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Pharmacol Rev. 2013 Jan 10;65(1):156-70. doi: 10.1124/pr.111.005611. Print 2013 Jan.

Integrating optogenetic and pharmacological approaches to study neural circuit function: current applications and future directions.

Author information

1
Departments of Psychiatry & Cell Biology and Physiology, UNC Neuroscience Center University of North Carolina at Chapel Hill, Chapel Hill, NC, USA. gstuber@med.unc.edu

Abstract

Optogenetic strategies to control genetically distinct populations of neurons with light have been rapidly evolving and widely adopted by the neuroscience community as one of the most important tool sets to study neural circuit function. Although optogenetics have already reshaped neuroscience by allowing for more precise control of circuit function compared with traditional techniques, current limitations of these approaches should be considered. Here, we discuss several strategies that combine optogenetic and contemporary pharmacological techniques to further increase the specificity of neural circuit manipulation. We also discuss recent advances that allow for the selective modulation of cellular function and gene expression with light. In addition, we outline a novel application of optogenetic circuit analysis for causally addressing the role of pathway-specific neural activity in mediating alterations in postsynaptic transcriptional processing in genetically defined neurons. By determining how optogenetic activation of specific neural circuits causally contributes to alterations in gene expression in a high-throughput fashion, novel biologic targets for future pharmacological intervention may be uncovered. Lastly, extending this experimental pipeline to selectively target pharmacotherapies to genetically defined neuronal populations or circuits will not only provide more selective control of neural circuits, but also may lead to the development of neural circuit specific pharmacological therapeutics.

PMID:
23319548
PMCID:
PMC3565921
DOI:
10.1124/pr.111.005611
[Indexed for MEDLINE]
Free PMC Article

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