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丙戊酸治疗后大鼠脊髓挫伤中胶质纤维酸性蛋白(GFAP)表达降低及功能恢复改善。

Decreased GFAP expression and improved functional recovery in contused spinal cord of rats following valproic acid therapy.

作者信息

Darvishi Marzieh, Tiraihi Taki, Mesbah-Namin Seyed A, Delshad AliReza, Taheri Taher

机构信息

Department of Anatomical Sciences, Faculty of Medical Sciences, Tarbiat Modares University, Tehran, Iran.

出版信息

Neurochem Res. 2014 Dec;39(12):2319-33. doi: 10.1007/s11064-014-1429-5. Epub 2014 Sep 10.

Abstract

Many studies have illustrated that much of the post-traumatic degeneration of the spinal cord cells is caused by the secondary mechanism. The aim of this study is to evaluate the effect of the anti-inflammatory property of valproic acid (VPA) on injured spinal cords (SC). The rats with the contused SC received intraperitoneal single injection of VPA (150, 200, 300, 400 or 500 mg/kg) at 2, 6, 12 and 24 h post-injury. Basso-Beattie-Bresnahan (BBB) test and H-reflex evaluated the functional outcome for 12 weeks. The SC were investigated 3 months post-injury using morphometry and glial fibrillary acid protein (GFAP) expression. Reduction in cavitation, H/M ratio, BBB scores and GFAP expression in the treatment groups were significantly more than that of the untreated one (P < 0.05). The optimal improvement in the condition of the contused rats was in the ones treated at the acute phase of injury with 300 mg/kg of VPA at 12 h post-injury, they had the highest increase in BBB score and decrease in astrogliosis and axonal loss. We conclude that treating the contused rats with 300 mg/kg of VPA at 12 h post-injury improves the functional outcome and reduces the traumatized SC gliosis.

摘要

许多研究表明,脊髓细胞创伤后退变大多是由继发性机制引起的。本研究旨在评估丙戊酸(VPA)的抗炎特性对脊髓损伤(SC)的影响。脊髓挫伤的大鼠在损伤后2、6、12和24小时接受腹腔单次注射VPA(150、200、300、400或500mg/kg)。Basso-Beattie-Bresnahan(BBB)试验和H反射评估12周的功能结果。损伤后3个月,使用形态测量法和胶质纤维酸性蛋白(GFAP)表达对脊髓进行研究。治疗组的空洞形成、H/M比值、BBB评分和GFAP表达的降低明显多于未治疗组(P<0.05)。脊髓挫伤大鼠状况的最佳改善出现在损伤急性期12小时接受300mg/kg VPA治疗的大鼠中,它们的BBB评分增加最多,星形胶质细胞增生和轴突损失减少。我们得出结论,损伤后12小时用300mg/kg VPA治疗脊髓挫伤大鼠可改善功能结果并减少创伤脊髓的胶质细胞增生。

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