Friday, July 23, 2010

Directly controlling 'fear' cells in the brain.

LeDoux and collaborators have done the clever experiment (in rats) of introducing an optically activated molecular label into cells in the amygdala thought to be causal in fear conditioning. Activation of these cells by light just after presentation of a auditory sensory cue (but with no aversive stimulus) caused the rats to exhibit behavioral fear responses when the cue was subsequently presented.

Humans and animals can learn that specific sensory cues in the environment predict aversive events through a form of associative learning termed fear conditioning. This learning occurs when the sensory cues are paired with an aversive event occuring in close temporal proximity. Activation of lateral amygdala (LA) pyramidal neurons by aversive stimuli is thought to drive the formation of these associative fear memories; yet, there have been no direct tests of this hypothesis. Here we demonstrate that viral-targeted, tissue-specific expression of the light-activated channelrhodopsin (ChR2) in LA pyramidal cells permitted optical control of LA neuronal activity. Using this approach we then paired an auditory sensory cue with optical stimulation of LA pyramidal neurons instead of an aversive stimulus. Subsequently presentation of the tone alone produced behavioral fear responses. These results demonstrate in vivo optogenetic control of LA neurons and provide compelling support for the idea that fear learning is instructed by aversive stimulus-induced activation of LA pyramidal cells.

1 comment:

shorter college georgia said...

Thank you for sharing us this information. This is a great study but I think we need to test a bit more in order to arrive to a conclusion. But I think it makes sense in overall aspect so this facts can be considered when we talk about fear conditioning.

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