自然科学版
陕西师范大学学报(自然科学版)
运动生物学专题
RNSP改善APP/PS1小鼠海马线粒体质量与学习记忆能力的研究
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闫清伟1*, 色里玛2, 巴桑次仁2, 格桑罗布2, 田青3
(1 西藏民族大学 体育学院, 陕西 咸阳 712082;2 西藏甘露藏药股份有限公司, 西藏 拉萨 851400;3 西藏民族大学 教育学院,陕西 咸阳 712082)
闫清伟,男,讲师,博士,主要研究方向运动生化与营养。Email:yan2004@126.com
摘要:
为探讨藏药七十味珍珠丸(ratanasampil,RNSP)对阿尔茨海默症(Alzheimer’s disease, AD)病理中海马线粒体融合、分裂及学习记忆能力的影响,以APP/PS1小鼠为实验对象,利用Morris 水迷宫、RTPCR、透射电镜、ELISA等实验手段,对小鼠的空间学习记忆能力,线粒体融合、分裂,线粒体形态结构及功能的关键指标进行了系统检测。结果表明:持续给药RNSP 12周,可改善APP/PS1小鼠空间学习记忆能力,上调APP/PS1小鼠海马线粒体融合相关基因即线粒体融合蛋白(mitofusin1/2, mfn1,mfn2)基因和视神经萎缩症蛋白质1(optic atrophy protein1,Opa1)基因的mRNA,下调线粒体分裂基因动力相关蛋白质1(dynaminrelated protein 1,Drp1)基因的mRNA,改善线粒体形态结构,上调海马ATP合成酶基因(ATP Synthetase C)的mRNA及ATP水平。结果提示,RNSP改善APP/PS1小鼠学习记忆能力的机制,可能与RNSP对该模型小鼠海马线粒体融合、分裂及后续能量代谢的改善有关。
关键词:
阿尔茨海默症;七十味珍珠丸;线粒体;融合与分裂;能量代谢;学习记忆
收稿日期:
2018-03-12
中图分类号:
G804.7
文献标识码:
A
文章编号:
16724291(2019)03005707
基金项目:
西藏自治区自然科学基金(2016ZR1520);西藏甘露藏药横向项目;西藏民族大学重大项目培育计划
Doi:
Effect of RNSP on mitochondrial quality and learning and memory abilities in hippocampus of APP/PS1 mice
YAN Qingwei1*, SE Lima2, BA SANG Ciren2, GE SANG Luobu2, TIAN Qing3
(1 School of Physical Education, Xizang Minzu University, Xianyang 712082, Shaanxi,China;2 Tibet Ganlu Tibetan Medicine Co.Ltd, Lhasa 851400, Tibet, China;3 School of Education, Xizang Minzu University, Xianyang 712082, Shaanxi, China)
Abstract:
In order to investigate the effect of Tibetan medicine ratanasampil (RNSP) on the hippocampal mitochondrial fusion, fission and the ability of learning and memory in Alzheimer′s disease (AD), APP/PS1 mice were used as experimental subjects in. The spatial learning and memory ability of the APP/PS1 mice, the mitochondrial fusion and fission, the mitochondrial morphology and function of the mice were tested respectively by means of Morris water maze, RTPCR, transmission electron microscopy, ELISA and so on. The results showed that continuous administration of RNSP for 12 weeks could improve the spatial learning and memory ability of APP/PS1 mice, upregulate the expression of mitochondrial fusion genes mfn1, Mfn2 and Opa1 in the hippocampus of APP/PS1 mice, downregulate the expression of mitochondrial fission gene Drp1, improve the morphological structure of mitochondria, and upregulate the expression of ATP Synthetase C and ATP level in the hippocampus. It is suggested that the mechanism of RNSP improving the learning and memory abilities of APP/PS1 mice may be related to the improvement of mitochondrial fusion, fission and subsequent energy metabolism in hippocampus of APP/PS1 mice induced by RNSP.
KeyWords:
Alzheimer′s disease; ratanasampil(RNSP); mitochondria; fusion and fission; energy metabolism; learning and memory