Article(id=1291404318326907901, tenantId=1146029695717560320, journalId=1246415772164075586, issueId=1291404284806030089, articleNumber=null, orderNo=null, doi=10.13699/j.cnki.1001-6821.2025.04.014, pmid=null, cstr=null, oa=null, hot=null, price=null, onlineType=0, articleFormat=0, articleType=null, articleTypeStr=null, receivedDate=1722182400000, receivedDateStr=2024-07-29, revisedDate=null, revisedDateStr=null, acceptedDate=null, acceptedDateStr=null, onlineDate=1785824382621, onlineDateStr=2026-08-04, pubDate=1740672000000, pubDateStr=2025-02-28, doiRegisterDate=null, doiRegisterDateStr=null, onlineIssueDate=1785824382621, onlineIssueDateStr=2026-08-04, onlineJustAcceptDate=null, onlineJustAcceptDateStr=null, onlineFirstDate=null, onlineFirstDateStr=null, sourceXml=null, magXml=null, createTime=1785824382620, creator=13701087609, updateTime=1785824382620, updator=13701087609, issue=Issue{id=1291404284806030089, tenantId=1146029695717560320, journalId=1246415772164075586, year='2025', volume='41', issue='4', pageStart='451', pageEnd='600', issueExtLink='null', onlineDate='null', pubDate='1740672000000', pubDateStr='2025-02-28', beforeIssueId=null, nextIssueId=null, price=null, status=1, issueComplete=1, articleOrder=1, issueType=-1, specialIssue=null, createTime=1785824374629, creator='13701087609', updateTime=1785824374629, updator='13701087609', preIssue=null, nextIssue=null, articleTotal=null, ext=null, issueFiles=null, downloadFileDto=null}, startPage=517, endPage=521, ext={EN=ArticleExt(id=1291404318796669950, articleId=1291404318326907901, tenantId=1146029695717560320, journalId=1246415772164075586, language=EN, title=Mechanism of Danzhi Jiangtang capsule in improving kidney tissue injury in db/db mice, columnId=1246531407326105792, journalTitle=Chinese Journal of Clinical Pharmacology, columnName=Clinical and Basic Bridging Research, runingTitle=null, highlight=null, articleAbstract=
Objective To investigate the protective effect of Danzhi Jiangtang capsule on kidney of db/db mice with diabetic kidney disease (DKD) and its effects on the autophagy-lysosomal pathway.
Methods The db/db mice were randomly divided into model group (0.2 mL·d-1 0.9% NaCl), positive control group (45 mg·kg-1·d-1 irbesartan) and experimental-H, -M, -L groups (1 800, 900 and 450 mg·kg-1·d-1 Danzhi Jiangtang capsule), and another db/m mice were taken as blank group (0.2 mL·d-1 0.9% NaCl), which were continuously infused for 8 weeks. The expression levels of sequestosome1 (P62), microtubule-associated protein light chain 3 (LC3), transcription factor EB (TFEB), lysosomal associated membrane protein 1 (LAMP-1) and cathepsin D (CTSD) were detected in renal tissues by Western blot.
Results The relative expression levels of P62 protein in blank group, model group, positive control group and experimental-H,-M,-L groups were 1.00±0.04, 7.66±0.27, 3.52±0.11, 2.21±0.09, 2.86±0.10 and 4.05±0.16; the LC3Ⅱ/Ⅰ levels were 1.00±0.02, 0.17±0.01, 0.71±0.08, 0.86±0.05, 0.80±0.04 and 0.73±0.06; the TFEB protein levels were 1.00±0.01, 0.17±0.01, 0.30±0.01, 0.63±0.01, 0.45±0.01 and 0.42±0.01; the LAMP-1 protein levels were 1.00±0.01, 0.28±0.02, 0.42±0.01, 0.77±0.00, 0.55±0.03 and 0.40±0.02; the CTSD protein levels were 1.00±0.04, 0.27±0.03, 0.47±0.04, 0.73±0.02, 0.63±0.01 and 0.52±0.02. The differences between the above indexes in the experimental-H, -M, -L groups and the model group were statistically significant (all P<0.01).
Conclusion Danzhi Jiangtang capsule can improved renal damage in db/db mice, which may be related to the repair of autophagy-lysosome pathway, accelerate clearance of abnormal proteins and degradation of organelles.
, authors=Nou-bing RUAN
1a, Zhao-hui FANG
2, 3, Jin-ju LI
1a, Qi XU
1b, Yu-fan LI
1a, Ke-xin HU
1a, authorsList=Nou-bing RUAN, Zhao-hui FANG, Jin-ju LI, Qi XU, Yu-fan LI, Ke-xin HU, authorCompany=null, correspAuthors=Zhao-hui FANG, 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=1291404319320957951, articleId=1291404318326907901, tenantId=1146029695717560320, journalId=1246415772164075586, language=CN, title=丹蛭降糖胶囊改善db/db小鼠肾组织损伤的作用机制, columnId=1246531407485489349, journalTitle=中国临床药理学杂志, columnName=临床与基础桥接研究, runingTitle=null, highlight=null, articleAbstract=
目的 探讨丹蛭降糖胶囊对糖尿病肾病(DKD)db/db小鼠肾保护作用及对自噬-溶酶体途径的影响。
方法 将db/db小鼠随机分为模型组(0.2 mL·d-1 0.9% NaCl)、阳性对照组(45 mg·kg-1·d-1厄贝沙坦)和高、中、低剂量实验组(1 800、900、450 mg·kg-1·d-1丹蛭降糖胶囊),另以db/m小鼠作为空白组(0.2 mL·d-1 0.9% NaCl),连续灌胃给药8周。用蛋白质印迹法检测肾组织选择性自噬接头蛋白p62(P62)、微管相关蛋白轻链3(LC3)、转录因子EB(TFEB)、溶酶体关联膜蛋白1(LAMP-1)、组织蛋白酶Cathepsin D(CTSD)的相对表达水平。
结果 空白组、模型组、阳性对照组和高、中、低剂量实验组P62蛋白相对表达水平分别为1.00±0.04、7.66±0.27、3.52±0.11、2.21±0.09、2.86±0.10和4.05±0.16,LC3Ⅱ/Ⅰ分别为1.00±0.02、0.17±0.01、0.71±0.08、0.86±0.05、0.80±0.04和0.73±0.06,TFEB蛋白相对表达水平分别为1.00±0.01、0.17±0.01、0.30±0.01、0.63±0.01、0.45±0.01和0.42±0.01,LAMP-1蛋白相对表达水平分别为1.00±0.01、0.28±0.02、0.42±0.01、0.77±0.00、0.55±0.03和0.40±0.02,CTSD蛋白相对表达水平分别为1.00±0.04、0.27±0.03、0.47±0.04、0.73±0.02、0.63±0.01和0.52±0.02。高、中、低剂量实验组的上述指标与模型组比较,在统计学上差异有统计学意义(均P<0.01)。
结论 丹蛭降糖胶囊可改善db/db小鼠肾损害,可能与修复自噬-溶酶体途径,激活自噬,加速清除异常蛋白质和降解细胞器有关。
, authors=阮诺冰
1a, 方朝晖
2, 3, 李金菊
1a, 许奇
1b, 李瑜璠
1a, 胡可心
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阮诺冰(1996-),女,博士研究生,主要研究方向为中医药防治内分泌疾病方面的研究
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2.Department of Endocrinology, The First Affiliated Hospital of Anhui University of Chinese Medicine, Hefei 230031, Anhui Province, China
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1b.Graduate School, Anhui University of Chinese Medicine, Hefei 230031, Anhui Province, China, bio=null, bioImg=null, bioContent=null, aboutCorrespAuthor=null), CN=AuthorExt(id=1291404323100024863, tenantId=1146029695717560320, journalId=1246415772164075586, articleId=1291404318326907901, authorId=1291404322919669788, language=CN, stringName=许奇, firstName=null, middleName=null, lastName=null, prefix=null, suffix=null, authorComment=null, nameInitials=null, affiliation=null, department=null, xref=
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