Journal
MICROSCOPY AND MICROANALYSIS
Volume 27, Issue 2, Pages 450-456Publisher
CAMBRIDGE UNIV PRESS
DOI: 10.1017/S1431927621000076
Keywords
CCI; GFAP; nestin; neuropathic pain; stem cells
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The study investigated the efficacy of intravenously injected mesenchymal stem cells in treating neuropathic pain either before or after its induction. Results showed that the stem cells had reached the cerebral cortex and exhibited anti-inflammatory effects. The injected group with MSCs before induction showed few stem cells expressing specific proteins, while the group injected after induction showed numerous proliferated stem cells expressing these proteins in the cerebral cortex.
The present study aims to investigate the efficacy of intravenously injected mesenchymal stem cells (MSCs) in treating neuropathic pain either before or after its induction by a chronic constriction injury (CCI) model. Rats were divided into four groups: control group, neuropathic group, and treated groups (pre and postinduction) with i.v. mononuclear cells (10(6) cell/mL). For these rats, experimental testing for both thermal and mechanical hyperalgesia was evaluated. The cerebral cortex of the rats was dissected, and immunohistochemical analysis using anti-proliferating cell nuclear antigen (PCNA), CD117, nestin, and glial fibrillary acidic protein was performed. Our results showed that a single injection of MSCs (either preemptive/or post-CCI) produced equipotent effects on allodynia, mechanical hyperalgesia, and thermal response. Immunohistochemical analysis showed that the stem cells have reached the cerebral cortex. The injected group with MSCs before CCI showing few stem cells expressed PCNA, CD117, and nestin in the cerebral cortex. The group injected with MSCs after CCI, showing numerous recently proliferated CD117-, nestin-, PCNA-positive stem cells in the cerebral cortex. In conclusion, our findings demonstrate that the most probable effect of i.v. stem cells is the central anti-inflammatory effect, which opens concerns about how stem cells circulating in systemic administration to reach the site of injury.
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