Article(id=1319291177577329180, tenantId=1146029695717560320, journalId=1255847919539208197, issueId=1319291166823142311, articleNumber=null, orderNo=null, doi=10.13193/j.issn.1673-7717.2026.09.006, 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=1792473127978, onlineDateStr=2026-10-20, pubDate=1788969600000, pubDateStr=2026-09-10, doiRegisterDate=null, doiRegisterDateStr=null, onlineIssueDate=1792473127978, onlineIssueDateStr=2026-10-20, onlineJustAcceptDate=null, onlineJustAcceptDateStr=null, onlineFirstDate=null, onlineFirstDateStr=null, sourceXml=null, magXml=null, createTime=1792473127978, creator=13701087609, updateTime=1792473127978, updator=13701087609, issue=Issue{id=1319291166823142311, tenantId=1146029695717560320, journalId=1255847919539208197, year='2026', volume='44', issue='9', pageStart='1', pageEnd='258', issueExtLink='null', onlineDate='null', pubDate='1788969600000', pubDateStr='2026-09-10', beforeIssueId=null, nextIssueId=null, price=null, status=1, issueComplete=1, articleOrder=1, issueType=1, specialIssue=null, createTime=1792473125414, creator='13701087609', updateTime=1792473357559, updator='13701087609', preIssue=null, nextIssue=null, articleTotal=null, ext={EN=IssueExt(id=1319292140618896016, tenantId=1146029695717560320, journalId=1255847919539208197, issueId=1319291166823142311, language=EN, specialIssueTitle=, coverIllustrator=null, specialIssueEditor=, specialIssueAbout=), CN=IssueExt(id=1319292140618896017, tenantId=1146029695717560320, journalId=1255847919539208197, issueId=1319291166823142311, language=CN, specialIssueTitle=, coverIllustrator=null, specialIssueEditor=, specialIssueAbout=)}, issueFiles=null, downloadFileDto=null}, startPage=32, endPage=36, ext={EN=ArticleExt(id=1319291177791238685, articleId=1319291177577329180, tenantId=1146029695717560320, journalId=1255847919539208197, language=EN, title=Effects of Different Concentrations of Yinyanghuo (Epimedii Folium) Extract on Osteogenic Differentiation of Rats Adipose-Derived Stem Cells, columnId=1256183361521967297, journalTitle=Chinese Archives of Traditional Chinese Medicine, columnName=Target on National Project, runingTitle=null, highlight=null, articleAbstract=
Objective

To investigate the effects of different concentrations of Yinyanghuo (Epimedii Folium) extract on osteogenic differentiation of the rats adipose-derived stem cells (ADSCs).

Methods

Five healthy, nulliparous SPF-grade female SD rats were used to isolate and culture the ADSCs. The obtained third-generation ADSCs were stained with Alizarin Red and Oil Red O to evaluate their osteogenic and adipogenic differentiation abilities after being cultured with 1, 10, 50, 100 μmol/L Yinyanghuo (Epimedii Folium) extract. Then, the third-generation ADSCs were divided into a blank group, a resveratrol group (100 μmol/L) and Yinyanghuo (Epimedii Folium) extract groups. According to the different concentrations of Yinyanghuo (Epimedii Folium) extract, four subgroups were created, namely Ⅰ~Ⅳ groups (1, 10, 50, 100 μmol/L). After 7 days of culture, qRT-PCR and Western blotting were performed to detect the expression levels of LIM domain-containing protein Ajuba (Ajuba), Runx-related transcription factor 2 (Runx2), alkaline phosphatase (ALP) in the ADSCs.

Results

The resveratrol group and Yinyanghuo (Epimedii Folium) extract I to IV groups all upregulated the expression levels of Runx2 gene and protein, as well as ALP gene, with the best effect observed in the 100 μmol/L Yinyanghuo (Epimedii Folium) extract group (P<0.01). As for the expression levels of ALP protein, the resveratrol group exhibited a stronger promoting effect than the Yinyanghuo (Epimedii Folium) extract I to IV groups (P<0.01). The resveratrol group and Yinyanghuo (Epimedii Folium) extract groups I to IV all downregulated the expression levels of Ajuba gene and protein (P<0.01, P<0.05), with the resveratrol group showing a stronger gene inhibitory effect at the same concentration.

Conclusion

Both Yinyanghuo (Epimedii Folium) extract and resveratrol can promote the osteogenic differentiation of adipose-derived stem cells, but the promoting effect of Yinyanghuo (Epimedii Folium) extract is more significant and effective. Both can also inhibit adipogenic differentiation, with Yinyanghuo (Epimedii Folium) extract exhibiting weaker inhibition than resveratrol in the short term. With the extension of intervention time, further research is needed to investigate the trend in the future.

, authors=Lei SHU, Bing LIAO, Haiquan LIU, authorsList=Lei SHU, Bing LIAO, Haiquan LIU, authorCompany=null, correspAuthors=Haiquan LIU, 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=1319291178214863390, articleId=1319291177577329180, tenantId=1146029695717560320, journalId=1255847919539208197, language=CN, title=探明不同浓度淫羊藿对大鼠脂肪干细胞成骨分化的影响, columnId=1256183362172142382, journalTitle=中华中医药学刊, columnName=国家项目点击, runingTitle=null, highlight=null, articleAbstract=
目的

探明淫羊藿醇提物对大鼠脂肪干细胞(adipose-derived stem cells,ADSCs)成骨分化的影响。

方法

取5只健康未生育SPF级SD雌性大鼠进行分离、培养脂肪干细胞,获得第3代ADSCs用茜素红和油红O染色,用1、10、50和100 μmol/L淫羊藿醇提物培养,评价其成骨和成脂分化能力。将第3代ADSCs分为空白组、白藜芦醇组(100 μmol/L)、淫羊藿醇提物Ⅰ~Ⅳ组(1、10、50、100 μmol/L),培养7 d后对脂肪干细胞LIM结构域蛋白Ajuba(LIM domain-containing protein ajuba,Ajuba)、Runt相关转录因子2(Runx-related transcription factor 2,Runx2)、碱性磷酸酶(Alkaline phosphatase,ALP)表达水平进行qRT-PCR、Western-blotting检测。

结果

白藜芦醇组和不同浓度(1、10、50、100 μmol/L)淫羊藿醇提物组均能促进Runx2基因和蛋白、ALP的基因表达水平(P<0.01);且与白藜芦醇组比较,100 μmol/L淫羊藿醇提物组显示出更强的促进作用(P<0.01)。在ALP蛋白的表达水平方面,白藜芦醇组的促进作用优于淫羊藿I~IV组(P<0.01)。白藜芦醇组和不同浓度(1、10、50、100 μmol/L)淫羊藿醇提物组均会抑制Ajuba基因表达(P<0.01,P<0.05),其中白藜芦醇组在相同浓度下表现出较强的基因抑制作用。

结论

淫羊藿醇提物与白藜芦醇均能促进脂肪干细胞成骨分化,但淫羊藿醇提物的促进作用更明显,效果更显著,两者均能抑制成脂分化,而在短期内白藜芦醇抑制成脂分化更优。随着干预的时间延长,随后的趋势有待进一步研究。

, authors=舒雷, 廖冰, 刘海全, authorsList=舒雷, 廖冰, 刘海全, authorCompany=null, correspAuthors=刘海全, authorNote=

舒雷(1998-),男,湖北荆州人,硕士在读,研究方向:中医药防治骨质疏松症。

, correspAuthorsNote=
刘海全(1977-),男,河北滦县人,主任中医师,博士研究生导师,博士,研究方向:中医药防治骨质疏松。E-mail:。
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舒雷(1998-),男,湖北荆州人,硕士在读,研究方向:中医药防治骨质疏松症。

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舒雷(1998-),男,湖北荆州人,硕士在读,研究方向:中医药防治骨质疏松症。

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探明不同浓度淫羊藿对大鼠脂肪干细胞成骨分化的影响
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舒雷 , 廖冰 , 刘海全
中华中医药学刊 | 国家项目点击 2026,44(9): 32-36
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中华中医药学刊 |国家项目点击 2026 , 44 (9) : 32 -36
探明不同浓度淫羊藿对大鼠脂肪干细胞成骨分化的影响
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舒雷, 廖冰, 刘海全
作者信息
  • 广州中医药大学惠州医院(惠州市中医医院),广东 惠州 516001
通讯作者:
刘海全(1977-),男,河北滦县人,主任中医师,博士研究生导师,博士,研究方向:中医药防治骨质疏松。E-mail:。
作者简介:

舒雷(1998-),男,湖北荆州人,硕士在读,研究方向:中医药防治骨质疏松症。

Effects of Different Concentrations of Yinyanghuo (Epimedii Folium) Extract on Osteogenic Differentiation of Rats Adipose-Derived Stem Cells
Lei SHU, Bing LIAO, Haiquan LIU
Affiliations
  • Huizhou Hospital of Guangzhou University of Chinese Medicine (Huizhou Hospital ofTraditional Chinese Medicine), Huizhou 516001, Guangdong, China
出版时间: 2026-09-10 doi: 10.13193/j.issn.1673-7717.2026.09.006
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目的

探明淫羊藿醇提物对大鼠脂肪干细胞(adipose-derived stem cells,ADSCs)成骨分化的影响。

方法

取5只健康未生育SPF级SD雌性大鼠进行分离、培养脂肪干细胞,获得第3代ADSCs用茜素红和油红O染色,用1、10、50和100 μmol/L淫羊藿醇提物培养,评价其成骨和成脂分化能力。将第3代ADSCs分为空白组、白藜芦醇组(100 μmol/L)、淫羊藿醇提物Ⅰ~Ⅳ组(1、10、50、100 μmol/L),培养7 d后对脂肪干细胞LIM结构域蛋白Ajuba(LIM domain-containing protein ajuba,Ajuba)、Runt相关转录因子2(Runx-related transcription factor 2,Runx2)、碱性磷酸酶(Alkaline phosphatase,ALP)表达水平进行qRT-PCR、Western-blotting检测。

结果

白藜芦醇组和不同浓度(1、10、50、100 μmol/L)淫羊藿醇提物组均能促进Runx2基因和蛋白、ALP的基因表达水平(P<0.01);且与白藜芦醇组比较,100 μmol/L淫羊藿醇提物组显示出更强的促进作用(P<0.01)。在ALP蛋白的表达水平方面,白藜芦醇组的促进作用优于淫羊藿I~IV组(P<0.01)。白藜芦醇组和不同浓度(1、10、50、100 μmol/L)淫羊藿醇提物组均会抑制Ajuba基因表达(P<0.01,P<0.05),其中白藜芦醇组在相同浓度下表现出较强的基因抑制作用。

结论

淫羊藿醇提物与白藜芦醇均能促进脂肪干细胞成骨分化,但淫羊藿醇提物的促进作用更明显,效果更显著,两者均能抑制成脂分化,而在短期内白藜芦醇抑制成脂分化更优。随着干预的时间延长,随后的趋势有待进一步研究。

淫羊藿醇提物  /  脂肪干细胞  /  白藜芦醇  /  成骨分化  /  成脂分化
Objective

To investigate the effects of different concentrations of Yinyanghuo (Epimedii Folium) extract on osteogenic differentiation of the rats adipose-derived stem cells (ADSCs).

Methods

Five healthy, nulliparous SPF-grade female SD rats were used to isolate and culture the ADSCs. The obtained third-generation ADSCs were stained with Alizarin Red and Oil Red O to evaluate their osteogenic and adipogenic differentiation abilities after being cultured with 1, 10, 50, 100 μmol/L Yinyanghuo (Epimedii Folium) extract. Then, the third-generation ADSCs were divided into a blank group, a resveratrol group (100 μmol/L) and Yinyanghuo (Epimedii Folium) extract groups. According to the different concentrations of Yinyanghuo (Epimedii Folium) extract, four subgroups were created, namely Ⅰ~Ⅳ groups (1, 10, 50, 100 μmol/L). After 7 days of culture, qRT-PCR and Western blotting were performed to detect the expression levels of LIM domain-containing protein Ajuba (Ajuba), Runx-related transcription factor 2 (Runx2), alkaline phosphatase (ALP) in the ADSCs.

Results

The resveratrol group and Yinyanghuo (Epimedii Folium) extract I to IV groups all upregulated the expression levels of Runx2 gene and protein, as well as ALP gene, with the best effect observed in the 100 μmol/L Yinyanghuo (Epimedii Folium) extract group (P<0.01). As for the expression levels of ALP protein, the resveratrol group exhibited a stronger promoting effect than the Yinyanghuo (Epimedii Folium) extract I to IV groups (P<0.01). The resveratrol group and Yinyanghuo (Epimedii Folium) extract groups I to IV all downregulated the expression levels of Ajuba gene and protein (P<0.01, P<0.05), with the resveratrol group showing a stronger gene inhibitory effect at the same concentration.

Conclusion

Both Yinyanghuo (Epimedii Folium) extract and resveratrol can promote the osteogenic differentiation of adipose-derived stem cells, but the promoting effect of Yinyanghuo (Epimedii Folium) extract is more significant and effective. Both can also inhibit adipogenic differentiation, with Yinyanghuo (Epimedii Folium) extract exhibiting weaker inhibition than resveratrol in the short term. With the extension of intervention time, further research is needed to investigate the trend in the future.

Yinyanghuo (Epimedii Folium) extract  /  adipose-derived stem cells  /  resveratrol  /  osteogenic differentiation  /  adipogenic differentiation
舒雷, 廖冰, 刘海全. 探明不同浓度淫羊藿对大鼠脂肪干细胞成骨分化的影响. 中华中医药学刊, 2026 , 44 (9) : 32 -36 . DOI: 10.13193/j.issn.1673-7717.2026.09.006
Lei SHU, Bing LIAO, Haiquan LIU. Effects of Different Concentrations of Yinyanghuo (Epimedii Folium) Extract on Osteogenic Differentiation of Rats Adipose-Derived Stem Cells[J]. Chinese Archives of Traditional Chinese Medicine, 2026 , 44 (9) : 32 -36 . DOI: 10.13193/j.issn.1673-7717.2026.09.006
  • 国家自然科学基金项目(82174147)
  • 广东省基础与应用基础研究基金项目(2021A1515011271)
  • 广东省中医药局科研项目(20213019)
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2026年第44卷第9期
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doi: 10.13193/j.issn.1673-7717.2026.09.006
  • 首发时间:2026-10-20
  • 出版时间:2026-09-10
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基金
国家自然科学基金项目(82174147)
广东省基础与应用基础研究基金项目(2021A1515011271)
广东省中医药局科研项目(20213019)
作者信息
    广州中医药大学惠州医院(惠州市中医医院),广东 惠州 516001

通讯作者:

刘海全(1977-),男,河北滦县人,主任中医师,博士研究生导师,博士,研究方向:中医药防治骨质疏松。E-mail:。
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2种不同金属材料的力学参数
科
Family
属数
Number of
genus
种数
Number of
species
占总种数比例
Percentage of
total species (%)
属
Genus
种数
Number of
species
占总种数比例
Percentage of total
species (%)
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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