{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,3]],"date-time":"2026-10-03T01:43:36Z","timestamp":1790991816559,"version":"4.1.0"},"reference-count":44,"publisher":"Journal of Neurosurgery Publishing Group (JNSPG)","issue":"3","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2023,3,1]]},"abstract":"<jats:sec>\n<jats:title>OBJECTIVE<\/jats:title>\n<jats:p>The objective of this study was to test whether regenerating motor axons from a donor nerve can travel in a retrograde fashion using sensory branches to successfully reinnervate a motor nerve end organ.<\/jats:p>\n<\/jats:sec>\n<jats:sec>\n<jats:title>METHODS<\/jats:title>\n<jats:p>This study has two parts. In part I, rats (n = 30) were assigned to one of five groups for obturator nerve (ON)\u2013to\u2013femoral nerve transfer: group 1, ON-to\u2013saphenous nerve (SN) distal stump; group 2, ON-to-SN proximal stump without femoral nerve proper (FNP) injury; group 3, ON-to-SN proximal stump with FNP crush injury; group 4, ON-to-SN proximal stump with FNP transection injury; and group 5, gold standard transfer, ON-to\u2013motor femoral nerve (MFN) branch. At 8 weeks, retrograde labeling was done from the distal MFN, and the spinal cords were examined to assess the degree of obturator motor axon regeneration across the five groups. In part II, only group 4 was examined (n = 8). Through use of immunostaining and optical tissue clearing methods, the nerve transfer networks were cleared and imaged using light-sheet fluorescence microscopy to visualize the regeneration pathways in 2D and 3D models at 2- and 8-week time points.<\/jats:p>\n<\/jats:sec>\n<jats:sec>\n<jats:title>RESULTS<\/jats:title>\n<jats:p>Proximal FNP transection (group 4) enabled a significantly higher number of retrogradely regenerated motor axons compared with control groups 1\u20133. Moreover, group 4 had modest, but nonsignificant, superiority of motor neuron counts compared with the positive control group, group 5. Optical tissue clearing demonstrated that the axons traveled in a retrograde fashion from the recipient sensory branch to the FNP mixed stump, then through complex turns, down to distal branches. Immunostaining confirmed the tissue clearing findings and suggested perineurium disruption as a means by which axons could traverse across fascicular boundaries.<\/jats:p>\n<\/jats:sec>\n<jats:sec>\n<jats:title>CONCLUSIONS<\/jats:title>\n<jats:p>Sensory branches can transmit regenerating axons from donor nerves back to main mixed recipient nerves, then distally toward target organs. The extent of retrograde regeneration is markedly influenced by the type and severity of injury sustained by the recipient nerve. Using a sensory branch as a bridge for retrogradely regenerating axons can open new potential horizons in nerve repair surgery for severely injured mixed nerves.<\/jats:p>\n<\/jats:sec>","DOI":"10.3171\/2022.6.jns22734","type":"journal-article","created":{"date-parts":[[2022,8,5]],"date-time":"2022-08-05T12:52:20Z","timestamp":1659703940000},"page":"858-867","source":"Crossref","is-referenced-by-count":5,"title":["Successful retrograde regeneration using a sensory branch for motor nerve transfer"],"prefix":"10.3171","volume":"138","author":[{"given":"Saud","family":"Alzahrani","sequence":"first","affiliation":[{"name":"Department of Clinical Neurosciences, University of Calgary;"},{"name":"Hotchkiss Brain Institute, University of Calgary;"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Harley","family":"Brito da Silva","sequence":"additional","affiliation":[{"name":"Department of Clinical Neurosciences, University of Calgary;"},{"name":"Hotchkiss Brain Institute, University of Calgary;"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Tak-Ho","family":"Chu","sequence":"additional","affiliation":[{"name":"Department of Clinical Neurosciences, University of Calgary;"},{"name":"Hotchkiss Brain Institute, University of Calgary;"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Zain","family":"Tariq","sequence":"additional","affiliation":[{"name":"Department of Clinical Neurosciences, University of Calgary;"},{"name":"Hotchkiss Brain Institute, University of Calgary;"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Daniel","family":"Umansky","sequence":"additional","affiliation":[{"name":"Department of Clinical Neurosciences, University of Calgary;"},{"name":"Hotchkiss Brain Institute, University of Calgary;"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"David A.","family":"Elliott","sequence":"additional","affiliation":[{"name":"Hotchkiss Brain Institute Advanced Microscopy Platform, University of Calgary, Alberta, Canada"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Rajiv","family":"Midha","sequence":"additional","affiliation":[{"name":"Department of Clinical Neurosciences, University of Calgary;"},{"name":"Hotchkiss Brain Institute, University of Calgary;"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"1754","reference":[{"issue":"237","key":"b1","series-title":"Indication and results. 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