期刊
CNS NEUROSCIENCE & THERAPEUTICS
卷 27, 期 8, 页码 919-929出版社
WILEY
DOI: 10.1111/cns.13651
关键词
calcium; locomotor recovery; neuronal apoptosis; oxidative stress; spinal cord injury
资金
- Ministry of Food and Drug Safety [19182MFDS408, 20182MFDS423]
This study demonstrates that local/immediate administration of the calcium chelator BAPTA is strongly neuroprotective following severe spinal cord injury. The use of BAPTA inhibited neuronal apoptosis and reactive oxygen species generation, leading to improved preservation of electrophysiological function and better behavioral recovery.
Aim Despite animal evidence of a role of calcium in the pathogenesis of spinal cord injury, several studies conducted in the past found calcium blockade ineffective. However, those studies involved oral or parenteral administration of Ca++ antagonists. We hypothesized that Ca++ blockade might be effective with local/immediate application (LIA) at the time of neural injury. Methods In this study, we assessed the effects of LIA of BAPTA (1,2-bis (o-aminophenoxy) ethane-N, N, N ', N'-tetraacetic acid), a cell-permeable highly selective Ca++ chelator, after spinal cord transection (SCT) in mice over 4 weeks. Effects of BAPTA were assessed behaviorally and with immunohistochemistry. Concurrently, BAPTA was submitted for the first time to multimodality assessment in an in vitro model of neural damage as a possible spinal neuroprotectant. Results We demonstrate that BAPTA alleviates neuronal apoptosis caused by physical damage by inhibition of neuronal apoptosis and reactive oxygen species (ROS) generation. This translates to enhanced preservation of electrophysiological function and superior behavioral recovery. Conclusion This study shows for the first time that local/immediate application of Ca++ chelator BAPTA is strongly neuroprotective after severe spinal cord injury.
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