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升血饮联合阿伐曲泊帕治疗化疗致血小板减少症临床研究 被引量:4
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作者 张美玲 王艳昕 《陕西中医》 CAS 2022年第11期1547-1550,共4页
目的:探讨升血饮联合阿伐曲泊帕治疗化疗致血小板减少症疗效及对血小板相关免疫球蛋白(PAIg)、血小板反应蛋白1(THBS-1)、血小板膜蛋白-140(GMP-140)的影响。方法:选取118例化疗致血小板减少症患者为研究对象,随机分为观察组、对照组,每... 目的:探讨升血饮联合阿伐曲泊帕治疗化疗致血小板减少症疗效及对血小板相关免疫球蛋白(PAIg)、血小板反应蛋白1(THBS-1)、血小板膜蛋白-140(GMP-140)的影响。方法:选取118例化疗致血小板减少症患者为研究对象,随机分为观察组、对照组,每组59例。对照组以阿伐曲泊帕治疗,观察组以升血饮联合阿伐曲泊帕治疗。比较两组患者的临床疗效、中医症候积分、血小板计数水平、炎症损伤指标及治疗安全性。结果:治疗后观察组患者的总有效率为91.53%,高于对照组的74.58%(P<0.05)。治疗后观察组神疲乏力、纳差食少、少气懒言、腰膝酸软症候积分均低于对照组(P<0.05)。治疗后观察组血小板计数(PLT)、血小板压积(PCT)水平高于对照组,血小板分布宽度(PDW)、血小板平均体积(MPV)水平低于对照组(P<0.05)。观察组治疗后PAIg、THBS-1、GMP-140水平均低于对照组(P<0.05)。两组不良反应发生率比较差异无统计学意义(P>0.05)。结论:升血饮联合阿伐曲泊帕治疗化疗致血小板减少症疗效显著,能够改善患者的中医症候,增加血小板计数,抑制PAIg、THBS-1、GMP-140等炎症损伤因子的表达,且治疗安全性较好。 展开更多
关键词 血小板减少症 化疗 阿伐曲泊帕 升血饮 中医症候 血小板计数 炎症损伤因子
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两种方法修复磨牙残根残冠的临床比较
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作者 邬优盛 方丽敏 《浙江创伤外科》 2021年第1期130-131,共2页
目的探讨铸造金属桩核与纤维树脂桩核修复磨牙残根残冠的临床疗效病牙体损伤以及对患者血清炎性因子的影响。方法回顾分析2018年1月至2020年6月在本院治疗的收治的进行根管治疗后的残根残冠患者65例,共80颗患牙,各40例。对照组采用铸造... 目的探讨铸造金属桩核与纤维树脂桩核修复磨牙残根残冠的临床疗效病牙体损伤以及对患者血清炎性因子的影响。方法回顾分析2018年1月至2020年6月在本院治疗的收治的进行根管治疗后的残根残冠患者65例,共80颗患牙,各40例。对照组采用铸造金属桩核治疗,观察组则纤维树脂桩核,对比两组患者治疗前后的临床疗效指标以及炎症因子指标包括IL-6、TNF-a水平,以及不良反应合并发症情况。结果观察组在治疗结束后治疗有效率明显高于对照组(P<0.05);修复后对照组与观察组的IL-6、TNF-a水平同入组时相比均升高,且对照组术后IL-6、TNF-a水平高于观察组(P<0.05)。结论应用纤维树脂桩核修复残根残冠可提高患者治疗有效率,降低炎性反应,减轻牙体损伤,无明显不良反应。 展开更多
关键词 铸造金属桩核 纤维树脂桩核 残根残冠修复、牙体损伤炎症因子
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Punicalagin protects bovine endometrial epithelial cells against lipopolysaccharide-induced inflammatory injury 被引量:9
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作者 An LYU Jia-jia CHEN +5 位作者 Hui-chuan WANG Xiao-hong YU Zhi-cong ZHANG Ping GONG Lin-shu JIANG Feng-hua LIU 《Journal of Zhejiang University-Science B(Biomedicine & Biotechnology)》 SCIE CAS CSCD 2017年第6期481-491,共11页
Objective:Bovine endometritis is one of the most common reproductive disorders in cattle.The aim of this study was to investigate the anti-inflammation potential of punicalagin in lipopolysaccharide(LPS)-induced bo... Objective:Bovine endometritis is one of the most common reproductive disorders in cattle.The aim of this study was to investigate the anti-inflammation potential of punicalagin in lipopolysaccharide(LPS)-induced bovine endometrial epithelial cells(bE ECs)and to uncover the underlying mechanisms.Methods:bE ECs were stimulated with different concentrations(1,10,30,50,and 100μg/ml)of LPS for 3,6,9,12,and 18 h.MTT assay was used to assess cell viability and to identify the conditions for inflammatory injury and effective concentrations of punicalagin.Quantitative real-time polymerase chain reaction(q RT-PCR)was used to assess gene expression of pro-inflammatory cytokines.Western blotting was used to assess levels of inflammation-related proteins.Results:Treatment of b EECs with 30μg/ml LPS for 12 h induced cell injury and reduced cell viability.Punicalagin(5,10,or 20μg/ml)pretreatment significantly decreased LPS-induced productions of interleukin(IL)-1β,IL-6,IL-8,and tumor necrosis factor-α(TNF-α)in bE ECs.Molecular research showed that punicalagin inhibited the activation of the upstream mediator nuclear factor-κB(NF-κB)by suppressing the production of inhibitorκBα(IκBα)and phosphorylation of p65.Results also indicated that punicalagin can suppress the phosphorylation of mitogen-activated protein kinases(MAPKs)including p38,c-Jun N-terminal kinase(JNK),and extracellular signal-regulated kinase(ERK).Conclusions:Punicalagin may attenuate LPS-induced inflammatory injury and provide a potential option for the treatment of dairy cows with Escherichia coli endometritis. 展开更多
关键词 Bovine endometrial epithelial cell CYTOKINE Inflammatory injury PUNICALAGIN
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