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4篇 您的检索式:作者名="Sinai Li"
    题名 作者 年代 出处 被引量
1Effects of Wen Dan Tang on insomnia-related anxiety and levels of the brain-gut peptide Ghrelin显示文摘Ghrelin, a brain-gut peptide that induces anxiety and other abnormal emotions, contributes to the effects of insomnia on emotional behavior. In contrast, the traditional Chinese Medicine remedy Wen Dan Tang reduces insomnia-related anxiety, which may perhaps correspond to changes in the brain-gut axis. This suggests a possible relationship between Wen Dan Tang's pharmacological mechanism and the brain-gut axis. Based on this hypothesis, a sleep-deprived rat model was induced and Wen Dan Tang was administered using oral gavage during model establishment. Wen Dan Tang significantly reduced insomnia-related anxiety and prevented Ghrelin level decreases following sleep deprivation, especially in the hypothalamus. Increased expression of Ghrelin receptor mRNA in the hypothalamus was also observed, suggesting that reduced anxiety may be a result of Wen Dan Tang's regulation of Ghrelin-Ghrelin receptors.Liye Wang Yuehan Song Feng Li Yan Liu Jie Ma Meng Mao Fengzhi Wu Ying Wu Sinai Li Binghe Guan Xiaolan Liu 2014Neural Regeneration Research2014,9,2:16
2Synthesis of two mono-deoxy β-cyclodextrin derivatives as useful tools for confirming DIBAL-H promoted bis-de-O-methylation mechanism显示文摘Diisobutylaluminium 氢化物(DIBAL-H ) 支持 permethylated -cyclodextrin 的第二等的边界 regioselective bis-de-O-methylation (给 diol 2 的 -CD) 。获得卓见进这显著 regioselective 行为的机制,有在 2 位置或 3 位置的白酒功能的二相应 permethylated CD 在我们的以前的学习被综合。作为对这个工作进一步的步,二混合物负担得起相应 2-deoxy 和 3-deoxy permethylated CD 衍生物(19 和 16 ) 的 2,2-azobisisobutyronitrile 在礼品与 tributyltin 氢化物受到 deoxygenation 反应。这二混合物的结构被 1D 和 2D NMR 和 HRMS 描绘。混合物 16 和 19 是不能的与建议那 O-2A 的 DIBAL-H 反应, O-3B 为 DIBAL-H 是必要的 permethylated 的支持的 bis-de-O-methylation 反应 CD。Su Long Xiao De Min Zhou Ming Yang Fei Yu Li He Zhang Pierre Sinay Yong Min Zhang 2012Chinese Chemical Letters2012,23,12:1
3查看详情显示文摘Hamamoto R Furukawa Y Morita M Iimura Y SiNai F.P Li M Yagyu R Nakamural Y 0,,:1
4Cucurbitacin E inhibits the proliferation of hepatoma cells in vitro and in vivo through induction of G2/M phase arrest显示文摘Objective Cucurbitacins are the highly oxygenated tetracyclic triterpenes,which are predominantly found in the Cucurbitaceae family but are also present in several other families of the plant kingdom.A number of compounds of this group have been investigated for their cytotoxic,hepatoprotective,anti-inflammatory,cardiovascular and anti-diabetic activities.In China,the cucurbitacin preparation,which contains mostly cucurbitacin B and cucurbitacin E,has been clinically used for the treatment of the primary liver carcinoma.It has been previously reported that cucurbitacin E could produce cytotoxicity against a variety of cancer cells,and various mechanisms were implicated in its cytotoxic effect.The present study is to investigate the effect of cucurbitacin E on hepatoma cells in vitro and in vivo and to study their potential mechanisms of action.Methods The MTT assay was used to assess the viability of human HepG2 and BEL7402 hepatoma cells in vitro after treatment with different concentrations of cucurbitacin E.The cell cycle distribution was determined by flowcytometric analysis after propidium iodide(PI)staining.The cell cycle-related proteins were detected using western blotting analysis.Implanted mouse hepatoma H22 model was built to evaluate the growth inhibitory effect of cucurbitacin E in vivo in mice.Results Our studies found that cucurbitacin E(10-300 nM)produced anti-proliferative effect on human HepG2 and BEL7402 hepatoma cells in vitro without cytotoxicity.According to flowcytometric analysis,cucurbitacin E arrested the cell cycle at G2/M phase in both HepG2 and BEL7402 hepatoma cells after 24 h treatment.Cucurbitacin E induced the decrease in the level of CDK1 protein and the increase in the level of p21 protein,but had no effect on the levels of cyclin A,cyclin B1 and Cdc25C protein.In in vivo anti-tumor experiment,cucurbitacin E had significant inhibitory effects on the growth of mouse H22 hepatoma cells.Conclusions Cucurbitacin E inhibited the proliferation of hepatoma cells in vitro and in vivo,at least in part,through induction of cell cycle arrest at G2/M phase,which was mediated by concomitant upregulation of p21 and downregulation of CDK1.We consider that cucurbitacin E may be useful in the treatment of liver cancer.LI Yan-chun1,MA En-long1,DENG Yi-hui2,JING Yong-kui3(1.Department of Pharmacology,Shenyang Pharmaceutical University,Shenyang 110016,China 2.Department of Pharmaceutics,Shenyang Pharmaceutical University,Shenyang 110016,China 3.Department of Medicine,Mount Sinai School of Medicine,New York,USA) 2008沈阳药科大学学报2008,25,S1:0
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