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The Periodic Table03:25

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As early chemists discovered more elements, they realized that various elements could be grouped by their similar chemical behaviors. One such grouping includes lithium (Li), sodium (Na), and potassium (K). All of these elements are shiny, conduct heat and electricity well, and have similar chemical properties. A second grouping includes calcium (Ca), strontium (Sr), and barium (Ba), which also are shiny, good conductors of heat and electricity, and have chemical properties in common. However,...
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The Measurement and Treatment of Suppression in Amblyopia
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Critical periods in amblyopia.

Takao K Hensch1, Elizabeth M Quinlan2

  • 1FM Kirby Neurobiology Center,Boston Children's Hospital,Harvard Medical School,Boston,Massachusetts.

Visual Neuroscience
|June 16, 2018
PubMed
Summary

Synaptic plasticity in the visual cortex, crucial for development and amblyopia treatment, is actively constrained by molecular brakes in adults. Lifting these brakes restores plasticity, offering new hope for treating vision disorders.

Keywords:
AcetylcholineDark exposureGABAHDACPSD-95ParvalbuminPerineuronal net

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Area of Science:

  • Neuroscience
  • Developmental Biology
  • Ophthalmology

Background:

  • Monocular deprivation induces ocular dominance shifts, a key model for synaptic plasticity during a critical period.
  • Visual plasticity is constrained by development, limiting amblyopia recovery in adults.
  • Understanding these constraints is vital for developing effective amblyopia treatments.

Purpose of the Study:

  • To investigate the molecular and cellular mechanisms controlling critical periods of plasticity in the primary visual cortex (V1).
  • To explore how plasticity is actively constrained in adults and if these constraints can be overcome.
  • To assess the potential for reactivating plasticity for amblyopia treatment in adults.

Main Methods:

  • Utilized mouse models with advanced molecular, genetic, and imaging tools.
  • Examined the neurobiology of critical period initiation and termination.
  • Investigated molecular mechanisms that regulate synaptic plasticity.

Main Results:

  • Plasticity is not lost with age but actively constrained by molecular 'brakes' that up-regulate developmentally.
  • Lifting these molecular brakes enhances plasticity in the adult visual cortex.
  • Experimental manipulations can reactivate plasticity in adult animals.

Conclusions:

  • The closure of critical periods is an active, regulated process, not merely passive decay.
  • Targeting molecular brakes offers a promising strategy for treating adult amblyopia.
  • Mechanistic insights into critical periods can guide clinical interventions for vision restoration.