Kunming Medical University, School of Rehabilitation, Kunming, China.
Turk Neurosurg. 2023;33(1):77-86. doi: 10.5137/1019-5149.JTN.37469-21.2.
To explore the efficacy and possible mechanisms of Low-intensity focused ultrasound (LIFU) in alleviating spasticity caused by Spinal cord injury (SCI).
We selected male Sprague?Dawley rats as subjects and performed transverse injuries on the T9 vertebra of their spinal cord (SC) to build SCI. On the 7th day after SCI, LIFU treatment was performed below the SCI segment once a day for 20 min, for 4 consecutive weeks. During treatment, a pressure sensor was used to assess the degree of spasticity. After treatment, the SC tissues from the treatment sites of the SCI+LIFU(-) and SCI+LIFU(+) groups were extracted, and high-throughput sequencing was performed to identify the changes in proteomics. In addition, expression of the growth associated protein 43 (Gap43) was validated by western blotting.
The behavioral results suggested that after 2 weeks of SCI, the rats were significantly induced to have a spastic reaction (p < 0.05), while after 4 weeks of LIFU treatment, the spastic response of rats was significantly improved (p < 0.05). Western blot analysis showed a significant increase in Gap43 expression in the SCI+LIFU(-) group compared with the sham group, whereas after 4 weeks of LIFU treatment, Gap43 protein expression was significantly decreased (p < 0.05).
The results of this study showed that LIFU is an alternative treatment that can effectively relieve spastic reactions caused by SCI, possibly by reducing abnormal neuroplasticity or axon regeneration below the SCI segment.
探讨低强度聚焦超声(LIFU)缓解脊髓损伤(SCI)所致痉挛的疗效及可能机制。
选用雄性 Sprague-Dawley 大鼠为研究对象,对 T9 椎体脊髓进行横断损伤,建立 SCI 模型。SCI 后第 7 天,在 SCI 节段下方每天进行一次 LIFU 治疗,每次 20 min,连续治疗 4 周。治疗过程中采用压力传感器评估痉挛程度。治疗结束后,提取 SCI+LIFU(-)和 SCI+LIFU(+)组 SCI 治疗部位的脊髓组织,进行高通量测序以鉴定蛋白质组学的变化。此外,通过 Western blot 验证生长相关蛋白 43(Gap43)的表达。
行为学结果表明,SCI 后 2 周大鼠明显出现痉挛反应(p<0.05),而 LIFU 治疗 4 周后,大鼠的痉挛反应明显改善(p<0.05)。Western blot 分析显示,与假手术组相比,SCI+LIFU(-)组 Gap43 表达显著增加,而经过 4 周的 LIFU 治疗后,Gap43 蛋白表达明显下降(p<0.05)。
本研究结果表明,LIFU 是一种有效的治疗方法,可有效缓解 SCI 引起的痉挛反应,其可能机制是减少 SCI 节段以下的异常神经可塑性或轴突再生。