首页|淫黄葛合剂通过抑制铁死亡改善AD模型小鼠认知功能

淫黄葛合剂通过抑制铁死亡改善AD模型小鼠认知功能

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目的:研究淫黄葛合剂(icariin-astragaloside IV-puerarin mixture,Yin-Huang-Ge mixture,YHG)对阿尔茨海默病(Alzheimer disease,AD)模型小鼠认知功能障碍和脑组织铁死亡的影响,并探讨其机制。方法:将APP/PS1小鼠采用随机数字表法分为APP/PS1组、YHG治疗(APP/PS1+YHG)组和艾地苯醌(idebenone,IDE)治疗(APP/PS1+IDE)组,同月龄C57BL/6J小鼠为正常组。连续给药1个月后,采用Morris水迷宫检测小鼠的学习记忆能力,尼氏染色观察小鼠海马的形态学改变,电镜下观察各组小鼠神经元超微结构改变情况,Western blot检测海马组织中铁死亡抑制蛋白 1(ferroptosis suppressor protein 1,FSP1)的表达。ELISA检测辅酶Q10(coenzyme Q10,CoQ10)、还原型辅酶Q10(coenzyme Q10 H2,CoQ10H2)和4-羟基壬烯醛(4-hydroxynonenal,4-HNE)含量;生化试剂盒检测丙二醛(malondialdehyde,MDA)含量。结果:与正常组相比,APP/PS1小鼠学习记忆能力下降,海马CA3区神经元细胞排列松散,形状不规则;海马神经元线粒体皱缩,嵴不完整,膜密度增高;脑内FSP1蛋白表达降低(P<0。05);CoQ10和CoQ10H2水平均显著降低(P<0。01);4-HNE与MDA水平显著升高(P<0。01)。使用YHG和IDE后,小鼠学习记忆能力提高;海马CA3区神经元结构较模型组排列紧密,形状规则;线粒体结构相对清晰,线粒体膜相对正常,嵴较完整;脑内FSP1蛋白表达显著升高(P<0。05);CoQ10和CoQ10H2水平均显著升高(P<0。05);4-HNE与MDA水平显著降低(P<0。01)。结论:YHG可以改善AD小鼠认知功能,其机制可能与通过激活FSP1/CoQ10信号通路抑制铁死亡有关。
Icariin-astragaloside IV-puerarin mixture improves cognition in AD model mice by inhibiting ferroptosis
AIM:Study the effects of icariin-astragaloside IV-puerarin mixture(Yin-Huang-Ge mixture,YHG)on cognitive dysfunction and brain tissue ferroptosis in Alzheimer disease(AD)model mice,and explore its mecha-nism.METHODS:APP/PS1 mice were randomly divided into APP/PS1 group,icariin-astragaloside IV-puerarin mixture(APP/PS1+YHG)group,and idebenone(APP/PS1+IDE)group using a random number table method.C57BL/6J mice of the same age were selected as the normal group.After one month of continuous administration,Morris water maze was used to test the learning and memory abilities of mice.Nissl staining was used to observe the morphological changes in the hippocampus of mice.The ultrastructure of neurons in each group of mice was observed under electron microscopy.West-ern blot was used to detect the expression of FSP1 protein in hippocampal tissue.ELISA detection of coenzyme Q10(CoQ10),CoQ10H2,and 4-hydroxynonenal(4-HNE)content.Biochemical reagent kit is used to detect malondialde-hyde(MDA)content.RESULTS:Compared with the normal group,APP/PS1 mice showed decreased learning and mem-ory abilities,with loosely arranged and irregularly shaped hippocampal CA3 neurons.Hippocampal neurons exhibit mito-chondrial shrinkage,incomplete cristae,and increased membrane density.The expression of FSP1 protein in the brain de-creased(P<0.05).The levels of CoQ10 and CoQ10H2 were both reduced(P<0.01).The levels of 4-HNE and MDA in-creased(P<0.01).After using icariin-astragaloside IV-puerarin mixture and idebenone,the learning and memory abili-ties of mice were improved.The neuronal structure in the hippocampal CA3 region is more tightly arranged and has a regu-lar shape compared to the model group.The mitochondrial structure is relatively clear,the mitochondrial membrane is rel-atively normal,and the cristae are relatively intact.The expression of FSP1 protein in the brain increased(P<0.05).The levels of CoQ10 and CoQ10H2 both increased(P<0.05).The levels of 4-HNE and MDA were significantly reduced(P<0.01).CONCLUSION:The icariin-astragaloside IV-puerarin mixture can improve cognition in AD mice,and its mecha-nism may be related to inhibiting ferroptosis by activating the FSP1/CoQ10 signaling pathway.

icariin-astragaloside IV-puerarin mixtureAlzheimer diseasecognitionferroptosisFSP1/CoQ10 signaling pathawy

赵炎、贺小平、胡文竹、钟健民、郝雅煊、董贤慧

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河北中医药大学,河北省心脑血管病中医药防治研究重点实验室,河北 石家庄 050091

淫黄葛合剂 阿尔茨海默病 认知 铁死亡 FSP1/CoQ10信号通路

2024

中国病理生理杂志
中国病理生理学会

中国病理生理杂志

CSTPCD北大核心
影响因子:1.065
ISSN:1000-4718
年,卷(期):2024.40(12)