Jimena Perez Sanchez
Postdoctoral Research Scientist
Research Interests
I am interested the mechanisms by which the spinal cord can select somatosensory information that is relevant to navigate in the natural world, in normal and pathological conditions. My research focuses on the neural circuits that drive painful stimuli; from the activation of sensory neurons in the periphery, to descending pathways that modulate this information in the spinal cord. The spinal cord is an ideal system to study plastic changes that occur after injury because it is a relatively simple neural circuit, with direct input from sensory neurons and a measurable output. While a ‘taxonomic’ neurophysiological characterisation of different neuronal subpopulations may yield important insights, it also requires the understanding of how information is processed within these circuits.
I use electrophysiology, but also imaging and behavioural assays, to study the impact of changes in sensory afferents and dorsal horn neurons in the spinal cord. I believe that the combination of two-photon microscopy with electrophysiology can give powerful insight into the mechanisms of spinal cord plasticity in normal and pathological conditions.
Recent publications
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In vivo calcium imaging reveals directional sensitivity of C‐low threshold mechanoreceptors
Journal article
Semizoglou E. et al, (2025), The Journal of Physiology
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Characterising the stimulus-response function of mouse C-Low threshold mechanoreceptors to mechanical stimuliin vivo
Preprint
Semizoglou E. et al, (2024)
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A humanized chemogenetic system inhibits murine pain-related behavior and hyperactivity in human sensory neurons
Journal article
Perez-Sanchez J. et al, (2023), Science Translational Medicine, 15
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Inhibition of sensory neuron driven acute, inflammatory, and neuropathic pain using a humanised chemogenetic system
Journal article
Sanchez JP. et al, (2023)
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Composite Fibrin and Carbon Microfibre Implant to Modulate Postraumatic Inflammation after Spinal Cord Injury
Journal article
Escarrat V. et al, (2023), Cells, 12, 839 - 839