Skip to main content
Log in

The cerebellar nuclear afferent and efferent connections with the lateral reticular nucleus in the cat as studied with retrograde transport of WGA-HRP

  • Published:
Anatomy and Embryology Aims and scope Submit manuscript

Summary

The cerebellar nuclear projection from the lateral reticular nucleus (NRL) was studied in 29 cats by means of retrograde axonal transport after implantation of the crystalline wheat germ agglutinin-horseradish peroxidase (WGA-HRP) complex in the cerebellar nuclei. It was confirmed that all the cerebellar nuclei receive afferent fibres from the NRL with the strongest termination in the ipsilateral interposed nuclei. In addition, these experiments give evidence of a previously unrecognized topical pattern in the projection to the interposed nuclei, arranged according to the same principle as in the projection to the immediately overlying cerebellar cortex. Thus, the anterior interposed nucleus receives fibres from all parts of the main NRL, its rostral part especially from laterally situated neurons, while subsequent more caudal parts from more medially situated neurons, while the posterior interposed nucleus receives fibres mainly from the dorsomedial part of the main NRL.

The cerebellar nuclear projection to the NRL was investigated in 15 cats using retrograde transport after ventral microiontophoretical ejections of the WGA-HRP complex in the main NRL. The contralateral rostral fastigial nucleus was confirmed as the main origin of this projection, but projecting neurons were, in addition, discovered rostrally in the anterior interposed and dentate nuclei on the same side. No topical differences could be observed following ejections in different parts of the NRL; the majority of the projecting neurons were always concentrated along the ventral and lateral borders of the fastigial nucleus and in the adjacent medial part of the anterior interposed nucleus.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  • Angaut P (1970) The ascending projections of the nucleus interpositus posterior of the cat cerebellum: an experimental anatomical study using silver impregnation methods. Brain Res 24:377–394

    Google Scholar 

  • Batton RR III, Jayaraman A, Ruggiero D, Carpenter MB (1977) Fastigial efferent projections in the monkey: an autoradiographic study. J Comp Neurol 174:281–306

    Google Scholar 

  • Bishop GA, McCrea RA, Kitai ST (1976) Afferent projections to the nucleus interpositus anterior (NIa) and lateral nucleus (LN) of the cat cerebellum. Anat Rec 184:360

    Google Scholar 

  • Brodal A (1972) Cerebrocerebellar pathways. Anatomical data and some functional implications. Acta Neurol Scand 48:153–195

    Google Scholar 

  • Brodal A (1981) Neurological anatomy in relation to clinical medicine. Oxford Univ Press, New York London

    Google Scholar 

  • Brodal P (1975) Demonstration of a somatotopically organized projection onto the paramedian lobule and the anterior lobe from the lateral reticular nucleus: an experimental study with the horseradish peroxidase method. Brain Res 95:221–239

    Google Scholar 

  • Brodal P, Dietrichs E, Bjålie JG, Nordby T, Walberg F (1983) Is lectine-coupled horseradish peroxidase taken up and transported by undamaged as well as by damaged fibres in the central nervous system? Brain Res 278:1–9

    Google Scholar 

  • Brodal P, Dietrichs E, Walberg F (1986) Do pontocerebellar mossy fibres give off collaterals to the cerebellar nuclei? An experimental study in the cat with implantation of crystalline HRP-WGA. Neurosci Res 4:12–24

    Google Scholar 

  • Brooks VB, Thach WT (1981) Cerebellar control of posture and movement. In: Brooks VB (ed) Handbook of physiology, section 1: the nervous system, vol 2. Motor control. Am Physiol Soc. Bethesda, Maryland

    Google Scholar 

  • Chan-Palay V (1977) Cerebellar dentate nucleus: organization, cytology and transmitters. Springer, Berlin Heidelberg New York

    Google Scholar 

  • Chan-Palay V, Palay SL, Brown JT, van Itallie C (1977) Sagittal organization of olivocerebellar and reticulocerebellar projections: autoradiographic studies with 35S-methionine. Exp Brain Res 30:561–576

    Google Scholar 

  • Chen R, Gibson AR, Houk JC, Robinson FR (1983) Distribution of terminals in cerebellar cortex and their relative absence in the deep cerebellar nuclei from three major sources of mossy fibres in the cat. Soc Neurosci Proc 251:4

    Google Scholar 

  • Cohen D, Chambers WW, Sprague JM (1958) Experimental study of the efferent projections from the cerebellar nuclei to the brainstem of the cat. J Comp Neurol 109:233–259

    Google Scholar 

  • Corvaja N, Grofová I, Pompeiano O, Walberg F (1977) The lateral reticular nucleus in the cat — I. An experimental anatomical study of its spinal and supraspinal afferent connections. Neuroscience 2:537–553

    Google Scholar 

  • Courville J, Faraco-Cantin F (1980) Topography in the olivo-cerebellar projection: an experimental study in the cat with an autoradiographic tracing method. In: Courville J, de Montigny C, Lamarre Y (eds) The inferior olivary nucleus: anatomy and physiology. Raven Press, New York, pp 235–277

    Google Scholar 

  • Dietrichs E (1983) Cerebellar nuclear afferents from the lateral reticular nucleus in the cat. Brain Res 288:320–324

    Google Scholar 

  • Dietrichs E, Walberg F (1979) The cerebellar projection from the lateral reticular nucleus as studied with retrograde transport of horseradish peroxidase. Anat Embryol 155:273–290

    Google Scholar 

  • Dietrichs E, Walberg F (1985) The cerebellar nucleo-olivary and olivo-cerebellar nuclear projections in the cat as studied with anterograde and retrograde transport in the same animal after implantation of crystalline WGA-HRP. II. The fastigial nucleus. Anat Embryol 173:253–261

    Google Scholar 

  • Dietrichs E, Walberg F (1986) The cerebellar nucleo-olivary and olivocerebellar nuclear projections in the cat as studied with anterograde and retrograde transport in the same animal after implantation of crystalline WGA-HRP. III. The interposed nuclei. Brain Res 373:373–383

    Google Scholar 

  • Dietrichs E, Walberg F, Nordby T (1985) Cerebellar nucleo-olivary and olivo-cerebellar nuclear projections in the cat as studied with anterograde and retrograde transport in the same animal after implantation of crystalline WGA-HRP. I. The dentate nucleus. Neurosci Res 3:52–70

    Google Scholar 

  • Eccles JC, Ito M, Szentagothai J (1967) The cerebellum as a neuronal machine. Springer, Berlin Heidelberg New York

    Google Scholar 

  • Eller T, Chan-Palay V (1976) Afferents to the cerebellar lateral nucleus. Evidence from retrograde transport of horseradish peroxidase after pressure injections through micropipettes. J Comp Neurol 166:285–301

    Google Scholar 

  • Fukushima K, Peterson BW, Uchino Y, Coulter JD, Wilson VJ (1977) Direct fastigiospinal fibres in the cat. Brain Res 126:538–542

    Google Scholar 

  • Gerrits NM, Voogd J (1987) The projection of the nucleus reticularis tegmenti pontis and adjacent regions of the pontine nuclei to the central cerebellar nuclei in the cat. J Comp Neurol 258:52–69

    Google Scholar 

  • Gibson AR, Hansma DI, Houk JC, Robinson FR (1984) A sensitive low artifact TMB procedure for the demonstration of WGA-HRP in the CNS. Brain Res 298:235–241

    Google Scholar 

  • Gonatas NK, Harper C, Mizutani T, Gonatas JO (1979) Superior sensitivity of conjugates of horseradish peroxidase with wheat germ agglutinin for studies of retrograde axonal transport. J Histochem Cytochem 27:728–734

    Google Scholar 

  • Groenewegen HJ, Voogd J (1977) The parasagittal zonation within the olivocerebellar projection, I. Climbing fiber distribution in the vermis of the cat cerebellum. J Comp Neurol 174:417–488

    Google Scholar 

  • Groenewegen HJ, Voogd J, Freedman SL (1979) The parasagittal zonation within the olivocerebellar projection. II. Climbing fiber distribution in the intermediate and hemispheric parts of the cerebellum. J Comp Neurol 183:551–602

    Google Scholar 

  • Hoddevik GH (1978) The projection from the nucleus reticularis tegmenti pontis onto the cerebellum in the cat. A study using the methods of anterograde degeneration and retrograde axonal transport of horseradish peroxidase. Anat Embryol 153:227–242

    Google Scholar 

  • Hrycyshyn AW, Flumerfelt DA (1981) A light microscopic investigation of the afferent connections of the lateral reticular nucleus in the cat. J Comp Neurol 197:477–502

    Google Scholar 

  • Hrycyshyn AW, Flumerfelt BA, Anderson WA (1982) A horseradish peroxidase study of the projections from the lateral reticular nucleus to the cerebellum in the rat. Anat Embryol 165:1–18

    Google Scholar 

  • Ito M (1984) The cerebellum and neural control. Raven press, New York, pp 141–142

    Google Scholar 

  • Ito M, Yoshida M, Obata K, Kawai N, Udo M (1970) Inhibitory control of intracerebellar nuclei by the Purkinje cell axons. Exp Brain Res 10:64–80

    Google Scholar 

  • Kitai ST, DeFrance JF, Hatada K, Kennedy DT (1974) Electrophysiological properties of lateral reticular nucleus cells: II. Synaptic activation. Exp Brain Res 21:419–432

    Google Scholar 

  • Künzle H (1973) The topographic organization of spinal afferents to the lateral reticular nucleus of the cat. J Comp Neurol 149:103–116

    Google Scholar 

  • Llinàs RR (1981) Electrophysiology of the cerebellar networks. In: Brooks VB (ed) Handbook of physiology, section 1: the nervous system, vol 2. Motor control. Am Physiol Soc, Bethesda, Maryland

    Google Scholar 

  • Martin GF, King JS, Dom R (1974) The projections of the deep cerebellar nuclei of the opposum, Didelphis marsupialis virginiana. J Hirnforsch 15:545–573

    Google Scholar 

  • Martin GF, Andrezik J, Crutcher K, Linauts M, Panneton M (1977) The lateral reticular nucleus of the opposum (Didelphis virginiana). II. Connections. J Comp Neurol 174:151–186

    Google Scholar 

  • Matsushita M, Hosoya Y (1978) The location of spinal projection neurons in the cerebellar nuclei (cerebellospinal tract neurons) of the cat. A study with the horseradish peroxidase technique. Brain Res 142:237–248

    Google Scholar 

  • Matsushita M, Ikeda M (1970) Olivary projections to the cerebellar nuclei in the cat. Exp Brain Res 10:488–500

    Google Scholar 

  • Matsushita M, Ikeda M (1976) Projections from the lateral reticular nucleus to the cerebellar cortex and nuclei in the cat. Exp Brain Res 24:403–421

    Google Scholar 

  • McCrea RA, Bishop GA, Kitai ST (1977) Electrophysiological and horseradish peroxidase studies of precerebellar afferents to the nucleus interpositus anterior. II. Mossy fiber system. Brain Res 122:215–228

    Google Scholar 

  • Mesulam M-M (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

    Google Scholar 

  • Mori J, Hori N, Katsuda N (1981) A new method for application of horseradish peroxidase into a restricted area of the brain. Brain Res Bull 6:19–22

    Google Scholar 

  • Naus CG, Flumerfelt BA, Hrycyshyn AW (1985) An HRP-TMB ultra-structural study of rubral afferents in the rat. J Comp Neurol 239:453–465

    Google Scholar 

  • Oka H, Yoshida K, Yamamoto T, Samejima A (1985) Organization of afferent connections to the lateral and interpositus cerebellar nuclei from the brainstem relay nuclei: a horseradish peroxidase study in the cat. Neurosci Res 2:321–333

    Google Scholar 

  • Pugh WW, Kalia M (1982) Differential uptake of peroxidase (HRP) and peroxidase-lectin (HRP-WGA) conjugate injected in the nodose ganglion of the cat. J Histochem Cytochem 30:887–894

    Google Scholar 

  • Qvist H (1989) Demonstration of axonal branching of fibres from certain precerebellar nuclei to the cerebellar cortex and nuclei. A retrograde fluorescent double-labelling study in the cat. Exp Brain Res (in press)

  • Qvist H, Dietrichs E (1986) Afferents to the lateral reticular nucleus from the oculomotor region. I. The Edinger-Westphal nucleus. Anat Embryol 175:261–269

    Google Scholar 

  • Qvist H, Dietrichs E, Walberg F (1984) An ipsilateral projection from the red nucleus to the lateral reticular nucleus in the cat. Anat Embryol 170:327–330

    Google Scholar 

  • Russchen FT, Groenewegen HJ, Voogd J (1976) Reticulocerebellar connections in the cat. An autoradiographic study. Acta Morphol Neerl-Scand 14:245–246

    Google Scholar 

  • Saint-Cyr JA (1983) The projection from the motor cortex to the inferior olive in the cat. An experimental study using axonal transport techniques. Neuroscience 10:667–684

    Google Scholar 

  • Shokunbi MT, Hrycyshyn AW, Flumerfelt BA (1985) Spinal projections to the lateral reticular nucleus in the rat: a retrograde labelling study using horseradish peroxidase. J Comp Neurol 239:216–226

    Google Scholar 

  • Shokunbi MT, Hrycyshyn AW, Flumerfelt BA (1986) A horseradish peroxidase study of the rubral and cortical afferents to the lateral reticular nucleus in the rat. J Comp Neurol 248:441–454

    Google Scholar 

  • Thomas DN, Kaufman RP, Sprague JM, Chambers WW (1956) Experimental studies of the vermal cerebellar projections in the brain stem of the cat (fastigiobulbar tract). J Anat 90:371–385

    Google Scholar 

  • Trojanowski JQ, Gonatas JO, Gonatas NK (1981a) A light and electron microscopic study of the intraneuronal transport of horseradish peroxidase and wheat germ agglutinin-peroxidase conjugates of the rat visual system. J Neurocytol 10:441–456

    Google Scholar 

  • Trojanowski JQ, Gonatas JO, Gonatas NK (1981b) Conjugates of horseradish peroxidase (HRP) with cholera toxin and wheat germ agglutinin are superior to free HRP as orthogradely transported markers. Brain Res 223:381–385

    Google Scholar 

  • Trojanowski JQ, Gonatas JO, Gonatas NK (1982) Horseradish peroxidase (HRP) conjugates of cholera toxin and lectins are more sensitive retrogradely transported markers than free HRP. Brain Res 231:33–50

    Google Scholar 

  • Tsukahara N, Bando T, Murakami F, Oda Y (1983) Properties of cerebello-precerebellar reverberating circuits. Brain Res 274:249–259

    Google Scholar 

  • van der Want JJL, Voogd J (1987) Ultrastructural identification and localization of climbing fiber terminals in the fastigial nucleus of the cat. J Comp Neurol 258:81–90

    Google Scholar 

  • van der Want JJL, Gerrits NM, Voogd J (1987) Autoradiography of mossy fiber terminals in the fastigial nucleus of the cat. J Comp Neurol 258:70–80

    Google Scholar 

  • Walberg F (1952) The lateral reticular nucleus of the medulla oblongata in mammals. J Comp Neurol 96:283–343

    Google Scholar 

  • Walberg F, Dietrichs E (1986) Is there a reciprocal connection between the red nucleus and the interposed cerebellar nuclei? Conclusions based on observations of anterograde and retrograde transport of peroxidase-labelled lectin in the same animal. Brain Res 397:73–85

    Google Scholar 

  • Walberg F, Pompeiano O (1960) Fastigiofugal fibers to the lateral reticular nucleus. An experimental study in the cat. Exp Neurol 2:40–53

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Qvist, H. The cerebellar nuclear afferent and efferent connections with the lateral reticular nucleus in the cat as studied with retrograde transport of WGA-HRP. Anat Embryol 179, 471–483 (1989). https://doi.org/10.1007/BF00319590

Download citation

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00319590

Key words

Navigation