Next-Generation Tools to Study Autonomic Regulation In Vivo

被引:6
|
作者
Mukerjee, Snigdha [1 ]
Lazartigues, Eric [1 ,2 ,3 ]
机构
[1] Louisiana State Univ, Hlth Sci Ctr, Dept Pharmacol & Expt Therapeut, New Orleans, LA 70112 USA
[2] Louisiana State Univ, Hlth Sci Ctr, Neurosci & Cardiovasc Ctr Excellence, New Orleans, LA 70112 USA
[3] Southeast Louisiana Vet Hlth Care Syst, New Orleans, LA 70112 USA
基金
美国国家卫生研究院;
关键词
Autonomic regulation; Optogenetics; Calcium sensors; DREADD; SYMPATHETIC-NERVE ACTIVITY; OPTOGENETIC STIMULATION; TRANSGENIC MICE; NEURONS; ACTIVATION; BRAIN; LIGHT; HYPERTENSION; MODULATION; EXPRESSION;
D O I
10.1007/s12264-018-0319-2
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
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.
引用
收藏
页码:113 / 123
页数:11
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