首页|环黄芪醇促进脊髓损伤小鼠运动功能恢复及皮质神经元再生的相关机制

环黄芪醇促进脊髓损伤小鼠运动功能恢复及皮质神经元再生的相关机制

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背景:前期研究证实,环黄芪醇能够促进坐骨神经损伤修复,且环黄芪醇能够激活端粒酶反转录酶进一步参与外周感觉神经元轴突再生的调节.但环黄芪醇是否可以激活皮质神经元轴突再生仍然未知,尤其是环黄芪醇是否参与脊髓损伤修复过程中运动功能的恢复.目的:探究环黄芪醇对小鼠脊髓损伤后运动功能恢复的影响,以及环黄芪醇促进皮质神经元再生的相关机制.方法:①将12只ICR小鼠随机分为溶剂组、环黄芪醇组,每组6只,构建脊髓损伤模型后分别腹腔注射含2%吐温20和5%二甲基亚砜的PBS、环黄芪醇(20 mg/kg),连续给药12周,使用BMS运动功能评分评估小鼠肢体运动功能;②体外培养E14胎鼠大脑皮质神经元,分为二甲基亚砜组与环黄芪醇组,分别用二甲基亚砜、0.5 μmol/L环黄芪醇体外培养3 d;③E7孕鼠分为溶剂组与环黄芪醇组,分别腹腔注射含2%吐温20和5%二甲基亚砜的PBS、20 mg/kg环黄芪醇,连续给药7 d,分离出胎鼠大脑皮质,体外培养皮质神经元3 d;④对胎鼠大脑皮质神经元进行Tuj1免疫荧光染色,分析Tuj1阳性细胞的轴突长度,验证环黄芪醇对皮质神经元轴突再生的作用;对胎鼠大脑皮质神经元进行Tuj1、端粒酶反转录酶双标免疫荧光染色,分析环黄芪醇对端粒酶反转录酶表达的影响;蛋白免疫印迹分析胎鼠大脑皮质神经元中端粒酶反转录酶蛋白的相对表达;⑤将6只ICR小鼠随机分为溶剂组、环黄芪醇组,每组3只,构建脊髓损伤模型后分别腹腔注射含2%吐温20和5%二甲基亚砜的PBS和环黄芪醇(20 mg/kg),连续给药7 d,蛋白免疫印迹检测脊髓组织中端粒酶反转录酶蛋白的相对表达.结果与结论:①脊髓损伤后环黄芪醇治疗4,6,8,12周,环黄芪醇组小鼠运动功能评分显著高于溶剂组(P<0.000 1);脊髓损伤后环黄芪醇治疗7 d,环黄芪醇组小鼠脊髓组织中端粒酶反转录酶蛋白相对表达量显著高于溶剂组(P<0.05);②Tuj1免疫荧光染色结果显示,0.5 μmol/L环黄芪醇组体外干预的皮质神经元轴突长度显著大于二甲基亚砜组(P<0.001),腹腔注射20 mg/kg环黄芪醇组的皮质神经元轴突长度显著大于溶剂组(P<0.01);③端粒酶反转录酶免疫荧光染色结果显示,0.5 μmol/L环黄芪醇组体外干预的皮质神经元的端粒酶反转录酶荧光强度显著大于二甲基亚砜组(P<0.01);④蛋白免疫印迹检测显示,0.5 μmol/L环黄芪醇组体外干预的皮质神经元中端粒酶反转录酶蛋白相对表达量显著高于二甲基亚砜组(P<0.05),腹腔注射20 mg/kg环黄芪醇组的皮质神经元中端粒酶反转录酶蛋白相对表达量显著高于溶剂组(P<0.05).结果表明,环黄芪醇能够促进皮质神经元轴突生长并改善小鼠脊髓损伤后运动功能,这一现象可能与端粒酶反转录酶的表达升高有关.
Cycloastragenol promotes motor function recovery and cortical neuron regeneration in mice with spinal cord injury
BACKGROUND:Previous studies have confirmed that cycloastragenol can promote the repair of sciatic nerve injuries,and activate telomerase reverse transcriptase to further participate in the regulation of axonal regeneration of peripheral sensory neurons.However,it remains unknown whether cycloastragenol can activate the axonal regeneration of cortical neurons,particularly whether it is involved in the restoration of motor function during spinal cord injury recovery.OBJECTIVE:To investigate the effects of cycloastragenol on the restoration of motor function in mice with spinal cord injury,as well as the related mechanisms by which cycloastragenol promotes cortical neuron regeneration.METHODS:(1)Twelve ICR mice were randomly divided into a solvent group and a cycloastragenol group,with six mice in each group.Mice were given intraperitoneal injections of PBS containing 2%Tween 20 and 5%dimethyl sulfoxide(DMSO)(the solvent group)and cycloastragenol(20 mg/kg),respectively.The treatment lasted for 12 weeks,and the motor function of the mouse limbs was assessed using the Basso Mouse Scale.(2)E14 fetal mouse cortical neurons were cultured in vitro and divided into a DMSO group and a cycloastragenol group,with the neurons being treated with DMSO and 0.5 μmol/L cycloastragenol for 3 days in vitro.(3)E7 pregnant mice were divided into a solvent group and a cycloastragenol group.After continuous intraperitoneal injections of PBS containing 2%Tween 20 and 5%DMSO and 20 mg/kg cycloastragenol for 7 continuous days,the fetal mouse cortex was harvested.The cortical neurons were then cultured in vitro for 3 days.(4)Tuj1 immunofluorescence staining was performed on fetal rat cortical neurons to analyze the axon length of Tuj1-positive cells,validating the effect of cycloastragenol on axonal regeneration of cortical neurons.Fetal mouse cortical neurons were subjected to dual-label immunofluorescence staining for Tuj1 and telomerase reverse transcriptase,in order to analyze the effect of cycloastragenol on the expression of telomerase reverse transcriptase.Western blot assay was used to detect the relative expression of telomerase reverse transcriptase in cortical neurons of fetal mice.(5)Six ICR mice were randomized into a solvent group and a cycloastragenol group(n=3 per group).After modeling,mice in the two groups received continuous intraperitoneal injections of PBS containing 2%Tween 20 and 5%DMSO and 20 mg/kg cycloastragenol,respectively,for 7 days.The relative expression of telomerase reverse transcriptase protein in spinal cord tissue was detected by western blot assay.RESULTS AND CONCLUSION:(1)After 4,6,8,and 12 weeks of treatment with cycloastragenol,the motor function scores of the mice in the cycloastragenol group were significantly higher than those in the solvent group(P<0.000 1).The relative protein expression of telomerase reverse transcriptase in the spinal cord tissues of mice in the cycloastragenol group was significantly higher than that in the solvent group after 7 days of cycloastragenol treatment(P<0.05).(2)The results of Tuj1 immunofluorescence staining showed that the axon length of neurons cultured in vitro in the 0.5 μmol/L cycloastragenol group was significantly greater than that in the DMSO group(P<0.001),and the axon length of neurons in the 20 mg/kg cycloastragenol intraperitoneal injection group was significantly greater than that in the solvent group(P<0.01).(3)The results of telomerase reverse transcriptase immunofluorescence staining indicated that the fluorescence intensity of telomerase reverse transcriptase in cortical neurons cultured in vitro in the 0.5 μmol/L cycloastragenol group was significantly higher than that of the DMSO group(P<0.01).(4)Western blot analysis showed that the relative expression of telomerase reverse transcriptase protein in cortical neurons cultured in vitro in the 0.5 μmol/L cycloastragenol group was significantly higher than that in the DMSO group(P<0.05).Similarly,the relative expression of telomerase reverse transcriptase protein in cortical neurons in the 20 mg/kg cycloastragenol intraperitoneal injection group was significantly higher than that in the solvent group(P<0.05).These findings indicate that cycloastragenol promotes axonal growth of cortical neurons and improves motor function in mice after spinal cord injury,which may be associated with elevated expression of telomerase reverse transcriptase.

cycloastragenolcortical neuronsaxonal growthtelomerase reverse transcriptasemotor functionspinal cord injuryengineered animal model

陶紫晗、赛吉拉夫

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苏州大学苏州医学院骨科研究所,江苏省 苏州市 215031

环黄芪醇 皮质神经元 轴突生长 端粒酶反转录酶 运动功能 脊髓损伤 工程化动物模型

2025

中国组织工程研究
中国康复医学会,《中国组织工程研究与临床康复》杂志社

中国组织工程研究

北大核心
影响因子:1.387
ISSN:2095-4344
年,卷(期):2025.29(20)