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作 者:孙源 王丹阳 孙晶 白亚娟 范蓓[2,3] 宋洪波 吉建邦[1,3,5] 卢聪 王凤忠[1,2,3] SUN Yuan;WANG Danyang;SUN Jing;BAI Yajuan;FAN Bei;SONG Hongbo;JI Jianbang;LU Cong;WANG Fengzhong(National Nanfan Research Institute(Sanya),Chinese Academy of Agricultural Sciences,Sanya,Hainan 572024,China;Institute of Food Science and Technology,Chinese Academy of Agricultural Sciences,Beijing 100193,China;Sanya Institute,Hainan Academy of Agricultural Sciences,Sanya,Hainan 572025,China;College of Food Science,Fujian Agriculture and Forestry University,Fuzhou,Fujian 350002,China;Haikou Key Laboratory of Areca Processing Research,Haikou,Hainan 570100,China)
机构地区:[1]三亚中国农业科学院国家南繁研究院,海南三亚572024 [2]中国农业科学院农产品加工研究所,北京100193 [3]海南省农业科学院三亚研究院,海南三亚572025 [4]福建农林大学食品科学学院,福建福州350002 [5]海口市槟榔加工研究重点实验室,海南海口570100
出 处:《热带作物学报》2024年第6期1252-1261,共10页Chinese Journal of Tropical Crops
基 金:三亚中国农业科学院国家南繁研究院“南繁专项”2022年院院联合攻关项目(No.YYLH05);三亚中国农业科学院国家南繁研究院“南繁专项”2023年重点项目(No.ZDXM2302);国家重点研发计划项目(No.2022YFD1600303)。
摘 要:本研究通过建立过氧化氢(H_(2)O_(2))诱导的SH-SY5Y神经细胞氧化应激模型,旨在探究槟榔碱对氧化应激诱导神经细胞损伤的保护作用及其作用机制。采用CCK-8法检测细胞活力,采用分光光度法检测乳酸脱氢酶(LDH)释放、丙二醛(MDA)含量、超氧化物歧化酶(SOD)和过氧化氢酶(CAT)活性,采用流式细胞术检测细胞凋亡、线粒体膜电位,采用Western blot技术检测Nrf2、HO-1、Keap1、Bcl-2、Bax、Caspase-3的表达。结果表明:槟榔碱干预均能有效降低细胞凋亡并显著上调线粒体膜电位;在提高SOD、CAT水平的同时降低MDA水平;140μmol/L槟榔碱处理能够显著上调Nrf2、HO-1、Bcl-2蛋白的表达(P<0.001,P<0.0001),并下调Keap1、Bax、Caspase-3蛋白的表达(P<0.001,P<0.0001)。表明槟榔碱能够有效改善H_(2)O_(2)诱导的氧化应激损伤,其作用机制与激活Nrf2/HO-1信号通路、提升细胞抗氧化活力、调控Bcl-2/Bax/Caspase-3信号通路和抑制细胞凋亡有关。The aim of this study was to explore the protective effect of arecoline on the cell model of H_(2)O_(2)-induced oxidative stress damaged model in SH-SY5Y cells and elucidate its mechanism.Cell viability was detected by CCK-8 assay.Spectrophotometry was used to detect LDH release,MDA,SOD,and CAT contents.Flow cytometry was used to detect cell apoptosis and mitochondrial membrane potential.Western blot was used to detect the expressions of Nrf2,HO-1,Keap1,Bcl-2,Bax and Caspase-3.Arecoline could reduce cell apoptosis and significantly increase mitochondrial membrane potential.The level of SOD elucidateand CAT increased while the level of MDA decreased.Arecoline 140μmol/L group could significantly up-regulate the protein expression of Nrf2,HO-1 and Bcl-2(P<0.001,P<0.0001),and down-regulate the protein expression of Keap1,Bax and Caspase-3(P<0.001,P<0.0001).Conclusions:arecoline can effectively improve H_(2)O_(2)-induced oxidative stress injury in SH-SY5Y cell by activating the Nrf2/HO-1 signaling pathway,enhancing the activities of antioxidant enzymes and regulating the oxidation reduction system of cells,as well as regulating the Bcl-2/Bax/Caspase-3 signaling pathway and inhibiting cell apoptosis.
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