Table 13.
Inosine
| Paper | Animal model and injury model | Intervention and timing | Experimental groups |
Reported outcomes: Histologic/biochemical/physiological Behavioral |
|---|---|---|---|---|
| Conta Spinal Cord2008 |
Model: “Adult” Female Long-Evans Rats Injury: T9/T10 NYU Impactor 10g × 25 mm |
Inosine IP • 100 mg/kg starting @ 15min or 3w PI, then twice daily for 1 week Inosine SQ • 100 mg/kg starting @ 15min PI, then twice daily for 6 weeks |
SCI + • Inosine IP (n = 10) • Inosine SQ (n = 8) • Vehicle (n = 28) |
Histologic/Biochemical/Physiological: Reduced the volume fraction of ED1 positive profiles around the lesion site only in the group with continuous 6 week inosine delivery. Behavioral: Not reported. |
| Bohnert J Neurotrauma2007 |
Model: Female Guinea Pigs, ∼400g Injury: T10 Lateral Hemisection |
Inosine SQ through an osmotic minipump • 10 mM at 0.25 μL/h for 1 month started @ 3 months PI |
SCI + • Inosine • Vehicle n = 15/group |
Histologic/Biochemical/Physiological: Retrograde and anterograde tracing of spinal cord tracts indicated that inosine induced regenerative sprouting of ascending and descending tracts up to the lesion site. This regeneration was enhanced when inosine therapy was combined with oscillating field stimulation (OFS). Behavioral: 5 months after injury or 2 months after treatment, Inosine mediated a significant recovery of CTM receptive fields. |
| Liu Spinal Cord2006 |
Model: Male SD Rats, 200–220g Injury: T8-T9 Clip Compression 95g × 1 min |
Inosine IP • 75 mg/kg @ 2h, 12h or 24h |
SCI + • Inosine • Saline n = 6/group |
Histologic/Biochemical/Physiological: At 3 days post injury, Inosine given as late as 12h, significantly reduced apoptosis (TUNEL labeling) and degenerative areas in the spinal cord (H&E stain). Behavioral: Not reported. |
SCI: spinal cord injury; h: hour, hours; w: week, weeks; PI: post-injury;
T8: thoracic vertebra 8; IP: intraperitoneal; SC: subcutaneous;
CTM: cutaneus trunci muscle; SD rats: Sprague-Dawley rats.