Transneuronal pathways to the vestibulocerebellum

The α‐herpes virus (pseudorabies, PRV) was used to observe central nervous system (CNS) pathways associated with the vestibulocerebellar system. Retrograde transneuronal migration of α‐herpes virions from specific lobules of the gerbil and rat vestibulo‐cerebellar cortex was detected immunohistochemically. Using a time series analysis, progression of infection along polyneuronal cerebellar afferent pathways was examined. Pressure injections of >20 nanoliters of a 108 plaque forming units (pfu) per ml solution of virus were sufficient to initiate an infectious locus which resulted in labeled neurons in the inferior olivary subnuclei, vestibular nuclei, and their afferent cell groups in a progressive temporal fashion and in growing complexity with increasing incubation time. We show that climbing fibers and some other cerebellar afferent fibers transported the virus retrogradely from the cerebellum within 24 hours. One to three days after cerebellar infection discrete cell groups were labeled and appropriate laterality within crossed projections was preserved. Subsequent nuclei labeled with PRV after infection of the flocculus/paraflocculus, or nodulus/uvula, included the following: vestibular (e.g., z) and inferior olivary nuclei (e.g., dorsal cap), accessory oculomotor (e.g., Darkschewitsch n.) and accessory optic related nuclei, (e.g., the nucleus of the optic tract, and the medial terminal nucleus); noradrenergic, raphe, and reticular cell groups (e.g., locus coeruleus, dorsal raphe, raphe pontis, and the lateral reticular tract); other vestibulocerebellum sites, the periaqueductal gray, substantia nigra, hippocampus, thalamus and hypothalamus, amygdala, septal nuclei, and the frontal, cingulate, entorhinal, perirhinal, and insular cortices. However, there were differences in the resulting labeling between infection in either region. Double‐labeling experiments revealed that vestibular efferent neurons are located adjacent to, but are not included among, flocculus‐projecting supragenual neurons. PRV transport from the vestibular labyrinth and cervical muscles also resulted in CNS infections. Virus propagation in situ provides specific connectivity information based on the functional transport across synapses. The findings support and extend anatomical data regarding vestibulo‐olivo‐cerebellar pathways. © 1996 Wiley‐Liss, Inc.

[1]  F A Miles,et al.  THE “ERROR” SIGNALS SUBSERVING ADAPTIVE GAIN CONTROL IN THE PRIMATE VESTIBULO‐OCULAR REFLEX , 1981, Annals of the New York Academy of Sciences.

[2]  E. Irle,et al.  Afferents to the ventral tegmental nucleus of gudden in the mouse, rat, and cat , 1984, The Journal of comparative neurology.

[3]  D. Robinson Movement control: Implications of neural networks for how we think about brain function , 1992 .

[4]  J. Cadet,et al.  Involvement of nigrotecto-reticulospinal pathways in the iminodipropionitrile (IDPN) model of spasmodic dyskinesias: a 2-deoxy-d-[1-14C]glucose study in the rat , 1989, Brain Research.

[5]  J R Augustine,et al.  The insular lobe in primates including humans. , 1985, Neurological research.

[6]  J. Cornwall,et al.  Afferent and efferent connections of the laterodorsal tegmental nucleus in the rat , 1990, Brain Research Bulletin.

[7]  E. Aantaa,et al.  Studies of vestibular cortical areas with short-living 15O2 isotopes. , 1983, ORL; journal for oto-rhino-laryngology and its related specialties.

[8]  N. Gerrits,et al.  The rostral dorsal cap and ventrolateral outgrowth of the rabbit inferior olive receive a GABAergic input from dorsal group Y and the ventral dentate nucleus , 1994, The Journal of comparative neurology.

[9]  S G Lisberger,et al.  The neural basis for learning of simple motor skills. , 1988, Science.

[10]  W. Precht,et al.  Anatomical studies on the nucleus reticularis tegmenti pontis in the pigmented rat. I. Cytoarchitecture, topography, and cerebral cortical afferents , 1986, The Journal of comparative neurology.

[11]  O B Paulson,et al.  Focal increase of blood flow in the cerebral cortex of man during vestibular stimulation. , 1985, Brain : a journal of neurology.

[12]  M. Ito,et al.  Neural design of the cerebellar motor control system. , 1972, Brain research.

[13]  M. Caria,et al.  Vestibular projections to hypothalamic supraoptic and paraventricular nuclei. , 1993, Archives italiennes de biologie.

[14]  P. Strick,et al.  Multiple output channels in the basal ganglia. , 1993, Science.

[15]  G. Tseng,et al.  Efferent connections from the external cuneate nucleus to the medulla oblongata in the gerbil , 1994, Brain Research.

[16]  J. S. Schneider,et al.  Substantia nigra projection to medullary reticular formation: Relevance to oculomotor and related motor functions in the cat , 1985, Neuroscience Letters.

[17]  R. Vertes,et al.  Projections of the dorsal raphe nucleus to the brainstem: PHA‐L analysis in the rat , 1994, The Journal of comparative neurology.

[18]  P E Sharp,et al.  Influences of vestibular and visual motion information on the spatial firing patterns of hippocampal place cells , 1995, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[19]  J. Simpson,et al.  The accessory optic system of rabbit. I. Basic visual response properties. , 1988, Journal of neurophysiology.

[20]  E. Mugnaini,et al.  Fine structure of the dorsal cap of the inferior olive and its GAB aergic and non‐Gabaergic input from the nucleus prepositus hypoglossi in rat and rabbit , 1993, The Journal of comparative neurology.

[21]  J. Bernard Topographical organization of olivocerebellar and corticonuclear connections in the rat—An WGA‐HRP study: I. Lobules IX, X, and the flocculus , 1987, The Journal of comparative neurology.

[22]  N. Delhaye-bouchaud,et al.  Enlargement of olivo-cerebellar microzones in the agranular cerebellum of adult rats , 1994, Brain Research.

[23]  Jean K. Moore,et al.  Nigrotectal projection to the inferior colliculus: Horseradish peroxidase transport and tyrosine hydroxylase immunohistochemical studies in rats, cats, and bats , 1989, The Journal of comparative neurology.

[24]  D. Pélisson,et al.  Vestibuloocular reflex inhibition and gaze saccade control characteristics during eye-head orientation in humans. , 1988, Journal of neurophysiology.

[25]  A. Robbins,et al.  Specific pseudorabies virus infection of the rat visual system requires both gI and gp63 glycoproteins , 1993, Journal of virology.

[26]  E. Dietrichs,et al.  The interconnection between the vestibular nuclei and the nodulus: a study of reciprocity , 1988, Brain Research.

[27]  O J Grüsser,et al.  Thalamic connections of the vestibular cortical fields in the squirrel monkey (Saimiri sciureus) , 1992, The Journal of comparative neurology.

[28]  R. Blanks,et al.  Projections of medial terminal accessory optic nucleus, ventral tegmental nuclei, and substantia nigra of rabbit and rat as studied by retrograde axonal transport of horseradish peroxidase , 1985, The Journal of comparative neurology.

[29]  G. Blatt,et al.  The olivocerebellar projection to the uvula in the mouse , 1983, The Journal of comparative neurology.

[30]  O. Grüsser,et al.  Corticofugal connections between the cerebral cortex and brainstem vestibular nuclei in the macaque monkey , 1994, The Journal of comparative neurology.

[31]  J. Schwaber,et al.  Neurotropic properties of pseudorabies virus: uptake and transneuronal passage in the rat central nervous system , 1990, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[32]  A. Fuchs,et al.  Floccular efferents in the rhesus macaque as revealed by autoradiography and horseradish peroxidase , 1985, The Journal of comparative neurology.

[33]  Isao Kato,et al.  Direct projection from the nucleus of the optic tract to the medial vestibular nucleus in the cat , 1993, Neuroscience Research.

[34]  O. Pompeiano,et al.  Responses of locus coeruleus neurons to convergent neck and vestibular inputs. , 1989, Acta oto-laryngologica. Supplementum.

[35]  Detection of pseudorabies virus DNA in the inner ear of intranasally infected BALB/c mice with nucleic acid hybridization in situ , 1986, Journal of virology.

[36]  G. Holstege,et al.  Dorsal mesencephalic projections to pons, medulla, and spinal cord in the cat: Limbic and non‐limbic components , 1992, The Journal of comparative neurology.

[37]  P. Buisseret,et al.  The X zone and CX subzone of the cerebellum in the rat , 1993, Neuroscience Research.

[38]  A. Fuchs,et al.  Anatomical connections of the primate pretectal nucleus of the optic tract , 1994, The Journal of comparative neurology.

[39]  J H Anderson,et al.  Brainstem Fos expression following acute unilateral labyrinthectomy in the rat. , 1992, Neuroreport.

[40]  A. Loewy,et al.  CNS innervation of airway-related parasympathetic preganglionic neurons: a transneuronal labeling study using pseudorabies virus , 1993, Brain Research.

[41]  Richard F. Thompson,et al.  Lesions of the inferior olivary complex cause extinction of the classically conditioned eyeblink response , 1985, Brain Research.

[42]  K. Semba,et al.  Dual projections of single cholinergic and aminergic brainstem neurons to the thalamus and basal forebrain in the rat , 1993, Brain Research.

[43]  J. Saint-Cyr,et al.  Comparative topography of projections from the mesodiencephalic junction to the inferior olive, vestibular nuclei, and upper cervical cord in the cat , 1988, The Journal of comparative neurology.

[44]  T. Kubo,et al.  Neuropharmacology of motion sickness and emesis. A review. , 1993, Acta oto-laryngologica. Supplementum.

[45]  L. Rinaman,et al.  Pseudorabies virus infection of the rat central nervous system: ultrastructural characterization of viral replication, transport, and pathogenesis , 1993, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[46]  W. Precht,et al.  Anatomical studies on the nucleus reticularis tegmenti pontis in the pigmented rat. II. Subcortical afferents demonstrated by the retrograde transport of horseradish peroxidase , 1986, The Journal of comparative neurology.

[47]  Q. Pittman,et al.  Vasopressin-induced motor effects: Localization of a sensitive site in the amygdala , 1992, Brain Research.

[48]  B. J. Yates,et al.  Responses of neurons in the rostral ventrolateral medulla of the cat to natural vestibular stimulation , 1993, Brain Research.

[49]  L. Enquist,et al.  Two α-herpesvirus strains are transported differentially in the rodent visual system , 1991, Neuron.

[50]  A. Wilson,et al.  Transneuronal labelling of CNS neurons with herpes simplex virus , 1994, Progress in Neurobiology.

[51]  G. Kaufman,et al.  Fos-defined activity in rat brainstem following centripetal acceleration , 1992, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[52]  A. Fuchs,et al.  Afferents to the flocculus of the cerebellum in the rhesus macaque as revealed by retrograde transport of horseradish peroxidase , 1985, The Journal of comparative neurology.

[53]  N. Takeda,et al.  Effect of unilateral vestibular stimulation on histamine release from the hypothalamus of rats in vivo. , 1993, Journal of neurophysiology.

[54]  R. Swenson,et al.  The afferent connections of the inferior olivary complex in rats. An anterograde study using autoradiographic and axonal degeneration techniques , 1983, Neuroscience.

[55]  G. C. Thompson,et al.  Distribution and origin of serotoninergic afferents to guinea pig cochlear nucleus , 1995, The Journal of comparative neurology.

[56]  A. Loewy,et al.  CNS cell groups projecting to the submandibular parasympathetic preganglionic neurons in the rat: a retrograde transneuronal viral cell body labeling study , 1992, Brain Research.

[57]  J. Voogd,et al.  Organization of inferior olivary projections to the flocculus and ventral paraflocculus of the rat cerebellum , 1992, The Journal of comparative neurology.

[58]  S. Lisberger,et al.  Neural basis for motor learning in the vestibuloocular reflex of primates. I. Changes in the responses of brain stem neurons. , 1994, Journal of neurophysiology.

[59]  J. Adams,et al.  GABAergic neurons in the mammalian inferior olive and ventral medulla detected by glutamate decarboxylase immunocytochemistry , 1992, The Journal of comparative neurology.

[60]  D. Armstrong,et al.  Firing patterns of Purkinje cells in the cat cerebellum for different maintained positions of the limbs. , 1973, Brain research.

[61]  R. Tomlinson,et al.  Combined eye-head gaze shifts in the primate. II. Interactions between saccades and the vestibuloocular reflex. , 1986, Journal of neurophysiology.

[62]  J. Card,et al.  Spatiotemporal responses of astrocytes, ramified microglia, and brain macrophages to central neuronal infection with pseudorabies virus , 1993, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[63]  K. Brizzee,et al.  Conditioned taste aversion and motion sickness in cats and squirrel monkeys 1.2 , 2022 .

[64]  R. Llinás,et al.  Oscillatory properties of guinea‐pig inferior olivary neurones and their pharmacological modulation: an in vitro study. , 1986, The Journal of physiology.

[65]  H. Fujisawa,et al.  The accessory optic system of rodents: A whole‐mount HRP study , 1984, The Journal of comparative neurology.

[66]  P. Strick,et al.  Anatomical evidence for cerebellar and basal ganglia involvement in higher cognitive function. , 1994, Science.

[67]  A. Perachio,et al.  Translabyrinth electrical stimulation for the induction of immediate-early genes in the gerbil brainstem , 1994, Brain Research.

[68]  L. Schramm,et al.  Peripheral and central pathways regulating the kidney: a study using pseudorabies virus , 1993, Brain Research.

[69]  G. Volsi,et al.  Effects of noradrenaline on the firing rate of vestibular neurons , 1993, Neuroscience.

[70]  C. I. Zeeuw,et al.  Olivary projecting neurons in the nucleus of Darkschewitsch in the cat receive excitatory monosynaptic input from the cerebellar nuclei , 1994, Brain Research.

[71]  L. Enquist,et al.  Innervation of the heart and its central medullary origin defined by viral tracing. , 1994, Science.

[72]  A. Berthoz,et al.  Neurons responding to whole-body motion in the primate hippocampus , 1994, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[73]  G. Ugolini Specificity of rabies virus as a transneuronal tracer of motor networks: Transfer from hypoglossal motoneurons to connected second‐order and higher order central nervous system cell groups , 1995, The Journal of comparative neurology.

[74]  A. Loewy,et al.  A general pattern of CNS innervation of the sympathetic outflow demonstrated by transneuronal pseudorabies viral infections , 1989, Brain Research.

[75]  N. Barmack,et al.  Cholinergic projection to the dorsal cap of the inferior olive of the rat, rabbit, and monkey , 1993, The Journal of comparative neurology.

[76]  A. Loewy,et al.  CNS projections to the pterygopalatine parasympathetic preganglionic neurons in the rat: a retrograde transneuronal viral cell body labeling study , 1990, Brain Research.