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Published on: May 12, 2018
Optogenetic Approach for Investigating Descending Control of Nociception in Ex Vivo Spinal Cord Preparation
Volodymyr Krotov1, Ivan Blashchak1, Jayden Moore1
1Department of Molecular Biophysics and Sensory Signaling, Bogomoletz Institute of Physiology, Kyiv, Ukraine.
None:
Nociception is critically shaped by descending modulation of spinal circuits, yet its cellular and synaptic mechanisms remain poorly defined. Elucidating these mechanisms is technically challenging, as it requires simultaneous activation of primary afferents and descending fibers while monitoring the functioning of individual spinal neurons. Here, we present a method to investigate the influence of the rostral ventromedial medulla (RVM), a principal supraspinal structure mediating descending modulation, on the activity of spinal lamina I neurons. Our approach combines electrophysiological recordings in ex vivo intact spinal cord preparation with optogenetics, granting several advantages. First, ex vivo preparation spares rostrocaudal and mediolateral spinal architecture, preserving lamina I as well as primary afferent and descending inputs. Second, virally mediated channelrhodopsin-2 (ChR2) expression enables selective photostimulation of RVM-originating fibers. When coupled with patch-clamp recordings, this photostimulation allows identifying postsynaptic inputs from RVM to spinal neurons and revealing RVM-dependent presynaptic inhibition of primary afferent inputs. Overall, our approach is well-suited for investigating both pre- and postsynaptic mechanisms of descending modulation in physiological and pathological pain conditions. Key features • Rapid preparation procedure that grants access to lamina I neurons while preserving spinal cord architecture, including primary afferents and descending inputs. • Optogenetic approach allowing functional studies of RVM-dependent descending modulation. • Ability to assess RVM fiber-dependent presynaptic inhibition of synaptic transmission between primary afferents and lamina I neurons.

