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A study of neuronal circuitry mediating the saccadic suppression in the rabbit

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Summary

Stimulation of the deep layers of the superior colliculus (SC) evoked an IPSP in the relay cells of the lateral geniculate nucleus (LGN). The latency of the JPSP ranged from 3.3 to 4.7 ms with an average of 3.87±0.56 ms (S.D.). The IPSP from SC stimulation was proposed to be mediated by the recurrent inhibitory circuit to LGN, since the recurrent inhibitory interneurones in the thalamic reticular nucleus (R) responded to the same stimulation with a latency of 2.14±0.43 ms, which was 1.73 ms shorter than the latency of the IPSP in LGN relay cells. This was in good agreement with our previous observation that the recurrent interneurones always fired about 1.8 ms prior to the onset of the recurrent IPSP in LGN (Lo and Xie 1987b). The recurrent inhibitory interneurones could also be excited by stimulation of the central lateral nucleus (CL) with a very short latency (0.57±0.15 ms), suggesting a monosynaptic connection between the central lateral nucleus and the reticular recurrent interneurones. This suggestion was supported by the fact that CL neurones, which projected to the striate cortex (Cx), were antidromically excited by stimulation of the caudal part of R where the recurrent inhibitory interneurones were situated. CL neurone's response to stimulation of the deep layers of SC (SC-CL response) has a latency of 1.68±0.56 ms, which was comparable with the difference between the latency of SC-R response and that of CL-R response, just as expected from the notion that the saccadic suppression is mediated by a circuit of SC (deep layers) -CL-R-LGN.

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References

  • Bartlett JR, Doty RW Sr, Lee BB, Sakahara H (1976) Influence of saccadic eye movements on geniculostriate excitability in normal monkeys. Exp Brain Res 25: 487–509

    Google Scholar 

  • Beeler GW Jr (1967) Visual threshold changes resulting from spontaneous saccadic eye movements. Vision Res 7: 769–775

    Google Scholar 

  • Cesaro P, Nguyen-Legros J, Pollin B, Laplante S (1985) Single intralaminar thalamic neurons project to cerebral cortex, striatum and nucleus reticularis thalami. A retrograde anatomical tracing study in the rat. Brain Res 325: 29–37

    Google Scholar 

  • Collewijn H (1969) Changes in visual evoked responses during the fast phase of optokinetic nystagmus in the rabbit. Vision Res 9: 803–814

    Google Scholar 

  • Graham J, Berman N (1981) Origins of the pretectal and tectal projections to the central lateral nucleus in the cat. Neurosci Lett 26: 209–214

    Google Scholar 

  • Hall WC, May PJ (1984) The anatomical basis for sensorimotor transformations in the superior colliculus. In: Neff WD (ed) Contributions to sensory physiology, Vol. 8. Academic Press Inc, New York, pp 1–40

    Google Scholar 

  • Harting JK, Hall WC, Diamond IT, Martin GF (1973) Anterograde degeneration study of the superior colliculus in Tuaia glis: evidence for a subdivision between superficial and deep layers. J Comp Neurol 148: 361–386

    Google Scholar 

  • Huerta MF, Harting JK (1984) Connectional organization of the superior colliculus. Trends Neurosci 7: 286–289

    Google Scholar 

  • Kawamura S, Fukushima N, Hattori S, Kudo M (1980) Laminar segregation of cells of origin of ascending projections from the superficial layers of the superior colliculus in the cat. Brain Res 184: 486–490

    Google Scholar 

  • Latour PL (1962) Visual threshold during eye movements. Vision Res 2: 261–262

    Google Scholar 

  • Lo F-S (1981) Synaptic organization of the lateral geniculate nucleus of the rabbit: lack of feed-forward inhibition. Brain Res 221: 387–392

    Google Scholar 

  • Lo F-S (1985) Responses of the rabbit lateral geniculate neurones to electrical stimulation of the visual cortex. Chinese J Physiol Sci 1: 129–136

    Google Scholar 

  • Lo F-S (1986) Connections between the visual cortex and the rostral thalamus in the rabbit. Chinese J Physiol Sci 2: 369–376

    Google Scholar 

  • Lo F-S (1987) Mutual inhibition between recurrent inhibitory interneurones in the geniculocortical pathway of the rabbit. Chinese J Physiol Sci 3: 1–6

    Google Scholar 

  • Lo F-S, Xie G-Y (1987a) Control of recurrent inhibition of the lateral geniculate nucleus by afferents from the superior colliculus of the rabbit. A possible mechanism of saccadic suppression. Exp Brain Res 68: 421–427

    Google Scholar 

  • Lo F-S, Xie G-Y (1987b) Location of interneurones in the recurrent inhibitory circuit of the rabbit lateral geniculate nucleus. Exp Brain Res 66: 83–90

    Google Scholar 

  • Martinez MA, Velayos JL (1981) Afferent connections of the centralis lateralis and paracentralis thalamic nuclei in the cat. Neurosci Lett [Suppl] 7: S109

    Google Scholar 

  • Michael JA, Stark L (1967) Electrophysiological correlates of saccadic suppression. Exp Neurol 17: 233–246

    Google Scholar 

  • Nguyen-Legros J, Cesaro P, Pollin B, Laplante S, Gay M (1982) Thalamostriatal neurons with collateral projection onto the rostral reticular thalamic nucleus: anatomical study in the rat by retrograde axonal transport of iron-dextran and horseradish peroxidase. Brain Res 249: 147–152

    Google Scholar 

  • Noda H (1975) Depression in the excitability of relay cells of lateral geniculate nucleus following saccadic eye movements in the cat. J Physiol (Lond) 249: 87–102

    Google Scholar 

  • Sawyer CH, Everett JW, Green JD (1954) The rabbit diencephalon in stereotaxic coordinates. J Comp Neurol 101: 801–824

    Google Scholar 

  • Schiller PH, Stryker M (1972) Single-unit recording and stimulation in superior colliculus of the alert rhesus monkey. J Neurophysiol 35: 915–924

    Google Scholar 

  • Schlag J, Schlag-Rey M (1971) Induction of oculomotor responses from thalamic internal medullary lamina in the cat. Exp Neurol 1: 956–980

    Google Scholar 

  • Schlag J, Lehtinen I, Schlag-Rey M (1974) Neuronal activity before and during eye movements in thalamic internal medullary lamina of the cat. J Neurophysiol 37: 982–995

    Google Scholar 

  • Schlag J, Schlag-Rey M, Peck CK, Joseph JP (1980) Visual responses of thalamic neurons depending on the direction of gaze and the position of targets in space. Exp Brain Res 40: 170–184

    Google Scholar 

  • Stryker MP, Schiller PH (1975) Eye and head movements evoked by electrical stimulation of monkey superior colliculus. Exp Brain Res 23: 103–112

    Google Scholar 

  • Urban I, Richard P (1972) A stereotaxic atlas of the New Zealand rabbit's brain. Charles C Thomas, Springfield Illinois

    Google Scholar 

  • Zuber BL, Stark L (1966) Saccadic suppression: elevation of visual threshold associated with saccadic eye movements. Exp Neurol 16: 65–79

    Google Scholar 

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Lo, F.S. A study of neuronal circuitry mediating the saccadic suppression in the rabbit. Exp Brain Res 71, 618–622 (1988). https://doi.org/10.1007/BF00248755

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  • DOI: https://doi.org/10.1007/BF00248755

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