Literature DB >> 7589290

Magnocellular and parvocellular divisions of pigeon nucleus isthmi differentially modulate visual responses in the tectum.

S R Wang1, Y C Wang, B J Frost.   

Abstract

The electrophysiological responses of 162 tectal cells to computer-generated visual stimuli were extracellularly recorded from 24 homing pigeons before and after injecting either lidocaine or N-methyl-D-aspartate (NMDA) into the nucleus isthmi pars magnocellularis (Imc) or the nucleus isthmi pars parvocellularis (Ipc). Micro-injections of lidocaine into Imc resulted in a significant reduction of firing rate in 80% of tectal cells, whose excitatory receptive fields (ERFs) were localized within the ERF of the Imc cell where the lidocaine was injected. In contrast, when lidocaine was injected into Ipc under identical circumstances it had no effect on the visually driven activity of 68% of tectal cells. However, when the excitatory amino acid NMDA was injected into Ipc it produced a significant reduction in the visually driven firing of 75% of tectal neurons when their ERFs were within the isthmic ERF, while similar application of NMDA into Imc had no effect on the visually driven response of 94% of tectal neurons. When the ERFs of tectal cells were localized outside the ERF of the isthmic cell where the chemical was injected, Imc-injected lidocaine had no effect in 9 out of 10 tectal cells, whereas Ipc-injected NMDA increased firing in 7 out of 17 tectal cells. Therefore, it is suggested that the Imc-tectal fibers participate in a positive feedback pathway and the Ipc-tectal fibers are involved in a negative feedback pathway.

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Year:  1995        PMID: 7589290     DOI: 10.1007/BF00231973

Source DB:  PubMed          Journal:  Exp Brain Res        ISSN: 0014-4819            Impact factor:   1.972


  53 in total

1.  A projection from the parabigeminal nucleus to the pulvinar nucleus in Galago.

Authors:  I T Diamond; D Fitzpatrick; M Conley
Journal:  J Comp Neurol       Date:  1992-02-15       Impact factor: 3.215

2.  Visual response characteristics of neurons in the nucleus isthmi magnocellularis and nucleus isthmi parvocellularis of pigeons.

Authors:  Y C Wang; B J Frost
Journal:  Exp Brain Res       Date:  1991       Impact factor: 1.972

3.  Nucleus isthmi: its contribution to tectal acetylcholinesterase and choline acetyltransferase in the frog Rana pipiens.

Authors:  M T Wallace; A J Ricciuti; E R Gruberg
Journal:  Neuroscience       Date:  1990       Impact factor: 3.590

4.  Release of exqenous glycine in the pigeon optic tectum during stimulation of a midbrain nucleus.

Authors:  J C Reubi; M Cuénod
Journal:  Brain Res       Date:  1976-08-13       Impact factor: 3.252

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Authors:  E R Gruberg; S B Udin
Journal:  J Comp Neurol       Date:  1978-06-01       Impact factor: 3.215

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Authors:  F J Hock
Journal:  Behav Neural Biol       Date:  1983-07

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Authors:  L S Jen; Z G Dai; K F So
Journal:  Neurosci Lett       Date:  1984-10-12       Impact factor: 3.046

8.  Anatomy and physiology of a binocular system in the frog Rana pipiens.

Authors:  E R Gruberg; J Y Lettvin
Journal:  Brain Res       Date:  1980-06-23       Impact factor: 3.252

9.  Visual field topography in the frog's nucleus isthmi.

Authors:  S J Wang; K Yan; Y T Wang
Journal:  Neurosci Lett       Date:  1981-04-09       Impact factor: 3.046

10.  The organization of the parabigemino-tectal projections in the opossum.

Authors:  R Méndez-Otero; C E Rocha-Miranda; V H Perry
Journal:  Brain Res       Date:  1980-09-29       Impact factor: 3.252

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  2 in total

1.  Response properties of visual neurons in the turtle nucleus isthmi.

Authors:  Debajit Saha; David Morton; Michael Ariel; Ralf Wessel
Journal:  J Comp Physiol A Neuroethol Sens Neural Behav Physiol       Date:  2010-10-22       Impact factor: 1.836

2.  Neuronal circuitry and discharge patterns controlling eye movements in the pigeon.

Authors:  Yang Yang; Yan Yang; Shu-Rong Wang
Journal:  J Neurosci       Date:  2008-10-15       Impact factor: 6.167

  2 in total

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