Affiliated with Université Laval & CERVO Research Centre

Epidural optogenetics for controlled analgesia.

TitleEpidural optogenetics for controlled analgesia.
Publication TypeJournal Article
Year of Publication2016
AuthorsBonin RP, Wang F, Desrochers-Couture M, Secka AGa, Boulanger M-E, Côté DC, De Koninck Y
JournalMol Pain
Volume12
Date Published2016
ISSN1744-8069
KeywordsAfferent Pathways, Analgesia, Epidural, Animals, Male, Mice, Inbred C57BL, Nociception, Opsins, Optical Fibers, Optogenetics, Sensory Receptor Cells
Abstract

BACKGROUND: Optogenetic tools enable cell selective and temporally precise control of neuronal activity; yet, difficulties in delivering sufficient light to the spinal cord of freely behaving animals have hampered the use of spinal optogenetic approaches to produce analgesia. We describe an epidural optic fiber designed for chronic spinal optogenetics that enables the precise delivery of light at multiple wavelengths to the spinal cord dorsal horn and sensory afferents.RESULTS: The epidural delivery of light enabled the optogenetic modulation of nociceptive processes at the spinal level. The acute and repeated activation of channelrhodopsin-2 expressing nociceptive afferents produced robust nocifensive behavior and mechanical sensitization in freely behaving mice, respectively. The optogenetic inhibition of GABAergic interneurons in the spinal cord dorsal horn through the activation of archaerhodopsin also produced a transient, but selective induction of mechanical hypersensitivity. Finally, we demonstrate the capacity of optogenetics to produce analgesia in freely behaving mice through the inhibition of nociceptive afferents via archaerhodopsin.CONCLUSION: Epidural optogenetics provides a robust and powerful solution for activation of both excitatory and inhibitory opsins in sensory processing pathways. Our results demonstrate the potential of spinal optogenetics to modulate sensory behavior and produce analgesia in freely behaving animals.

DOI10.1177/1744806916629051
Alternate JournalMol Pain
PubMed ID27030718
PubMed Central IDPMC4955967