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PRECLINICAL PUBLICATION · 2019

Mild Traumatic Brain Injury Causes Nociceptive Sensitization through Spinal Chemokine Upregulation.

Mouse / TBI

Evidence by therapy association

Study details and outcomes are extracted in the context of a specific intervention. Separate associations are retained rather than silently merged.

PMID 31863005 ↗2019Reported benefit

Mild Traumatic Brain Injury Causes Nociceptive Sensitization through Spinal Chemokine Upregulation.

MouseTBIClosed-head / concussionC57Bl/6JMaleIntrathecal for ondansetron, 5,7-dihydroxytryptamine and spinal SCH527123; systemic injection for p-chlorophenylalanine, desipramine and systemic SCH527123Ondansetron 1 or 3 micrograms in 10 microlitres intrathecal…Ondansetron and intrathecal SCH527123 given on post-injury day 3; systemic SCH5…

Model: Closed-head mild traumatic brain injury delivered by a stereotaxic impactor mounted at a 40 degree angle with a 5 mm tip, impact velocity 5.8 to 6.0 m/s, dwell time 0.2 s and impact depth 5 mm over the right S1 somatosensory cortex under isoflurane anaesthesia, with no skull fractures observed; sham animals had the device discharged in air

Mild closed-head injury produced mechanical hypersensitivity peaking over 72 h and resolving by around 14 days, together with raised spinal CXCR2, CXCL1 and CXCL2 (and CXCL3 at day 7) and increased GFAP and IBA-1 staining. Intrathecal ondansetron dose-dependently reversed hypersensitivity, with the…

Extraction: extract · Subtype source: rule · Supplied extraction confidence: 0.9. Machine-extracted fields require source verification.