| Literature DB >> 30560436 |
Snigdha Mukerjee1, Eric Lazartigues2,3,4.
Abstract
The recent development of tools to decipher the intricacies of neural networks has improved our understanding of brain function. Optogenetics allows one to assess the direct outcome of activating a genetically-distinct population of neurons. Neurons are tagged with light-sensitive channels followed by photo-activation with an appropriate wavelength of light to functionally activate or silence them, resulting in quantifiable changes in the periphery. Capturing and manipulating activated neuron ensembles, is a recently-designed technique to permanently label activated neurons responsible for a physiological function and manipulate them. On the other hand, neurons can be transfected with genetically-encoded Ca2+ indicators to capture the interplay between them that modulates autonomic end-points or somatic behavior. These techniques work with millisecond temporal precision. In addition, neurons can be manipulated chronically to simulate physiological aberrations by transfecting designer G-protein-coupled receptors exclusively activated by designer drugs. In this review, we elaborate on the fundamental concepts and applications of these techniques in research.Entities:
Keywords: Autonomic regulation; Calcium sensors; DREADD; Optogenetics
Mesh:
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Year: 2018 PMID: 30560436 PMCID: PMC6357278 DOI: 10.1007/s12264-018-0319-2
Source DB: PubMed Journal: Neurosci Bull ISSN: 1995-8218 Impact factor: 5.203