Skip to main content
Log in

Pallidofugal projections to thalamus and midbrain: A quantitative antidromic activation study in monkeys and cats

  • Published:
Experimental Brain Research Aims and scope Submit manuscript

Summary

The projections of monkey medial globus pallidus (and of cat entopeduncular nucleus) to thalamus and midbrain were studied with antidromic activation in order to determine the number of pallidal neurons sending axonal branches to the two sites. The animals were anesthetized with pentobarbital and several movable electrodes were used to stimulate the thalamic nuclear complex ventralis anterior — ventralis lateralis (VA-VL), the nucleus “centre médian” (CM), and the midbrain nucleus tegmenti pedunculopontinus (TPP). The responses of pallidal neurons were recorded with extracellular microelectrodes. In 3 monkeys 99% and 87% of 145 medial pallidal neurons responded antidromically to stimulation of VA-VL and TPP respectively. Reciprocal collision tests demonstrated that 86% of the 145 neurons sent axonal branches to the two sites. By comparison in 2 cats the tests demonstrated that 72% of 46 entopeduncular neurons branched to VA-VL and TPP. In 2 monkeys 68% of 53 medial pallidal neurons were shown to branch to VA-VL and CM thalamic nuclei. In the monkeys, the latencies of responses indicate that all pallidofugal fibers have the same mean conduction rate: 6 m/s. The fibers appear to branch profusely in VA-VL where less current was required to activate neurons antidromically than in TPP. The location of neurons in the medial pallidum is weakly correlated with the location of stimulation points in VA-VL activating the neurons antidromically at low threshold, suggesting some topography in the pallidothalamic projection. However there is no particular localization of medial pallidal neurons with and without branching projections. Apart from one exception, the 162 neurons recorded in the lateral pallidum failed to respond antidromically to the stimulation sites. We conclude that the great majority of medial pallidal neurons can send signals to both the thalamus and the midbrain in the cat and in the monkey.

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

  • Carpenter MB, Strominger NL (1967) Efferent fiber projections of the subthalamic nucleus in the rhesus monkey. A comparison of the efferent projections of the subthalamic nucleus, the substantia nigra and globus pallidus. Am J Anat 121: 41–72

    Google Scholar 

  • Carter DA, Fibiger HC (1978) The projections of the entopeduncular nucleus and globus pallidus in rat as demonstrated by autoradiography and horseradish peroxidase histochemistry. J Comp Neurol 177: 113–114

    Google Scholar 

  • DeLong M (1971) Activity of pallidal neurons during movement. J Neurophysiol 34: 414–427

    Google Scholar 

  • Deniau JM, Hammond C, Riszk A, Feger J (1978) Electrophysiological properties of identified output neurons of the rat substantia nigra (pars compacta and pars reticulata): Evidence for the existence of branched neurons. Exp Brain Res 32: 409–422

    Google Scholar 

  • Filion M, Harnois C (1978) A comparison of projections of entopeduncular neurons to the thalamus, the midbrain and the habenula in the cat. J Comp Neurol 181: 763–780

    Google Scholar 

  • Forman D, Ward JW (1957) Responses to electrical stimulation of caudate nucleus in cats in chronic experiments. J Neurophysiol 20: 230–243

    Google Scholar 

  • Fuller H, Schlag JD (1976) Determination of antidromic excitation by the collision test: Problems of interpretation. Brain Res 112: 283–298

    Google Scholar 

  • Gasser HS, Grundfest H (1939) Axon diameters in relation to the spike dimensions and the conduction velocity in mammalian A fibers. Am J Physiol 127: 393–414

    Google Scholar 

  • Grofova I (1975) The identification of striatal and pallidal neurons projecting to substantia nigra. An experimental study by means of retrograde axonal transport of horseradish peroxidase. Brain Res 91: 286–291

    Google Scholar 

  • Harnois C, Filion M (1980) Pallidal neurons branching to the thalamus and to the midbrain in the monkey. Brain Res 186: 222–225

    Google Scholar 

  • Hopkins DA (1977) Basal ganglia projections to the brain stem in the rat, cat and monkey. In: Lakke JPWF, Korf J, Wesseling H (eds) Parkinson's disease — concepts and prospects. Exerpta Medica, Amsterdam Oxford (Exerpta medica international congress series no 429, pp 11–24)

    Google Scholar 

  • Jones EG, Leavitt RY (1974) Retrograde axonal transport and the demonstration of non-specific projections to the cerebral cortex and striatum from thalamic intralaminar nuclei in the rat, cat and monkey. J Comp Neurol 154: 349–378

    Google Scholar 

  • Kievit J, Kuypers GJM (1975) Subcortical afferents to the frontal lobe in the rhesus monkey studied by means of retrograde horseradish peroxidase transport. Brain Res 85: 261–266

    Google Scholar 

  • Kim R, Nakana A, Jayaraman A, Carpenter MB (1976) Projections of the globus pallidus and adjacent structures: An autoradiographic study in the monkey. J Comp Neurol 169: 263–290

    Google Scholar 

  • Kuo JC, Carpenter MB (1973) Organization of pallidothalamic projections in the rhesus monkey. J Comp Neurol 151: 201–256

    Google Scholar 

  • Larsen KD, McBride RL (1979) The organization of feline entopeduncular nucleus projections: Anatomical studies. J Comp Neurol 184: 293–308

    Google Scholar 

  • Larsen KD, Sutin J (1978) Output organization of the feline entopeduncular and subthalamic nuclei. Brain Res 157: 21–31

    Google Scholar 

  • Laursen AM (1962) Movements evoked from the region of the caudate nucleus in cats. Acta Physiol Scand 54: 175–184

    Google Scholar 

  • Lee LA, Crossman AR, Slater P (1980) The neurological basis of striatally induced head-turning in the rat: The effects of lesions in putative output pathways. Neuroscience 5: 73–79

    Google Scholar 

  • McLennan H, Emmons PR, Plummer PM (1964) Some behavioral effects of stimulation of the caudate nucleus in unrestrained cats. Can J Physiol Pharmacol 42: 329–339

    Google Scholar 

  • Moon Edley S, Graybiel AM (1980) Connections of the nucleus tegmenti pedunculopontinis, pars compacta (TPc) in cat. Anat Rec 196: 129A

  • Nauta HJW (1974) Efferent projections of the caudate nucleus, pallidal complex and subthalamic nucleus in the cat. Doctoral dissertation, Case Western Reserve Univ., No. 4322

  • Nauta HJW (1979) Projections of the pallidal complex: An autoradiographic study in the cat. Neuroscience 4: 1853–1873

    Google Scholar 

  • Nauta WJH, Mehler WR (1966) Projections of the lentiform nucleus in the monkey. Brain Res 1: 3–42

    Google Scholar 

  • Nomura J, Mizuno N, Sugimoto T (1980) Direct projections from the pedunculopontine tegmental nucleus to the subthalamic nucleus in the cat. Brain Res 196: 223–227

    Google Scholar 

  • Parent A, Gravel S, Olivier A (1979) The extrapyramidal and limbic systems relationship at the globus pallidus level: A comparative histochemical study in the rat, cat and monkey. Adv Neurol 24: 1–11

    Google Scholar 

  • Siegel S (1956) Non parametric statistics for the behavioral sciences. McGraw-Hill, New York

    Google Scholar 

  • Van Der Kooy D, Carter DA (1981) The organization of the efferent projections and striatal afferents of the entopeduncular nucleus and adjacent areas in the rat. Brain Res 211: 15–36

    MathSciNet  MATH  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Additional information

Supported by the Medical Research Council of Canada

Part of doctoral dissertation

Studentship award from the Conseil de la recherche en sante du Québec

Associate professor at the Dept. of Physiology of Laval University in Québec

Rights and permissions

Reprints and permissions

About this article

Cite this article

Harnois, C., Filion, M. Pallidofugal projections to thalamus and midbrain: A quantitative antidromic activation study in monkeys and cats. Exp Brain Res 47, 277–285 (1982). https://doi.org/10.1007/BF00239387

Download citation

  • Received:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00239387

Key words

Navigation