The Effect of Short-Term Sensory Deprivation on Rote Learning

1966 ◽  
Vol 64 (1) ◽  
pp. 127-133 ◽  
Author(s):  
Cabot L. Jaffee
1993 ◽  
Vol 53 (6) ◽  
pp. 1231-1234 ◽  
Author(s):  
D.Curtis Lawson ◽  
Susan S. Schiffman ◽  
Theodore N. Pappas

2013 ◽  
Vol 110 (4) ◽  
pp. 999-1008 ◽  
Author(s):  
Anne E. Takesian ◽  
Vibhakar C. Kotak ◽  
Neeti Sharma ◽  
Dan H. Sanes

Sensory deprivation, such as developmental hearing loss, leads to an adjustment of synaptic and membrane properties throughout the central nervous system. These changes are thought to compensate for diminished sound-evoked activity. This model predicts that compensatory changes should be synergistic with one another along each functional pathway. To test this idea, we examined the excitatory thalamic drive to two types of cortical inhibitory interneurons that display differential effects in response to developmental hearing loss. The inhibitory synapses made by fast-spiking (FS) cells are weakened by hearing loss, whereas those made by low threshold-spiking (LTS) cells remain strong but display greater short-term depression ( Takesian et al. 2010 ). Whole-cell recordings were made from FS or LTS interneurons in a thalamocortical brain slice, and medial geniculate (MG)-evoked postsynaptic potentials were analyzed. Following hearing loss, MG-evoked net excitatory potentials were smaller than normal at FS cells but larger than normal at LTS cells. Furthermore, MG-evoked excitatory potentials displayed less short-term depression at FS cells and greater short-term depression at LTS cells. Thus deprivation-induced adjustments of excitatory synapses onto inhibitory interneurons are cell-type specific and parallel the changes made by the inhibitory afferents.


eLife ◽  
2018 ◽  
Vol 7 ◽  
Author(s):  
Paola Binda ◽  
Jan W Kurzawski ◽  
Claudia Lunghi ◽  
Laura Biagi ◽  
Michela Tosetti ◽  
...  

Sensory deprivation during the post-natal ‘critical period’ leads to structural reorganization of the developing visual cortex. In adulthood, the visual cortex retains some flexibility and adapts to sensory deprivation. Here we show that short-term (2 hr) monocular deprivation in adult humans boosts the BOLD response to the deprived eye, changing ocular dominance of V1 vertices, consistent with homeostatic plasticity. The boost is strongest in V1, present in V2, V3 and V4 but absent in V3a and hMT+. Assessment of spatial frequency tuning in V1 by a population Receptive-Field technique shows that deprivation primarily boosts high spatial frequencies, consistent with a primary involvement of the parvocellular pathway. Crucially, the V1 deprivation effect correlates across participants with the perceptual increase of the deprived eye dominance assessed with binocular rivalry, suggesting a common origin. Our results demonstrate that visual cortex, particularly the ventral pathway, retains a high potential for homeostatic plasticity in the human adult.


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