1. 甘肃中医药大学
2. 深圳市罗湖区人民医院
3. 深圳市罗湖区中医院
4. 甘肃省定西市第二人民医院
5. 上海中医药大学附属龙华医院
6. 甘肃中医药大学深圳市罗湖区人民医院深圳市罗湖区中医院甘肃省定西市第二人民医院上海中医药大学附属龙华医院
纸质出版:2019
移动端阅览
[1]马春林,吴红彦,崔淑梅,朱凯敏,刘佳楠,兰美华,王爱琳.黑逍遥散对APP/PS1双转基因小鼠海马CREB1蛋白及其磷酸化表达的影响[J].中医杂志,2019,60(17):1499-1503.
MA Chunlin, WU Hongyan, CUI Shumei, et al. Effect of Heixiaoyao Powder(黑逍遥散) on CREB1 Protein and Its Phosphorylation Expression in Hippocampus of APP/PS1 Double Transgenic Mice[J]. Journal of Traditional Chinese Medicine2019, 60(17): 1499-1503.
[1]马春林,吴红彦,崔淑梅,朱凯敏,刘佳楠,兰美华,王爱琳.黑逍遥散对APP/PS1双转基因小鼠海马CREB1蛋白及其磷酸化表达的影响[J].中医杂志,2019,60(17):1499-1503. DOI: 10.13288/j.11-2166/r.2019.17.014.
MA Chunlin, WU Hongyan, CUI Shumei, et al. Effect of Heixiaoyao Powder(黑逍遥散) on CREB1 Protein and Its Phosphorylation Expression in Hippocampus of APP/PS1 Double Transgenic Mice[J]. Journal of Traditional Chinese Medicine2019, 60(17): 1499-1503. DOI: 10.13288/j.11-2166/r.2019.17.014.
目的探讨黑逍遥散治疗阿尔茨海默病的可能作用机制。方法 30只APP/PS1双转基因雄性小鼠随机分为模型组、盐酸多奈哌齐组、黑逍遥散组
每组10只。同月龄、同种系的野生型C57BL/6雄性小鼠10只设为空白组。黑逍遥散组给予黑逍遥散6 g/(kg·d)灌胃
盐酸多奈哌齐组给予盐酸多奈哌齐片3. 25 mg/(kg·d)灌胃
模型组、空白组给予双蒸水0. 2 ml/10 g灌胃
各组均每日灌胃1次
连续3个月。采用Morris水迷宫于实验结束第1~5天进行定位航行实验观察逃避潜伏期
第6天开展空间搜索实验记录跨原平台次数。采用免疫组化法检测小鼠海马CA1、CA3及DG区环腺苷酸应答元件结合蛋白1 (CREB1)及磷酸化环腺苷酸应答元件结合蛋白1 (p-CREB1)表达。结果与空白组比较
模型组小鼠第1~5天逃避潜伏期明显延长
第6天跨原平台次数明显减少
小鼠海马CA1、CA3及DG区CREB1及p-CREB1蛋白表达显著降低(P <0. 05或P <0. 01)。与模型组比较
盐酸多奈哌齐组和黑逍遥散组各时间点逃避潜伏期均缩短
第6天跨原平台次数明显增加
小鼠海马CA1、CA3及DG区CREB1、p-CREB1蛋白表达显著升高(P <0. 05或P <0. 01)。黑逍遥散组和盐酸多奈哌齐组各指标组间比较差异无统计学意义(P> 0. 05)。结论黑逍遥散可能通过调节海马CREB1及其磷酸化表达发挥防治阿尔茨海默病的作用。
Objective To investigate the possible mechanism of action of Heixiaoyao Powder( 黑逍遥散) in the treatment of Alzheimer’ s disease. Methods A total of 30 APP/PS1 double transgenic male mice were randomly divided into a model group
a donepezil hydrochloride group and a Heixiaoyao Powder group
with 10 rats in each group. Ten wild-type C57 BL/6 male mice of the same age and same strain were set as blank group. The Heixiaoyao Powder group was given 6 g/( kg·d) by intragastric administration
and donepezil hydrochloride was given 3. 25 mg/( kg·d) to the donepezil hydrochloride group. The model group and the blank group were given double distilled water 0. 2 ml/10 g by gavage. All groups were intragastrically administered once a day for 3 months. The Morris water maze was used to observe the escape latency during the 1 st to 5 th day of the experiment
and the space search experiment was recorded on the 6 th day to record the number of times across the original platform. The expression of cyclic adenosine responsive element binding protein 1( CREB1) and phosphorylated cyclic adenosine responsive element binding protein 1( p-CREB1) in mouse hippocampal CA1
CA3 and DG regions were detected by immunohistochemistry. Results Compared with the blank group
the escape latency of the model group was significantly prolonged on the 1 st to 5 th day
and the number of trans-platforms was significantly decreased on the 6 th day. The expression of CREB1 and p-CREB1 protein in the hippocampus CA1
CA3 and DG areas was significantly decreased( P < 0. 05 or P < 0. 01). Compared with the model group
the escape latency of the donepezil hydrochloride group and the Heixiaoyao Powder group was shortened at each time point
and the number of trans-platforms increased significantly on the 6 th day. The expression of CREB1 and p-CREB1 protein in the hippocampus CA1
CA3 and DG areas of the mice increased significantly( P < 0. 05 or P < 0. 01). There was no significant difference between the indicators of Heixiaoyao Powder and Donepezil Hydrochloride( P > 0. 05). Conclusion Heixiaoyao Powder may play a role in the prevention and treatment of Alzheimer’s disease by regulating hippocampal CREB1 and its phosphorylation expression.
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