Book contents
- OptogeneticsFrom Neuronal Function to Mapping and Disease Biology
- Optogenetics
- Copyright page
- Dedication
- Contents
- Contributors
- Foreword
- Preface
- Part I Optogenetics in Model Organisms
- Part II Opsin Biology, Tools, and Technology Platform
- Part III Optogenetics in Neurobiology, Brain Circuits, and Plasticity
- 12 Optogenetics for Neurological Disorders: What Is the Path to the Clinic?
- 13 Optogenetic Control of Astroglia
- 14 Optogenetics for Neurohormones and Neuropeptides: Focus on Oxytocin
- 15 Optogenetic Approaches to Investigating Brain Circuits
- 16 Optogenetic Mapping of Neuronal Connections and their Plasticity
- Part IV Optogenetics in Learning, Neuropsychiatric Diseases, and Behavior
- Part V Optogenetics in Vision Restoration and Memory
- Part VI Optogenetics in Sleep, Prosthetics, and Epigenetics of Neurodegenerative Diseases
- Index
- Plate Section (PDF Only)
- References
12 - Optogenetics for Neurological Disorders: What Is the Path to the Clinic?
from Part III - Optogenetics in Neurobiology, Brain Circuits, and Plasticity
Published online by Cambridge University Press: 28 April 2017
Edited by
Book contents
- OptogeneticsFrom Neuronal Function to Mapping and Disease Biology
- Optogenetics
- Copyright page
- Dedication
- Contents
- Contributors
- Foreword
- Preface
- Part I Optogenetics in Model Organisms
- Part II Opsin Biology, Tools, and Technology Platform
- Part III Optogenetics in Neurobiology, Brain Circuits, and Plasticity
- 12 Optogenetics for Neurological Disorders: What Is the Path to the Clinic?
- 13 Optogenetic Control of Astroglia
- 14 Optogenetics for Neurohormones and Neuropeptides: Focus on Oxytocin
- 15 Optogenetic Approaches to Investigating Brain Circuits
- 16 Optogenetic Mapping of Neuronal Connections and their Plasticity
- Part IV Optogenetics in Learning, Neuropsychiatric Diseases, and Behavior
- Part V Optogenetics in Vision Restoration and Memory
- Part VI Optogenetics in Sleep, Prosthetics, and Epigenetics of Neurodegenerative Diseases
- Index
- Plate Section (PDF Only)
- References
- Type
- Chapter
- Information
- OptogeneticsFrom Neuronal Function to Mapping and Disease Biology, pp. 169 - 180Publisher: Cambridge University PressPrint publication year: 2017
References
Bergey, G. K., Morrell, M. J., et al., (2015). Long-term treatment with responsive brain stimulation in adults with refractory partial seizures. Neurology 84(8): 810–817.CrossRefGoogle ScholarPubMed
Berndt, A., Lee, S. Y., et al., (2014). Structure-guided transformation of channelrhodopsin into a light-activated chloride channel. Science 344(6182): 420–424.CrossRefGoogle ScholarPubMed
Boyden, E. S., Zhang, F., et al., (2005). Millisecond-timescale, genetically targeted optical control of neural activity. Nat Neurosci 8(9): 1263–1268.CrossRefGoogle ScholarPubMed
Carr, F. B. and Zachariou, V. (2014). Nociception and pain: lessons from optogenetics. Front Behav Neurosci 8: 69.CrossRefGoogle ScholarPubMed
Cavanaugh, J., Monosov, I. E., et al., (2012). Optogenetic inactivation modifies monkey visuomotor behavior. Neuron 76(5): 901–907.CrossRefGoogle ScholarPubMed
Chiang, C. C., Ladas, T. P., et al., (2014). Seizure suppression by high frequency optogenetic stimulation using in vitro and in vivo animal models of epilepsy. Brain Stimul 7(6): 890–899.CrossRefGoogle ScholarPubMed
Gerits, A., Farivar, R., et al., (2012). Optogenetically induced behavioral and functional network changes in primates. Curr Biol 22(18): 1722–1726.CrossRefGoogle Scholar
Gerits, A. and Vanduffel, W. (2013). Optogenetics in primates: a shining future? Trends Genet 29(7): 403–411.CrossRefGoogle ScholarPubMed
Gradinaru, V., Mogri, M., et al., (2009). Optical deconstruction of Parkinsonian neural circuitry. Science 324(5925): 354–359.CrossRefGoogle ScholarPubMed
Gradinaru, V., Zhang, F., et al., (2010). Molecular and cellular approaches for diversifying and extending optogenetics. Cell 141(1): 154–165.CrossRefGoogle ScholarPubMed
Gunaydin, L. A., Yizhar, O., et al., (2010). Ultrafast optogenetic control. Nat Neurosci 13(3): 387–392.CrossRefGoogle ScholarPubMed
Han, X. (2012). Optogenetics in the nonhuman primate. Prog Brain Res 196: 215–233.CrossRefGoogle ScholarPubMed
Han, X., Chow, B. Y., et al., (2011). A high-light sensitivity optical neural silencer: development and application to optogenetic control of non-human primate cortex. Front Syst Neurosci 5: 18.CrossRefGoogle ScholarPubMed
Jazayeri, M., Lindbloom-Brown, Z., et al., (2012). Saccadic eye movements evoked by optogenetic activation of primate V1. Nat Neurosci 15(10): 1368–1370.CrossRefGoogle Scholar
Jin, X., Tecuapetla, F., et al., (2014). Basal ganglia subcircuits distinctively encode the parsing and concatenation of action sequences. Nat Neurosci 17(3): 423–430.CrossRefGoogle Scholar
Krook-Magnuson, E., Armstrong, C., et al., (2013). On-demand optogenetic control of spontaneous seizures in temporal lobe epilepsy. Nat Commun 4: 1376.CrossRefGoogle ScholarPubMed
Krook-Magnuson, E. and Soltesz, I. (2015). Beyond the hammer and the scalpel: selective circuit control for the epilepsies. Nat Neurosci 18(3): 331–338.CrossRefGoogle Scholar
Krook-Magnuson, E., Szabo, G. G., et al., (2014). Cerebellar directed optogenetic intervention inhibits spontaneous hippocampal seizures in a mouse model of temporal lobe epilepsy. eNeuro 1(1): e.2014.CrossRefGoogle Scholar
Kros, L., Rooda, O. H. Eelkman, et al., (2015). Cerebellar output controls generalized spike-and-wave discharge occurrence. Ann Neurol 77(6): 1027–1049.CrossRefGoogle Scholar
Lammel, S., Tye, K. M., et al., (2014). Progress in understanding mood d isorders: optogenetic dissection of neural circuits. Genes Brain Behav 13(1): 38–51.CrossRefGoogle Scholar
Montgomery, K. L., Yeh, A. J., et al., (2015). Wirelessly powered, fully internal optogenetics for brain, spinal and peripheral circuits in mice. Nat Methods 12(10): 969–974.CrossRefGoogle ScholarPubMed
Nature Video. (2010). Method of the Year 2010: Optogenetics. from https://www.youtube.com/watch?v=I64X7vHSHOE.Google Scholar
Ozden, I., Wang, J., et al., (2013). A coaxial optrode as multifunction write-read probe for optogenetic studies in non-human primates. J Neurosci Methods 219(1): 142–154.CrossRefGoogle ScholarPubMed
Paz, J. T., Davidson, T. J., et al., (2013). Closed-loop optogenetic control of thalamus as a tool for interrupting seizures after cortical injury. Nat Neurosci 16(1): 64–70.CrossRefGoogle ScholarPubMed
Raimondo, J. V., Kay, L., et al., (2012). Optogenetic silencing strategies differ in their effects on inhibitory synaptic transmission. Nat Neurosci 15(8): 1102–1104.CrossRefGoogle ScholarPubMed
Tonnesen, J., Sorensen, A. T., et al., (2009). Optogenetic control of epileptiform activity. Proc Natl Acad Sci U S A 106(29): 12162–12167.CrossRefGoogle ScholarPubMed
Wykes, R. C., Heeroma, J. H., et al., (2012). Optogenetic and potassium channel gene therapy in a rodent model of focal neocortical epilepsy. Sci Transl Med 4(161): 161ra152.CrossRefGoogle Scholar
Zemelman, B. V., Lee, G. A., et al., (2002). Selective photostimulation of genetically chARGed neurons. Neuron 33(1): 15–22.CrossRefGoogle ScholarPubMed
- 1
- Cited by