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Karl Lashley
wanted to know where in brain memories stored
lesioned parts of cortex and effects of lesions on maze performance
engram is distributed and not stored in specific region
Engram
enduring offline physical and/or chemical changes that were elicited by learning and underlie newly formed memory associations
Engram cells
cells that constitute critical cellular components of given engram
activated by learning experience, physically or chemically modified by learning experience, reactivated by subsequent presentation of stimuli present at learning experience
fear conditioning
pair tone with shock
set of engram cells undergo plasticity and allocated to that engram
lesioning engram cells abolishes memory of fear conditioning
Immediate Early Genes
genes that are rapidly and transiently expressed in response to neural activation
associated with neural plasticity (ex. c-Fos and Arc)
c-Fos used to identify engram cells
Optogenetics
reversible lesion
light sensitive protiens (opsins) expressed in specific population of neurons, don’t respond to any chemical but light instead
fast temporal res, implanted optic fiber does damage and possible heating
Tagging an Engram
Virus injected into region
if neuron expresses c-Fos and is off Doxycycline, generates optogenetic protein chennelrhodopsin (ChR2)
Engram complex
entire brain-wide engram supporting a memory that is stored in sets of engram cell ensembles in different brain regions connected via an engram cell pathway