益智胶囊对大鼠学习记忆障碍及β -淀粉样肽神经毒性的影响

X. Jiang-ping, Wu Hang-yu, Li Lin, S. Sha
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引用次数: 0

摘要

目的:探讨益直胶囊(CYZ主要由我科从何首蓼、人参和淫羊藿中提取纯化,定量有效成分均大于50%)对大鼠学习记忆障碍和-淀粉样蛋白诱导的神经毒性的影响。方法:用不同剂量的CYZ灌胃SD大鼠,连续8 d,每天2次。各组大鼠腹腔注射氢溴酸东莨菪碱(Sco),分别进行Morris水迷宫实验和步进实验,探讨大鼠学习记忆能力的变化。体外培养大鼠皮层原代神经元7 d后,在添加淀粉样肽25 - 35 (a25 - 35)前后分别加入含有CYZ的血清,观察CYZ对神经毒性的保护作用程度。采用MTT法测定培养基中乳酸脱氢酶水平。莫里斯结果与对照组相比,大鼠在水迷宫测试需要显著下降的时间在寻找水面下的平台从19.5±11.40,8.5±2.39,8.8±3.07,7.4±3.87秒,分别在step-though测试,潜伏期从22.70±23.07,148.50±124.02,176.50±143.36,196.60±128.00秒而错误数量降低了从14.20±7.74,7.50±8.02,3.40±4.43,2.50±3.10,分别均具有统计学显著性。此外,在培养的原代神经元中,培养基中LDH水平从3670.2±437.65急剧下降到864.5±371.69和1444±635.18 U L, MTT测试中A评分从0.68±0.193上升到0.93±0.009和0.96±0.239,表明CYZ能有效抵抗a25 - 35诱导的神经毒性。结论:CYZ对体外学习记忆功能障碍和神经毒性有较好的治疗作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effects of Capsule Yi‐Zhi on Learning and Memory Disorder and β‐Amyloid Peptide Induced Neurotoxicity in Rats
Objective: To investigate the effects of Capsule Yi-Zhi (CYZ is extracted and purified by our department mainly from Polygonum Multiflorum, Ginseng and Korean Epimedium herb, among which quantitatively effective ingredients are more than 50%.) on learning and memory disorder and â-amyloid protein induced neurotoxicity in rats. Methods: Various doses of CYZ were administered to Sprague-Dawley (SD) rats for 8 days, twice a day. Then scopolamine hydrobromide (Sco) intraperitoneal injection was performed on each rat and the Morris water maze test and step-though test were carried out respectively to explore the changes of the rats’ learning and memory capacities. Primary rat cortex neurons were cultured in vitro for 7 days and then, serum containing CYZ was added to neurons before or after the addition of â Amyloid peptide25–35 (Aâ25–35) to see the extent of CYZ’s protectiveness on neurotoxicity. MTT assay and test of level of LDH in the culture media were performed to achieve this aim. Results Compared with control group, rats in Morris water maze test required significantly decreased time in finding the platform under the water surface from 19.5 ± 11.40 to 8.5 ± 2.39, 8.8 ± 3.07, and 7.4 ± 3.87 sec, respectively, and in step-though test, the latent period rose from 22.70 ± 23.07 to 148.50 ± 124.02, 176.50 ± 143.36, and 196.60 ± 128.00 sec and the error number decreased from 14.20 ± 7.74 to 7.50 ± 8.02, 3.40 ± 4.43 and 2.50 ± 3.10 respectively, all with statistical significance. Moreover, in cultured primary neurons, the dramatic drop of LDH level in culture media from 3670.2 ± 437.65 to 864.5 ± 371.69 and 1444 ± 635.18 U L and the high A scores rising from 0.68 ± 0.193 to 0.93 ± 0.009 and 0.96 ± 0.239 in MTT test indicated that CYZ could effectively resist the neurotoxicity induced by Aâ25–35. Conclusions: CYZ presented promising effects on learning and memory dysfunction and Aâ induced neurotoxicity in vitro.
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