The ability to change behavior likely depends on the selective strengthening and weakening of brain synapses. The cellular models of synaptic plasticity, long-term potentiation (LTP) and depression (LTD) of synaptic strength, can be expressed by the synaptic insertion or removal of AMPA receptors (AMPARs), respectively. We here present an overview of studies that have used animal models to show that such AM PAR trafficking underlies several experience-driven phenomena-from neuronal circuit formation to the modification of behavior. We argue that monitoring and manipulating synaptic AMPAR trafficking represents an attractive means to study cognitive function and dysfunction in animal models.
机构:
Univ N Carolina, Dept Cell Biol & Physiol, Chapel Hill, NC 27514 USA
Univ N Carolina, Neurosci Ctr, Chapel Hill, NC 27514 USAUniv N Carolina, Dept Cell Biol & Physiol, Chapel Hill, NC 27514 USA
Diering, Graham H.
Huganir, Richard L.
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机构:
Johns Hopkins Univ, Sch Med, Solomon H Snyder Dept Neurosci, Baltimore, MD 21205 USA
Johns Hopkins Univ, Kavli Neurosci Discovery Inst, Baltimore, MD 21205 USAUniv N Carolina, Dept Cell Biol & Physiol, Chapel Hill, NC 27514 USA