Article(id=1321425929507815908, tenantId=1146029695717560320, journalId=1235980733773295621, issueId=1321425881147495164, articleNumber=null, orderNo=null, doi=10.20251/j.cnki.1003-3734.2026.18.009, pmid=null, cstr=null, oa=null, hot=null, price=null, onlineType=0, articleFormat=0, articleType=null, articleTypeStr=null, receivedDate=null, receivedDateStr=null, revisedDate=null, revisedDateStr=null, acceptedDate=1767542400000, acceptedDateStr=2026-01-05, onlineDate=1792982092500, onlineDateStr=2026-10-26, pubDate=1790697600000, pubDateStr=2026-09-30, doiRegisterDate=null, doiRegisterDateStr=null, onlineIssueDate=1792982092500, onlineIssueDateStr=2026-10-26, onlineJustAcceptDate=null, onlineJustAcceptDateStr=null, onlineFirstDate=null, onlineFirstDateStr=null, sourceXml=null, magXml=null, createTime=1792982092500, creator=13701087609, updateTime=1792982092500, updator=13701087609, issue=Issue{id=1321425881147495164, tenantId=1146029695717560320, journalId=1235980733773295621, year='2026', volume='35', issue='18', pageStart='1905', pageEnd='2016', issueExtLink='null', onlineDate='null', pubDate='1790697600000', pubDateStr='2026-09-30', beforeIssueId=null, nextIssueId=null, price=null, status=1, issueComplete=1, articleOrder=1, issueType=-1, specialIssue=null, createTime=1792982080970, creator='13701087609', updateTime=1792982834300, updator='13701087609', preIssue=null, nextIssue=null, articleTotal=null, ext={EN=IssueExt(id=1321429040930599029, tenantId=1146029695717560320, journalId=1235980733773295621, issueId=1321425881147495164, language=EN, specialIssueTitle=, coverIllustrator=null, specialIssueEditor=, specialIssueAbout=), CN=IssueExt(id=1321429040930599030, tenantId=1146029695717560320, journalId=1235980733773295621, issueId=1321425881147495164, language=CN, specialIssueTitle=, coverIllustrator=null, specialIssueEditor=, specialIssueAbout=)}, issueFiles=null, downloadFileDto=null}, startPage=1968, endPage=1976, ext={EN=ArticleExt(id=1321425929658810853, articleId=1321425929507815908, tenantId=1146029695717560320, journalId=1235980733773295621, language=EN, title=Investigating the mechanisms of total alkaloids of Strychnos against myasthenia gravis in a rat model, columnId=null, journalTitle=Chinese Journal of New Drugs, columnName=null, runingTitle=null, highlight=null, articleAbstract=
Objective:

To investigate the therapeutic effect of MQZZJ (total alkaloids of Strychnos) on experimental autoimmune myasthenia gravis (EAMG) rats and to elucidate its underlying mechanisms.

Methods:

The EAMG rat model was established by immunizing female Lewis rats with the R97-116 peptide fragment. Rats were assigned to different groups and treated with MQZZJ (0.35, 0.7, and 1.4 mg·kg-1) or prednisone (4.2 mg·kg-1). The therapeutic effects and potential mechanisms were evaluated by monitoring the Lennon score and rotarod falling speed, measuring serum levels of acetylcholine receptor antibody (AChR-Ab), IgG, IgG1, IgG2b, IFN-γ, IL-17, and TGF-β, and detecting the CD4+/CD8+ ratio in peripheral blood lymphocytes.

Results:

MQZZJ significantly reduced the Lennon score, increased the rotarod falling speed, and reduced serum levels of AChR-Ab, IgG, and the IgG2b subtype. It also significantly decreased serum IL-17 and IFN-γ levels, increased serum TGF-β levels, and reduced the CD4+/CD8+ ratio.

Conclusion:

MQZZJ can markedly ameliorate myasthenic symptoms in EAMG rats. The mechanism may be related to inhibiting AChR-Ab production, reducing the CD4+/CD8+ ratio, modulating immune dysfunction, and alleviating abnormal inflammation.

, authors=Han-xing LIU1, Xing HUANG1, Xue-chun WU1, Lu LI1, Bin-bin DAI1, Xin-zhuang ZHANG1, Liang CAO1, Yong-wen ZHANG2, Wei XIAO1, *, authorsList=Han-xing LIU, Xing HUANG, Xue-chun WU, Lu LI, Bin-bin DAI, Xin-zhuang ZHANG, Liang CAO, Yong-wen ZHANG, Wei XIAO, authorCompany=null, correspAuthors=Wei XIAO, 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=1321425929931440614, articleId=1321425929507815908, tenantId=1146029695717560320, journalId=1235980733773295621, language=CN, title=马钱子总碱治疗重症肌无力大鼠模型的机制研究, columnId=1236330556003242277, journalTitle=中国新药杂志, columnName=实验研究, runingTitle=null, highlight=null, articleAbstract=
目的:

探讨马钱子总碱对实验性自身免疫性重症肌无力(experimental autoimmune myasthenia gravis, EAMG)大鼠的疗效及其作用机制。

方法:

Lewis雌性大鼠采用R97-116肽段免疫法构建EAMG模型,马钱子总碱(0.35、0.7、1.4 mg·kg-1)和泼尼松(4.2 mg·kg-1)分别对其进行分组给药治疗。通过记录大鼠Lennon评分和跌落时的转棒速度,测定血清抗乙酰胆碱受体抗体(anti-acetylcholine receptor antibody, AChR-Ab)、免疫球蛋白G(immunoglobulin G, IgG)、免疫球蛋白G1(immunoglobulin G1, IgG1)、免疫球蛋白G2b(immunoglobulin G2b, IgG2b)、干扰素-γ(interferon-γ, IFN-γ)、白细胞介素-17(interleukin 17, IL-17)和转化生长因子-β(transforming growth factor-β, TGF-β)水平,检测外周血淋巴细胞CD4+/CD8+比例等相关指标,考察其药效并探究可能的作用机制。

结果:

马钱子总碱能显著降低Lennon评分,显著升高跌落时的转棒速度,显著降低血清AChR-Ab、IgG和IgG2b亚型水平。马钱子总碱显著降低了血清IL-17和IFN-γ含量,升高血清TGF-β含量,显著降低外周血淋巴细胞CD4+/CD8+比例。

结论:

马钱子总碱能明显改善EAMG大鼠肌无力的症状,其作用机制可能与抑制AChR-Ab的生成、降低CD4+/CD8+比例、调节免疫功能紊乱和机体异常炎性状态有关。

, authors=刘涵星1, 黄醒1, 吴雪纯1, 李璐1, 代斌斌1, 张新庄1, 曹亮1, 张永文2, 肖伟1, *, authorsList=刘涵星, 黄醒, 吴雪纯, 李璐, 代斌斌, 张新庄, 曹亮, 张永文, 肖伟, authorCompany=null, correspAuthors=肖伟, authorNote=

刘涵星,男,硕士,主要从事中药新药药理毒理研究。E-mail: 。

, correspAuthorsNote=
* 肖伟,男,教授,博士生导师,主要从事中药新药研发及过程质量控制研究。E-mail: 。
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刘涵星,男,硕士,主要从事中药新药药理毒理研究。E-mail: 。

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刘涵星,男,硕士,主要从事中药新药药理毒理研究。E-mail: 。

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马钱子总碱治疗重症肌无力大鼠模型的机制研究
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刘涵星 1 , 黄醒 1 , 吴雪纯 1 , 李璐 1 , 代斌斌 1 , 张新庄 1 , 曹亮 1 , 张永文 2 , 肖伟 1, *
中国新药杂志 | 实验研究 2026,35(18): 1968-1976
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中国新药杂志 |实验研究 2026 , 35 (18) : 1968 -1976
马钱子总碱治疗重症肌无力大鼠模型的机制研究
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刘涵星1 , 黄醒1, 吴雪纯1, 李璐1, 代斌斌1, 张新庄1, 曹亮1, 张永文2, 肖伟1, *
作者信息
  • 1中药制药过程控制与智能制造技术全国重点实验室(江苏康缘药业股份有限公司),南京 211112
  • 2南京中医药大学,南京 210023
通讯作者:
* 肖伟,男,教授,博士生导师,主要从事中药新药研发及过程质量控制研究。E-mail: 。
作者简介:

刘涵星,男,硕士,主要从事中药新药药理毒理研究。E-mail: 。

Investigating the mechanisms of total alkaloids of Strychnos against myasthenia gravis in a rat model
Han-xing LIU1 , Xing HUANG1, Xue-chun WU1, Lu LI1, Bin-bin DAI1, Xin-zhuang ZHANG1, Liang CAO1, Yong-wen ZHANG2, Wei XIAO1, *
Affiliations
  • 1State Key Laboratory of Technologies for Chinese Medicine Pharmaceutical Process Control and Intelligent Manufacture (Jiangsu Kanion Pharmaceutical Co., Ltd.), Nanjing 211112, China
  • 2Nanjing University of Chinese Medicine, Nanjing 210023, China
出版时间: 2026-09-30 doi: 10.20251/j.cnki.1003-3734.2026.18.009
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目的:

探讨马钱子总碱对实验性自身免疫性重症肌无力(experimental autoimmune myasthenia gravis, EAMG)大鼠的疗效及其作用机制。

方法:

Lewis雌性大鼠采用R97-116肽段免疫法构建EAMG模型,马钱子总碱(0.35、0.7、1.4 mg·kg-1)和泼尼松(4.2 mg·kg-1)分别对其进行分组给药治疗。通过记录大鼠Lennon评分和跌落时的转棒速度,测定血清抗乙酰胆碱受体抗体(anti-acetylcholine receptor antibody, AChR-Ab)、免疫球蛋白G(immunoglobulin G, IgG)、免疫球蛋白G1(immunoglobulin G1, IgG1)、免疫球蛋白G2b(immunoglobulin G2b, IgG2b)、干扰素-γ(interferon-γ, IFN-γ)、白细胞介素-17(interleukin 17, IL-17)和转化生长因子-β(transforming growth factor-β, TGF-β)水平,检测外周血淋巴细胞CD4+/CD8+比例等相关指标,考察其药效并探究可能的作用机制。

结果:

马钱子总碱能显著降低Lennon评分,显著升高跌落时的转棒速度,显著降低血清AChR-Ab、IgG和IgG2b亚型水平。马钱子总碱显著降低了血清IL-17和IFN-γ含量,升高血清TGF-β含量,显著降低外周血淋巴细胞CD4+/CD8+比例。

结论:

马钱子总碱能明显改善EAMG大鼠肌无力的症状,其作用机制可能与抑制AChR-Ab的生成、降低CD4+/CD8+比例、调节免疫功能紊乱和机体异常炎性状态有关。

重症肌无力  /  马钱子总碱  /  抗乙酰胆碱受体抗体  /  CD4+/CD8+  /  细胞因子
Objective:

To investigate the therapeutic effect of MQZZJ (total alkaloids of Strychnos) on experimental autoimmune myasthenia gravis (EAMG) rats and to elucidate its underlying mechanisms.

Methods:

The EAMG rat model was established by immunizing female Lewis rats with the R97-116 peptide fragment. Rats were assigned to different groups and treated with MQZZJ (0.35, 0.7, and 1.4 mg·kg-1) or prednisone (4.2 mg·kg-1). The therapeutic effects and potential mechanisms were evaluated by monitoring the Lennon score and rotarod falling speed, measuring serum levels of acetylcholine receptor antibody (AChR-Ab), IgG, IgG1, IgG2b, IFN-γ, IL-17, and TGF-β, and detecting the CD4+/CD8+ ratio in peripheral blood lymphocytes.

Results:

MQZZJ significantly reduced the Lennon score, increased the rotarod falling speed, and reduced serum levels of AChR-Ab, IgG, and the IgG2b subtype. It also significantly decreased serum IL-17 and IFN-γ levels, increased serum TGF-β levels, and reduced the CD4+/CD8+ ratio.

Conclusion:

MQZZJ can markedly ameliorate myasthenic symptoms in EAMG rats. The mechanism may be related to inhibiting AChR-Ab production, reducing the CD4+/CD8+ ratio, modulating immune dysfunction, and alleviating abnormal inflammation.

myasthenia gravis  /  total alkaloids of Strychnos  /  AChR-Ab  /  CD4+/CD8+  /  cytokines
刘涵星, 黄醒, 吴雪纯, 李璐, 代斌斌, 张新庄, 曹亮, 张永文, 肖伟. 马钱子总碱治疗重症肌无力大鼠模型的机制研究. 中国新药杂志, 2026 , 35 (18) : 1968 -1976 . DOI: 10.20251/j.cnki.1003-3734.2026.18.009
Han-xing LIU, Xing HUANG, Xue-chun WU, Lu LI, Bin-bin DAI, Xin-zhuang ZHANG, Liang CAO, Yong-wen ZHANG, Wei XIAO. Investigating the mechanisms of total alkaloids of Strychnos against myasthenia gravis in a rat model[J]. Chinese Journal of New Drugs, 2026 , 35 (18) : 1968 -1976 . DOI: 10.20251/j.cnki.1003-3734.2026.18.009
  • 江苏省基础研究计划自然科学基金资助项目:前沿引领技术基础研究专项资助项目(BK20232014)
  • 中药制药过程控制与智能制造技术全国重点实验室目标资助项目(SKL2023D01001)
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2026年第35卷第18期
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doi: 10.20251/j.cnki.1003-3734.2026.18.009
  • 首发时间:2026-10-26
  • 出版时间:2026-09-30
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  • 录用日期:2026-01-05
基金
江苏省基础研究计划自然科学基金资助项目:前沿引领技术基础研究专项资助项目(BK20232014)
中药制药过程控制与智能制造技术全国重点实验室目标资助项目(SKL2023D01001)
作者信息
    1中药制药过程控制与智能制造技术全国重点实验室(江苏康缘药业股份有限公司),南京 211112
    2南京中医药大学,南京 210023

通讯作者:

* 肖伟,男,教授,博士生导师,主要从事中药新药研发及过程质量控制研究。E-mail: 。
参考文献
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2种不同金属材料的力学参数
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鹅膏菌科Amanitaceae 2 11 5.26 鹅膏菌属 Amanita 10 4.78
小菇科 Mycenaceae 2 12 5.74 丝盖伞属 Inocybe 5 2.39
多孔菌科 Polyporaceae 8 14 6.70 蜡蘑属 Laccaria 5 2.39
红菇科 Russulaceae 3 23 11.00 小皮伞属 Marasmius 6 2.87
小菇属 Mycena 11 5.26
光柄菇属 Pluteus 5 2.39
红菇属 Russula 17 8.13
栓菌属 Trametes 5 2.39
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