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在大鼠坐骨神经横断模型中,盐酸法舒地尔通过[具体通路]增强功能恢复。

Augmentation of functional recovery via pathway by Fasudil Hydrochloride in a rat sciatic nerve transection model.

作者信息

Wang Hai, Fang Fang, Jing Xing, Xu Dan, Ren Zhenyu, Dou Shuang, Xie Yun, Zhuang Yuehong

机构信息

Department of Orthopedics, First Affiliated Hospital, Fujian Medical University, Fuzhou, 350004, Fujian, China.

Department of Orthopedics, National Regional Medical Center, Binhai Campus of the First Affiliated Hospital, Fujian Medical University, Fuzhou, 350212, China.

出版信息

J Orthop Translat. 2024 Jun 20;47:74-86. doi: 10.1016/j.jot.2024.06.006. eCollection 2024 Jul.

Abstract

BACKGROUNDS

The functional recovery after peripheral nerve injury remains unsatisfactory. This study aims to perform a comprehensive evaluation of the efficacy of Fasudil Hydrochloride at treating the sciatic nerve transection injury in rats and the mechanism involved.

MATERIALS AND METHODS

In animal experiments, 75 Sprague Dawley rats that underwent transection and repair of the right sciatic nerve were divided into a control, Fasudil, and Fas + LY group, receiving daily intraperitoneal injection of saline, Fasudil Hydrochloride (10 mg/kg), and Fasudil Hydrochloride plus LY294002 (5 mg/kg), respectively. At day 3 after surgery, the expression of ROCK2, p-PI3K, and p-AKT in L DRG and the lumbosacral enlargement was determined using Western blotting. At day 7 and 14, axon density in the distal stump was evaluated with immunostaining using the anti-Neurofilament-200 antibody. At day 30, retrograde tracing by injecting Fluoro-gold in the distal stump was performed. Three months after surgery, remyelination was analyzed with immostaining using the anti-MPZ antibody and the transmission electron microscope; Moreover, Motion-Evoked Potential, and recovery of sensorimotor functions was evaluated with a neuromonitor, Footprint, Hot Plate and Von Frey Filaments, respectively. Moveover, the Gastrocnemius muscles were weighed, and then underwent H&E staining, and staining of the neuromuscular junction using α-Bungarotoxin to evaluate the extent of atrophy and degeneration of the endplates in the Gastrocnemius. In vitro, spinal motor neurons (SMNs) and dorsal root ganglia (DRG) were cultured to examine the impact of Fasudil Hydrochloride and LY294002 on the axon outgrowth.

RESULTS

Three days after injury, the expression of ROCK2 increased significantly (P<0.01), and Fasudil application significantly increased the expression of p-PI3K and p-AKT in L DRG and the lumbosacral enlargement (P < 0.05). At day 7 and 14 after surgery, a higher axon density could be observed in the Fasudil group(P < 0.05). At day 30 after surgery, a larger number of motor and sensory neurons absorbing Fluoro-gold could be observed in the Fasudil group (P < 0.01) Three months after surgery, a greater thickness of myelin sheath could be observed in the Fasudil group (P < 0.05). The electrophysiological test showed that a larger amplitude of motion-evoked potential could be triggered in the Fasudil group (P < 0.01). Behavioral tests showed that a higher sciatic function index and a lower threshold for reacting to heat and mechanical stimuli could be measured in the Fasudil group. (P < 0.01). The wet weight ratio of the Gastrocnemius muscles and the area of the cross section of its myofibrils were greater in the Fasudil group (P < 0.01), which also demonstrated a higer ratio of axon-endplate connection and a larger size of endplates (P < 0.05). And there were no significant differences for the abovementioned parameters between the control and Fas + LY groups (P>0.05). In vitro studies showed that Fasudil could significantly promote axon growth in DRG and SMNs, and increase the expression of p-PI3K and p-AKT, which could be abolished by LY294002 (P < 0.05).

CONCLUSIONS

Fasudil can augment axon regeneration and remyelination, and functional recovery after sciatic nerve injury by activating the PI3K/AKT pathway.

THE TRANSLATIONAL POTENTIAL OF THIS ARTICLE

The translation potential of this article is that we report for the first time that Fasudil Hydrochloride has a remarkable efficacy at improving axon regeneration and remyelination following a transection injury of the right sciatic nerve in rats through the ROCK/PI3K/AKT pathway, which has a translational potential to be used clinically to treat peripheral nerve injury.

摘要

背景

周围神经损伤后的功能恢复仍不尽人意。本研究旨在全面评估盐酸法舒地尔治疗大鼠坐骨神经横断损伤的疗效及其相关机制。

材料与方法

在动物实验中,将75只接受右侧坐骨神经横断和修复的Sprague Dawley大鼠分为对照组、法舒地尔组和法舒地尔+LY组,分别每日腹腔注射生理盐水、盐酸法舒地尔(10mg/kg)和盐酸法舒地尔加LY294002(5mg/kg)。术后第3天,采用蛋白质免疫印迹法检测腰段背根神经节(L DRG)和腰骶膨大处ROCK2、p-PI3K和p-AKT的表达。术后第7天和14天,使用抗神经丝蛋白-200抗体通过免疫染色评估远端残端的轴突密度。术后第30天,通过向远端残端注射荧光金进行逆行示踪。术后3个月,使用抗髓磷脂蛋白零(MPZ)抗体免疫染色和透射电子显微镜分析髓鞘再生情况;此外,分别使用神经监测仪、足迹分析、热板法和von Frey细丝评估运动诱发电位以及感觉运动功能的恢复情况。另外,称量腓肠肌重量,然后进行苏木精-伊红(H&E)染色,并用α-银环蛇毒素对神经肌肉接头进行染色,以评估腓肠肌终板萎缩和变性程度。在体外,培养脊髓运动神经元(SMNs)和背根神经节(DRG),以研究盐酸法舒地尔和LY294002对轴突生长的影响。

结果

损伤后3天,ROCK2表达显著增加(P<0.01),应用法舒地尔可显著增加L DRG和腰骶膨大处p-PI3K和p-AKT的表达(P < 0.05)。术后第7天和14天,法舒地尔组的轴突密度更高(P < 0.05)。术后第30天,法舒地尔组可观察到更多摄取荧光金的运动和感觉神经元(P < 0.01)。术后3个月,法舒地尔组的髓鞘厚度更大(P < 0.05)。电生理测试表明,法舒地尔组可触发更大振幅的运动诱发电位(P < 0.01)。行为测试表明,法舒地尔组的坐骨神经功能指数更高,对热和机械刺激的反应阈值更低(P < 0.01)。法舒地尔组腓肠肌的湿重比及其肌原纤维横截面积更大(P < 0.01),其轴突-终板连接比例也更高,终板尺寸更大(P < 0.05)。对照组和法舒地尔+LY组之间上述参数无显著差异(P>0.05)。体外研究表明,法舒地尔可显著促进DRG和SMNs中的轴突生长,并增加p-PI3K和p-AKT的表达,而LY294002可消除这种作用(P < 0.05)。

结论

法舒地尔可通过激活PI3K/AKT通路增强坐骨神经损伤后的轴突再生、髓鞘再生及功能恢复。

本文的转化潜力

本文的转化潜力在于我们首次报道盐酸法舒地尔通过ROCK/PI3K/AKT通路对大鼠右侧坐骨神经横断损伤后的轴突再生和髓鞘再生具有显著疗效,具有临床治疗周围神经损伤的转化潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eb87/11245988/5fe522acaace/ga1.jpg

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