| Literature DB >> 29679548 |
Carolin Meyer1, Habib Bendella2, Svenja Rink3, Robin Gensch4, Robert Seitz4, Gregor Stein5, Marilena Manthou6, Theodora Papamitsou7, Makoto Nakamura8, Bertil Bouillon9, Mary Galea10, Peter Batchelor11, Sarah Dunlop12, Doychin Angelov13.
Abstract
Myelotomy is a surgical procedure allowing removal of extravasated blood and necrotic tissue that is thought to attenuate secondary injury as well as promote recovery in experimental spinal cord injury (SCI) models and humans. Here we examined in rat whether myelotomy at 48 h after low-thoracic compressive SCI provided any benefit over a 12 week period. Compared to animals receiving SCI alone, myelotomy worsened BBB scores (p < 0.05) and also did not improve plantar stepping, ladder climbing, urinary bladder voiding or sensory function (thermal latency) during the 12-week period. Quantitative analyses of tissue sections at 12 weeks showed that myelotomy also did not reduce lesion volume nor alter immunohistochemical markers of axons in spared white matter bridges, microglia, astrocytes or serotinergic fibres. However, myelotomy reduced synaptophysin expression, a marker of synaptic plasticity. We conclude that further studies are required to evaluate myelotomy after SCI. (142 words).Entities:
Keywords: Bladder and sensory function; Cellular markers; Locomotor; Myelotomy; Rat; Spinal cord injury
Mesh:
Year: 2018 PMID: 29679548 DOI: 10.1016/j.expneurol.2018.04.011
Source DB: PubMed Journal: Exp Neurol ISSN: 0014-4886 Impact factor: 5.330