Article(id=1221483550319231623, tenantId=1146029695717560320, journalId=1189982191388893191, issueId=1221483541674774769, articleNumber=null, orderNo=null, doi=10.16438/j.0513-4870.2020-0421, pmid=null, cstr=null, oa=null, hot=null, price=null, onlineType=0, articleFormat=0, articleType=null, articleTypeStr=research-article, receivedDate=1585238400000, receivedDateStr=2020-03-27, revisedDate=1590508800000, revisedDateStr=2020-05-27, acceptedDate=null, acceptedDateStr=null, onlineDate=1769153972463, onlineDateStr=2026-01-23, pubDate=1605110400000, pubDateStr=2020-11-12, doiRegisterDate=null, doiRegisterDateStr=null, onlineIssueDate=1769153972463, onlineIssueDateStr=2026-01-23, onlineJustAcceptDate=null, onlineJustAcceptDateStr=null, onlineFirstDate=null, onlineFirstDateStr=null, sourceXml=null, magXml=null, createTime=1769153972463, creator=13701087609, updateTime=1769153972463, updator=13701087609, issue=Issue{id=1221483541674774769, tenantId=1146029695717560320, journalId=1189982191388893191, year='2020', volume='55', issue='11', pageStart='2491', pageEnd='2750', issueExtLink='null', onlineDate='null', pubDate='null', beforeIssueId=null, nextIssueId=null, price=null, status=1, issueComplete=1, articleOrder=1, issueType=-1, specialIssue=null, createTime=1769153970402, creator=13701087609, updateTime=1769154342560, updator=13701087609, preIssue=null, nextIssue=null, ext={EN=IssueExt(id=1221485102668890897, tenantId=1146029695717560320, journalId=1189982191388893191, issueId=1221483541674774769, language=EN, specialIssueTitle=, coverIllustrator=null, specialIssueEditor=, specialIssueAbout=), CN=IssueExt(id=1221485102673085202, tenantId=1146029695717560320, journalId=1189982191388893191, issueId=1221483541674774769, language=CN, specialIssueTitle=, coverIllustrator=null, specialIssueEditor=, specialIssueAbout=)}, issueFiles=null}, startPage=2651, endPage=2656, ext={EN=ArticleExt(id=1221483550864491167, articleId=1221483550319231623, tenantId=1146029695717560320, journalId=1189982191388893191, language=EN, title=Therapeutic effects of artesunate on cytomegalovirus pneumonia in mice, columnId=1190335348761793317, journalTitle=Acta Pharmaceutica Sinica, columnName=Original Articles, runingTitle=null, highlight=null, articleAbstract=
To investigate the therapeutic effect of artesunate on mouse cytomegalovirus pneumonia, the BALB/c-nu mice were infected with murine cytomegalovirus-green fluorescent protein (MCMV-GFP) by nose dropping method. The experimental protocol was approved by the Medical Laboratory Animal Ethics Committee of Guangzhou Medical University. The BALB/c-nu mice were randomly divided into five groups:control group, MCMV pneumonia group, and artesunate (60, 120, and 240 mg·kg-1) groups. The survival rate, weights, and virus loads in lungs among the groups were observed. The degree of histopathologic changes in lungs was assessed directly by hematoxylin-eosin (HE) assay. MCMV-GFP expression was assessed by immunofluorescence. In addition, reverse transcription polymerase chain reaction (RT-PCR) analysis was performed to investigate the content of major immediate early 1 (Mie1) mRNA, and enzyme-linked immunosorbent assay (ELISA) was used to detect the changes of inflammatory factors, interleukin 10 (IL-10), IL-6, and tumor necrosis factor-α (TNF-α). Western blot analysis was used to detect the expression of the changes of nuclear factor-kappa B (NF-κB) signaling pathways in total proteins. Compared with MCMV group, artesunate (120 mg·kg-1) significantly increased body weights of MCMV-infected nude mice over 30 days, and decreased the viral titer in lung homogenate, lung inflammation, and histological severity. Moreover, the administration of artesunate (120 mg·kg-1) could downregulate the expression of phospho-NF-κB (p-NF-κB) p65 in the lungs of mice. The present study suggested that artesunate can protect the immunocompromised mice from MCMV-induced interstitial pneumonia via downregulating NF-κB signaling pathway, thus attenuating inflammation in the lungs.
, correspAuthors=Ai-ping QIN, Xi-yong YU, authorNote=null, correspAuthorsNote=null, copyrightStatement=Copyright ©2020 Acta Pharmaceutica Sinica. All rights reserved., copyrightOwner=null, extLink=null, articleAbsUrl=null, sourceXml=null, magXml=null, pdfUrl=null, pdf=null, pdfFileSize=null, pdfExtLink=null, richHtmlUrl=null, mobilePdfUrl=null, reviewReport=null, pdfFirstPage=null, abstractGraph=null, abstractGraphContent=null, abstractVideo=null, citation=null, cebUrl=null, magXmlContent=null, mapNumber=null, authorCompany=null, fund=null, authors=null, authorsList=Ping WANG, Sheng CHEN, Xiao-tao HUANG, Xiao-mei XIAO, Qing-ping ZHAN, Ai-ping QIN, Xi-yong YU), CN=ArticleExt(id=1221483552328303335, articleId=1221483550319231623, tenantId=1146029695717560320, journalId=1189982191388893191, language=CN, title=青蒿琥酯对小鼠巨细胞病毒性肺炎的治疗作用, columnId=1190335348896011050, journalTitle=药学学报, columnName=研究论文, runingTitle=null, highlight=null, articleAbstract=
为了探索青蒿琥酯对小鼠巨细胞病毒性肺炎的治疗作用及其机制,应用滴鼻法建立携带绿色荧光蛋白的小鼠巨细胞病毒(murine cytomegalovirus-green fluorescent protein,MCMV-GFP)感染的巨细胞病毒性肺炎模型。动物福利和实验过程均遵循广州医科大学动物伦理委员会的规定。将BALB/c-nu小鼠随机分为5组:空白对照组、巨细胞病毒肺炎模型组、青蒿琥酯60、120和240 mg·kg-1组。观察小鼠生存期和肺组织病理变化,并进一步进行分子机制研究。分别采用苏木精-伊红(hematoxylin-eosin,HE)染色法检测肺组织的病理变化;荧光定量PCR(polymerase chain reaction)方法检测肺组织中MCMV主要即刻早期基因1(major immediate early 1,Mie1)mRNA的表达;免疫荧光法检测MCMV-GFP的表达;ELISA法(enzyme-linked immunosorbent assay)检测肺上清炎症因子白细胞介素6(interleukin 6,IL-6)、IL-10和肿瘤坏死因子α(tumor necrosis factor α,TNF-α)的含量;Western blot法检测感染后肺组织NF-κB(nuclear factor-κB)通路的变化;绘制小鼠体重变化和生存曲线图。结果显示,MCMV感染模型组小鼠肺组织出现大量炎症细胞浸润,肺组织结构破坏。青蒿琥酯(120 mg·kg-1)治疗后的小鼠肺部炎症减轻,肺泡结构明显好转。与MCMV感染模型组相比,青蒿琥酯(120和240 mg·kg-1)剂量组治疗后,小鼠肺部病毒复制水平降低,青蒿琥酯(120 mg·kg-1)剂量组可显著降低促炎因子IL-6和TNF-α水平并增加抗炎因子IL-10的水平;磷酸化NF-κB蛋白表达明显下降,治疗组小鼠体重增加,生存期延长。上述结果表明,青蒿琥酯具有抑制MCMV感染小鼠肺炎的作用,通过抑制NF-κB炎症信号通路的激活,减轻肺组织炎症因子IL-6和TNF-α的释放,并增加抗炎因子IL-10的表达,从而实现减轻肺部组织炎症的作用。
, correspAuthors=秦爱萍, 余细勇, authorNote=null, correspAuthorsNote=
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Effects of artesunate (ART) on weight and mortality of murine cytomegalovirus (MCMV) infected mice. A: Body weight change was monitored following infection for 40 days. Median with interquartile range of 10 mice per experimental group; B: Survival time of mice was recorded over 40 days. n = 10, x±s. ***P < 0.001 vs MCMV group. Ctrl: Control , figureFileSmall=IrGZQrYVsaiAin+8w1GZDg==, figureFileBig=ETuhdodROgnCROL1riqV8g==, tableContent=null), ArticleFig(id=1221483556824596594, tenantId=1146029695717560320, journalId=1189982191388893191, articleId=1221483550319231623, language=EN, label=null, caption=null, figureFileSmall=uk8ugeFkrcAlf+ODiERTZw==, figureFileBig=mdrYVXJylg99IhJOOwjQ5g==, tableContent=null), ArticleFig(id=1221483556904288381, tenantId=1146029695717560320, journalId=1189982191388893191, articleId=1221483550319231623, language=CN, label=Figure 2, caption=
Hematoxylin-eosin (HE)-stained sections of MCMV infected-mice lungs at 21 days post-infection compared to the phosphate buffered saline (PBS)-infected mice lungs. A: Control group; B: MCMV group; C: ART group (60 mg·kg-1); D: ART group (120 mg·kg-1); E: ART group (240 mg·kg-1). Scale bar: 200 μm , figureFileSmall=uk8ugeFkrcAlf+ODiERTZw==, figureFileBig=mdrYVXJylg99IhJOOwjQ5g==, tableContent=null), ArticleFig(id=1221483557030117517, tenantId=1146029695717560320, journalId=1189982191388893191, articleId=1221483550319231623, language=EN, label=null, caption=null, figureFileSmall=FSeOaH82bFWCtO4+jyjqPA==, figureFileBig=Bxjh41mB4yz98CaGYELIDg==, tableContent=null), ArticleFig(id=1221483557143363737, tenantId=1146029695717560320, journalId=1189982191388893191, articleId=1221483550319231623, language=CN, label=Figure 3, caption=
Effects of ART on MCMV replication in lung tissues. Mice were infected with MCMV-GFP. After treatment for 3 days with artesunate, lung sections were stained for MCMV-expressed GFP (green in the merge images). Nuclei were stained with DAPI (blue). Scale bar: 50 μm. A: Control group; B: MCMV group; C: ART group (60 mg·kg-1); D: ART group (120 mg·kg-1); E: ART group (240 mg·kg-1); F: Immune fluorescence identification of mice lungs was analyzed; G: The expression of Mie1 mRNA in lung tissues of MCMV-infected mice. n = 5, x±s. ##P < 0.01, ####P < 0.000 1 vs control; *P < 0.05, **P < 0.01, ***P < 0.001 vs MCMV group. GFP: Green fluorescent protein; DAPI: 4', 6-Diamidino-2-phenylindole; Mie1: Major immediate early 1 , figureFileSmall=FSeOaH82bFWCtO4+jyjqPA==, figureFileBig=Bxjh41mB4yz98CaGYELIDg==, tableContent=null), ArticleFig(id=1221483557227249823, tenantId=1146029695717560320, journalId=1189982191388893191, articleId=1221483550319231623, language=EN, label=null, caption=null, figureFileSmall=v6/a6fxtb5mtoEC6fY+KAA==, figureFileBig=LTqJltrvvJHcmN0DGL9AvA==, tableContent=null), ArticleFig(id=1221483557365661868, tenantId=1146029695717560320, journalId=1189982191388893191, articleId=1221483550319231623, language=CN, label=Figure 4, caption=
Effects of ART on inflammatory factors in lung tissues. The expression levels of interleukin 10 (IL-10), tumor necrosis factor α (TNF-α), and IL-6 in lung supernatants were measured by enzyme-linked immunosorbent assay (ELISA). n = 5, x±s. #P < 0.05, ####P < 0.000 1 vs control; *P < 0.05, ***P < 0.001 vs MCMV group , figureFileSmall=v6/a6fxtb5mtoEC6fY+KAA==, figureFileBig=LTqJltrvvJHcmN0DGL9AvA==, tableContent=null), ArticleFig(id=1221483557487296694, tenantId=1146029695717560320, journalId=1189982191388893191, articleId=1221483550319231623, language=EN, label=null, caption=null, figureFileSmall=LpmFnzNxi8uN5LKPCPiGyA==, figureFileBig=4kBP86M+NrKU8J8zrElyeg==, tableContent=null), ArticleFig(id=1221483557617320126, tenantId=1146029695717560320, journalId=1189982191388893191, articleId=1221483550319231623, language=CN, label=Figure 5, caption=
Expression of nuclear factor-kappa B (NF-κB) and phospho-NF-κB (p-NF-κB) in MCMV-infected mice lungs after ART treatment (60, 120, and 240 mg·kg-1) were detected. Representative Western blot images of NF-κB and p-NF-κB were presented and analyzed. n = 5, x ± s.*P < 0.05, **P < 0.01 vs MCMV group. 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