Article(id=1322245666785579775, tenantId=1146029695717560320, journalId=1235980733773295621, issueId=1322245649572156020, articleNumber=null, orderNo=null, doi=null, 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=1612108800000, acceptedDateStr=2021-02-01, onlineDate=1793177533097, onlineDateStr=2026-10-28, pubDate=1619712000000, pubDateStr=2021-04-30, doiRegisterDate=null, doiRegisterDateStr=null, onlineIssueDate=1793177533097, onlineIssueDateStr=2026-10-28, onlineJustAcceptDate=null, onlineJustAcceptDateStr=null, onlineFirstDate=null, onlineFirstDateStr=null, sourceXml=null, magXml=null, createTime=1793177533097, creator=13701087609, updateTime=1793177533097, updator=13701087609, issue=Issue{id=1322245649572156020, tenantId=1146029695717560320, journalId=1235980733773295621, year='2021', volume='30', issue='8', pageStart='673', pageEnd='768', issueExtLink='null', onlineDate='null', pubDate='1619712000000', pubDateStr='2021-04-30', beforeIssueId=null, nextIssueId=null, price=null, status=1, issueComplete=1, articleOrder=1, issueType=-1, specialIssue=null, createTime=1793177528994, creator='13701087609', updateTime=1793177643007, updator='13701087609', preIssue=null, nextIssue=null, articleTotal=null, ext={EN=IssueExt(id=1322246127831863562, tenantId=1146029695717560320, journalId=1235980733773295621, issueId=1322245649572156020, language=EN, specialIssueTitle=, coverIllustrator=null, specialIssueEditor=, specialIssueAbout=), CN=IssueExt(id=1322246127831863563, tenantId=1146029695717560320, journalId=1235980733773295621, issueId=1322245649572156020, language=CN, specialIssueTitle=, coverIllustrator=null, specialIssueEditor=, specialIssueAbout=)}, issueFiles=null, downloadFileDto=null}, startPage=740, endPage=746, ext={EN=ArticleExt(id=1322245666986906368, articleId=1322245666785579775, tenantId=1146029695717560320, journalId=1235980733773295621, language=EN, title=Study on the neurotoxic effects of harmine and its derivatives DH-004 in mice, columnId=null, journalTitle=Chinese Journal of New Drugs, columnName=null, runingTitle=null, highlight=null, articleAbstract=
Objective: To study the neurotoxicity of DH-004, a derivative of harmine (HM).
Methods: IL-1β, TNF-α, IL-12 and IL-6 in the brain of mice were determined by enzyme-linked immunosorbent assay (ELISA). Morphological changes of neurons in cerebral cortex of mice were detected by Nissl staining. Real-time fluorescence quantitative reverse transcription polymerase chain reaction (qRT-PCR) was used to detect ionized calcium binding adaptor molecule-1 (Iba-1) mRNA expression in brain tissue. Iba-1 protein expression in brain tissue was detected by Western-Blot.
Results: ELISA results showed that except for the insignificant changes of IL-6 in each dose group, the expression levels of the other three inflammatory factors with HM-treated mice in the brain tissues were the highest. After the same dose of DH-004 was given, the expression levels of inflammatory factors in the cerebellum tissues were significantly decreased compared with HM-treated mice (P<0.01). The results of Nisier staining, qRT-PCR and Western-Blot showed that compared with the blank control group, HM group had serious and dose-dependent damage to the cortical nerve cells of mice. The expression levels of Iba-1 mRNA and Iba-1 protein in HM group were up-regulated compared with the corresponding blank control group (P<0.01), after the same dose of DH-004 was given, the expression levels of Iba-1 mRNA and Iba-1 protein in cerebellum tissues were significantly down-regulated compared with HM group (P<0.01).
Conclusion: HM can induce the activation of microglia cells in mice, then the activated microglia cells promote the release of inflammatory factors, leading to nerve tissue damage. While DH-004 can inhibit the activation of microglia cells, thus reducing the release of inflammatory factors and reducing neurotoxicity.
, authors=Ruzenisa·abudula
1, 2, Hui-jing GAO
2, Yue-hong GONG
2, Li-mei WEN
2, Yi GAO
1, 2, Jian-hua WANG
2, Bei CHEN
2, authorsList=Ruzenisa·abudula, Hui-jing GAO, Yue-hong GONG, Li-mei WEN, Yi GAO, Jian-hua WANG, Bei CHEN, authorCompany=null, correspAuthors=Jian-hua WANG, Bei CHEN, 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=1322245667259536129, articleId=1322245666785579775, tenantId=1146029695717560320, journalId=1235980733773295621, language=CN, title=去氢骆驼蓬碱及其衍生物DH-004暴露对小鼠神经系统毒性作用研究, columnId=1236330556003242277, journalTitle=中国新药杂志, columnName=实验研究, runingTitle=null, highlight=null, articleAbstract=
目的: 研究去氢骆驼蓬碱(harmine,HM)及其衍生物1-(4-甲氧基)苯基-9-丁基-β-咔啉(DH-004)对脑神经毒性的作用。
方法: 免疫吸附测定法(ELISA)测定小鼠脑组织中IL-1β,TNF-α,IL-12和IL-6含量;尼氏染色法检测小鼠大脑皮质神经细胞形态改变;实时荧光定量逆转录聚合酶链反应法(qRT-PCR)检测脑组织中离子钙接头蛋白(ionized calcium binding adaptor molecule-1,Iba-1)基因的表达水平;蛋白免疫印迹法(Western-Blot)检测脑组织中Iba-1蛋白的表达水平。
结果: ELISA实验结果显示,除了IL-6因子在各剂量组的含量变化不明显,其余3个因子HM处理组小鼠脑组织中的表达量最高,给予相同剂量的DH-004后,与HM处理组相比,小脑组织中炎症因子表达出现显著下降(P<0.01)。尼氏染色、qRT-PCR、Western-Blot实验结果显示,与空白组相比,HM给药组对小鼠皮质神经细胞损伤严重,且有剂量依赖性;HM组Iba-1mRNA和Iba-1蛋白表达水平较相应的空白组明显上调(P<0.01),给予相同剂量的DH-004后,与HM处理组相比,小脑组织中Iba-1mRNA和Iba-1蛋白表达水平显著下调(P<0.01)。
结论: HM可能诱导小鼠小胶质细胞的活化,激活的小胶质细胞促使炎症因子释放增加,导致神经组织损伤;而DH-004可能抑制小胶质细胞活化,从而减少炎症因子释放,减轻神经毒性。
, authors=茹则妮萨·阿卜杜拉
1, 2, 高惠静
2, 巩月红
2, 文丽梅
2, 高旖
1, 2, 王建华
2, 陈蓓
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1College of Pharmaceutical Sciences, Xinjiang Medical University, Urumqi 830000, China
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1新疆医科大学药学院,乌鲁木齐 830000
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茹则妮萨·阿卜杜拉,女,在读硕士研究生,研究方向:抗包虫药物新制剂。E-mail:2441527648@qq.com。
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茹则妮萨·阿卜杜拉,女,在读硕士研究生,研究方向:抗包虫药物新制剂。E-mail:2441527648@qq.com。
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1College of Pharmaceutical Sciences, Xinjiang Medical University, Urumqi 830000, China
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1新疆医科大学药学院,乌鲁木齐 830000
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