Summary
Neuronal cell populations giving rise to cerebellar projections in the turtle, Pseudemys scripta elegans, were analysed following injections of horseradish peroxidase into the cerebellar cortex. The most prominent retrograde cell labeling occurred bilaterally within the caudal rhombencephalon and especially in the ventral portion of the inferior reticular field. Based on the structural parameters of the labeled cells (size, dendritic tree), their location and laterality of projection, attempts were made to identify cell groups similar to the inferior olive, the lateral funicular (reticular) nucleus and the perihypoglossal complex of other vertebrates. There were some labeled neurons within the descending and principal trigeminal nuclei, but few if any within the dorsal column nuclear complex. Cerebellar projections on the other hand clearly arose from the n.vestibularis inferior and n.vestibularis dorsolateralis on both sides.
While there was little evidence for labeled cells located in a similar position as the pontine nuclei of higher vertebrates, a conspicuous number of neurons were observed in meso-diencephalic regions. Confirming the findings of Reiner and Karten (1978) characteristic accumulations of cells were seen in the nucleus opticus tegmenti, in the ipsilateral mesencephalic tegmentum and lateral and ventral to the ipsilateral nucleus pretectalis. Additional neurons were found in the periventricular hypothalamus, the nucleus of the fasciculus longitudinalis medialis and in the n.interstitialis of flm on both sides as well as in the red nucleus.
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Abbreviations
- A:
-
rhombencephalic cell population
- Ab:
-
n.nervi abducentis
- Ap:
-
cell population at the spino-medullary level
- B:
-
rhombencephalic cell population
- C:
-
rhombencephalic cell population
- Cbl:
-
cerebellum
- CoM:
-
n.cochlearis dorsalis magnocellularis
- D:
-
rhombencephalic cell population
- DC:
-
dorsal column nuclear complex
- Fa:
-
n.nervi facialis
- FLM:
-
n. of flm
- flm:
-
fasciculus longitudinalis medialis
- GL:
-
n.geniculatus lateralis
- Hg:
-
n.motorius nervi hypoglossi
- Hy:
-
hypothalamus
- ICP:
-
n.interstitialis commissuralis posterior
- IFLM:
-
n.interstitialis of flm
- IsM:
-
n. isthmi, pars magnocellularis
- MTg:
-
mesencephalic tegmentum
- Om:
-
n.nervi oculomotorii
- om:
-
nervus oculomotorius
- OT:
-
optic tectum
- ot:
-
optic tract
- OTg:
-
n.opticus tegmenti
- PHg:
-
perihypoglossal region
- PrT:
-
pretectum
- Prt:
-
n.praetectalis
- RaI:
-
n.raphes inferior
- RaS:
-
n.raphes superior
- RFI:
-
reticular formation, inferior field
- RFIs:
-
reticular formation, isthmic field
- RFM:
-
reticular formation, medial field
- Ru:
-
n.ruber
- So:
-
n.tractus solitarii
- To:
-
n.nervi trochlearis
- tr:
-
nervus trigeminus
- TrM:
-
n.motorius nervi trigemini
- TrMe:
-
n.mesencephalicus nervi trigemini
- TrP:
-
n.princeps nervi trigemini
- VeDl:
-
n.vestibularis dorsolateralis
- VeI:
-
n.vestibularis inferior
- VeVl:
-
n.vestibularis ventrolateralis
- VgMD:
-
n.motorius dorsalis nervi vagi
References
Andrezik JA, King JS (1977) The lateral reticular nucleus of the opossum (Didelphis virginiana). I. Conformation, cytology and synaptology. J Comp Neurol 174: 119–150
Armstrong DM (1974) Functional significance of connections of the inferior olive. Physiol Rev 54: 358–417
Bangma GC, ten Donkelaar HJ, de Boer-van Huizen R, Pellegrino A (1981) Afferent connections of the cerebellum in various types of reptiles. Neurosci Lett 7: S119
Bortolami RE, Callegari E, Lucchi ML (1972) Anatomical relationship between mesencephalic trigeminal nucleus and cerebellum in the duck. Brain Res 47: 317–329
Brauth SE, Karten HJ (1977) Direct accessory optic projections to the vestibulo-cerebellum: A possible channel for oculomotor control systems. Exp Brain Res 28: 73–84
Brodal A, Kawamura K (1980) Olivocerebellar projection: A review. Adv Anat Embryol Cell Biol 64: 1–140
Brodal A, Kristiansen K, Jansen J (1950) Experimental demonstration of a pontine homologue in birds. J Comp Neurol 92: 23–69
Brodal P (1980) The cortical projection to the nucleus reticularis tegmenti pontis in the rhesus monkey. Exp Brain Res 38: 19–28
Brodal P (1982) Further observations on the cerebellar projections from the pontine nuclei and the nucleus reticularis tegmenti pontis in the rhesus monkey. J Comp Neurol 204: 44–55
Chan-Palay V (1977) Cerebellar dentate nucleus; organization, cytology and transmitter. Springer, Berlin Heidelberg New York
Chiba M (1980) Patterns of organization of comments on the corticopontine projection in the cat with the pontocerebellar projection. J Hirnforsch 21: 89–99
Clarke PGH (1977) Some visual and other connections to the cerebellum of the pigeon. J Comp Neurol 174: 535–552
Cochran SL, Hackett JT (1977) The climbing fiber afferent system of the frog. Brain Res 121: 362–367
Courville J, Brodal A (1966) Rubro-cerebellar connections in the cat: An experimental study with silver impregnation methods. J Comp Neurol 126: 471–486
Courville J, de Montigny C, Lamarre Y (1980) The inferior olivary nucleus. Anatomy and physiology. Raven Press, New York
Cruce WLR, Nieuwenhuys R (1974) The cell masses in the brain stem of the turtle Testudo hermanni; a topographical and topological analysis. J Comp Neurol 156: 277–306
Crutcher KA, Humbertson AO Jr, Martin GF (1978) The origin of brainstem-spinal pathways in the North American Opossum (Didelphis virginiana). Studies using the horseradish peroxidase method. J Comp Neurol 179: 169–194
Dietrichs E, Walberg F (1979) The cerebellar projection from the lateral reticular nucleus as studied with retrograde transport of horseradish peroxidase. Anat Embryol (Berl) 155: 273–290
Donkelaar HJ ten, Kusama A, de Boer-van Huizen R (1980) Cells of origin of pathways descending to the spinal cord in some quadrupedal reptiles. J Comp Neurol 192: 827–851
Dubbeldam JL, Karten HJ (1978) The trigeminal system in the pigeon (Columba livia). I. Projections of the Gasserian Ganglion. J Comp Neurol 180: 661–678
Ebbesson SOE (1969) Brain stem afferents from the spinal cord in a sample of reptilian and amphibian species. Ann NY Acad Sci 167: 80–101
Finger TE (1978) Cerebellar afferents in teleost catfish (Ictaluridae). J Comp Neurol 181: 173–182
Freedman SL, Voogd J, Vielvoye GJ (1977) Experimental evidence for climbing fibers in the avian cerebellum. J Comp Neurol 175: 243–252
Fuller PM (1974) Projections of the vestibular complex in the bullfrog (Rana catesbeiana). Brain Behav Evol 10: 157–169
Gould BB (1980) Organization of afferents from the brain stem nuclei to the cerebellar cortex in the cat. Adv Anat Embryol Cell Biol 62: 1–90
Gray TS, Hazlett JC, Martin GF (1981) Organization of projections from the gracile, medial cuneate and lateral cuneate nuclei in the North American Opossum. Horseradish peroxidase study of the cells projecting to the cerebellum, thalamus and spinal cord. Brain Behav Evol 18: 140–156
Griffin G, Watkins LR, Mayer DJ (1979) HRP pellet and slow-release gels: Two new techniques for greater localization and sensitivity. Brain Res 168: 595–601
Groenewegen HJ, Voogd J (1979) The parasagittal zonation within the olivocerebellar projection. I. Climbing fiber distribution in the vermis of cat cerebellum. J Comp Neurol 174: 417–488
Hall JA, Foster RE, Ebner FF, Hall WC (1977) Visual cortex in a reptile, the turtle (Pseudemys scripta and chrysemys picta). Brain Res 130: 197–216
Hanker JS, Yates PE, Metz CB, Rustioni A (1977) A new specific sensitive and non-carcinogenic reagent for the demonstration of horseradish peroxidase. Histochem J 9: 789–792
Hartman-von Monakow K, Akert K, Künzle H (1981) Projections of precentral, premotor and prefrontal cortex to the basilar pontine grey and to the nucleus reticularis tegmenti pontis in the monkey (Macaca fascicularis). Schweiz Arch Neurol Neurochir Psychiatr 129: 189–208
Hazlett JC, Dom R, Martin GF (1972) Spino-bulbar, spinothalamic and medial lemniscal connections in the American opossum, Didelphis marsupialis virginiana. J Comp Neurol 146: 95–118
Hrycyshyn AW, Flumerfelt BA (1981) A light microscopic investigation of the afferent connections of the lateral reticular nucleus in the cat. J Comp Neurol 197: 477–502
Ikeda M (1979) Projections from the spinal and the principal sensory nuclei of the trigeminal nerve to the cerebellar cortex in the cat, as studied by retrograde transport of horseradish peroxidase. J Comp Neurol 184: 567–586
Joseph BS, Whitlock DG (1968) Central projections of selected spinal dorsal roots in anuran amphibians. Anat Rec 160: 279–288
Kamei I, Shiosaka S, Senba E, Takagi H, Sakanaka M, Inagaki S, Takatsuki K, Nakai K, Imai H, Itakura T, Komai N, Tohyama M (1981) Comparative anatomy of the distribution of catecholamines within the inferior olivary complex from teleosts to primates. J Comp Neurol 202: 125–134
Karten HJ, Finger TE (1976) A direct thalamo-cerebellar pathway in pigeon and catfish. Brain Res 102: 335–338
Kimoto Y, Satoh K, Sakumoto T, Tohyama M, Shimizu N (1978) Afferent fiber connections from the lower brain stem to the rat cerebellum by the horseradish peroxidase method combined with MAO staining with special reference to noradrenergic neurons. J Hirnforsch 19: 85–100
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
Kotchabhakdi N, Hoddevik GH, Walberg F (1978) Cerebellar afferent projections from the perihypoglossal nuclei: An experimental study with the method of retrograde axonal transport of horseradish peroxidase. Exp Brain Res 31: 13–30
Kotchabhakdi N, Hoddevik GH, Walberg F (1980) The reticulocerebellar projection in the cat as studied with retrograde transport of horseradish peroxidase. Anat Embryol (Berl) 160: 341–360
Künzle H (1973) The topographic organization of spinal afferents to the lateral reticular nucleus of the cat. J Comp Neurol 149: 103–116
Künzle H (1975) Autoradiographic tracing of the cerebellar projections from the lateral reticular nucleus in the cat. Exp Brain Res 22: 255–266
Künzle H (1982) Dorsal root projections to the cerebellum in turtle. Exp Brain Res 45: 464–466
Künzle H, Woodson W (1982) Meso-diencephalic and other target regions of ascending spinal projections in the turtle, Pseudemys scripta elegans. J Comp Neurol (in press)
Lipp HP, Schwegler H (1980) Improved transport of horseradish peroxidase after injection with a non-ionic tetergent (Nonidet P-40) into mouse cortex and observations on the relationship between spread at the injection site and amount of transported label. Neurosci Lett 20: 49–54
Llinás R, Hillman DE (1969) Physiological and morphological organization of the cerebellar circuits in various vertebrates. In: Llinás R (ed) Neurobiology of cerebellar evolution and development. AMA, Chicago, pp 43–73
Martin GF, Dom R, Katz S, King J (1974) The organization of projection neurons in the opossum red nucleus. Brain Res 78: 17–34
McCrea RA, Baker R, Delgado-Garcia J (1979) Afferent and efferent organization of the prepositus hypoglossi nucleus. Prog Brain Res 50: 653–665
Mesulam MM (1978) Tetramethyl benzidine for horseradish peroxidase neurohistochemistry: A non-carcinogenic blue reaction product with superior sensitivity for visualizing neural afferents and efferents. J Histochem Cytochem 26: 106–117
Mihailoff GA, Burne RA, Azizi SA, Norell G, Woodward DJ (1981) The pontocerebellar system in the rat: An HRP study. II. Hemispheral components. J Comp Neurol 197: 559–578
Miller MR, Kasahara M (1979) The cochlear nuclei of some turtles. J Comp Neurol 185: 221–236
Molenaar GJ (1978) The sensory trigeminal system of a snake in the possession of infrared receptors. II. The central projections of the trigeminal nerve. J Comp Neurol 179: 137–152
Mugnaini E, Dahl AL (1975) Mode of distribution of aminergic fibers in the cerebellar cortex of the chicken. J Comp Neurol 162: 417–432
Mugnaini E, Atluri RL, Houk JC (1974) Fine structure of granular layer in turtle cerebellum with emphasis on large glomeruli. J Neurophysiol 37: 1–29
Parent A (1973) Distribution of monoamine-containing nerve terminals in the brain of the painted turtle, Chrysemys picta. J Comp Neurol 148: 153–166
Parent A (1976) Striatal afferent connections in the turtle (Chrysemys picta) as revealed by retrograde axonal transport of horseradish peroxidase. Brain Res 108: 25–36
Reiner A, Karten H (1978) A bisynaptic retinocerebellar pathway in the turtle. Brain Res 150: 163–169
Reiner A, Brauth SE, Kitt CA, Karten HJ (1980) Basal ganglionic pathways to the tectum: Studies in reptiles. J Comp Neurol 193: 565–589
Saigal RP, Karamanlidis AN, Voogd J, Mangana O, Michaloudi H (1980a) Secondary trigeminocerebellar projections in sheep studied with horseradish peroxidase tracing method. J Comp Neurol 189: 537–553
Saigal RP, Karamanlidis AN, Voogd J, Michaloudi H, Mangana O (1980b) Cerebellar afferents from the motor nuclei of cranial nerves, the nucleus of the solitary tract and nuclei coeruleus and parabrachialis in sheep, demonstrated with retrograde transport of horseradish peroxidase. Brain Res 197: 200–206
Schwab ME, Javoy-Agid F, Agid Y (1978) Labeled wheat germ agglutinin (WGA) as a new, highly sensitive retrograde tracer in the rat brain hippocampal system. Brain Res 152: 145–150
Schwarz IE, Schwarz DWF (1980) Afferents to the cerebellar cortex of turtles studied by means of the horseradish peroxidase technique. Anat Embryol (Berl) 160: 39–52
Simon H, Moal LeM, Calas A (1979) Efferents and afferents of the ventral tegmental-A 10 region studied after local injection of (3H)leucine and horseradish peroxidase. Brain Res 178: 17–40
Somana R, Walberg F (1980) A re-examination of the cerebellar projections from the gracile, main and external cuneate nuclei in the cat. Brain Res 186: 33–42
Somana R, Kotchabhakdi N, Walberg F (1980) Cerebellar afferents from the trigeminal sensory nuclei in the cat. Exp Brain Res 38: 57–64
Taber-Pierce E, Hoddevik GH, Walberg F (1977) The cerebellar projection from the raphe nuclei in the cat as studied with the method of retrograde transport of horseradish peroxidase. Anat Embryol (Berl) 152: 73–88
Tohyama M (1976) Comparative anatomy of cerebellar catecholamine innervation from teleosts to mammals. J Hirnforsch 17: 43–60
Wiesendanger M, Rüegg DG, Wiesendanger R (1979) The corticopontine system in primates: Anatomical and functional considerations. In: Massion J, Sasaki K (eds) Cerebrocerebellar interactions. Elsevier/North Holland, Amsterdam, pp 45–65
Winfield JA, Hendrickson A, Kimm J (1978) Anatomical evidence that the medial terminal nucleus of the accessory optic tract in mammals provides a visual mossy fiber input to the flocculus. Brain Res 151: 175–182
Woodson W, Künzle H (1982) Distribution and structural characterization of neurons giving rise to descending spinal projections in the turtle, Pseudemys scripta elegans. J Comp Neurol (in press)
Yamamoto K, Tohyama M, Shimizu N (1977) Comparative anatomy of the topography of catecholamine containing neuron system in the brain stem from birds to teleosts. J Hirnforsch 18: 229–240
Zemlan FP, Leonard CM, Kow LM, Pfaff DW (1978) Ascending tracts of the lateral columns of the rat spinal cord. A study using the silver impregnation and horseradish peroxidase techniques. Exp Neurol 62: 298–334
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Supported by the Swiss National Science Foundation (grant No. 3.433.78 and No. 3.505.79) and the Dr. Eric Slack-Gyr Stiftung, Zürich
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Künzle, H. Supraspinal cell populations projecting to the cerebellar cortex in the turtle (Pseudemys scripta elegans). Exp Brain Res 49, 1–12 (1983). https://doi.org/10.1007/BF00235536
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DOI: https://doi.org/10.1007/BF00235536