GSK-3 Inhibitor Promotes Neuronal Cell Regeneration and Functional Recovery in a Rat Model of Spinal Cord Injury.
Fei LeiWen HeXinggui TianQingzhong ZhouLipeng ZhengJianping KangYueming SongDaxiong FengPublished in: BioMed research international (2019)
The reparative process following spinal cord injury (SCI) is extremely complicated. Cells in the microenvironment express multiple inhibitory factors that affect axonal regeneration over a prolonged period of time. The axon growth inhibitory factor glycogen synthase kinase-3 (GSK-3) is an important factor during these processes. TDZD-8 (4-benzyl-2-methyl-1,2,4-thiadiazolidine-3,5-dione) is the most effective and specific non-ATP-competitive inhibitor of GSK-3. Here, we show that administering TDZD-8 after SCI was associated with significantly inhibited neuronal apoptosis, upregulated GAP-43 expression, increased density of cortical spinal tract fibers around areas of injury, and increased Basso, Beattie, and Bresnahan (BBB) scores in the lower limbs. These findings support the notion that GSK-3 inhibitors promote neuronal cell regeneration and lower limb functional recovery.
Keyphrases
- spinal cord injury
- pi k akt
- cell cycle arrest
- stem cells
- spinal cord
- signaling pathway
- lower limb
- neuropathic pain
- induced apoptosis
- single cell
- cell therapy
- oxidative stress
- cell death
- poor prognosis
- endoplasmic reticulum stress
- cerebral ischemia
- wound healing
- cell proliferation
- tyrosine kinase
- long non coding rna
- optic nerve
- optical coherence tomography