The postnatal development of visual callosal connections in the absence of visual experience or of the eyes

1980 ◽  
Vol 39 (4) ◽  
Author(s):  
G.M. Innocenti ◽  
D.O. Frost
Keyword(s):  
Postnatal Development ◽  
Visual Experience ◽  
Callosal Connections

Functional postnatal development of the rat primary visual cortex and the role of visual experience: Dark rearing and monocular deprivation

1994 ◽  
Vol 34 (6) ◽  
pp. 709-720 ◽  
Author(s):  
Michela Fagiolini ◽  
Tommaso Pizzorusso ◽  
Nicoletta Berardi ◽  
Luciano Domenici ◽  
Lamberto Maffei
Keyword(s):  
Visual Cortex ◽  
Postnatal Development ◽  
Primary Visual Cortex ◽  
Visual Experience ◽  
Monocular Deprivation ◽  
Dark Rearing

scholarly journals Lack of visual experience does not affect the retinotopic organization of visual cortico-callosal connections.

2012 ◽  
Vol 12 (9) ◽  
pp. 1358-1358
Author(s):  
A. Bock ◽  
M. Saenz ◽  
G. Boynton ◽  
H. Bridge ◽  
I. Fine
Keyword(s):  
Visual Experience ◽  
Callosal Connections ◽  
Retinotopic Organization

scholarly journals Experience-dependent development of NMDAR1 subunit expression in the lateral geniculate nucleus

1999 ◽  
Vol 16 (4) ◽  
pp. 781-789 ◽  
Author(s):  
MARK A. FAVA ◽  
KEVIN R. DUFFY ◽  
KATHRYN M. MURPHY
Keyword(s):  
Visual Cortex ◽  
Postnatal Development ◽  
Lateral Geniculate Nucleus ◽  
Critical Period ◽  
Visual Experience ◽  
Monocular Deprivation ◽  
Lateral Geniculate ◽  
Subunit Expression ◽  
Complete Reversal ◽  
Eye Opening

Monocular deprivation early in postnatal development leads to anatomical and physiological changes in the lateral geniculate nucleus (LGN) and visual cortex. Many of these changes are dependent upon activation of the NMDA receptor. We have examined the role of visual experience in modifying NMDAR1 subunit expression in the LGN of animals reared with various forms of visual deprivation. Following monocular deprivation initiated either at eye opening or at the peak of the critical period, there were approximately 20% fewer NMDAR1-immunopositive neurons in the deprived laminae of the LGN. The loss of NMDAR1-immunopositive neurons was found throughout both the binocular and monocular segments of the LGN and after monocular deprivation until just 3 weeks of age. These results indicate that the loss of NMDAR1 in the LGN following monocular deprivation does not simply reflect changes in the visual cortex. The loss of NMDAR1 expression was not necessarily permanent. Initiation of binocular vision at the peak of the critical period ameliorated the effect of monocular deprivation and the introduction of a period of reverse occlusion led to a complete reversal. Taken together, the results show that the expression of the NMDAR1 subunit in the LGN can be modified by the pattern of visual experience during postnatal development.

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