基于PINK1/Parkin信号通路研究细叶远志皂苷对AD模型小鼠脑组织线粒体自噬的影响 点击下载
论文标题: 基于PINK1/Parkin信号通路研究细叶远志皂苷对AD模型小鼠脑组织线粒体自噬的影响
英文标题:
中文摘要: 目的:探讨细叶远志皂苷(TEN)对阿尔茨海默病(AD)模型小鼠脑组织线粒体自噬的影响。方法:将50只雄性APP/PS1双转基因小鼠随机分为模型组、TEN中剂量+3-甲基腺嘌呤(3-MA)组[TEN40mg/(kg·d)+自噬抑制剂3-MA30mg/(kg·d)]和TEN低、中、高剂量组[20、40、80mg/(kg·d)],每组10只;另将10只同系野生型小鼠作为正常对照组。各给药组小鼠灌胃相应药液,正常对照组和模型组小鼠灌胃0.3%羧甲基纤维素钠溶液,每天给药1次,给药体积为0.01mL/g,连续给药3个月。末次给药后,检测神经元内微管相关蛋白1轻链3(LC3)的阳性表达水平[以积分光密度(IOD)计],脑组织线粒体中LC3、泛素结合蛋白p62、CathepsinD、Rab7、人第10号染色体缺失的磷酸酶及张力蛋白同源基因诱导的假定激酶1(PINK1)、E3泛素连接酶(Parkin)mRNA的表达量和LC3、p62、PINK1、Parkin蛋白的表达量。结果:与正常对照组比较,模型组小鼠神经元内LC3的IOD值和脑组织线粒体中LC3、p62、PINK1、ParkinmRNA及其蛋白的表达量均显著升高(P<0.05或P<0.01),CathepsinD、Rab7mRNA的表达量均显著降低(P<0.05或P<0.01)。与模型组比较,TEN低、中、高剂量组小鼠神经元内LC3的IOD值(除TEN低、中剂量组外)和脑组织线粒体中LC3、CathepsinD、Rab7、PINK1(除TEN低剂量组外)、Parkin(除TEN低剂量组外)mRNA的表达量以及LC3(除TEN中剂量组外)、PINK1(除TEN高剂量组显著降低外)、Parkin(除TEN低剂量组显著降低外)蛋白的表达量均显著升高(P<0.05或P<0.01),p62mRNA(除TEN低剂量组外)及其蛋白的表达量均显著降低(P<0.05或P<0.01)。与TEN中剂量组比较,TEN中剂量+3-MA组小鼠上述指标的变化均被显著抑制(P<0.05或P<0.01)。结论:TEN可通过激活PINK1/Parkin信号通路来诱导AD模型小鼠脑组织线粒体自噬,增强溶酶体功能。
英文摘要: OBJECTIVE:To investig ate the effects of tenuifolin (TEN)on brain mitochondrial autophagy in Aizheimer ’s disease(AD)model mice. METHODS :Totally 50 male APP/PS1 double transgenic mice were randomly divided into model group,TEN medium-dose+ 3-MA group [TEN 40 mg/(kg·d)+autophagy inhibitor 3-MA 30 mg/(kg·d)] and TEN low-dose , medium-dose and high-dose groups [ 20,40,80 mg/(kg·d)],with 10 mice in each group. In addition ,10 wild-type homologous mice were included in normal control group. Administration groups were intragastrically given corresponding drug solution ;normal control group and model group were intragastrically given 0.3% sodium carboxymethyl cellulose solution ,once a day ,0.01 mL/g, for consecutive 3 months. After last administration ,positive expression [measured by integrated optical density (IOD)] of microtubule associated protein 1 light chain 3(LC3)in neuron was detected ;mRNA expressions of LC3,ubiquitin-binding protein p62,Cathepsin D ,Rab7,phosphatase and tensin homolog deleted on chromosome ten gene-induced putative kinase 1(PINK1) and E 3 ligase(Parkin)as well as protein expressions of LC 3,p62,PINK1 and Parkin were detected in brain mitochondria. RESULTS:Compared with normal control group ,IOD value of LC 3 in neuron as well as mRNA and protein expressions of LC 3, p62,PINK1 and Parkin in brain mitochondria were all increased significantly in model group (P<0.05 or P<0.01),while mRNA expressions of Cathepsin D and Rab 7 were decreased significantly (P<0.05 or P<0.01). Compared wit h model group ,IOD values of LC 3(except for TEN low-dose and medium-dose groups ) in neuron ,mRNA expressions of LC 3,Cathepsin D ,Rab7, PINK1(except for TEN low-dose group )and Parkin (except for TEN low-dose group ) in brain mitochondria as well as protein expressions of LC 3 (except for TEN medium-dose group),PINK1(except fo r TEN high-dose group decreased significantly)and Parkin (except for TEN low-dose group decreased significantly )were increased significantly in TEN low-dose , medium-dose and high-dose groups (P<0.05 or P<0.01);mRNA(except for TEN low-dose group )and protein expressions of p62 were decreased significantly (P<0.05 or P<0.01). Compared with TEN medium-dose group ,the changes of above indexes were inhibited significantly in TEN medium-dose + 3-MA group (P<0.05 or P<0.01). CONCLUSIONS :TEN can induce mitophagy in brain tissue of AD model mice by activating PINK 1/Parkin signaling pathway and improve lysosome function.
期刊: 2021年第32卷第22期
作者: 陆晓华,金桂芳,余河汉,杨红
英文作者: LU Xiaohua ,JIN Guifang,YU Hehan ,YANG Hong
关键字: 细叶远志皂苷;阿尔茨海默病;PINK1/Parkin信号通路;线粒体自噬;APP/PS1双转基因小鼠
KEYWORDS: Tenuifolin;Alzheimer’s disease ;PINK1/Parkin signaling pathway ;Mitochondrial autophagy ;APP/PS1 double
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