Article(id=1317115086280446623, tenantId=1146029695717560320, journalId=1255847919539208197, issueId=1317114999827452826, articleNumber=null, orderNo=null, doi=10.13193/j.issn.1673-7717.2026.06.022, 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=null, acceptedDateStr=null, onlineDate=1791954307383, onlineDateStr=2026-10-14, pubDate=1781020800000, pubDateStr=2026-06-10, doiRegisterDate=null, doiRegisterDateStr=null, onlineIssueDate=1791954307383, onlineIssueDateStr=2026-10-14, onlineJustAcceptDate=null, onlineJustAcceptDateStr=null, onlineFirstDate=null, onlineFirstDateStr=null, sourceXml=null, magXml=null, createTime=1791954307383, creator=13701087609, updateTime=1791954307383, updator=13701087609, issue=Issue{id=1317114999827452826, tenantId=1146029695717560320, journalId=1255847919539208197, year='2026', volume='44', issue='6', pageStart='1', pageEnd='258', issueExtLink='null', onlineDate='null', pubDate='1781020800000', pubDateStr='2026-06-10', beforeIssueId=null, nextIssueId=null, price=null, status=1, issueComplete=1, articleOrder=1, issueType=-1, specialIssue=null, createTime=1791954286772, creator='13701087609', updateTime=1791958677365, updator='13701087609', preIssue=null, nextIssue=null, articleTotal=null, ext={EN=IssueExt(id=1317133415753831385, tenantId=1146029695717560320, journalId=1255847919539208197, issueId=1317114999827452826, language=EN, specialIssueTitle=, coverIllustrator=null, specialIssueEditor=, specialIssueAbout=), CN=IssueExt(id=1317133415753831386, tenantId=1146029695717560320, journalId=1255847919539208197, issueId=1317114999827452826, language=CN, specialIssueTitle=, coverIllustrator=null, specialIssueEditor=, specialIssueAbout=)}, issueFiles=null, downloadFileDto=null}, startPage=126, endPage=130, ext={EN=ArticleExt(id=1317115087920419488, articleId=1317115086280446623, tenantId=1146029695717560320, journalId=1255847919539208197, language=EN, title=Proteomics Study on Protection of Dopamine Cell in Mice with Parkinson’s Disease, columnId=1256183361521967297, journalTitle=Chinese Archives of Traditional Chinese Medicine, columnName=Target on National Project, runingTitle=null, highlight=null, articleAbstract=
Objective To explore the mechanism of verbascoside (VB) on dopamine cell protection in the mice with Parkinson's disease (PD).
Methods A total of 63 C57/BL male mice were enrolled as the experimental subjects and randomly divided into blank control group, 1-methyl-4-phenyl-1, 2, 3, 6-tetrahydropyridine (MPTP) group, 10 mg/kg group, 30 mg/kg group, 60 mg/kg group, 120 mg/kg group and 180 mg/kg group, with 9 mice in each group. After successful modeling, the behavioral changes of the mice were evaluated by mining, climbing pole and hanging experiments. Hematoxylin-eosin (HE) and Nissl staining were used to evaluate the neuron counts in the substantia nigra of the mice. Immunohistochemistry method and immunofluorescence staining were used to evaluate the tyrosine hydroxylase (TH) -positive and positive cell counts in the substantia nigra, respectively. Western blotting was used to detect the expression of TH protein in the substantia nigra of the mice. HE staining was used to evaluate liver and kidney cell morphology and cell count. Finally, the optimal dose group screened for proteomic analysis was performed.
Results (1) In the mine experiment, the total distance and the distance of the 120 mg/kg group were higher than those of the MPTP group and other concentration gradient groups (all P<0.05). In the pole climbing experiment, the pole climbing time of the 120 mg/kg group was both higher than that of the MPTP group and other concentration gradient groups (all P<0.05). In the pole climbing experiment, the pole climbing time of the 120 mg/kg group was both higher than that of the pole climbing experiment. The suspension scores of the MPTP group and the other concentration gradient groups (all P<0.05). In the suspension experiment, the suspension scores of the 120 mg/kg group were higher than those of the MPTP group and the 10 mg/kg group (all P<0.05). (2) In HE staining, Niss-type staining and immunohistochemistry method, the cell count and tan pixel proportion of the 120 mg/kg group were higher than those of the MPTP group and other concentration gradient groups (all P<0.05). (3) In immunofluorescence, the average fluorescence intensity of the 120 mg/kg group was higher than that of the MPTP group and other concentration gradient groups (all P<0.05). (5) In Western blotting, the relative expression of TH in the 120 mg/kg group was higher than that in the MPTP group and other concentration gradient groups (all P<0.05). (6) Proteomic analysis showed that compared with the 120 mg/kg group and the MPTP group, there were 181 proteins with statistical differences, including 83 up-regulated proteins and 98 down-regulated proteins. There were up to 85 differential proteins localized to the nucleus of subcellular nucleus, and gene ontology (GO) functional analysis showed that there were up to 6 biological processes directly related to immunity (BP). KEGG pathway analysis showed the highest level of enrichment with arginine biosynthesis (all P<0.05).
Conclusion VB with the dose of 120 mg/kg has a protective effect on DA neurons in PD mice, and this protective effect may be related to a variety of biological processes including arginine biosynthesis.
, authors=Huan XIA
1, Shan YANG
1, Xiaoxiao ZHU
2, Zihao WANG
1, Peishan LI
1, Qian CAI
3, Xinling YANG
4, authorsList=Huan XIA, Shan YANG, Xiaoxiao ZHU, Zihao WANG, Peishan LI, Qian CAI, Xinling YANG, authorCompany=null, correspAuthors=Xinling YANG, 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=1317115088201437857, articleId=1317115086280446623, tenantId=1146029695717560320, journalId=1255847919539208197, language=CN, title=毛蕊花糖苷对帕金森病小鼠多巴胺细胞保护作用的蛋白组学研究, columnId=1256183362172142382, journalTitle=中华中医药学刊, columnName=国家项目点击, runingTitle=null, highlight=null, articleAbstract=
目的 探索毛蕊花糖苷(Verbascoside,VB)对帕金森病(Parkinson's disease,PD)小鼠多巴胺细胞保护作用的机制。
方法 纳入63只C57/BL雄性小鼠为实验对象,随机分为空白对照组、MPTP组、10 mg/kg组、30 mg/kg组、60 mg/kg组、120 mg/kg组、180 mg/kg组,每组9只。造模成功后采用矿场、爬杆、悬挂实验评估小鼠行为学改变。采用苏木精-伊红(Hematoxylin-Eosin,HE)、尼氏染色评估小鼠黑质区神经元计数。采用免疫组化和免疫荧光染色分别评估黑质区TH阳性、阳性细胞计数。采用Western blotting检测小鼠黑质区酪氨酸羟化酶(Tyrosine hydroxylase,TH)蛋白的表达情况。采用HE染色评估肝脏和肾脏细胞形态和细胞计数。最后筛选的最佳剂量组黑质组织进行蛋白组学分析。
结果 (1)矿场实验中,120 mg/kg组总路程和中央区的路程均高于MPTP组和其他各浓度梯度组(均P<0.05);爬杆实验中,120 mg/kg组爬杆时间均低于MPTP组和其他各浓度梯度组(均P<0.05);悬挂实验中,120 mg/kg组悬挂评分均高于MPTP组和10 mg/kg组(均P<0.05)。(2)HE染色、尼氏染色和免疫组化中,120 mg/kg组细胞计数、棕褐色像素占比均高于MPTP组和其他各浓度梯度组(均P<0.05)。(3)免疫荧光中,120 mg/kg组平均荧光强度均高于MPTP组和其他各浓度梯度组(均P<0.05)。(5)Western blotting中,TH在120 mg/kg组小鼠中的相对表达量均高于MPTP组和其他各浓度梯度组(均P<0.05)。(6)蛋白组学分析显示120 mg/kg组和MPTP组比较,具有统计学差异的蛋白质合计181个,其中上调蛋白83个,下调蛋白98个;亚细胞定位于细胞核的差异蛋白最多有85个,且基因本体(Gene Ontology,GO)功能分析显示最多有6个与免疫直接相关的生物过程(Biological Process,BP);KEGG通路分析显示与精氨酸生物合成的富集度水平最高(均P<0.05)。
结论 120 mg/kg的VB对PD小鼠的DA神经元具有保护作用,且该保护作用可能与包括精氨酸生物合成在内的多种生物过程有关。
, authors=夏欢
1, 杨珊
1, 朱筱潇
2, 王子豪
1, 李沛珊
1, 蔡倩
3, 杨新玲
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夏欢(1987-),男,湖北咸宁人,主治医师,博士在读,研究方向:帕金森病的诊断与治疗。
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