Possible Pathways for Cerebellar Modulation of Autonomic Responses: Micturition

REFERENCES

• Schmahmann JD, Sharman JC. The cerebellar cognitive affective syndrome. Brain 1998; 121: 561–79.
   PubMed Web of Science ®Google Scholar
• Moruzzi G. Paleocerebellar inhibition of vasomotor and respiratory carotid sinus reflexes. J Neurophysiol 1940; 3: 20–31.
   Google Scholar
• Moruzzi G. Problems in cerebellar physiology. Spring-field: Thomas; 1950.
   Google Scholar
• Chambers WW. Electrical stimulation of the interior of the cerebellum in the cat. Am J Anat 1947; 80: 55–93.
   PubMedGoogle Scholar
• Zanchetti A, Zoccolini A. Autonomic hypothalamic outbursts elicited by cerebellar stimulation. J Neurophy-siol 1954; 17: 475–83.
   PubMed Web of Science ®Google Scholar
• Chambers WW, Sprague TM. Functional localization in the cerebellum. I: Organization in longitudinal cortico-nuclear zones and their contribution to the control of posture, both extrapyramidal and pyramidal. J Comp Neurol 1955; 103: 105–29.
   Google Scholar
• Chambers WW, Sprague TM. Functional localization in the cerebellum. II: Somatotopic organization in the cortex and nuclei. Arch Neurol Psychiat 1955; 74: 653–80.
   PubMedGoogle Scholar
• Ban TK, Inoue S, Ozaki S, Kurotsu T. Interrelation between anterior lobe cerebellum and hypothalamus in rabbit. Med J Osaka Univ 1956; 7: 101–15.
   Google Scholar
• Dow RS, Moruzzi G. The physiology and pathology of the cerebellum. Minneapolis: Univ Minnesota Press; 1958.
   Google Scholar
• Miura M, Reis DJ. Cerebellum: A pressor response elicited from the fastigial nucleus and its efferent pathway in brain stem. Brain Res 1969; 13: 595–9.
   PubMed Web of Science ®Google Scholar
• Martner J. Cerebellar influences on cerebellar mechan-isms. Acta Physiol Scand 1975; (Suppl 425): 1–42.
   Google Scholar
• Bradley WE, Teague CT. Cerebellar influence on the micturition reflex. Exp Neurol 1969; 23: 399–411.
   PubMed Web of Science ®Google Scholar
• Nishizawa O, Ebina K, Sugaya K, Noto H, Satoh K, Kohama T, Harada T, Tsuchida S. Effect of cerebellec-tomy on reflex micturition in the decerebrate dog as determined by urodynamic evaluation. Urol Int 1989; 44: 152–6.
   PubMed Web of Science ®Google Scholar
• Nardulli R, Monitillo V, Losavio E, Fiore P, Nicolardi G, Megna G. Urodynamic evaluation of 12 ataxic subjects: neurophysiopathologi c considerations. Funct Neurol 1992; 7: 223–5.
   PubMedGoogle Scholar
• Siffert J, Poussaint TY, Goumnerova LC, Scott RI\4, LaValley B, Tarbell NJ, Pomeroy SL. Neurological dysfunction associated with postoperative cerebellar mutism. J Neurooncol 2000; 48: 75–81.
   Google Scholar
• Golanov EV, Reis DJ. Vasodilation evoked from medulla and cerebellum is coupled to bursts of cortical EEG activity in rats. Am J Physiol 1995; 268: R454–67.
   PubMedGoogle Scholar
• Gjone R, Setekleiv J. Exitatory and inhibitory responses to stimulation of the cerebral cortex of the cat. Acta Physiol Scand 1963; 95: 337–48.
   Google Scholar
• Andrew J, Nathan PW. Lesions of the anterior frontal lobes and disturbances of micturition and defaecation. Brain 1964; 87: 233–62.
   PubMed Web of Science ®Google Scholar
• Maurice-Williams RS. Micturition symptoms in frontal tumours. J Neurol Neurosurg Psychiat 1974; 37: 431–6.
   PubMed Web of Science ®Google Scholar
• Marson L. Identification of central nervous system neurons that innervate the bladder body, bladder base, or external urethral sphincter of female rats: a transneuronal
   Google Scholar
• Zermann D-H, Ishigooka M, Doggweiler R, Schmidt RA. Central autonomic innervation of the lower urinarytract—a neuroanatomy study. World J Urol 1998; 16: 417–22.
   Google Scholar
• Grill WM, Erokwu BO, Hadziefendic S, Haxhiu MA. Extended survival time following pseudorabies virus injection labels the suprapontine neural network controlling the bladder and urethra in the rat. Neurosci Lett 1999; 270: 63–6.
   PubMed Web of Science ®Google Scholar
• Blok BF, Willemsen AT, Holstege G. A PET study on brain control of micturition in humans. Brain 1997; 120: 111–21.
   PubMed Web of Science ®Google Scholar
• Blok BFM, Hostege G. The central nervous system control of micturition in cats and humans. Behav Brain Res 1998; 92: 119–25.
   PubMed Web of Science ®Google Scholar
• Schmahmann JD, Pandya DN. The cerebrocerebellar system. Int Rev Neurobiol 1997; 41: 31–60.
   PubMed Web of Science ®Google Scholar
• Dietrichs E. Cerebellar autonomic function: Direct hypothalamocerebellar pathway. Science 1984; 223: 591–3.
   PubMed Web of Science ®Google Scholar
• Haines DE, Dietrichs E. An HRP study of hypothala-mocerebellar and cerebellohypothalamic connections in squirrel monkey (Saimiri squireus). J Comp Neurol
   Google Scholar
• Haines DE, Dietrichs E, Sowa TE. Hypothalamocere-bellar and cerebellohypothalamic pathways: A review and hypothesis concerning cerebellar circuits which may in uence autonomic centers and affective behavior. Brain Behav Evol 1984; 24: 198–220.
   Google Scholar
• Haines DE, May PJ, Dietrichs E. Neuronal connections between the cerebellar nuclei and hypothalamus in Macaca fascicularis: Cerebello-visceral circuits. J Comp Neurol 1990; 299: 106–22.
   Google Scholar
• Dietrichs E, Røste GK, R ste LS, Qvist HL, Haines DE. The hypothalamocerebellar projection in the cat: Branching and nuclear termination. Arch Ital Biol
   Google Scholar
• Dietrichs E, Zheng Z-H. Are hypothalamo-cerebellar fibres collaterals from the hypothalamo-spinal projec-
   Google Scholar
• Dietrichs E, Haines DE. Do the same hypothalamic neurons project to both amygdala and cerebellum? Brain
   Google Scholar
• Dietrichs E, Haines DE. Do hypothalamocerebellar fibres terminate in all layers of the cerebellar cortex?
   Google Scholar
• Haines DE, Dietrichs E, Culberson JL, Sowa TE. The organization of hypothalamocerebellar cortical fibres in
   Google Scholar
• Panula P, Pirvola U, Auvinen S, Airaksinen MS. Histamine-immunoreactive nerve fibers and terminals
   Google Scholar
• Panula P, Tagaki H, Yamalodani A, Tokyama M, Wada H, Kotlainen E. Histamine-containing nerve fibers innervate human cerebellum. Neurosci Lett 1993; 160:
   Web of Science ®Google Scholar
• Li W-C, Tang X-H, Li H-Z, Wang J-J. Histamine excites rat cerebellar granule cells in vitro through H1 and H2 receptors. J Physiol 1999; 93: 239–44.
   Google Scholar
• Tian L, Wen Y-Q, Li H-Z, Zuo C-C, Wang J-J. Histamine excites rat cerebellar Purkinje cells via H2 receptors in vitro. Neurosci Res 2000; 36: 61–6.
   Google Scholar
• Dietrichs E, Haines DE. Demonstration of hypothala-mocerebellar and cerebellohypothalamic fibres in a prosimian primate (Galago crassicaudatus). Anat Embryo' 1984; 170: 313–8.
   PubMedGoogle Scholar
• Cavdar S, San T, Aker R, Sehirli U, Onat F. Cerebellar connections to the dorsomedial and posterior nuclei of the hypothalamus in the rat. J Anat 2001; 198: 37–45.
   Google Scholar
• Dietrichs E, Haines DE, Røste GK, Røste LS. Hypotha-lamocerebellar and cerebellohypothalamic projections: Circuits for regulating nonsomatic cerebellar activity? Histol Histopathol 1994; 9: 603–14.
   Google Scholar
• Haines DE, Dietrichs E, Mihailoff GA, McDonald EF. The cerebellar-hypothalamic axis: Basic circuits and clinical observations. Int Rev Neurobiol 1997; 41: 83–107.
   PubMed Web of Science ®Google Scholar
• Aas J-E, Brodal P. Demonstration of topographically organized projections from the hypothalamus to the pontine nuclei: An experimental anatomical study in the cat. J Comp Neurol 1988; 268: 313–28.
   Google Scholar
• Aas J-E, Brodal P. Demonstration of a mamillo-ponto-cerebellar pathway. Eur J Neurosci 1989; 1: 61–74.
   PubMedGoogle Scholar
• Haines DE, Dietrichs E. On the organization of interconnections between the cerebellum and hypotha-lamus. In: King JS, editor. New concepts in cerebellar neurobiology. New York: Alan R Liss; 1987. p. 113–49.
   Google Scholar
• Haines DE, Dietrichs E. Non-somatic cerebellar circuits: A broader view of cerebellar involvement in locomotion. J Motor Behav 1989; 21: 518–25.
   PubMed Web of Science ®Google Scholar
• Dietrichs E, Haines DE. Interconnections between hypothalamus and cerebellum. Anat Embryo' 1989; 179: 207–20.
   PubMedGoogle Scholar
• Min B-I, Oomura Y, Katafuchi T. Responses of lateral hypothalamic neuronal activity to fastigial nucleus stimulation. J Neurophysiol 1989; 61: 1178–84.
   Google Scholar
• Katafuchi T, Koizumi K. Fastigial inputs to paraven-tricular neurosecretory neurones studied by extra- and intracellular recordings in rats. J Physiol 1990; 421: 535–51.
   PubMed Web of Science ®Google Scholar
• Pu Y-M, Wang J-J, Wang T, Yu Q-X. Cerebellar interpositus nucleus modulates neuronal activity of lateral hypothalamic area. NeuroReport 1995; 6: 985–8.
   Google Scholar
• Dietrichs E. Cerebellar cortical afferents from the periaqueductal grey in the cat. Neurosci Lett 1983; 41: 21–6.
   PubMed Web of Science ®Google Scholar
• Barrington FJF. The effect of lesions of the hind- and mid-brain on micturition in the cat. Q J Exp Physiol Cogn Med 1925; 15: 81–102.
   Google Scholar
• Nishizawa O, Sugaya K, Shimoda N. Pontine and spinal modulation of the micturition reflex. Scand J Urol Nephrol 1995; 29 (Suppl 175): 15–9.
   PubMedGoogle Scholar
• Valentino RJ, Miselis RR, Pavcovich LA. Pontine regulation of pelvic viscera: pharmacological target for pelvic visceral dysfunction. Trends Pharmacol Sci 1999; 20: 253–60.
   Google Scholar
• Rocha I, Bumstock G, Spyer KM. Effects on urinary bladder function and arterial blood pressure of the activation of putative purine receptors in brainstem areas. Auton Neurosci 2001; 88: 6–15.
   Google Scholar
• Dietrichs E. Divergent axon collaterals to cerebellum and amygdala from neurons in the parabrachial nucleus, the nucleus locus coeruleus and some adjacent nuclei. Anat Embryo' 1985; 172: 375–82.
   PubMedGoogle Scholar
• Homma Y, Nonaka S, Matsuyama K, Mori S. Fastigio-fugal projections to the brainstem nuclei in the cat: an anterograde PHA-L tracing study. Neurosci Res 1995; 23: 89–102.
   PubMedGoogle Scholar
• Teune TM, van der Burg J, van der Moer J, Voogd J, Ruigrok TJH. Topography of cerebellar nuclear projec-tions to the brain stem in the rat. Progr Brain Res 2000; 124: 141–72.
   PubMedGoogle Scholar
• Dietrichs E. Cerebellar cortical and nuclear afferents from the feline locus coeruleus complex. Neuroscience 1988; 27: 77–91.
   PubMed Web of Science ®Google Scholar
• Olson L, Fuxe K. On the projections from the locus coeruleus noradrenaline neurons: the cerebellar innerva-tion. Brain Res 1971; 28: 165–71.
   PubMed Web of Science ®Google Scholar
• Foote SL, Bloom Fb„ Aston-Jones G. Nucleus locus ceruleus: new evidence of anatomical and physiological specificity. Physiol Rev 1983; 63: 844–914.
   Google Scholar
• Del Bo A, Rosina A. Potential disynaptic pathways connecting the fastigial pressor area and the paraven-tricular nucleus of the hypothalamus in the rat. Neurosci Lett 1986; 71: 37–42.
   PubMed Web of Science ®Google Scholar
• Carpenter MB, Batton RR III. Connections of the fastigial nucleus in the cat and monkey. Exp Brain Res 1982; (Suppl 6): 250–91.
   Google Scholar
• Andrezik JA, Dormer KJ, Foreman RD, Person RJ. Fastigial nucleus projections to the brain stem in beagles: pathway for autonomic regulation. Neuroscience 1984; 11: 497–507.
   PubMed Web of Science ®Google Scholar
• Newman DB, Ginsberg CY. Brainstem reticular nuclei that project to the cerebellum in rats: a retrograde tracer study. Brain Behav Evol 1992; 39: 24–68.
   PubMed Web of Science ®Google Scholar
• Pierce ET, Hoddevik GH, Walberg F. The cerebellar projection from the raphe nuclei in the cat as studied with the method of retrograde transport of horseradish peroxidase. Anat Embryol 1977; 152: 73–87.
   Google Scholar
• Kotchabhakdi N, Hoddevik GH, Walberg F. The reticulocerebellar projection in the cat as studied with retrograde transport of horseradish peroxidase. Anat Embryol 1980; 160: 341–59.
   Google Scholar
• Zheng Z-H, Dietrichs E, Walberg F. Cerebellar afferent fibres from the dorsal motor vagal nucleus in the cat. Neurosci Lett 1982; 32: 113–8.
   Google Scholar
• Somana R, Walberg F. Cerebellar afferents from the nucleus of the solitary tract. Neurosci Lett 1979; 11: 41–7.
   PubMed Web of Science ®Google Scholar
• Harper R1\4, Woo MA, Alger JR. Visualization of sleep influences on cerebellar and brainstem cardiac and respiratory control mechanisms. Brain Res Bull 2000; 53: 125–31.
   Google Scholar
• Blok BF, Sturms LM, Hostege G. A PET study on cortical and subcortical control of pelvic floor muscu-lature in women. J Comp Neurol 1997; 389: 535–44.
   Google Scholar