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Organization of cingulo-ponto-cerebellar connections in the cat

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Summary

This study deals with three different aspects of the organization of connections from the cingulate gyrus to the cerebellum. (1) With the use of wheat germ agglutinin-horseradish peroxidase as a retrograde tracer, the distribution of cingulate neurons projecting to the pontine nuclei was studied. Retrogradely labeled cells were found in layer 5 in all parts of the cingulate gyrus. Average densities of cingulopontine cells were similar in the different cytoarchitectonic subdivisions, although some density gradients were observed. The projection was found to be remarkably strong. Average densities of corticopontine cells in the cingulate gyrus ranged from 500–700 cells per mm2 cortical surface, and the total number of neurons was in the range of 75000–105000 (n=4). (2) A topographical organization of terminal fields of fibers originating in different parts of the cingulate gyrus was demonstrated with the combined use of anterograde degeneration and anterograde transport of wheat germ agglutinin-horseradish peroxidase. Terminal fibers originating in different zones of the cingulate gyrus were distributed in a patchy mosaic within a narrow band along the ventromedial aspect of the pontine nuclei. (3) We confirm, with the combined use of lesions in the cingulate gyrus and injections of wheat germ agglutinin-horseradish peroxidase in the ventral paraflocculus, that there is considerable overlap between terminal fibers originating in the cingulate gyrus, and cells retrogradely labeled from the ventral paraflocculus. The role of the ventral paraflocculus as a receiver of “limbic” input is discussed.

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References

  • Aas J-E, Brodal P (1988) Demonstration of topographically organized projections from the hypothalamus to the pontine nuclei: an experimental anatomical study in the cat. J Comp Neurol 268:313–328

    Google Scholar 

  • Aas J-E, Brodal P (1989) Demonstration of a mamillo-ponto-cerebellar pathway a multi-tracer study. Eur J Neurosci 1:61–74

    Google Scholar 

  • Abdel-Kader GA (1968) The organization of the cortico-pontine system of the rabbit. J Anat 102:165–181

    Google Scholar 

  • Anderson ME, DeVito JL (1987) An analysis of potentially converging inputs to the rostral ventral thalamic nucleus of the cat. Exp Brain Res 68:260–276

    Google Scholar 

  • Bjaalie JG (1985) Distribution in areas 18 and 19 of neurons projecting to the pontine nuclei: a quantitative study in the cat with retrograde transport of HRP-WGA. Exp Brain Res 57:585–597

    Google Scholar 

  • Bjaalie JG (1986) Distribution of corticopontine neurons in visual areas of the middle suprasylvian sulcus: Quantitative studies in the cat. Neuroscience 18:1013–1033

    Google Scholar 

  • Bjaalie JG (1989) The cortico pontine projection from area 20 and surrounding areas in the cat: terminal fields and distribution of cells of origin as compared to other visual cortical areas. Neuroscience 29:81–93

    Google Scholar 

  • Bjaalie JG (1990) The visual corticopontine system. Quantitative experimental neuroanatomical investigations in the cat. Thesis. Anatomical Institute, University of Oslo, Oslo

    Google Scholar 

  • Bjaalie JG, Brodal P (1983) Distribution in area 17 of neurons projecting to the pontine nuclei: a quantitative study in the cat with retrograde transport of HRP-WGA. J Comp Neurol 221:289–303

    Google Scholar 

  • Bjaalie JG, Brodal P (1989) Visual pathways to the cerebellum: segregation in the pontine nuclei of terminal fields from different visual cortical areas in the cat. Neuroscience 29:95–107

    Google Scholar 

  • Bjaalie JG, Diggle P (1990) Statistical analysis of corticopontine neuron distribution in visual areas 17, 18, and 19 of the cat. J Comp Neurol 295:15–32

    Google Scholar 

  • Bjaalie JG, Diggle PJ, Nikundiwe A, Karagülle T, Brodal P (1991) Spatial segregation between populations of pontocerebellar neurons. Statistical analysis of multivariate spatial interactions. Anat Rec (in press)

  • Blackstad TW, Bjaalie JG (1988) Computer programs for neuroanatomy: three-dimensional reconstruction and analysis of populations of cortical neurons and other bodies with a laminar distribution. Comput Biol Med 18:321–340

    Google Scholar 

  • Broch-Smith T, Brodal P (1990) Organization of the cortico-pontocerebellar pathway to the dorsal paraflocculus. An experimental study with anterograde and retrograde transport of WGA-HRP in the cat. Arch Ital Biol 128:249–271

    Google Scholar 

  • Brodal A, Høivik B (1964) Site and mode of termination of primary vestibulocerebellar fibres in the cat. An experimental study with silver impregnation methods. Arch Ital Biol 102:1–21

    Google Scholar 

  • Brodal P (1972) The corticopontine projection from the visual cortex in the cat. II. The projection from areas 18 and 19. Brain Res 39:319–335

    Google Scholar 

  • Brodal P (1978) The corticopontine projection in the rhesus monkey. Origin and principles of organization. Brain 101:251–283

    Google Scholar 

  • Brodal P (1982) The cerebropontocerebellar pathway: Salient features of its organization. In: Chan-Palay V, Palay S (eds) The Cerebellum — New Vistas. Exp Brain Res [Suppl 6] Springer, Berlin Heidelberg, pp 108–132

    Google Scholar 

  • Brodal P (1983) Principles of organization of the corticopontocerebellar projection to crus II in the cat with particular reference to the parietal cortical areas. Neuroscience 10:621–638

    Google Scholar 

  • Brodal P (1987) Organization of cerebropontocerebellar connections as studied with anterograde and retrograde transport of HRP-WGA in the cat. In: King JS (ed) New concepts in cerebellar Neurobiology. Liss, New York, pp 151–182

    Google Scholar 

  • Brodal P, Walberg F (1977) The pontine projection to the cerebellar anterior lobe. An experimental study in the cat with retrograde transport of horseradish peroxidase. Exp Brain Res 29:233–248

    Google Scholar 

  • Brooks VB (1986) How does the limbic system assist motor learning? A limbic comparator hypothesis. Brain Behav Evol 29:29–53

    Google Scholar 

  • Dhanarajan P, Rüegg DG, Wiesendanger M (1977) An anatomical investigation of the corticopontine projection in the primate (Saimiri sciureus). The projection from motor and somatosensory areas. Neuroscience 2:913–922

    Google Scholar 

  • Dietrichs E (1981) The cerebellar corticonuclear and nucleocortical projections in the cat as studied with anterograde and retrograde transport of horseradish peroxidase. Exp Brain Res 44:235–242

    Google Scholar 

  • Dietrichs E (1984) Cerebellar autonomic function: direct hypothalamocerebellar pathway. Science 223:591–593

    Google Scholar 

  • Dietrichs E, Haines DE (1989) Interconnections between hypothalamus and cerebellum. Anat Embryol 179:207–220

    Google Scholar 

  • Domesick VB (1969) Projections from the cingulate cortex in the rat. Brain Res 12:296–320

    Google Scholar 

  • Enger M, Brodal P (1985) Organization of corticopontocerebellar connections to the paramedian lobule in the cat. Anat Embryol 172:227–238

    Google Scholar 

  • Fink RP, Heimer L (1967) Two methods for selective silver impregnation of degenerating axons and their sysnaptic endings in the central nervous system. Brain Res 4:369–374

    Google Scholar 

  • Gerrits NM, Epema AH, Voogd J (1984) The mossy fiber projection of the nucleus reticularis tegmenti pontis to the flocculus and adjacent ventral paraflocculus in the cat. J Neurosci 11:627–644

    Google Scholar 

  • Glickstein M, May JG III, Mercier BE (1985) Corticopontine projection in the macaque: the distribution of labelled cortical cells after large injections of horseradish peroxidase in the pontine nuclei. J Comp Neurol 235:343–359

    Google Scholar 

  • Haines DE, Patrick GW, Satrulee P (1982) Organization of cerebellar corticonuclear fiber systems. Exp Brain Res [Suppl 6]:320–367

    Google Scholar 

  • Haines DE, Dietrichs E, Sowa TE (1986) Hypothalamo-cerebellar and cerebello-hypothalamic pathways: a review and hypothesis concerning cerebellar circuits which may influence autonomic centers and affective behavior. Brain Behav Evol 24:198–220

    Google Scholar 

  • Hoddevik GH (1978) The projection from the nucleus reticularis tegmenti pontins onto the cerebellum in the cat. Anat Embryol 153:227–242

    Google Scholar 

  • Isaacson RE (1982) The limbic system, 2nd edn. Plenum Press, New York

    Google Scholar 

  • Kalia M, Whitteridge D (1973) The visual areas in the splenial sulcus of the cat. J Physiol 232:275–283

    Google Scholar 

  • Korte GE, Mugnaini E (1979) The cerebellar projection of the vestibular nerve in the cat. J Comp Neurol 184:265–278

    Google Scholar 

  • Kotchabhakdi N, Walberg F (1978) Cerebellar afferent projections from the vestibular nuclei in the cat: an experimental study with the method of retrograde axonal transport of horseradish peroxidase. Exp Brain Res 31:591–604

    Google Scholar 

  • Leiner HC, Leiner AL, Dow RS (1986) Does the cerebellum contribute to mental skills? Behav Neurosci 100:443–454

    Google Scholar 

  • Mesulam M-M (1978) Tetramethyl benzidine for horseradish peroxidase neurochemistry: a non-carcinogenic blue reactionproduct with superior sensitivity for visualizing neural afferents and efferents. J Histochem Cytochem 26:106–117

    Google Scholar 

  • Mizuno N, Mochizuki K, Matsushima CAR, Sasaki K (1973) Projections from the parietal cortex to the brain stem nuclei in the cat, with special reference to the parietal cerebro-cerebellar system. J Comp Neurol 147:511–522

    Google Scholar 

  • Murray EA, Davidson M, Gaffan D, Olton DS, Suomi S (1989) Effects of fornix transection and cingulate cortical ablation on spatial memory in rhesus monkeys. Exp Brain Res 74:173–186

    Google Scholar 

  • Nikundiwe A, Bjaalie JG, Karagülle T, Blackstad TW, Brodal P (1989) Pontocerebellar connections to the dorsal and ventral paraflocculus. A multi-tracer and computer-reconstruction study in the cat. Eur J Neurosci [Suppl 2]:130

    Google Scholar 

  • Nudo RJ, Masterton RB (1990) Descending pathways to the spinal cord, III: Sites of origin of the corticospinal tract. J Comp Neurol 296:559–583

    Google Scholar 

  • Nyby O, Jansen J (1952) An experimental investigation of the corticopontine projection inMacaca mulatta. Skr Norske Videnskakad, I Mat-Nat Kl 3:1–47

    Google Scholar 

  • Øverby SE, Bjaalie JG, Brodal P (1989) Uneven densities of corticopontine neurons in the somatosensory cortex: a quantitative experimental study in the cat. Exp Brain Res 77:653–665

    Google Scholar 

  • Rose JE, Woolsey CN (1948) Structure and relations of the limbic cortex and anterior thalamic nuclei in the rabbit and cat. J Comp Neurol 89:279–347

    Google Scholar 

  • Rosenstock J, Field TD, Greene E (1977) The role of mammillary bodies in spatial memory. Exp Neurol 55:340–352

    Google Scholar 

  • Rosina A, Provini L (1987) Cerebellar transcommissural neurons. In: Glickstein M, Yeo C, Stein J (eds) Cerebellum and Neuronal Plasticity. Plenum Press, New York London, pp 63–82

    Google Scholar 

  • Saint-Cyr JA, Woodward DJ (1980a) A topographic analysis of limbic and somatic inputs to the cerebellar cortex in the rat. Exp Brain Res 40:13–22

    Google Scholar 

  • Saint-Cyr JA, Woodward DJ (1980b) Activation of mossy and climbing fiber pathways to the cerebellar cortex by stimulation of the fornix in the rat. Exp Brain Res 40:1–12

    Google Scholar 

  • Vilensky JA, Van Hoesen GW (1981) Corticopontine projections from the cingulate cortex in the rhesus monkey. Brain Res 205:391–395

    Google Scholar 

  • Wiesendanger R, Wiesendanger M (1982) The corticopontine system in the rat. I. Mapping of corticopontine neurons. J Comp Neurol 208:215–226

    Google Scholar 

  • Witter MP, Groenewegen HJ (1986) Connections of the parahippocampal cortex of the cat. IV. Subcortical efferents. J Comp Neurol 251:51–77

    Google Scholar 

  • Wyss JM, Sripanidkulchai K (1984) The topography of the mesencephalic and pontine projections from the cingulate cortex of the rat. Brain Res 293:1–15

    Google Scholar 

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This paper is dedicated to Professor Fred Walberg on the occasion of his 70th birthday

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Brodal, P., Bjaalie, J.G. & Aas, JE. Organization of cingulo-ponto-cerebellar connections in the cat. Anat Embryol 184, 245–254 (1991). https://doi.org/10.1007/BF01673259

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