinol. 286 (2008) 75-87
52. von Krosigk M., and Smith A.D. Descending projections from the substantia nigra and retrorubral field to the medullary and pontomedullary reticular formation. Eur. J. Neurosci. 3 (1991) 260-273
53. von Krosigk M., Smith Y., Bolam J.P., and Smith A.D. Synaptic organization of GABAergic inputs from the striatum and the globus pallidus onto neurons in the substantia nigra and retrorubral field which project to the medullary reticular formation. Neuroscience 50 (1992) 531-549
54. Wallace D.M., Magnuson D.J., and Gray T.S. The amygdalo-brainstem pathway: selective innervation of dopaminergic, noradrenergic and adrenergic cells in the rat. Neurosci. Lett. 97 (1989) 252-258
55. Wallace D.M., Magnuson D.J., and Gray T.S. Organization of amygdaloid projections to brainstem dopaminergic, noradrenergic, and adrenergic cell groups in the rat. Brain Res. Bull. 28 (1992) 447-454
56. Yamamoto M., Moritani M., Chang Z., Taki I., Tomita A., Ono T., Bae Y.-C., Shigenaga Y., and Yoshida A. The somatotopic organization of trigeminal premotoneurons in the cat brainstem. Brain Res. 1149 (2007) 111-117
57. Yasui, Y., Nakano, K., Nakagawa, Y., Kayahara, T., Shiroyama, T., Mizuno, N., 1992. Non-dopaminergic neurons in the substantia nigra project to the reticular formation around the trigeminal motor nucleus in the rat. Brain Res. 585, 361-366.
58. Yasui Y., Tsumori T., Ono K., and Kishi T. Nigral axon terminals are in contact with parvicellular reticular neurons which project to the motor trigeminal nucleus in the rat. Brain Res. 775 (1997) 219-224
59. Yasui Y., Tsumori T., Oka T., and Yokota S. Amygdaloid axon terminals are in contact with trigeminal premotor neurons in the parvicellular reticular formation of the rat oblongata. Brain Res. 1016 (2004) 129-134