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Quantitative proteomics analysis of Fructus Psoraleae-induced hepatotoxicity in rats 被引量:8
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作者 LI Zhi-Jian Abudumijiti Abulizi +10 位作者 XU Deng-Qiu Youlidouzi Maimaiti Silafu Aibai JIANG Zhen-Zhou ZHAO Guo-Lin WANG Tao Aiximujiang Refukati Zulikaer Maimaiti Yiliyaer Simayi CAO Chun-Yu ZHANG Lu-Yong 《Chinese Journal of Natural Medicines》 SCIE CAS CSCD 2020年第2期123-137,共15页
Fructus Psoraleae,which is commonly consumed for the treatment of osteoporosis,bone fracture,and leucoderma,induces liver injury.This study investigated the pathogenesis of the ethanol extract of Fructus Psoraleae(EEF... Fructus Psoraleae,which is commonly consumed for the treatment of osteoporosis,bone fracture,and leucoderma,induces liver injury.This study investigated the pathogenesis of the ethanol extract of Fructus Psoraleae(EEFP)-induced liver injury in rats.EEFP(1.35,1.80,and 2.25 g·kg^–1)was administrated to Sprague Dawley(SD)rats for 30 d.We measured liver chemistries,histopathology,and quantitative isobaric tags for relative and absolute quantitation(iTRAQ)-based protein profiling.EEFP demonstrated parameters suggestive of liver injury with changes in bile secretion,bile flow rate,and liver histopathology.iTRAQ analysis showed that a total of 4042 proteins were expressed in liver tissues of EEFP-treated and untreated rats.Among these proteins,81 were upregulated and 32 were downregulated in the treatment group.KEGG pathway analysis showed that the drug metabolic pathways of cytochrome P450,glutathione metabolism,glycerolipid metabolism,and bile secretion were enriched with differentially expressed proteins.The expression of key proteins related to the farnesoid X receptor(FXR),i.e.,the peroxisome proliferators-activated receptor alpha(PPAR-α),were downregulated,and multidrug resistance-associated protein 3(MRP3)was upregulated in the EEFP-treated rats.Our results provide evidence that EEFP may induce hepatotoxicity through various pathways.Furthermore,our study demonstrates changes in protein regulation using iTRAQ quantitative proteomics analysis. 展开更多
关键词 HEPATOTOXICITY itraq analysis Fructus Psoraleae FXR MRP3
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iTRAQ-based analysis of 17β-estradiol induced proteome in Chinese tongue sole Cynoglossus semilaevis
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作者 ZHU Ying LI Yangzhen +12 位作者 LI Hailong WANG Lei ZHANG Ning LIU Yang MENG Liang XU Xiwen DONG Zhongdian WEI Min GUO Hua CUI Zhongkai LI Xihong SHAO Changwei XU Wenteng 《Journal of Oceanology and Limnology》 SCIE CAS CSCD 2019年第5期1659-1668,共10页
The phenomenon of sex dimorphism prevails among many fi sh species. It has attracted the general research interest due to its close relationship to fi sh growth and thus aquaculture productivity. In Chinese tongue sol... The phenomenon of sex dimorphism prevails among many fi sh species. It has attracted the general research interest due to its close relationship to fi sh growth and thus aquaculture productivity. In Chinese tongue sole ( Cynoglossus semilaevis ), 17β-estradiol (E2) can be used reportedly to induce the feminization of fi sh, although the detailed regulatory network remained elusive. We treated the tongue sole fry before sex diff erentiation with E2 (10 and 30 μg/L) to identify potential targets of E2 in Chinese tongue sole. The E2 treatment indeed induced genetic male fi sh sex-reversal to phenotypic female. Using an iTRAQ-based comparative proteomic analysis, 409 proteins that diff erentially expressed after E2 induction were identifi ed, including 259 up-regulated and 150 down-regulated proteins. Furthermore, 19 diff erentially expressed proteins identifi ed in the comparative proteomic analysis were selected to assess their transcription and eight of them exhibited the same tendency. Functions of the eight proteins included mainly nucleotide and protein binding. Interestingly, a far upstream element-binding protein 3-like isoform exhibited the signifi cant upregulation both at transcription and translation levels after E2 treatment. This work identifi ed a set of candidate proteins for E2 response and deepened our understanding of E2 regulatory mechanism. 展开更多
关键词 Cynoglossus SEMILAEVIS 17Β-ESTRADIOL sex reversal PROTEOME itraq analysis
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梅花鹿茸不同生长时期转录组及蛋白组联合分析 被引量:1
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作者 慧芳 孙天霞 +2 位作者 薛东明 姜英男 赵雨 《吉林中医药》 2022年第8期975-979,共5页
目的了解鹿茸再生及快速生长过程中基因和蛋白的动态变化,阐明鹿茸生长发育机制。方法以梅花鹿(Cervus nippon Temminck)的鹿茸[初生期(PS)、快速生长期(RG)、骨化期(OS)鹿茸组织]作为实验材料,基于Illumina Hiseq和iTRAQ技术在转录和... 目的了解鹿茸再生及快速生长过程中基因和蛋白的动态变化,阐明鹿茸生长发育机制。方法以梅花鹿(Cervus nippon Temminck)的鹿茸[初生期(PS)、快速生长期(RG)、骨化期(OS)鹿茸组织]作为实验材料,基于Illumina Hiseq和iTRAQ技术在转录和蛋白水平进行分析,根据差异基因和差异蛋白结果筛选与鹿茸再生和快速生长有关的基因和蛋白。结果2组分别得到11294(PSvsRG)和4924(PSvsOS)个显著差异基因(DEGs),2组的蛋白组数据显示,分别得到236、211个差异蛋白(DAPs),相关性分析显示转录组和蛋白组数据相关性分析呈弱相关。在2组中分别有54、51个DEGs编码了其相应的DAPs,其中,在2组中分别得到35和20个在转录组和蛋白组中调节方向相同的DEGs和相应的DAPs。对候选基因/蛋白进行KEGG富集分析,分别富集到10和12个信号通路。其中,2组共同富集到的通路包括:血管平滑肌收缩、p53信号通路、黏着斑、蛋白质消化吸收、TGF-β信号通路、ECM-受体相互作用信号通路。只富集到快速生长期的信号通路包括:戊糖磷酸途径、糖酵解/糖异生、果糖和甘露糖代谢及代谢途径。只富集到骨化期的信号通路包括:破骨细胞分化、肌动蛋白细胞骨架的调节、紧密连接、RNA转运、mRNA监测途径信号通路。共有10个候选基因/蛋白(CALD1、THBS2S、COL9A、ALDO、COL1A、HSPG2、SIRPA、CSRP、MYH9、H1-5)注释到上述信号通路。结论在鹿茸生长发育期间许多基因和蛋白质在鹿茸快速生长期和骨化期表现出不同的丰度。转录组和蛋白组数据相关性较差。筛选出与鹿茸生长发育相关的蛋白为:CALD1、THBS2S、COL9A、ALDO、COL1A、HSPG2、SIRPA、CSRP、MYH9、H1-5以上结果为阐明鹿茸再生的分子机制提供了重要的理论依据。 展开更多
关键词 梅花鹿 转录组测序 蛋白组 itraq定量分析技术 鹿茸再生
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