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Differentiation of principal cells of the rat lateral geniculate body into two groups; fast and slow cells

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Summary

In urethane-anesthetized albino rats studies were made on mass potentials and/or unit activities of the lateral geniculate body (LGB) in response to single shock stimulation of optic tract (OT) and visual cortex (VC).

The previous finding that LGB mass responses to stimulation of the optic nerve comprise at least two postsynaptic waves (r1 and r2) with different peak times was confirmed by OT stimulation. It was found that the r1 wave had a lower threshold and a more rapid recovery process than the r2 wave.

Unit responses of principal (P) cells to maximal OT stimulation consisted of short-latency, single spikes (initial spike, IS), followed by long-latency, grouped discharges (late discharge, LD) repeated more than twice (LD1, LDr2 and so forth). Spontaneous discharges were almost completely suppressed after IS and each LD, suggesting that following these evoked discharges P cells underwent a phase of depressed excitability. The latency histogram of IS based upon 212 P cells had two peaks well-corresponding in time to the peaks of the r1 and r2 waves of the mass response, respectively. P cells were divided into the fast and slow groups according to whether their ISs occurred earlier or later than the trough separating the r1 and r2 waves. Typically, the fast cells had lower thresholds than the slow cells. The duration of the post-excitatory depression following IS and LD1 were shorter in the fast cells than in the slow cells. This same was found true with regard to the duration of depressed excitability following the antidromic firing. Examining the response patterns to OT stimulation of weak intensities, one characteristic difference between the two groups of P cells was found; the fast cells showed the IS without the succeeding LDs whereas the slow cells showed the LDs without the preceding IS.

A discussion was made on functional significance of the differentiation of P cells into two types.

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References

  • Adams, A.D., Forrester, J.M.: The projection of the rat's visual field on the cerebral cortex. Quart. J. exp. Physiol. 53, 327–336 (1968).

    Google Scholar 

  • Bishop, P.O., McLeod, J.G.: Nature of potentials associated with synaptic transmission in the lateral geniculate of cat. J. Neurophysiol. 17, 387–414 (1954).

    Google Scholar 

  • —, Davis, R.: The recovery of responsiveness of the sensory synapses in the lateral geniculate nucleus. J. Physiol. (Lond.) 150, 214–238 (1960).

    Google Scholar 

  • —, Burke, W., Davis, R.: The identification of single units in central visual pathway. J. Physiol. (Lond.) 162, 409–431 (1962).

    Google Scholar 

  • Burke, W., Sefton, A.J.: Discharge patterns of principal cells and inhibitory interneurons in lateral geniculate nucleus of rat. J. Physiol. (Lond.) 187, 201–212 (1966a).

    Google Scholar 

  • —: Recovery of responsiveness of cells of lateral geniculate nucleus of rat. J. Physiol. (Lond.) 187, 213–229 (1966b).

    Google Scholar 

  • —: Inhibitory mechanisms in lateral geniculate nucleus of rat. J. Physiol. (Lond.) 187, 231–246 (1966c).

    Google Scholar 

  • Cleland, B.G., Dubin, M.W., Levick, W.R.: Sustained and transient neurons in the cat retina and lateral geniculate nucleus. J. Physiol. (Lond.) 217, 473–496 (1971).

    Google Scholar 

  • Eccles, J.C., Eccles, R.M., Iggo, A., Ito, M.: Distribution of recurrent inhibition among motoneurones. J. Physiol. (Lond.) 159, 479–499 (1961).

    Google Scholar 

  • Fifková, E., Marsala, J.: Stereotaxic atlases for the cat, rabbit and rat. In: J. Bureš, M. Petráň and J. Zacher (Eds.). Electrophysiological Methods in Biological Research. New York: Academic Press 1967.

    Google Scholar 

  • Fukada, Y., Saito, H.: Phasic and tonic cells in the cat's lateral geniculate nucleus. Tohoku J. exp. Med. 106, 209–210 (1972).

    Google Scholar 

  • Fukuda, Y., Iwama, K.: Reticular inhibition of internuncial cells in the rat lateral geniculate body. Brain Res. 35, 107–118 (1971).

    Google Scholar 

  • —: A relation between latencies of initial and late spike discharges of rat lateral geniculate cells to optic tract stimulation. Brain Res. 37, 322–325 (1972).

    Google Scholar 

  • Fuster, J.M., Creutzfeldt, O.D., Straschill, M.: Intracellular recording of neuronal activity in the visual system. Z. vergl. Physiol. 49, 605–622 (1965).

    Google Scholar 

  • Hayhow, W.R., Sefton, A., Webb, C.: Primary optic centers of the rat in relation to terminal distribution of the crossed and uncrossed optic nerve fibers. J. comp. Neurol. 118, 295–322 (1962).

    Google Scholar 

  • Kato, H., Yamamoto, M., Nakahama, H.: Intracellular recordings from the lateral geniculate neurons of cats. Jap. J. Physiol. 21, 307–323 (1971).

    Google Scholar 

  • Krieg, W.J.S.: Connection of the cerebral cortex. I. The albino rat. A. Topography of the cortical area. J. comp. Neurol. 84, 221–275 (1946).

    Google Scholar 

  • Lund, R.D.: Uncrossed visual pathways of albino and hooded rats. Science 149, 1506–1507 (1965).

    Google Scholar 

  • Maekawa, K., Rosina, A.: Synaptic transmission in the sensory relay neurones of the thalamus. Progr. Brain Res., “Mechanisms of Synaptic Transmission”, Vol. 31, p. 259–264. Ed. by K. Akert and P.G. Waser. Amsterdam: Elsevier 1969.

    Google Scholar 

  • McIlwain, J.C., Creutzfeldt, O.D.: Microelectrode study of synaptic excitation and inhibition in the lateral geniculate nucleus of the cat. J. Neurophysiol. 30, 1–22 (1967).

    Google Scholar 

  • Noda, H., Iwama, K.: Unitary analysis of retino-geniculate response time in rats. Vision Res. 7, 205–213 (1967).

    Google Scholar 

  • Sefton, A.J., Swinburn, M.: Electrical activity of lateral geniculate nucleus and optic tract of the rat. Vision Res. 4, 315–328 (1964).

    Google Scholar 

  • Singer, W., Creutzfeldt, O.D.: Reciprocal lateral inhibition of on- and off-center neurones in the lateral geniculate body of the cat. Exp. Brain Res. 10, 311–330 (1970).

    Google Scholar 

  • Stone, J., Hoffmann, K.P.: Conduction velocity as a parameter in the organization of the afferent relay in the cat's lateral geniculate nucleus. Brain Res. 32, 454–459 (1971).

    Google Scholar 

  • Sumitomo, I., Ide, K., Iwama, K.: Maintained activity and responsiveness to flicker stimulation in rat lateral geniculate neurons. Physiol. Behav. 3, 955–959 (1968).

    Google Scholar 

  • —, Arikuni, T.: Conduction velocity of optic nerve fibers innervating lateral geniculate body and superior colliculus in the rat. Exp. Neurol. 25, 378–392 (1969).

    Google Scholar 

  • Sumitomo, I., Iwama, K., Arikuni, T.: A relation between visual field representation of rat lateral geniculate cells and conduction velocities of optic nerve fibers innervating them. Brain Res. 24, 333–335 (1970).

    Google Scholar 

  • Suzuki, H., Kato, E.: Binocular interaction at cat's lateral geniculate body. J. Neurophysiol. 29, 909–919 (1966).

    Google Scholar 

  • —: Postsynaptic inhibition in the lateral geniculate nucleus and its relation to “Recovery Cycle” of geniculate population response. Tohoku J. exp. Med. 92, 271–279 (1967).

    Google Scholar 

  • —, Takahashi, M.: Organization of lateral geniculate neurons in binocular inhibition. Brain Res. 23, 261–264 (1970).

    Google Scholar 

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Fukuda, Y. Differentiation of principal cells of the rat lateral geniculate body into two groups; fast and slow cells. Exp Brain Res 17, 242–260 (1973). https://doi.org/10.1007/BF00234664

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