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Design,delivery and efficacy testing of therapeutic nucleic acids used to inhibit hepatitis C virus gene expression in vitro and in vivo 被引量:9
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作者 Wolfgang H.Caselmann Matthias Serwe +3 位作者 Thomas Lehmann János Ludwig Brian S.Sproat Joachim W.Engels 《World Journal of Gastroenterology》 SCIE CAS CSCD 2000年第5期626-629,共4页
Despite major achievements in the treatment ofchronic hepatitis C with the combination ofinterferons and the nucleoside analog ribavirin themajority of patients with chronic hepatitis C virus(HCV) infection cannot be ... Despite major achievements in the treatment ofchronic hepatitis C with the combination ofinterferons and the nucleoside analog ribavirin themajority of patients with chronic hepatitis C virus(HCV) infection cannot be treated effectively.Toimprove this response rate we used antisensetechnologies to inhibit HCV translation as possibleadditional option for experimental treatment.Antisense oligodeoxynucleotides(ODN) are 展开更多
关键词 hepatitis C-like viruses/therapy gene expression in VITRO in vivo nucleic acids/therapeutic use CYTOMEGALOVIRUS
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Mechanism of exogenous nucleic acids and their precursors improving the repair of intestinal epithelium after 7-irradiation in mice 被引量:8
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作者 Da Xiang Cui~1 Guei Ying Zeng~2 Feng Wang~1 Jun Rong Xu~1 Dong Qing Ren~2 Yan Hai Guo~1 Fu Rong Tian~2 Xiao Jun Yan~1 Yu Hou~1 Cheng Zhi Su~1 1 Institute of Genetic Diagnosis of the Fourth Military Medical University,Xi’an 710032,China 2 Department of Irradiation Medicine of the Fourth Military Medical University,Xi’an 710032,China 《World Journal of Gastroenterology》 SCIE CAS CSCD 2000年第5期709-717,共9页
AIM To clone expressed genes associated withrepair of irradiation-damaged mice intestinalgland cells treated by small intestinal RNA,andto explore the molecular mechanism ofexogenous nucleic acids improving repair ofi... AIM To clone expressed genes associated withrepair of irradiation-damaged mice intestinalgland cells treated by small intestinal RNA,andto explore the molecular mechanism ofexogenous nucleic acids improving repair ofintestinal crypt.METHODS The animal mode of test group andcontrol group was established,forty-five micebeing irradiated by γ ray were treated with smallintestinal RNA as test group,forty mice beingirradiated by γ ray were treated withphysiological saline as control group,five micewithout irradiation were used as normal control,their jejunal specimens were collectedrespectively at 6h,12h,24h,4d and 8d afterirradiation.Then by using LD-PCR based onsubtractive hybridization,these gene fragmentsdifferentially expressed between test group andcontrol group were obtained,and then werecloned into T vectors as well as beingsequenced.Obtained sequences were screenedagainst.GeneBank,if being new sequences,they were submitted to GeneBank.RESULTS Ninety clones were associated withrepair of irradiation-damaged intestinal glandcells treated by intestinal RNA.These clonesfrom test group of 6h,12h,24h,4d and 8dwere respectively 18,22,25,13,12.By screening against GeneBank,18 of which werenew sequences,the others were dramaticallysimilar to the known sequences,mainly similarto hsp,Nmi,Dutt1,alkaline phosphatase,homeobox,anti-CEA ScFv antibody,arginine/serine kinase and BMP-4,repA.Eighteen genefragments were new sequences,their acceptnumbers in GeneBank were respectivelyAF240164-AF240181.CONCLUSION Ninety clones were obtained tobe associated with repair of irradiation-damagedmice intestinal gland cells treated by smallintestinal RNA,which may be related toabnormal expression of genes and matchedproteins of hsp,Nmi,Duttl,Na,K-ATPase,alkalineph-osphatase,glkA,single strandedreplicative centromeric gene as well as 18 newsequences. 展开更多
关键词 radiation ionizing INTESTINE small/injuries RNA gene expression nucleic acids/therapeutic use POLYMERASE chain reaction REPAIR intestinal EPITHELIUM MICE
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蛋白酶体抑制剂PS-341靶向干预多发性骨髓瘤骨髓间充质干细胞的实验研究
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作者 陆化 林如峰 +6 位作者 沈文怡 葛峥 刘澎 张建富 吴雨洁 费小明 李建勇 《中国误诊学杂志》 CAS 2007年第24期5708-5711,共4页
目的:分析蛋白酶体抑制剂PS-341对多发性骨髓瘤(MM)骨髓间充质干细胞(MSCs)凋亡及其对IL-6、IL-1β、SCF细胞因子表达的影响。方法:含10%FBS的1640培养液培养得到MSCs,流式细胞术(FCM)鉴定所培养细胞的表型,以终浓度分别为0 nmol/L、50 ... 目的:分析蛋白酶体抑制剂PS-341对多发性骨髓瘤(MM)骨髓间充质干细胞(MSCs)凋亡及其对IL-6、IL-1β、SCF细胞因子表达的影响。方法:含10%FBS的1640培养液培养得到MSCs,流式细胞术(FCM)鉴定所培养细胞的表型,以终浓度分别为0 nmol/L、50 nmol/L、100 nmol/L、150 nmol/L、200 nmol/L的PS-341作用MSCs 4 h,光学显微镜观察细胞形态改变,荧光显微镜下Annexin V-FITC/PI双染法观察细胞凋亡,反转录聚合酶链反应(RT-PCR)检测IL-6、IL-1β、SCF细胞因子表达的变化。结果:PS-341可诱导MSCs凋亡,与其浓度成正比;与对照组(0 nmol/L PS-341)比较,浓度分别为50 nmol/L、100 nmol/L、150 nmol/L、200 nmol/L的PS-341作用MSCs 4 h后明显抑制IL-6、IL-1β、SCF的表达(P<0.05);PS-341对IL-6和SCF的抑制与PS-341浓度成正相关(P<0.05),在初发/难治复发和完全缓解(CR)两组患者间均无显著差异;对IL-1β的抑制在CR组较初发/难治复发组更明显(P<0.05);PS-341作用后IL-1β表达的强弱对IL-6及SCF的表达无影响。结论:PS-341诱导MM患者MSCs凋亡和抑制其IL-6、IL-1β、SCF的表达,是PS-341有效治疗MM的靶点之一。 展开更多
关键词 硼酸化物/治疗应用 吡嗪类/治疗应用 蛋白酶抑制药/治疗应用 多发性骨髓瘤/药物疗法 骨髓细胞/药物作用 间质干细胞/药物作用 人类
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硼替佐米对K562细胞株粘附分子ICAM-1表达的影响
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作者 陆世丰 陆化 +4 位作者 刘澎 王永韧 王丽霞 张建富 李建勇 《中国误诊学杂志》 CAS 2007年第27期6472-6474,共3页
目的:探讨蛋白酶体抑制剂硼替佐米(万珂,Valcade)对白血病K562细胞株细胞问粘附分子(ICAM-1)表达的影响。方法:用含10%FBS的RPMI1640培养液体外培养K562细胞,分别用0、10、20、30、50、100 nmol/L的硼替佐米干预K562细胞6h后收集,用反... 目的:探讨蛋白酶体抑制剂硼替佐米(万珂,Valcade)对白血病K562细胞株细胞问粘附分子(ICAM-1)表达的影响。方法:用含10%FBS的RPMI1640培养液体外培养K562细胞,分别用0、10、20、30、50、100 nmol/L的硼替佐米干预K562细胞6h后收集,用反转录聚合酶链反应(RT-PCR)分析K562细胞ICAM-1表达的变化。并用20 nmol/L浓度硼替佐米作用K562细胞株不同时间(0,6,12,24,48h)分析K562细胞ICAM-1表达的变化。结果:硼替佐米明显抑制K562细胞ICAM-1的表达(P<0.05),在硼替佐米浓度为0~20 nmol/L时成正比关系,当浓度>20 nmol/L各组差异无显著性。以20 nmol/L浓度作用K562细胞株不同时间后,ICAM-1的表达较作用前明显下降.并且这种效应持续存在。结论:K562细胞株ICAM-1基因表达异常增高,硼替佐米可抑制其表达量。 展开更多
关键词 硼酸化物/药理学 吡嗪类/药理学 抗肿瘤药/治疗应用 胞间粘附分子1/药物作用/代谢 K562细胞/药物作用/代谢 白血病/药物疗法 体外研究
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Omega-6 for Body,Omega-3 for Brain:Balance for Brain Development in Children
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作者 J.Thomas BRENNA 《粮油食品科技》 2022年第3期16-22,共7页
Food must supply a balance of nutrients to support both brain and body.The human brain makes us uniquely human.Essential fatty acids are part of the metabolic pathways that define tissue structure and function.Omega-6... Food must supply a balance of nutrients to support both brain and body.The human brain makes us uniquely human.Essential fatty acids are part of the metabolic pathways that define tissue structure and function.Omega-6(O6)linoleic acid(LA6)has long been known to be required for skin structure,and as a precursor for inflammatory,thrombotic,immune,and other signaling molecules.Omega-3(O3)alpha-linolenic acid(ALA3)and particularly its long chain product docosahexaenoic acid(DHA3)has a key structural role in the brain,retina,and related neural tissue.In the 20 th century western world,inexpensive,high quality oils primarily from LA6-rich/O3-poor vegetable seed oils became dominant fats produced by the food industry.Provision of LA6-rich/O3-poor oils as the sole source of fat in the diets of pregnant animals causes O3 deficiency and poor brain development,primarily because high LA6 antagonizes metabolism of all O3,creating an artificial metabolic demand for O3.Data developed over the last 2~3 decades show that provision of low LA6 combined with preformed DHA3 optimizes brain function.Recent studies emphasize the importance of nutrition to support brain development,with newer findings showing particular importance of fatty acid balance in malnourished children.The World Health Organization(WHO)through the Codex Alimentarius(“Code for Food”)is increasingly recognizing the primacy of brain health and in part on that basis recently acted to recommend balanced fat for Ready-to-Use-Therapeutic Foods used to treat children with severe acute malnutrition.Similar principles are likely to be important in older persons.Industry now has the tools to adjust the composition of oils to support brain health throughout the life cycle. 展开更多
关键词 brain development docosahexaenoic acid Omega-3 Omega-6 high oleic oils severe acute malnutrition Ready to use therapeutic food fatty acid balance
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