Article(id=1317114964050039445, tenantId=1146029695717560320, journalId=1302318977290174537, issueId=1317114959243362461, articleNumber=null, orderNo=null, doi=10.19664/j.cnki.1002-2392.260197, pmid=null, cstr=null, oa=null, hot=null, price=null, onlineType=0, articleFormat=0, articleType=null, articleTypeStr=null, receivedDate=1743523200000, receivedDateStr=2025-04-02, revisedDate=1774886400000, revisedDateStr=2026-03-31, acceptedDate=null, acceptedDateStr=null, onlineDate=1791954278241, onlineDateStr=2026-10-14, pubDate=1792425600000, pubDateStr=2026-10-20, doiRegisterDate=null, doiRegisterDateStr=null, onlineIssueDate=1791954278241, onlineIssueDateStr=2026-10-14, onlineJustAcceptDate=null, onlineJustAcceptDateStr=null, onlineFirstDate=null, onlineFirstDateStr=null, sourceXml=null, magXml=null, createTime=1791954278241, creator=13701087609, updateTime=1791954278241, updator=13701087609, issue=Issue{id=1317114959243362461, tenantId=1146029695717560320, journalId=1302318977290174537, year='2026', volume='54', issue='10', pageStart='1', pageEnd='137', issueExtLink='null', onlineDate='null', pubDate='1792425600000', pubDateStr='2026-10-20', beforeIssueId=null, nextIssueId=null, price=null, status=1, issueComplete=1, articleOrder=1, issueType=1, specialIssue=null, createTime=1791954277096, creator='13701087609', updateTime=1792120134547, updator='13701087609', preIssue=null, nextIssue=null, articleTotal=null, ext={EN=IssueExt(id=1317810615909991147, tenantId=1146029695717560320, journalId=1302318977290174537, issueId=1317114959243362461, language=EN, specialIssueTitle=, coverIllustrator=null, specialIssueEditor=, specialIssueAbout=), CN=IssueExt(id=1317810615909991148, tenantId=1146029695717560320, journalId=1302318977290174537, issueId=1317114959243362461, language=CN, specialIssueTitle=, coverIllustrator=null, specialIssueEditor=, specialIssueAbout=)}, issueFiles=null, downloadFileDto=null}, startPage=21, endPage=26, ext={EN=ArticleExt(id=1317114964263948950, articleId=1317114964050039445, tenantId=1146029695717560320, journalId=1302318977290174537, language=EN, title=Study on the Anti-inflammatory Effects and Toxic Effects of Dendrobium Officinale Polysaccharides, columnId=null, journalTitle=Acta Chinese Medicine and Pharmacology, columnName=null, runingTitle=null, highlight=null, articleAbstract=
Objective: To evaluate the anti-inflammatory mechanism of Dendrobium officinale polysaccharides (DOP) as well as their acute and long-term toxicity, thereby providing a scientific basis for clinical application within a safe dosage range.
Methods: The anti-inflammatory mechanism of DOP was comprehensively investigated through in vitro cell experiments and in vivo animal studies. In the cell experiment, a mouse macrophage RAW264.7 inflammation model was established using lipopolysaccharide (LPS) stimulation. Different concentrations of DOP (50, 100, 200 μg/mL) were added, and the expression levels of inflammatory cytokines (TNF-α, IL-6, IL-1β) were measured. In the animal experiment, a xylene-induced ear edema model was used to observe the anti-inflammatory effect of DOP, and serum inflammatory cytokine levels were detected by ELISA. Additionally, acute toxicity tests and long-term toxicity tests were conducted to monitor mouse survival rate, body weight changes, biochemical indicators (ALT, AST, BUN, Cr), and to assess the risk of immune-allergic reactions.
Results: Cell experiment results showed that DOP significantly downregulated the expression levels of the inflammatory cytokines TNF-α, IL-6, and IL-1β in a dose-dependent manner (P<0.05). In animal experiments, DOP significantly reduced xylene-induced ear thickness and serum inflammatory cytokine levels in mice, demonstrating significant anti-inflammatory activity. In toxicity experiments, a high dose of DOP (5 000 mg/kg) reduced mouse survival rate to 40% and significantly inhibited body weight gain (P<0.05), while low to medium doses (50, 100, 200 mg/kg) showed no obvious acute toxicity. Long-term toxicity tests indicated that a high dose of DOP (200 mg/kg) significantly elevated liver and kidney function indicators ALT, AST, BUN, and Cr (P<0.05), suggesting that high doses may induce liver and kidney injury.
Conclusion: DOP exhibits significant anti-inflammatory effects with low toxicity within low to medium dosage ranges. However, potential acute toxicity and risk of liver and kidney injury exist at high doses. while also suggesting that long-term use requires caution and close monitoring of toxic reactions.
, authors=Yongqi ZHAO
1, Lihong LU
2, Shemin GUO
3, Sheng SHEN
4, authorsList=Yongqi ZHAO, Lihong LU, Shemin GUO, Sheng SHEN, authorCompany=null, correspAuthors=null, authorNote=null, correspAuthorsNote=null, copyrightStatement=null, 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, fund=null), CN=ArticleExt(id=1317114964570133143, articleId=1317114964050039445, tenantId=1146029695717560320, journalId=1302318977290174537, language=CN, title=铁皮石斛多糖的抗炎作用及毒性作用研究, columnId=1303760926633652690, journalTitle=中医药学报, columnName=实验研究, runingTitle=null, highlight=null, articleAbstract=
目的: 评估铁皮石斛多糖抗炎机制及急性和长期毒性,为其安全剂量范围内的临床应用提供科学依据。
方法: 通过细胞实验和动物实验综合研究铁皮石斛多糖的抗炎作用机制。在细胞实验中,选用LPS(脂多糖)刺激小鼠巨噬细胞RAW264.7建立炎症模型,分别加入不同浓度铁皮石斛多糖(50、100、200 μg/mL),检测炎症因子(TNF-α、IL-6、IL-1β)表达水平。在动物实验中,采用二甲苯诱导的耳肿胀模型,观察铁皮石斛多糖的抗炎效果,通过ELISA法检测血清中炎症因子水平。此外,在急性毒性试验及长期毒性试验中监测小鼠存活率、体质量变化、生化指标(ALT、AST、BUN、Cr),并评估其免疫过敏反应风险。
结果: 细胞实验结果显示,铁皮石斛多糖能显著下调炎症因子TNF-α、IL-6、IL-1β的表达水平(P<0.05,P<0.01),且呈剂量依赖性。在动物实验中,铁皮石斛多糖显著降低二甲苯诱导的小鼠耳厚度及血清炎症因子水平(P<0.05,P<0.01),表现出显著的抗炎活性。在急性毒性试验中,5 000 mg/kg高剂量铁皮石斛多糖导致小鼠存活率下降至40%并显著抑制体质量增长(P<0.05),而低剂量至中剂量(50、100、200 mg/kg)均未见明显急性毒性。长期毒性试验表明,高剂量铁皮石斛多糖(200 mg/kg)显著升高肝肾功能指标ALT、AST、BUN、Cr水平(P<0.05,P<0.01),提示高剂量可能引发肝肾损伤。
结论: 铁皮石斛多糖在低至中剂量范围内具有显著的抗炎作用,且毒性较低,但高剂量下存在潜在急性毒性及肝肾功能损伤风险,长期使用需谨慎并密切监测毒性反应。
, authors=赵永旗
1, 鲁丽红
2, 郭社民
3, 申晟
4, authorsList=赵永旗, 鲁丽红, 郭社民, 申晟, authorCompany=null, correspAuthors=null, authorNote=
赵永旗(1972-),男,副主任药师,研究方向:中药资源鉴定、炮制工艺与质量标准、中药药理及新药开发研究。
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1.Puyang People's Hospital, Puyang 457000, China, bio=null, bioImg=null, bioContent=null, aboutCorrespAuthor=null), CN=AuthorExt(id=1317504328689111045, tenantId=1146029695717560320, journalId=1302318977290174537, articleId=1317114964050039445, authorId=1317504328525533186, language=CN, stringName=赵永旗, firstName=null, middleName=null, lastName=null, prefix=null, suffix=null, authorComment=null, nameInitials=null, affiliation=null, department=null, xref=
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赵永旗(1972-),男,副主任药师,研究方向:中药资源鉴定、炮制工艺与质量标准、中药药理及新药开发研究。
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赵永旗(1972-),男,副主任药师,研究方向:中药资源鉴定、炮制工艺与质量标准、中药药理及新药开发研究。
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3.濮阳市产品质量检验检测中心食品药品检验所,河南 濮阳 457000, bio=null, bioImg=null, bioContent=null, aboutCorrespAuthor=null)}, companyList=[AuthorCompany(id=1317504326730372092, tenantId=1146029695717560320, journalId=1302318977290174537, articleId=1317114964050039445, xref=3., ext=[AuthorCompanyExt(id=1317504326747149309, tenantId=1146029695717560320, journalId=1302318977290174537, articleId=1317114964050039445, companyId=1317504326730372092, language=EN, country=null, province=null, city=null, postcode=null, companyName=null, departmentName=null, remark=
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