Article(id=1222466820943106171, tenantId=1146029695717560320, journalId=1189982191388893191, issueId=1222466818573324401, articleNumber=null, orderNo=null, doi=10.16438/j.0513-4870.2019-0198, pmid=null, cstr=null, oa=null, hot=null, price=null, onlineType=0, articleFormat=0, articleType=null, articleTypeStr=research-article, receivedDate=1553184000000, receivedDateStr=2019-03-22, revisedDate=1555516800000, revisedDateStr=2019-04-18, acceptedDate=null, acceptedDateStr=null, onlineDate=1769388402448, onlineDateStr=2026-01-26, pubDate=1560268800000, pubDateStr=2019-06-12, doiRegisterDate=null, doiRegisterDateStr=null, onlineIssueDate=1769388402448, onlineIssueDateStr=2026-01-26, onlineJustAcceptDate=null, onlineJustAcceptDateStr=null, onlineFirstDate=null, onlineFirstDateStr=null, sourceXml=null, magXml=null, createTime=1769388402448, creator=13701087609, updateTime=1769388402448, updator=13701087609, issue=Issue{id=1222466818573324401, tenantId=1146029695717560320, journalId=1189982191388893191, year='2019', volume='54', issue='6', pageStart='963', pageEnd='1144', issueExtLink='null', onlineDate='null', pubDate='null', beforeIssueId=null, nextIssueId=null, price=null, status=1, issueComplete=1, articleOrder=1, issueType=-1, specialIssue=null, createTime=1769388401883, creator=13701087609, updateTime=1769389420159, updator=13701087609, preIssue=null, nextIssue=null, ext={EN=IssueExt(id=1222471089591149021, tenantId=1146029695717560320, journalId=1189982191388893191, issueId=1222466818573324401, language=EN, specialIssueTitle=, coverIllustrator=null, specialIssueEditor=, specialIssueAbout=), CN=IssueExt(id=1222471089591149022, tenantId=1146029695717560320, journalId=1189982191388893191, issueId=1222466818573324401, language=CN, specialIssueTitle=, coverIllustrator=null, specialIssueEditor=, specialIssueAbout=)}, issueFiles=null}, startPage=1036, endPage=1040, ext={EN=ArticleExt(id=1222466821802938500, articleId=1222466820943106171, tenantId=1146029695717560320, journalId=1189982191388893191, language=EN, title=Therapeutic effects of artificial musk on acute ischemic stroke and subarachnoid hemorrhage in rats, columnId=1190335348761793317, journalTitle=Acta Pharmaceutica Sinica, columnName=Original Articles, runingTitle=null, highlight=null, articleAbstract=
The rat models of focal cerebral ischemic reperfusion and subarachnoid hemorrhage were used to evaluate the therapeutic effects of artificial musk to provide support for its clinical application. All animal experiments were performed following the regulations of the Animal Ethics Committee of Peking Union Medical College. The results showed that oral administration of artificial musk had significant protective effects on acute ischemic and hemorrhagic stroke. In the dose range of 10-200 mg·kg-1, the mortality, neurobehavioral and cerebral infarction volume of rats in model group indicated a clear dose dependent relationship. The effective dose of artificial musk is 10 mg·kg-1 in ischemic stroke and 200 mg·kg-1 in hemorrhagic stroke. These findings suggest that the treatments of artificial musk in ischemic stroke and in hemorrhagic stroke are different, and such differences should be noted for its clinical use.
, correspAuthors=Xiao-liang WANG, authorNote=null, correspAuthorsNote=null, copyrightStatement=Copyright ©2019 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=Ling WANG, Jiang LI, Shao-feng XU, Nan FENG, Shu ZHANG, Xiao-liang WANG), CN=ArticleExt(id=1222466824374046937, articleId=1222466820943106171, tenantId=1146029695717560320, journalId=1189982191388893191, language=CN, title=人工麝香对大鼠急性脑缺血再灌损伤和脑出血的实验治疗, columnId=1190335348896011050, journalTitle=药学学报, columnName=研究论文, runingTitle=null, highlight=null, articleAbstract=
采用大鼠局灶性脑缺血再灌注和蛛网膜下腔出血的动物模型,评价人工麝香对缺血性脑卒中和出血性脑卒中的治疗作用,为人工麝香的临床应用提供研究基础。所有动物实验都遵循北京协和医学院动物伦理委员会的规定。结果显示,大脑中动脉阻断或蛛网膜下腔出血5 min后灌胃给予人工麝香对急性缺血性和出血性脑卒中均具有明显的保护作用。在10~200 mg·kg-1剂量范围内,对模型大鼠的死亡率、神经行为学和脑梗死体积具有一定的量效关系。其中在缺血性脑卒中,人工麝香的有效剂量为10 mg·kg-1;在出血性脑卒中,其有效剂量为200 mg·kg-1。上述研究结果提示人工麝香在治疗缺血性脑卒中和出血性脑卒中时存在一定差别,临床使用中要给予区别。
, correspAuthors=王晓良, authorNote=null, correspAuthorsNote=
, copyrightStatement=版权所有©《药学学报》编辑部2019, copyrightOwner=null, extLink=null, articleAbsUrl=null, sourceXml=NJk1zrhg2T2N0o3VdlrAyQ==, magXml=H4Rti/+frI7F2T/pgUCz8w==, pdfUrl=null, pdf=zm1hVKMqcgRUSRyPA/PQow==, pdfFileSize=444343, pdfExtLink=null, richHtmlUrl=null, mobilePdfUrl=null, reviewReport=null, pdfFirstPage=null, abstractGraph=4iz6fXuxeQsbFnvgJ+nbCQ==, abstractGraphContent=null, abstractVideo=null, citation=null, cebUrl=null, magXmlContent=tS46PVscnm2zatYLJ3aAbw==, mapNumber=null, authorCompany=null, fund=null, authors=null, authorsList=王玲, 李江, 徐少锋, 冯楠, 章菽, 王晓良)}, authors=[Author(id=1222466934977848044, tenantId=1146029695717560320, journalId=1189982191388893191, articleId=1222466820943106171, orderNo=0, firstName=null, middleName=null, lastName=null, nameCn=null, orcid=null, stid=null, country=null, authorPic=null, dead=0, email=null, emailSecond=null, emailThird=null, correspondingAuthor=0, authorType=1, ext={EN=AuthorExt(id=1222466935078511349, tenantId=1146029695717560320, journalId=1189982191388893191, articleId=1222466820943106171, authorId=1222466934977848044, language=EN, stringName=Ling WANG, firstName=Ling, middleName=null, lastName=WANG, prefix=null, suffix=null, authorComment=null, nameInitials=null, affiliation=null, department=null, xref=
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15: 85-90., articleTitle=Protective effect of An-Gong-Niu-Huang-Wan (containing natural or artificial moschus) on experimental cerebral ischemia in rats, refAbstract=null)], funds=[Fund(id=1222466940044566619, tenantId=1146029695717560320, journalId=1189982191388893191, articleId=1222466820943106171, awardId=2012ZX09301002-004, language=CN, fundingSource=国家“重大新药创制”科技重大专项资助项目(2012ZX09301002-004), fundOrder=null, country=null), Fund(id=1222466940141035618, tenantId=1146029695717560320, journalId=1189982191388893191, articleId=1222466820943106171, awardId=BZ0150, language=CN, fundingSource=新药作用机制研究与药效评价北京市重点实验室(BZ0150), fundOrder=null, country=null)], companyList=[AuthorCompany(id=1222466934784910037, tenantId=1146029695717560320, journalId=1189982191388893191, articleId=1222466820943106171, xref=null, ext=[AuthorCompanyExt(id=1222466934789104342, tenantId=1146029695717560320, journalId=1189982191388893191, articleId=1222466820943106171, companyId=1222466934784910037, language=EN, country=null, province=null, city=null, postcode=null, companyName=null, departmentName=null, remark=1. Institute of Materia Medica, Chinese Academy of Medical Sciences and Peking Union Medical College, State Key Laboratory of Natural Products and Functions, Beijing 100050, China), AuthorCompanyExt(id=1222466934805881561, tenantId=1146029695717560320, journalId=1189982191388893191, articleId=1222466820943106171, companyId=1222466934784910037, language=CN, country=null, province=null, city=null, postcode=null, companyName=null, departmentName=null, remark=1.中国医学科学院、北京协和医学院药物研究所, 天然药物活性物质与功能国家重点实验室, 北京 100050)]), AuthorCompany(id=1222466934868796127, tenantId=1146029695717560320, journalId=1189982191388893191, articleId=1222466820943106171, xref=null, ext=[AuthorCompanyExt(id=1222466934872990432, tenantId=1146029695717560320, journalId=1189982191388893191, articleId=1222466820943106171, companyId=1222466934868796127, language=EN, country=null, province=null, city=null, postcode=null, companyName=null, departmentName=null, remark=2. Beijing Lianxin Pharmaceutical Co., Ltd., Beijing 102628, China), AuthorCompanyExt(id=1222466934881379041, tenantId=1146029695717560320, journalId=1189982191388893191, articleId=1222466820943106171, companyId=1222466934868796127, language=CN, country=null, province=null, city=null, postcode=null, companyName=null, departmentName=null, remark=2.北京联馨药业有限公司, 北京 102628)])], figs=[ArticleFig(id=1222466938056467403, tenantId=1146029695717560320, journalId=1189982191388893191, articleId=1222466820943106171, language=EN, label=null, caption=null, figureFileSmall=Wm6f9kml3ELNKO2fTKKYCw==, figureFileBig=4iz6fXuxeQsbFnvgJ+nbCQ==, tableContent=null), ArticleFig(id=1222466938203268050, tenantId=1146029695717560320, journalId=1189982191388893191, articleId=1222466820943106171, language=CN, label=Figure 1, caption=
Improvement in neurological behavior and infarct volume of RGX in rats after 2-h intraluminal suture occlusion of MCA and 24-h reperfusion. A and C: RGX (2, 10, 50 and 200 mg·kg-1) were orally administered 10 min after the onset of MCAO. B and D: RGX (10 mg·kg-1) were orally administered and MK-801 (0.1 mg·kg-1) were intraperitoneally given 10 min after the onset of MCAO. n = 10-31, x± SEM. ##P < 0.01 vs Sham group; **P < 0.01 vs tMCAO group , figureFileSmall=Wm6f9kml3ELNKO2fTKKYCw==, figureFileBig=4iz6fXuxeQsbFnvgJ+nbCQ==, tableContent=null), ArticleFig(id=1222466938303931355, tenantId=1146029695717560320, journalId=1189982191388893191, articleId=1222466820943106171, language=EN, label=null, caption=null, figureFileSmall=hvIgv9A5u5o0VKE7XNoWKA==, figureFileBig=VAvwz5U8FcviWJcinEpRTQ==, tableContent=null), ArticleFig(id=1222466938387817444, tenantId=1146029695717560320, journalId=1189982191388893191, articleId=1222466820943106171, language=CN, label=Figure 2, caption=
Effect of RGX (p.o.) on infarct volume in rat brain after 2-h intraluminal suture occlusion of MCA and 24-h reperfusion. The 2, 3, 5-triphenyltetrazolium chloride (TTC) stained coronal brain sections are from representative animals of Sham group (A), tMCAO group (B), and RGX (2, 10, 50 and 200 mg·kg-1)-treated group (C, D, E, and F), respectively. Drugs were orally administered 10 min after the onset of MCAO. Infarcted tissue is white, whereas live tissue is darkly stained by TTC , figureFileSmall=hvIgv9A5u5o0VKE7XNoWKA==, figureFileBig=VAvwz5U8FcviWJcinEpRTQ==, tableContent=null), ArticleFig(id=1222466938467509226, tenantId=1146029695717560320, journalId=1189982191388893191, articleId=1222466820943106171, language=EN, label=null, caption=null, figureFileSmall=UcbFHBtYThEXS7SgB5IMTg==, figureFileBig=S8t2EDbi9+LIx62oGBLp/w==, tableContent=null), ArticleFig(id=1222466938576561142, tenantId=1146029695717560320, journalId=1189982191388893191, articleId=1222466820943106171, language=CN, label=Figure 3, caption=
Improvement in neurological behavior of RGX in rotarod test of rats after 12-h and 24-h of SAH. RGX (10, 50 and 200 mg·kg-1) were orally administered 10 min after SAH. n = 10-22, x ± SEM. ##P < 0.01 vs Sham group; **P < 0.01 vs SAH group , figureFileSmall=UcbFHBtYThEXS7SgB5IMTg==, figureFileBig=S8t2EDbi9+LIx62oGBLp/w==, tableContent=null), ArticleFig(id=1222466938803053566, tenantId=1146029695717560320, journalId=1189982191388893191, articleId=1222466820943106171, language=EN, label=null, caption=null, figureFileSmall=j5b+DS1b3kP+8ite1iD07g==, figureFileBig=Ji2Dh6NxVg+mgFXx86W07w==, tableContent=null), ArticleFig(id=1222466938903715848, tenantId=1146029695717560320, journalId=1189982191388893191, articleId=1222466820943106171, language=CN, label=Figure 4, caption=
Improvement in latent period (A) and fall down times (B) of rotarod test of rats by dosing RGX after 12-h and 24-h of SAH. RGX (10, 50 and 200 mg·kg-1) were orally administered 10 min after SAH. n = 10-22, x± SEM. ##P < 0.01 vs Sham group; **P < 0.01 vs SAH group , figureFileSmall=j5b+DS1b3kP+8ite1iD07g==, figureFileBig=Ji2Dh6NxVg+mgFXx86W07w==, tableContent=null), ArticleFig(id=1222466939029544977, tenantId=1146029695717560320, journalId=1189982191388893191, articleId=1222466820943106171, language=EN, label=null, caption=null, figureFileSmall=rRfNyKWekg9cgfwt1LSD+w==, figureFileBig=S9mg77M9fi8sVHEpdcAvRw==, tableContent=null), ArticleFig(id=1222466939155374105, tenantId=1146029695717560320, journalId=1189982191388893191, articleId=1222466820943106171, language=CN, label=Figure 5, caption=
The photograph showed an example of SAH group (A), RGX (200 mg·kg-1)-treated group (B) and Sham group (C), respectively , figureFileSmall=rRfNyKWekg9cgfwt1LSD+w==, figureFileBig=S9mg77M9fi8sVHEpdcAvRw==, tableContent=null), ArticleFig(id=1222466939281203237, tenantId=1146029695717560320, journalId=1189982191388893191, articleId=1222466820943106171, language=EN, label=null, caption=null, figureFileSmall=null, figureFileBig=null, tableContent=
| Group | Total animal number | Dead animal number | Mortality/% |
| Sham | 10 | 0 | 0 |
| tMCAO | 42 | 21 | 50## |
| RGX | 2 mg·kg-1 | 22 | 10 | 45.4 |
| 10 mg·kg-1 | 12 | 2 | 16.7* |
| 50 mg·kg-1 | 12 | 2 | 16.7* |
| 200 mg·kg-1 | 13 | 1 | 7.7** |
), ArticleFig(id=1222466939377672235, tenantId=1146029695717560320, journalId=1189982191388893191, articleId=1222466820943106171, language=CN, label=Table 1, caption=
The effects of artificial musk (RGX) on mortality in rats after cerebral ischemia-reperfusion (tMCAO) for 24 h. ##P < 0.01 vs Sham group; *P < 0.05, **P < 0.01 vs tMCAO
, figureFileSmall=null, figureFileBig=null, tableContent=
| Group | Total animal number | Dead animal number | Mortality/% |
| Sham | 10 | 0 | 0 |
| tMCAO | 42 | 21 | 50## |
| RGX | 2 mg·kg-1 | 22 | 10 | 45.4 |
| 10 mg·kg-1 | 12 | 2 | 16.7* |
| 50 mg·kg-1 | 12 | 2 | 16.7* |
| 200 mg·kg-1 | 13 | 1 | 7.7** |
), ArticleFig(id=1222466939541250098, tenantId=1146029695717560320, journalId=1189982191388893191, articleId=1222466820943106171, language=EN, label=null, caption=null, figureFileSmall=null, figureFileBig=null, tableContent=
| Group | Total animal number | Dead animal number | Mortality/% |
| Sham | 10 | 0 | 0 |
| tMCAO | 19 | 7 | 36.8## |
| RGX | 10 mg·kg-1 | 16 | 5 | 31.3 |
| MK801 | 0.1 mg·kg-1 | 14 | 3 | 21.4 |
), ArticleFig(id=1222466939700633664, tenantId=1146029695717560320, journalId=1189982191388893191, articleId=1222466820943106171, language=CN, label=Table 2, caption=
Effects of single administration of RGX and MK801 on mortality in rats after tMCAO for 24 h. ##P < 0.01 vs Sham group
, figureFileSmall=null, figureFileBig=null, tableContent=
| Group | Total animal number | Dead animal number | Mortality/% |
| Sham | 10 | 0 | 0 |
| tMCAO | 19 | 7 | 36.8## |
| RGX | 10 mg·kg-1 | 16 | 5 | 31.3 |
| MK801 | 0.1 mg·kg-1 | 14 | 3 | 21.4 |
), ArticleFig(id=1222466939809685575, tenantId=1146029695717560320, journalId=1189982191388893191, articleId=1222466820943106171, language=EN, label=null, caption=null, figureFileSmall=null, figureFileBig=null, tableContent=
| Group | Total animal number | Dead animal number | Mortality/% |
| Sham | 10 | 0 | 0 |
| SAH | 31 | 9 | 29.0## |
| RGX | 10 mg·kg-1 | 16 | 5 | 31.2 |
| 50 mg·kg-1 | 15 | 5 | 33.3 |
| 200 mg·kg-1 | 12 | 1 | 7.7* |
), ArticleFig(id=1222466939901960269, tenantId=1146029695717560320, journalId=1189982191388893191, articleId=1222466820943106171, language=CN, label=Table 3, caption=
The effects of RGX on mortality in rats after subarachnoid hemorrhage (SAH) for 24 h. ##P < 0.01 vs Sham group; *P < 0.05 vs SAH group
, figureFileSmall=null, figureFileBig=null, tableContent=
| Group | Total animal number | Dead animal number | Mortality/% |
| Sham | 10 | 0 | 0 |
| SAH | 31 | 9 | 29.0## |
| RGX | 10 mg·kg-1 | 16 | 5 | 31.2 |
| 50 mg·kg-1 | 15 | 5 | 33.3 |
| 200 mg·kg-1 | 12 | 1 | 7.7* |
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