4-aminopyridine 抑制电压门 K+ 通道对斑马鱼脊髓损伤恢复的影响

Payge Hoffman, Karen Mruk
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引用次数: 0

摘要

脊髓损伤(SCI)每年影响 25 万至 50 万人。初次损伤后,细胞会出现一连串延迟的继发性反应,导致逐渐退化和永久性残疾。这种继发性过程的一部分是离子平衡紊乱。临床上使用 K+ 通道阻滞剂 4- 氨基吡啶(4-AP)来缓解多发性硬化症(MS)的症状。目前正在进行几项研究,以探索 4-AP 可能产生影响的其他领域,包括中风、创伤性脑损伤和 SCI 后的神经系统恢复。我们的研究目标是确定 4-AP 是否会影响斑马鱼(Danio rerio)的 SCI 恢复。我们利用转基因品系 Tg(gfap:EGFP)创建了脊髓横断并跟踪游泳恢复情况。我们发现,持续使用 10 μM 4-AP 可使游动距离增加 40%。实时成像显示,在 4-AP 存在的情况下,4-AP 会增加损伤部位的径向神经胶质细胞桥接。我们的结论是,10 μM 4-AP具有促进脊髓损伤后再生的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effect of Voltage-Gated K+ Channel Inhibition by 4-aminopyridine in Spinal Cord Injury Recovery in Zebrafish
Spinal cord injury (SCI) affects between 250,000 to 500,000 individuals annually. After the initial injury, a delayed secondary cascade of cellular responses occurs causing progressive degeneration and permanent disability. One part of this secondary process is disturbance of ionic homeostasis. The K+ channel blocker, 4-aminopyridine (4-AP), is used clinically to alleviate symptoms of multiple sclerosis (MS). Several ongoing studies are being conducted to explore additional areas where 4-AP may have an effect, including stroke, traumatic brain injury, and nervous system recovery after SCI. The goal of our study was to determine whether 4-AP affects recovery from SCI in zebrafish (Danio rerio). Using the transgenic line Tg(gfap:EGFP), we created a spinal transection and tracked swim recovery. We found that constant treatment with 10 μM 4-AP increases swimming distance 40%. Live imaging demonstrated that treatment with 4-AP increases radial glial cells bridging at the site of injury in the presence of 4-AP. We conclude that 10 μM 4-AP is pro-regenerative after SCI.
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