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PRECLINICAL PUBLICATION · 2017

Neuron and microglia/macrophage-derived FGF10 activate neuronal FGFR2/PI3K/Akt signaling and inhibit microglia/macrophages TLR4/NF-kB-dependent neuroinflammation to improve functional recovery after spinal cord injury.

Rat / Spinal cord injury

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 28981091 ↗2017Reported benefit

Neuron and microglia/macrophage-derived FGF10 activate neuronal FGFR2/PI3K/Akt signaling and inhibit microglia/macrophages TLR4/NF-kB-dependent neuroinflammation to improve functional recovery after spinal cord injury.

RatSpinal cord injuryCompressionSprague-DawleyIntravenous1 mg/kg per day; the pathway-inhibitor arm added LY294002 a…Started after surgery; exact interval not stated

Model: T9 laminectomy followed by vascular clip compression at 30 g force for 1 minute, producing a moderate crush injury; anaesthesia with 10% chloral hydrate 3.6 mL/kg intraperitoneally

Daily intravenous FGF10 at 1 mg/kg improved BBB and inclined plane scores from day 14 onward, reduced lesion cavity, motor neuron loss and apoptosis, and attenuated microglial and macrophage activation and pro-inflammatory cytokine release. Benefits were partially reversed by the PI3K inhibitor LY2…

Extraction: extract · Subtype source: rule · Supplied extraction confidence: 0.85. Machine-extracted fields require source verification.