Article(id=1322631321889911207, tenantId=1146029695717560320, journalId=1302319053441957962, issueId=1322631259684192984, articleNumber=null, orderNo=null, doi=10.7501j.issn.0253-2670.2026.19.015, pmid=null, cstr=null, oa=null, hot=0, price=null, onlineType=0, articleFormat=0, articleType=null, articleTypeStr=null, receivedDate=1772812800000, receivedDateStr=2026-03-07, revisedDate=null, revisedDateStr=null, acceptedDate=null, acceptedDateStr=null, onlineDate=1793269480439, onlineDateStr=2026-10-29, pubDate=null, pubDateStr=null, doiRegisterDate=null, doiRegisterDateStr=null, onlineIssueDate=1793269480439, onlineIssueDateStr=2026-10-29, onlineJustAcceptDate=null, onlineJustAcceptDateStr=null, onlineFirstDate=null, onlineFirstDateStr=null, sourceXml=null, magXml=null, createTime=1793269480439, creator=13701087609, updateTime=1793269480439, updator=13701087609, issue=Issue{id=1322631259684192984, tenantId=1146029695717560320, journalId=1302319053441957962, year='2026', volume='57', issue='19', pageStart='7501', pageEnd='7928', issueExtLink='null', onlineDate='null', pubDate='1791734400000', pubDateStr='2026-10-12', beforeIssueId=null, nextIssueId=null, price=null, status=1, issueComplete=1, articleOrder=1, issueType=1, specialIssue=null, createTime=1793269465608, creator='13701087609', updateTime=1793269554856, updator='13701087609', preIssue=null, nextIssue=null, articleTotal=null, ext={EN=IssueExt(id=1322631634101326494, tenantId=1146029695717560320, journalId=1302319053441957962, issueId=1322631259684192984, language=EN, specialIssueTitle=, coverIllustrator=null, specialIssueEditor=, specialIssueAbout=), CN=IssueExt(id=1322631634101326495, tenantId=1146029695717560320, journalId=1302319053441957962, issueId=1322631259684192984, language=CN, specialIssueTitle=, coverIllustrator=null, specialIssueEditor=, specialIssueAbout=)}, issueFiles=null, downloadFileDto=null}, startPage=7685, endPage=7696, ext={EN=ArticleExt(id=1322631323735404970, articleId=1322631321889911207, tenantId=1146029695717560320, journalId=1302319053441957962, language=EN, title=Yiqi Fumai Lyophilized Injection ameliorates heart failure induced by transverse aortic constriction via Piezo1/NO/cGMP pathway, columnId=null, journalTitle=Chinese Traditional and Herbal Drugs, columnName=null, runingTitle=null, highlight=null, articleAbstract=Objective To investigate whether Yiqi Fumai Lyophilized Injection [注射用益气复脉(冻干), YQFM] ameliorates myocardial hypertrophy and pressure overload-induced heart failure (HF) by upregulating the cardiac endothelial mechanosensitive ion channel Piezo1 and activating the nitric oxide (NO) signaling pathway. Methods A mouse HF model was prepared via transverse aortic constriction (TAC) surgery. Two weeks post-operation, mice received intraperitoneal injections of different doses of YQFM (0.13, 0.26, 0.53 g/kg) or captopril (20 mg/kg) for four weeks. Cardiac function was assessed by echocardiography. Pathological injury and fibrosis were evaluated by hematoxylin and eosin (HE) and Masson staining. Cardiac remodeling and cardiomyocyte hypertrophy were assessed by heart index, heart weight-to-tibia length ratio and wheat germ agglutinin (WGA) staining. Serum biochemical assays, qRT-PCR, Western blotting and immunofluorescence were employed to detect HF-related biomarkers and the expressions of key proteins in Piezo1/NO pathway. Results YQFM significantly improved TAC-induced cardiac dysfunction and remodeling (P < 0.05, 0.01), and alleviated histopathological disorganization, cardiomyocyte hypertrophy and myocardial fibrosis (P < 0.01). Mechanistic studies showed that YQFM reduced levels of cardiac injury markers cardiac troponin T (cTn-T) and N-terminal pro-B-type natriuretic peptide (NT-proBNP) in serum (P < 0.01), and significantly downregulated the expressions of hypertrophy-related genes natriuretic peptide A (Nppa), natriuretic peptide B (Nppb), myosin heavy chain 7 (Myh7) and fibrosis-related genes collagen type I alpha 1 chain (Col1a1), collagen type III alpha 1 chain (Col3a1) in cardiac tissue (P < 0.05, 0.01). YQFM significantly decreased the levels of follistatin-like 1 (Fstl1) and endothelin-1 (ET-1) (P < 0.05, 0.01), while elevating the levels of NO in serum and cardiac tissue and cyclic guanosine monophosphate (cGMP) in cardiac tissue (P < 0.01). Furthermore, YQFM significantly upregulated the expressions of Piezo1 protein and phosphorylated endothelial nitric oxide synthase (p-eNOS) in cardiac endothelial cells (P < 0.01). Conclusion YQFM improves cardiac function and remodeling, and inhibits cardiomyocyte hypertrophy in HF by upregulating endothelial Piezo1 expression and activating eNOS/NO signaling pathway., authors=DAI Sufang1, ZHAO Qingfei1, LIU Jincheng1, HUANG Zixuan1, XU Jinta1, LI Fang1, KOU Junping1, authorsList=DAI Sufang, ZHAO Qingfei, LIU Jincheng, HUANG Zixuan, XU Jinta, LI Fang, KOU Junping, authorCompany=1 Jiangsu Provincial Key Laboratory of Traditional Chinese Medicine Evaluation and Transformation, School of Traditional Chinese Pharmacy, China Pharmaceutical University, Nanjing 211198, China, correspAuthors=null, 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=1322631322128986536, articleId=1322631321889911207, tenantId=1146029695717560320, journalId=1302319053441957962, language=CN, title=注射用益气复脉(冻干)通过Piezo1/NO/cGMP通路改善主动脉弓缩窄诱导的心力衰竭, columnId=1304140191707456168, journalTitle=中草药, columnName=药理与临床, runingTitle=null, highlight=null, articleAbstract=目的 探讨注射用益气复脉(冻干)(Yiqi Fumai Lyophilized Injection,YQFM)通过上调心脏内皮机械敏感离子通道(piezo-type mechanosensitive ion channel component 1,Piezo1)激活一氧化氮(nitric oxide,NO)信号通路,从而抑制心肌肥大,改善压力超负荷所致心力衰竭(heart failure,HF)。方法 采用主动脉弓缩窄(transverse aortic constriction,TAC)手术制备小鼠HF模型,术后2周ip不同剂量YQFM(0.13、0.26、0.53 g/kg)和卡托普利(20 mg/kg)进行干预。药物干预4周后利用超声心动图评估心功能变化;采用苏木素-伊红(hematoxylin-eosin,HE)和Masson染色评价心脏病理损伤及纤维化程度;采用心脏指数、心脏质量与胫骨长度比值、小麦胚芽凝集素(wheat germ agglutinin,WGA)染色评价心脏重构和心肌细胞肥大程度;采用血清生化检测、qRT-PCR、Western blotting及免疫荧光染色等技术检测HF相关标志物及Piezo1/NO通路关键蛋白的表达变化。结果 YQFM显著改善TAC诱导的小鼠心功能障碍与心脏重构(P<0.05、0.01),并减轻组织结构紊乱、心肌细胞肥大和心肌纤维化(P<0.01)。机制研究表明YQFM降低血清心肌损伤标志物心肌肌钙蛋白T(cardiac troponin T,cTn-T)、N末端B型利钠肽前体(N-terminal pro-B-type natriuretic peptide,NT-proBNP)水平(P<0.01),显著下调心脏中肥大相关基因心房钠尿肽(natriuretic peptide A,Nppa)、B型利钠肽(natriuretic peptide B,Nppb)、肌球蛋白重链7(myosin heavy chain 7,Myh7)与纤维化相关基因I型胶原蛋白α1链(collagen type I alpha 1 chain,Col1a1)、Ⅲ型胶原蛋白α1链(collagen type III alpha 1 chain,Col3a1)的表达(P<0.05、0.01)。YQFM还可显著降低卵泡抑素样蛋白1(follistatin-like 1,Fstl1)和内皮素-1(endothelin-1,ET-1)含量(P<0.05、0.01),同时提升血清与心脏组织中NO及环磷酸鸟苷(cyclic guanosine monophosphate,cGMP)水平(P<0.01)。此外,YQFM显著上调心脏内皮细胞中Piezo1蛋白与磷酸化内皮型一氧化氮合酶(phosphorylated endothelial nitric oxide synthase,p-eNOS)的表达(P<0.01)。结论 YQFM通过上调内皮Piezo1表达并激活eNOS/NO通路,改善心脏功能与重构,抑制心肌细胞肥大,从而发挥抗HF作用。, authors=戴肃芳1, 赵庆飞1, 刘金成1, 黄子萱1, 许金塔1, 李芳1, 寇俊萍1, authorsList=戴肃芳, 赵庆飞, 刘金成, 黄子萱, 许金塔, 李芳, 寇俊萍, authorCompany=1 中国药科大学中药学院 江苏省中药评价与转化重点实验室, 江苏 南京 211198, correspAuthors=null, authorNote=戴肃芳: 戴肃芳(2002—),女,硕士研究生,从事中药心血管药理学研究。E-mail:17302232328@163.com, correspAuthorsNote=null, copyrightStatement=null, copyrightOwner=null, extLink=null, articleAbsUrl=null, sourceXml=null, magXml=null, pdfUrl=null, pdf=GEvYb0qJcsxDEZj7UFRU1w==, pdfFileSize=1645641, 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=国家自然科学基金面上项目 (82274140))}, authors=[Author(id=1324185325542711320, tenantId=1146029695717560320, journalId=null, articleId=1322631321889911207, orderNo=null, firstName=null, middleName=null, lastName=null, nameCn=null, orcid=null, stid=null, country=null, authorPic=null, dead=null, email=null, emailSecond=null, emailThird=null, correspondingAuthor=null, authorType=null, ext={EN=AuthorExt(id=null, tenantId=null, journalId=1302319053441957962, articleId=1322631321889911207, authorId=1324185325542711320, 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戴肃芳, 赵庆飞, 刘金成, 黄子萱, 许金塔, 李芳, 寇俊萍
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戴肃芳, 赵庆飞, 刘金成, 黄子萱, 许金塔, 李芳, 寇俊萍
作者信息
作者简介:
戴肃芳: 戴肃芳(2002—),女,硕士研究生,从事中药心血管药理学研究。E-mail:17302232328@163.com
Yiqi Fumai Lyophilized Injection ameliorates heart failure induced by transverse aortic constriction via Piezo1/NO/cGMP pathway
DAI Sufang, ZHAO Qingfei, LIU Jincheng, HUANG Zixuan, XU Jinta, LI Fang, KOU Junping
Affiliations
    1 Jiangsu Provincial Key Laboratory of Traditional Chinese Medicine Evaluation and Transformation, School of Traditional Chinese Pharmacy, China Pharmaceutical University, Nanjing 211198, China
doi: 10.7501j.issn.0253-2670.2026.19.015
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目的 探讨注射用益气复脉(冻干)(Yiqi Fumai Lyophilized Injection,YQFM)通过上调心脏内皮机械敏感离子通道(piezo-type mechanosensitive ion channel component 1,Piezo1)激活一氧化氮(nitric oxide,NO)信号通路,从而抑制心肌肥大,改善压力超负荷所致心力衰竭(heart failure,HF)。方法 采用主动脉弓缩窄(transverse aortic constriction,TAC)手术制备小鼠HF模型,术后2周ip不同剂量YQFM(0.13、0.26、0.53 g/kg)和卡托普利(20 mg/kg)进行干预。药物干预4周后利用超声心动图评估心功能变化;采用苏木素-伊红(hematoxylin-eosin,HE)和Masson染色评价心脏病理损伤及纤维化程度;采用心脏指数、心脏质量与胫骨长度比值、小麦胚芽凝集素(wheat germ agglutinin,WGA)染色评价心脏重构和心肌细胞肥大程度;采用血清生化检测、qRT-PCR、Western blotting及免疫荧光染色等技术检测HF相关标志物及Piezo1/NO通路关键蛋白的表达变化。结果 YQFM显著改善TAC诱导的小鼠心功能障碍与心脏重构(P<0.05、0.01),并减轻组织结构紊乱、心肌细胞肥大和心肌纤维化(P<0.01)。机制研究表明YQFM降低血清心肌损伤标志物心肌肌钙蛋白T(cardiac troponin T,cTn-T)、N末端B型利钠肽前体(N-terminal pro-B-type natriuretic peptide,NT-proBNP)水平(P<0.01),显著下调心脏中肥大相关基因心房钠尿肽(natriuretic peptide A,Nppa)、B型利钠肽(natriuretic peptide B,Nppb)、肌球蛋白重链7(myosin heavy chain 7,Myh7)与纤维化相关基因I型胶原蛋白α1链(collagen type I alpha 1 chain,Col1a1)、Ⅲ型胶原蛋白α1链(collagen type III alpha 1 chain,Col3a1)的表达(P<0.05、0.01)。YQFM还可显著降低卵泡抑素样蛋白1(follistatin-like 1,Fstl1)和内皮素-1(endothelin-1,ET-1)含量(P<0.05、0.01),同时提升血清与心脏组织中NO及环磷酸鸟苷(cyclic guanosine monophosphate,cGMP)水平(P<0.01)。此外,YQFM显著上调心脏内皮细胞中Piezo1蛋白与磷酸化内皮型一氧化氮合酶(phosphorylated endothelial nitric oxide synthase,p-eNOS)的表达(P<0.01)。结论 YQFM通过上调内皮Piezo1表达并激活eNOS/NO通路,改善心脏功能与重构,抑制心肌细胞肥大,从而发挥抗HF作用。
注射用益气复脉(冻干)  /  心力衰竭  /  心肌肥大  /  主动脉弓缩窄  /  Piezo1/NO/cGMP通路
Objective To investigate whether Yiqi Fumai Lyophilized Injection [注射用益气复脉(冻干), YQFM] ameliorates myocardial hypertrophy and pressure overload-induced heart failure (HF) by upregulating the cardiac endothelial mechanosensitive ion channel Piezo1 and activating the nitric oxide (NO) signaling pathway. Methods A mouse HF model was prepared via transverse aortic constriction (TAC) surgery. Two weeks post-operation, mice received intraperitoneal injections of different doses of YQFM (0.13, 0.26, 0.53 g/kg) or captopril (20 mg/kg) for four weeks. Cardiac function was assessed by echocardiography. Pathological injury and fibrosis were evaluated by hematoxylin and eosin (HE) and Masson staining. Cardiac remodeling and cardiomyocyte hypertrophy were assessed by heart index, heart weight-to-tibia length ratio and wheat germ agglutinin (WGA) staining. Serum biochemical assays, qRT-PCR, Western blotting and immunofluorescence were employed to detect HF-related biomarkers and the expressions of key proteins in Piezo1/NO pathway. Results YQFM significantly improved TAC-induced cardiac dysfunction and remodeling (P < 0.05, 0.01), and alleviated histopathological disorganization, cardiomyocyte hypertrophy and myocardial fibrosis (P < 0.01). Mechanistic studies showed that YQFM reduced levels of cardiac injury markers cardiac troponin T (cTn-T) and N-terminal pro-B-type natriuretic peptide (NT-proBNP) in serum (P < 0.01), and significantly downregulated the expressions of hypertrophy-related genes natriuretic peptide A (Nppa), natriuretic peptide B (Nppb), myosin heavy chain 7 (Myh7) and fibrosis-related genes collagen type I alpha 1 chain (Col1a1), collagen type III alpha 1 chain (Col3a1) in cardiac tissue (P < 0.05, 0.01). YQFM significantly decreased the levels of follistatin-like 1 (Fstl1) and endothelin-1 (ET-1) (P < 0.05, 0.01), while elevating the levels of NO in serum and cardiac tissue and cyclic guanosine monophosphate (cGMP) in cardiac tissue (P < 0.01). Furthermore, YQFM significantly upregulated the expressions of Piezo1 protein and phosphorylated endothelial nitric oxide synthase (p-eNOS) in cardiac endothelial cells (P < 0.01). Conclusion YQFM improves cardiac function and remodeling, and inhibits cardiomyocyte hypertrophy in HF by upregulating endothelial Piezo1 expression and activating eNOS/NO signaling pathway.
Yiqi Fumai Lyophilized Injection  /  heart failure  /  cardiac hypertrophy  /  transverse aortic constriction  /  Piezo1/NO/cGMP pathway
戴肃芳, 赵庆飞, 刘金成, 黄子萱, 许金塔, 李芳, 寇俊萍. 注射用益气复脉(冻干)通过Piezo1/NO/cGMP通路改善主动脉弓缩窄诱导的心力衰竭. 中草药, 2026 , 57 (19) : 7685 -7696 . DOI: 10.7501j.issn.0253-2670.2026.19.015
DAI Sufang, ZHAO Qingfei, LIU Jincheng, HUANG Zixuan, XU Jinta, LI Fang, KOU Junping. Yiqi Fumai Lyophilized Injection ameliorates heart failure induced by transverse aortic constriction via Piezo1/NO/cGMP pathway[J]. Chinese Traditional and Herbal Drugs, 2026 , 57 (19) : 7685 -7696 . DOI: 10.7501j.issn.0253-2670.2026.19.015

    国家自然科学基金面上项目 (82274140)

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2026年第57卷第19期
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doi: 10.7501j.issn.0253-2670.2026.19.015
  • 接收时间:2026-03-07
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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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