Literature DB >> 34031611

Surgical implantation of wireless, battery-free optoelectronic epidural implants for optogenetic manipulation of spinal cord circuits in mice.

Jose G Grajales-Reyes1,2, Bryan A Copits1, Ferrona Lie3,4, Yongjoon Yu3, Raudel Avila4, Sherri K Vogt1, Yonggang Huang4,5,6, Anthony R Banks3,5,6, John A Rogers5,6, Robert W Gereau7, Judith P Golden8.   

Abstract

The use of optogenetics to regulate neuronal activity has revolutionized the study of the neural circuitry underlying a number of complex behaviors in rodents. Advances have been particularly evident in the study of brain circuitry and related behaviors, while advances in the study of spinal circuitry have been less striking because of technical hurdles. We have developed and characterized a wireless and fully implantable optoelectronic device that enables optical manipulation of spinal cord circuitry in mice via a microscale light-emitting diode (µLED) placed in the epidural space (NeuroLux spinal optogenetic device). This protocol describes how to surgically implant the device into the epidural space and then analyze light-induced behavior upon µLED activation. We detail optimized optical parameters for in vivo stimulation and demonstrate typical behavioral effects of optogenetic activation of nociceptive spinal afferents using this device. This fully wireless spinal µLED system provides considerable versatility for behavioral assays compared with optogenetic approaches that require tethering of animals, and superior temporal and spatial resolution when compared with other methods used for circuit manipulation such as chemogenetics. The detailed surgical approach and improved functionality of these spinal optoelectronic devices substantially expand the utility of this approach for the study of spinal circuitry and behaviors related to mechanical and thermal sensation, pruriception and nociception. The surgical implantation procedure takes ~1 h. The time required for the study of behaviors that are modulated by the light-activated circuit is variable and will depend upon the nature of the study.

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Year:  2021        PMID: 34031611      PMCID: PMC9273129          DOI: 10.1038/s41596-021-00532-2

Source DB:  PubMed          Journal:  Nat Protoc        ISSN: 1750-2799            Impact factor:   17.021


  28 in total

1.  TRPV1-lineage neurons are required for thermal sensation.

Authors:  Santosh K Mishra; Sarah M Tisel; Peihan Orestes; Sonia K Bhangoo; Mark A Hoon
Journal:  EMBO J       Date:  2010-12-07       Impact factor: 11.598

2.  Flexible and fully implantable upconversion device for wireless optogenetic stimulation of the spinal cord in behaving animals.

Authors:  Ying Wang; Kai Xie; Haibing Yue; Xian Chen; Xuan Luo; Qinghai Liao; Ming Liu; Feng Wang; Peng Shi
Journal:  Nanoscale       Date:  2019-11-29       Impact factor: 7.790

3.  Wirelessly powered, fully internal optogenetics for brain, spinal and peripheral circuits in mice.

Authors:  Kate L Montgomery; Alexander J Yeh; John S Ho; Vivien Tsao; Shrivats Mohan Iyer; Logan Grosenick; Emily A Ferenczi; Yuji Tanabe; Karl Deisseroth; Scott L Delp; Ada S Y Poon
Journal:  Nat Methods       Date:  2015-08-17       Impact factor: 28.547

4.  Quantitative assessment of tactile allodynia in the rat paw.

Authors:  S R Chaplan; F W Bach; J W Pogrel; J M Chung; T L Yaksh
Journal:  J Neurosci Methods       Date:  1994-07       Impact factor: 2.390

5.  Spontaneous pain, both neuropathic and inflammatory, is related to frequency of spontaneous firing in intact C-fiber nociceptors.

Authors:  Laiche Djouhri; Stella Koutsikou; Xin Fang; Simon McMullan; Sally N Lawson
Journal:  J Neurosci       Date:  2006-01-25       Impact factor: 6.167

6.  A history of optogenetics: the development of tools for controlling brain circuits with light.

Authors:  Edward S Boyden
Journal:  F1000 Biol Rep       Date:  2011-05-03

Review 7.  Recent advances in neurotechnologies with broad potential for neuroscience research.

Authors:  Abraham Vázquez-Guardado; Yiyuan Yang; Amay J Bandodkar; John A Rogers
Journal:  Nat Neurosci       Date:  2020-11-16       Impact factor: 28.771

Review 8.  Insights Into Spinal Dorsal Horn Circuit Function and Dysfunction Using Optical Approaches.

Authors:  Erika K Harding; Samuel Wanchi Fung; Robert P Bonin
Journal:  Front Neural Circuits       Date:  2020-06-12       Impact factor: 3.492

Review 9.  Nociception and pain: lessons from optogenetics.

Authors:  Fiona B Carr; Venetia Zachariou
Journal:  Front Behav Neurosci       Date:  2014-03-25       Impact factor: 3.558

10.  Differential Regulation of Bladder Pain and Voiding Function by Sensory Afferent Populations Revealed by Selective Optogenetic Activation.

Authors:  Jennifer J DeBerry; Vijay K Samineni; Bryan A Copits; Christopher J Sullivan; Sherri K Vogt; Kathryn M Albers; Brian M Davis; Robert W Gereau
Journal:  Front Integr Neurosci       Date:  2018-02-12
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  3 in total

Review 1.  Optophysiology: Illuminating cell physiology with optogenetics.

Authors:  Peng Tan; Lian He; Yun Huang; Yubin Zhou
Journal:  Physiol Rev       Date:  2022-01-24       Impact factor: 37.312

2.  Site-specific mitochondrial dysfunction in neurodegeneration.

Authors:  Anežka Vodičková; Shon A Koren; Andrew P Wojtovich
Journal:  Mitochondrion       Date:  2022-02-16       Impact factor: 4.534

Review 3.  Emerging Optoelectronic Devices Based on Microscale LEDs and Their Use as Implantable Biomedical Applications.

Authors:  Haijian Zhang; Yanxiu Peng; Nuohan Zhang; Jian Yang; Yongtian Wang; He Ding
Journal:  Micromachines (Basel)       Date:  2022-07-04       Impact factor: 3.523

  3 in total

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