Literature DB >> 6173404

Efferent systems of the rabbit visual cortex: laminar distribution of the cells of origin, axonal conduction velocities, and identification of axonal branches.

H A Swadlow, T G Weyand.   

Abstract

Several efferent systems of visual area I in Dutch rabbits were studied with anatomical (horseradish peroxidase) and physiological (antidromic) methods. Anatomical studies provided information regarding the laminar origin of the projections to the contralateral hemisphere, visual area II, the dorsal lateral geniculate nucleus, and the superior colliculus. Physiological studies provided information regarding conduction velocities and multiple destinations of efferent axons. Both the callosal projection and the projection to V-II were shown to originate primarily in layer II-III. However, approximately 10-20% of the callosal projection and 20-40% of the projection to V-II originated in layers IV and V. In contrast, the projection to the dorsal lateral geniculate nucleus originated nearly exclusively in layer VI, while corticotectal neurons occurred primarily in layer V. A significant number of corticotectal neurons were, however, found in layer IV. Thus, the above efferent systems were found to differ in their principal laminar origin and in the diffuseness of that origin. The origins of corticocortical projections were considerably more diffuse than those of corticofugal projections. In addition to differences in laminar origin, efferent systems also differed significantly in the conduction velocities of their axons. The projection to visual area II and to the lateral geniculate nucleus consisted primarily of very slowly conducting axons, while the projection to the superior colliculus was fast conduction. The callosal projection consisted of both slow and fact conduction axons. Finally, the question of branching of V-I efferent axons was addressed. Although the laminar origin of the projections to the contralateral hemisphere and to visual area II overlapped considerably, none of these corticocortical axons could be shown to project to both locations or to a subcortical destination. In contrast, approximately one-third of corticotectal axons were shown to project a collateral into the thalamus. Although the destination of this collateral is unclear, it is medial to the lateral geniculate nucleus and may be the pulvinar.

Entities:  

Mesh:

Substances:

Year:  1981        PMID: 6173404     DOI: 10.1002/cne.902030415

Source DB:  PubMed          Journal:  J Comp Neurol        ISSN: 0021-9967            Impact factor:   3.215


  27 in total

1.  Voltage-sensitive dye imaging of neocortical spatiotemporal dynamics to afferent activation frequency.

Authors:  D Contreras; R Llinas
Journal:  J Neurosci       Date:  2001-12-01       Impact factor: 6.167

2.  Long-term potentiation of thalamocortical transmission in the adult visual cortex in vivo.

Authors:  A J Heynen; M F Bear
Journal:  J Neurosci       Date:  2001-12-15       Impact factor: 6.167

3.  Developmental inhibitory gate controls the relay of activity to the superficial layers of the visual cortex.

Authors:  C Rozas; H Frank; A J Heynen; B Morales; M F Bear; A Kirkwood
Journal:  J Neurosci       Date:  2001-09-01       Impact factor: 6.167

4.  Three channels of corticothalamic communication during locomotion.

Authors:  Mikhail G Sirota; Harvey A Swadlow; Irina N Beloozerova
Journal:  J Neurosci       Date:  2005-06-22       Impact factor: 6.167

5.  The impact of a corticotectal impulse on the awake superior colliculus.

Authors:  Yulia Bereshpolova; Carl R Stoelzel; Alexander G Gusev; Tatiana Bezdudnaya; Harvey A Swadlow
Journal:  J Neurosci       Date:  2006-02-22       Impact factor: 6.167

6.  Robust but delayed thalamocortical activation of dendritic-targeting inhibitory interneurons.

Authors:  Zhenjun Tan; Hang Hu; Z Josh Huang; Ariel Agmon
Journal:  Proc Natl Acad Sci U S A       Date:  2008-02-01       Impact factor: 11.205

7.  Temporal properties of feedforward and feedback pathways between the thalamus and visual cortex in the ferret.

Authors:  Farran Briggs; W Martin Usrey
Journal:  Thalamus Relat Syst       Date:  2005-06

8.  A cross-species comparison of corticogeniculate structure and function.

Authors:  J Michael Hasse; Farran Briggs
Journal:  Vis Neurosci       Date:  2017-11-16       Impact factor: 3.241

9.  The non-lemniscal auditory cortex in ferrets: convergence of corticotectal inputs in the superior colliculus.

Authors:  Victoria M Bajo; Fernando R Nodal; Jennifer K Bizley; Andrew J King
Journal:  Front Neuroanat       Date:  2010-05-21       Impact factor: 3.856

10.  Modulation of gamma-band activity across local cortical circuits.

Authors:  Farran Briggs; W Martin Usrey
Journal:  Front Integr Neurosci       Date:  2009-07-07
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.