Table 1 Pharmacologic repair strategy of spinal cord injury
From: Progression in translational research on spinal cord injury based on microenvironment imbalance
Medicine | Mechanism | Representative findings |
|---|---|---|
Microenvironmental regulator | ||
 Corticosteroids | • Upregulate the release of anti-inflammatory cytokines • Reduce the extravasation of inflammatory cells • Promote the survival of neurons | • NASCIS-1, NASCIS-2 and NASCIS-3 has been completed. • The controversial research is still being further clarified. |
 Minocycline | • Excellent lipid solubility206 • Reduce inflammatory response and prevent neuronal apoptosis207 | • Phase II study proved that minocycline can significantly improve the ASIA motor score for patients with SCI.208 • Phase III is underway |
 Riluzole | • Sodium channel blocker • Inhibiting excitotoxicity by reducing the release of presynaptic glutamate to inhibit excitotoxicity209 | • Phase I trial showed that Riluzole is effective in improving the ASIA score without serious adverse events • Phase II/III multicenter, randomized trial is in progress210,211 |
 Granulocyte-colony- stimulating factor (G-CSF) | • Promote differentiation and proliferation of granulocytes • Induce migration of bone marrow mesenchymal cells to SCI sites and inhibit apoptosis212 | • Phase I/II trial have shown that CSF can significantly improve motor function in patients with cervical and thoracic spinal cord injuries for 5 days.213 |
 Chondroitinase ABC (ChABC) | • Eliminate CSPG glycosaminoglycan (GAG) chains to achieve the inactivation of CSPGs94 • Promoting axonal regeneration | • Preclinical researches have shown that the superiority of ChABC in regulating the inhibitory environment214,215,216 |
 Ganglioside (GM-1) | • Downregulate caspase-3 and upregulate the expression of NGF • Maintain neuronal cell survival | • Phase I clinical trial conducted a preliminary assessment of the safety and effectiveness of GM-1 • Phase III trial shown that GM-1 did not show a significant difference in the improvement of the primary outcome measures. • More experiments are demonstrating the role of GM-1 in spinal cord injury. |
 Magnesium | • Block NMDA receptors to prevent glutamatergic excitotoxicity | • Preclinical studies have demonstrated that Magnesium has a neuroprotective effect on the rat model of SCI and optimizes motor functional outcome217 |
Neuroregenertive activator | ||
 Cethrin | • A recombinant of VX-210 • Involve the down-regulation of the RHOA pathway to promote axonal regeneration218 | • The phase I/IIa study has demonstrated the effectiveness of this medicine in improving motor function219 • Phase IIb/III trial is being carried out220 |
 Nogo-A antibodies | • The antibody of a myelin-derived axon growth inhibitor • Inhibit Nogo-A to facilitate nerve repair and reconstruction after SCI | • Nogo-A antibodies have proved an attraction in facilitating nerve regeneration in preclinical SCI trials, and a phase I research has been completed221,222 • Phase II placebo-controlled trial is underway |
 Basic fibroblast growth factor (bFGF) | • A ligand of tyrosine kinase receptor • Inhibit inflammatory response, glial scar and astrogliosis and stimulate axon regeneration • Neuroprotective function | • A preliminary Phase I clinical study has shown that FGF may have a positive effect in improving ASIA motor score • Phase I/II trial has evaluated with the unpublished conclusion223,224 |