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Afferent projections from the rat longus capitis muscle studied by transganglionic transport of HRP

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Summary

Using the method of transganglionic transport of horseradish peroxidase (HRP) according to Mesulam (1978), the course and central terminations of the afferents from the longus capitis muscle were studied in the rat. Application of HRP to the cut muscle nerves was followed by heavy labeling of a considerable number of cell bodies of different sizes in the spinal ganglia C2 and C3. The labeled central processes follow two distinct main routes: one to the external cuneate nucleus, which is known to project ipsilaterally to the cerebellum, the other to the central cervical nucleus (CCN) of the spinal cord. The latter nucleus contains dense arborizations and terminals of muscle afferents in close relationship to medium sized cells which project contralaterally to the cerebellum. This could be shown in double labeling experiments with HRP as a tracer for primary afferents and Nuclear yellow for the cerebellar pathway. The labeled area of CCN extends from the fourth cervical segment up to the medulla oblongata where it lies laterally adjacent to the hypoglossal nucleus, though clearly separated from the latter.

In the cervical part of CCN, dendrites of neck muscle motoneurons arborize within the area of afferent terminals.

Besides the external cuneate and the central cervical nuclei, afferent projections were seen in lamina X, partly in close contact with the central canal, and in more lateral areas of lamina VII. In contrast to results from studies on other neck muscles, no reaction product was observed in dorsal horn laminae I–VI.

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References

  • Abrahams VC (1981) Sensory and motor specialization in some muscles of the neck. Trends in Neuroscience 4:24–27

    Google Scholar 

  • Brodal A (1941) Die Verbindungen des Nucleus cuneatus externus mit dem Kleinhirn beim Kaninchen und bei der Katze. Experimentelle Untersuchungen. Z ges Neurol Psychiat 171:167–199

    Google Scholar 

  • Brodal A (1975) Neurological anatomy in relation to clinical medicine. 2nd ed. The Oxford University Press, London, Toronto

    Google Scholar 

  • Cervero F, Iggo A, Ogawa H (1976) Nociceptor-driven dorsal horn neurones in the lumbar spinal cord of the cat. Pain 2:5–24

    Google Scholar 

  • Cooke JD, Larson B, Oscarsson O, Sjölund B (1971) Origin and termination of cuneocerebellar tract. Exp Brain Res 13:339–358

    Google Scholar 

  • Corbin KB, Hinsey JC (1935) Intramedullary course of the dorsal root fibers of each of the first four cervical nerves. J Comp Neurol 63:119–126

    Google Scholar 

  • Cummings JF, Petras JM (1977) The origin of spinocerebellar pathways. 1. The nucleus cervicalis centralis of the cranial cervical spinal cord. J Comp Neurol 173:655–692

    Google Scholar 

  • Eccles JC, Fatt P, Landgren S, Winsbury GJ (1954) Spinal cord potentials, generated by volleys in the large muscle afferents. J Physiol Lond 125:590–606

    Google Scholar 

  • Ferraro A, Barrera SE (1935) The nuclei of the posterior funiculi in Macacus rhesus. An anatomic and experimental investigation. Arch Neurol Psychiat (Chicago) 33:262–275

    Google Scholar 

  • Gottschall J, Neuhuber W, Müntener M, Mysicka A (1980) The ansa Embryol 159:59–69

    Google Scholar 

  • Gottschall J, Zenker W, Neuhuber W, Mysicka A, Müntener M (1980) The sternomastoid muscle of the rat and its innervation. Muscle fiber composition, perikarya and axons of efferent and afferent neurons. Anat Embryol 160:285–300

    Google Scholar 

  • Grant G (1962) Projection of the external cuneate nucleus onto the cerebellum in the cat: An experimental study using silver methods. Exp Neurol 5:179–195

    Google Scholar 

  • Grant G, Arvidsson J, Robertson B, Ygge J (1979) Transganglionic transport of horseradish peroxidase in primary sensory neurons. Neuroscience Letters 12:23–28

    Google Scholar 

  • Heckmann Th, Bourassa ChM (1981) Lesions of the dorsal column nuclei or medial lemniscus of the cat: effect on motor performance. Brain Res 224:405–411

    Google Scholar 

  • Hirai N, Hongo T, Sasaki S (1978) Cerebellar projection and input organizations of the spinocerebellar tract arising from the central cervical nucleus of the cat. Brain Res 157:341–345

    Google Scholar 

  • Ishizuka N, Mannen H, Hongo T, Sasaki S (1979) Trajectory of group Ia afferent fibers stained with horseradish peroxidase in the lumbosacral cord of the cat: three dimensional reconstructions from serial sections. J Comp Neurol 186:189–212

    Google Scholar 

  • Hohnson JL jr, Welker WI, Pubols BH jr (1968) Somatotopic organization of raccoon dorsal column nuclei. J Comp Neurol 132:1–44

    Google Scholar 

  • Katan S, Gottschall J, Neuhuber W (1982) Simultaneous visualization of horseradish peroxidase and nuclear yellow in tissue sections for neuronal double labeling. Neuroscience Lett 28:121–126

    Google Scholar 

  • Kerr FWL (1961) Structural relation of the trigeminal spinal tract to upper cervical roots and the solitary nucleus of the cat. Exp Neurol 4:134–148

    Google Scholar 

  • Liu CN (1956) Afferent nerves to Clarke's and lateral cuneate nuclei in the cat. Arch Neurol Psychiat (Chicago) 75:67–77

    Google Scholar 

  • Lucas E, Willis WD (1974) Identification of muscle afferents which activate interneurons in the intermediate nucleus. J Neurophysiol 37:282–293

    Google Scholar 

  • Matsushita M, Ikeda M (1975) The central cervical nucleus as cell origin of a spinocerebellar tract arising from the cervical cord: a study in the cat using horseradish peroxidase. Brain Res 100:412–419

    Google Scholar 

  • Matsushita M, Hosoya Y (1979) Cells of origin of the spinocerebellar tract in the rat, studied with the method of retrograde transport of horseradish peroxidase. Brain Res 173:185–200

    Google Scholar 

  • Mesulam MM (1978) Tetramethylbenzidine 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 

  • Mesulam MM, Brushart TM (1979) Transganglionic and anterograde transport of horseradish peroxidase across dorsal root ganglia: A tetramethylbenzidine method for tracing central sensory connections of muscles and peripheral nerves. Neuroscience 4:1107–1117

    Google Scholar 

  • Müntener M, Gottschall J, Neuhuber W, Mysicka A (1980) The ansa cervicalis and the infrahyoid muscles of the rat. I. Anatomy; distribution, number and diameter of fiber types; motor units. Anat Embryol 159:49–57

    Google Scholar 

  • Mysicka A, Zenker W (1981) Central projections of muscle afferents from the sternomastoid nerve in the rat. Brain Res 211:257–265

    Google Scholar 

  • Oscarsson O (1965) Functional organization of the spino- and cuneocerebellar tracts. Physiol Rev 45:495–522

    Google Scholar 

  • Petras JM, Cummings JF (1975) Cervical spinocerebellar projections in the dog. Anat Rec 181:448

    Google Scholar 

  • Ramon y Cajal S (1909) Histologie du système nerveux de l'homme et des vertébrés. Vol I, Maloine, Paris

    Google Scholar 

  • Ranson SW, Davenport HK, Doles EA (1932) Intramedullary course of the dorsal root fibers of the first three cervical nerves. J Comp Neurol 54:1–12

    Google Scholar 

  • Rexed B (1952) The cytoarchitectonic organization of the spinal cord in the cat. J comp Neurol 96:415–495

    Google Scholar 

  • Rexed B (1954) A cytoarchitectonic atlas of the spinal cord of the cat. J Comp Neurol 100:297–378

    Google Scholar 

  • Richmond FJR, Scott DA, Abrahams VC (1978) Distribution of motoneurons to neck muscles biventer cervicis, splenius and complexus in cat. J Comp Neurol 181:451–463

    Google Scholar 

  • Rinvik E, Walberg F (1975) Studies on the cerebellar projections from the main and external cuneate nuclei in the cat by means of retrograde axonal transport of horseradish peroxidase. Brain Res 95:371–381

    Google Scholar 

  • Rosén I (1969) Localization in caudal brain stem and cervical spinal cord of neurones activated from forelimb group I afferents in the cat. Brain Res 16:55–71

    Google Scholar 

  • Shriver JE, Stein BM, Carpenter MB (1968) Central projections of spinal dorsal roots in monkey. I. Cervical and upper thoracic dorsal roots. Am J Anat 123:27–74

    Google Scholar 

  • Stacey MJ (1969) Free endings on skeletal muscle of the cat. J Anat (London) 105:231–254

    Google Scholar 

  • Stillhard G (1981) Musculi longus capitis et splenius der Ratte und innervierende Motoneurone. Acta Neuropathol 53:267–274

    Google Scholar 

  • Wiksten B (1975) The central cervical nucleus — a source of spinocerebellar fibers, demonstrated by retrograde transport of horseradish peroxidase. Neuroscience Lett 1:81–84

    Google Scholar 

  • Wiksten B (1979) The central cervical nucleus in the cat. I. A Golgi study. Exp Brain Res 36:143–154

    Google Scholar 

  • Wiksten B (1979) The central cervical nucleus in the cat. II. The cerebellar connections studied with retrograde transport of horseradish peroxidase. Exp Brain Res 36:155–173

    Google Scholar 

  • Wiksten B (1979) The central cervical nucleus in the cat. III. The cerebellar connections studied with anterograde transport of 3H-Leucine. Exp Brain Res 36:175–189

    Google Scholar 

  • Willis WD, Coggeshall RE (1975) Sensory mechanisms of the spinal cord. New York London

  • Yee J, Corbin KB (1939) The intramedullary course of the upper five, cervical dorsal root fibers in the rabbit. J Comp Neurol 70:297–304

    Google Scholar 

  • Zenker W, Mysicka A, Neuhuber W (1980) Dynamics of the transganglionic movement of horseradish peroxidase in primary sensory neurons. Cell Tissue Res 207:479–489

    Google Scholar 

Download references

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This investigation was supported by the EMDO-Stiftung Zürich

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Ammann, B., Gottschall, J. & Zenker, W. Afferent projections from the rat longus capitis muscle studied by transganglionic transport of HRP. Anat Embryol 166, 275–289 (1983). https://doi.org/10.1007/BF00305088

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