Literature DB >> 22322104

Potential utility of optogenetics in the study of depression.

Mary Kay Lobo1, Eric J Nestler, Herbert E Covington.   

Abstract

Novel antidepressants are needed to enhance the health and quality of life of the hundreds of millions of depressed individuals worldwide who remain inadequately treated with today's approaches. In reality, no new class of antidepressant medication has been introduced in over 50 years. This insufficiency of current drug treatments is evident to those eager to pursue invasive experimental options like that of deep brain stimulation. Encouragingly, human brain imaging studies and animal work implicate strong relationships between depressive symptoms and patterns of brain activity, which are now open to more empirical assessments using optogenetics. Recent advances in optogenetics permit control over specific subtypes of neurons or their afferent or efferent projections and can greatly further our understanding of the neural mechanisms involved in depression and the mechanism of action of deep brain stimulation and perhaps chemical antidepressants. Here, we discuss how optogenetic tools are being used to answer a broad range of molecular, cellular, and circuit-level questions pertaining to depression that, up until now, have been resistant to other experimental approaches. The emergence of optogenetic technology, when combined with the best-validated animal models of depression, will dramatically increase knowledge about the basic neurobiology of depression, as well as facilitate the development of more effective antidepressant treatments.
Copyright © 2012 Society of Biological Psychiatry. Published by Elsevier Inc. All rights reserved.

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Year:  2012        PMID: 22322104      PMCID: PMC3738208          DOI: 10.1016/j.biopsych.2011.12.026

Source DB:  PubMed          Journal:  Biol Psychiatry        ISSN: 0006-3223            Impact factor:   13.382


  98 in total

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Journal:  Nat Neurosci       Date:  2011-01-30       Impact factor: 24.884

2.  Regulation of parkinsonian motor behaviours by optogenetic control of basal ganglia circuitry.

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Review 3.  Animal models of neuropsychiatric disorders.

Authors:  Eric J Nestler; Steven E Hyman
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4.  Spatiotemporal control of small GTPases with light using the LOV domain.

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Journal:  Methods Enzymol       Date:  2011       Impact factor: 1.600

5.  Reciprocal limbic-cortical function and negative mood: converging PET findings in depression and normal sadness.

Authors:  H S Mayberg; M Liotti; S K Brannan; S McGinnis; R K Mahurin; P A Jerabek; J A Silva; J L Tekell; C C Martin; J L Lancaster; P T Fox
Journal:  Am J Psychiatry       Date:  1999-05       Impact factor: 18.112

6.  Targeted optogenetic stimulation and recording of neurons in vivo using cell-type-specific expression of Channelrhodopsin-2.

Authors:  Jessica A Cardin; Marie Carlén; Konstantinos Meletis; Ulf Knoblich; Feng Zhang; Karl Deisseroth; Li-Huei Tsai; Christopher I Moore
Journal:  Nat Protoc       Date:  2010-01-21       Impact factor: 13.491

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8.  The epidemiology of major depressive disorder: results from the National Comorbidity Survey Replication (NCS-R).

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Authors:  Michael Lutter; Ichiro Sakata; Sherri Osborne-Lawrence; Sherry A Rovinsky; Jason G Anderson; Saendy Jung; Shari Birnbaum; Masashi Yanagisawa; Joel K Elmquist; Eric J Nestler; Jeffrey M Zigman
Journal:  Nat Neurosci       Date:  2008-06-15       Impact factor: 24.884

10.  A high-light sensitivity optical neural silencer: development and application to optogenetic control of non-human primate cortex.

Authors:  Xue Han; Brian Y Chow; Huihui Zhou; Nathan C Klapoetke; Amy Chuong; Reza Rajimehr; Aimei Yang; Michael V Baratta; Jonathan Winkle; Robert Desimone; Edward S Boyden
Journal:  Front Syst Neurosci       Date:  2011-04-13
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  15 in total

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Authors:  Rachel J Sizemore; Sonja Seeger-Armbruster; Stephanie M Hughes; Louise C Parr-Brownlie
Journal:  J Neurophysiol       Date:  2016-02-17       Impact factor: 2.714

2.  Minimal time spiking in various ChR2-controlled neuron models.

Authors:  Vincent Renault; Michèle Thieullen; Emmanuel Trélat
Journal:  J Math Biol       Date:  2017-06-29       Impact factor: 2.259

3.  ∆FosB differentially modulates nucleus accumbens direct and indirect pathway function.

Authors:  Brad A Grueter; Alfred J Robison; Rachael L Neve; Eric J Nestler; Robert C Malenka
Journal:  Proc Natl Acad Sci U S A       Date:  2013-01-14       Impact factor: 11.205

4.  CB1 augments mGluR5 function in medial prefrontal cortical neurons to inhibit amygdala hyperactivity in an arthritis pain model.

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5.  Differential induction of FosB isoforms throughout the brain by fluoxetine and chronic stress.

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Journal:  Neuropharmacology       Date:  2015-07-09       Impact factor: 5.250

Review 6.  Using optogenetics to study habits.

Authors:  Kyle S Smith; Ann M Graybiel
Journal:  Brain Res       Date:  2013-01-10       Impact factor: 3.252

7.  Anhedonia and the brain reward circuitry in depression.

Authors:  Mitra Heshmati; Scott J Russo
Journal:  Curr Behav Neurosci Rep       Date:  2015-07-12

8.  Activin receptor signaling regulates cocaine-primed behavioral and morphological plasticity.

Authors:  Amy M Gancarz; Zi-Jun Wang; Gabrielle L Schroeder; Diane Damez-Werno; Kevin M Braunscheidel; Lauren E Mueller; Monica S Humby; Aaron Caccamise; Jennifer A Martin; Karen C Dietz; Rachael L Neve; David M Dietz
Journal:  Nat Neurosci       Date:  2015-06-01       Impact factor: 24.884

9.  Modulation of medial prefrontal cortical activity using in vivo recordings and optogenetics.

Authors:  Guangchen Ji; Volker Neugebauer
Journal:  Mol Brain       Date:  2012-10-08       Impact factor: 4.041

10.  Optogenetics as a neuromodulation tool in cognitive neuroscience.

Authors:  E A Claudia Pama; Lorenza S Colzato; Bernhard Hommel
Journal:  Front Psychol       Date:  2013-09-06
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