Article(id=1276976050781417953, tenantId=1146029695717560320, journalId=1276577828834349082, issueId=1276975955985961244, articleNumber=null, orderNo=null, doi=10.19540/j.cnki.cjcmm.20250925.801, pmid=null, cstr=null, oa=null, hot=null, price=null, onlineType=0, articleFormat=0, articleType=null, articleTypeStr=null, receivedDate=1752163200000, receivedDateStr=2025-07-11, revisedDate=null, revisedDateStr=null, acceptedDate=null, acceptedDateStr=null, onlineDate=1782384415573, onlineDateStr=2026-06-25, pubDate=1767196800000, pubDateStr=2026-01-01, doiRegisterDate=null, doiRegisterDateStr=null, onlineIssueDate=1782384415573, onlineIssueDateStr=2026-06-25, onlineJustAcceptDate=null, onlineJustAcceptDateStr=null, onlineFirstDate=null, onlineFirstDateStr=null, sourceXml=null, magXml=null, createTime=1782384415573, creator=13701087609, updateTime=1782384415573, updator=13701087609, issue=Issue{id=1276975955985961244, tenantId=1146029695717560320, journalId=1276577828834349082, year='2026', volume='51', issue='1', pageStart='1', pageEnd='300', issueExtLink='null', onlineDate='null', pubDate='1767196800000', pubDateStr='2026-01-01', beforeIssueId=null, nextIssueId=null, price=null, status=1, issueComplete=1, articleOrder=1, issueType=-1, specialIssue=null, createTime=1782384392973, creator='13701087609', updateTime=1782384484405, updator='13701087609', preIssue=null, nextIssue=null, articleTotal=null, ext={EN=IssueExt(id=1276976339546673871, tenantId=1146029695717560320, journalId=1276577828834349082, issueId=1276975955985961244, language=EN, specialIssueTitle=, coverIllustrator=null, specialIssueEditor=, specialIssueAbout=), CN=IssueExt(id=1276976339546673872, tenantId=1146029695717560320, journalId=1276577828834349082, issueId=1276975955985961244, language=CN, specialIssueTitle=, coverIllustrator=null, specialIssueEditor=, specialIssueAbout=)}, issueFiles=null, downloadFileDto=null}, startPage=232, endPage=240, ext={EN=ArticleExt(id=1276976051548975587, articleId=1276976050781417953, tenantId=1146029695717560320, journalId=1276577828834349082, language=EN, title=Mechanism study of modified Xiangsha Liujunzi Decoction in regulating intestinal HDL3 to ameliorate hepatic inflammation in hyperlipidemic mice, columnId=null, journalTitle=Chinese Journal of Traditional Chinese Medicine, columnName=null, runingTitle=null, highlight=null, articleAbstract=

This study aims to investigate the mechanism by which modified Xiangsha Liujunzi Decoction (M-XS) ameliorates hepatic inflammation in hyperlipidemic mice by regulating the intestinal high-density lipoprotein 3 (HDL3) level. Intestine-specific ATP-binding cassette transporter A1 (ABCA1) knockout mice (Abcal-Villin-cre-Tg) were randomized into 3 groups (n = 8): intestine-specific knockout group (Abcal△Vill), intestine-specific knockout mice fed a high-fat diet group (Abcal△Vill + HFD), and intestine-specific knockout with Chinese herbal medicine intervention group (Abcal△Vill + HFD + M-XS). Littermate control mice were randomly allocated into 3 groups (n = 8): blank group (Abcalfl/fl), high-fat diet group (Abcalfl/fl+HFD), and Chinese herbal medicine intervention group (Abcalfl/fl +HFD+M-XS). Except the Abcalfl/fl and Abcal△Vill groups, the other groups were fed a HFD for 10 weeks. Drug administration lasted for 6 weeks at a dose of 23.66 g·kg-1·d-1. Serum lipid profiles (four items), hepatic histopathology (HE and oil red O staining), and ileal histopathology (HE staining) were assessed. Ileal HDL3 levels were measured by ELISA, hepatic triacylglycerol (TG) levels by the GPO-PAP method, and co-localization of CD86 and Toll-like receptor 4 (TLR4) in the liver tissue by immunofluorescence. The mRNA levels of hepatic lipopolysaccharide-binding protein (LBP), nuclear factor kappa-light-chain-enhancer of activated B cells p65 (NF-κB p65), inhibitor of nuclear factor kappa-B alpha (IκBα), interleukin-6 (IL-6), tumor necrosis factor-alpha (TNF-α), and interleukin-1 beta (IL-1β) were determined by real-time PCR. The protein levels of ABCA1 and apolipoprotein A-I (apoA-I) in the ileum, as well as LBP, p-NF-κB, p-IκBα, IL-6, TNF-α, and IL-1β in the liver, were assessed by Western blot. Compared with the Abcalfl/fl group, the Abcalfl/fl +HFD group showed increased blood lipid levels, numerous vacuoles and lipid droplets in the liver, shortened intestinal villi, elevated hepatic TG level, reduced levels of HDL3, ABCA1, and apoA-I in the ileum, co-localization of CD86 and TLR4 in the liver, and up-regulated mRNA levels of LBP, NF-κB, IκBα, IL-6, TNF-α, and IL-1β as well as protein levels of LBP, p-NF-κB, p-IκBα, IL-6, TNF-α, and IL-1β in the liver (P<0.05). Compared with the Abcalfl/fl +HFD group, the Abcalfl/fl +HFD+M-XS group showed decreased blood lipid levels, reduced vacuoles and lipid droplets in the liver, increased intestinal villus length, decreased hepatic TG level, elevated levels of HDL3, ABCA1, and apoA-I in the ileum, weakened co-localization of CD86 and TLR4 in the liver, and down-regulated mRNA levels of LBP, NF-κB, IκBα, IL-6, TNF-α, and IL-1β and protein levels of LBP, p-NF-κB, p-IκBα, IL-6, TNF-α, and IL-1β (P<0.05). Compared with the Abcalfl/fl+HFD group, the AbcalVill+HFD group showed raised blood lipid levels, increased vacuoles and lipid droplets in the liver, elevated hepatic TG level, enhanced co-localization of CD86 and TLR4 in the liver, and up-regulated mRNA levels of LBP, NF-κB, IκBα, IL-6, TNF-α, and IL-1β and protein levels of LBP, p-NF-κB, p-IκBα, TNF-α, and IL-1β (P<0.05). Compared with the Abcalfl/fl+HFD+M-XS group, the Abcal△Vill+HFD+M-XS group showed raised blood lipid levels, increased vacuoles and lipid droplets in the liver, elevated hepatic TG level, enhanced co-localization of CD86 and TLR4 in the liver, and up-regulated mRNA levels of LBP, NF-κB, IκBα, IL-6, TNF-α, and IL-1β and protein levels of LBP, p-NF-κB, p-IκBα, IL-6, TNF-α, and IL-1β (P<0.05). In conclusion, modified Xiangsha Liujunzi Decoction ameliorates hepatic inflammation and corrects dyslipidemia by modulating intestinal HDL3 levels.

, authors=null, authorsList=Meng-zhu CHE, Qi ZHANG, Guo-yuan SUI, Dong-yu MIN, Lian-qun JIA, Guan-lin YANG, authorCompany=null, correspAuthors=Lian-qun JIA, Guan-lin YANG, 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=1276976053167976934, articleId=1276976050781417953, tenantId=1146029695717560320, journalId=1276577828834349082, language=CN, title=加味香砂六君子汤调控高脂血症小鼠肠源性HDL3改善肝脏炎症反应的机制研究, columnId=1276975994707775974, journalTitle=中国中药杂志, columnName=药理, runingTitle=null, highlight=null, articleAbstract=

探讨加味香砂六君子汤调控肠道高密度脂蛋白3(high-density lipoprotein 3, HDL3)水平改善高脂血症小鼠肝脏炎症的作用机制。将肠特异性ATP结合盒转运体A1(ATP-binding cassette transporter A1, ABCA1)基因敲除小鼠(Abcal-Villin-cre-Tg)随机分为3组,每组8只:肠特异性敲除组(Abcal△Vill组),肠特异性敲除高脂组(Abcal△Vill+HFD组),肠特异性敲除中药干预组(Abcal△Vill +HFD+M-XS组);同窝对照小鼠随机分为3组,每组8只:空白组(Abcalfl/fl组),高脂组(Abcalfl/fl +HFD组),中药干预组(Abcalfl/fl +HFD+M-XS组)。除Abcalfl/fl组和Abcal△Vill组外,其余组给予高脂饲料饲养10周。连续给药6周,给药剂量23.66 g·kg-1·d-1。检测各组小鼠血脂四项;肝脏HE、油红O染色及回肠HE染色观察病理情况;酶联免疫吸附测定法(ELISA)检测小鼠回肠HDL3水平;GPO-PAP法检测肝脏甘油三酯(triacylglycerol, TG)水平;免疫荧光检测肝脏组织CD86与Toll样受体4(Toll-like receptor 4, TLR4)共定位情况;real-time PCR检测肝脏脂多糖结合蛋白(lipopolysaccharide-binding protein, LBP)、核转录因子-κB p65(nuclear factor kappa-light-chain-enhancer of activated B cells p65, NF-κB p65)、核因子-κBα抑制蛋白(inhibitor of nuclear factor kappa-B alpha, IκBα)、白细胞介素6(interleukin-6, IL-6)、肿瘤坏死因子-α(tumor necrosis factor alpha, TNF-α)、白细胞介素-1β(interleukin-1 beta, IL-1β)mRNA表达;Western blot检测回肠ABCA1、载脂蛋白A-I(apolipoprotein A-I, apoA-I)及肝脏LBP、p-NF-κB、p-IκBα、IL-6、TNF-α和IL-1β蛋白表达。结果显示,与Abcalfl/fl组比,Abcalfl/fl +HFD组血脂水平升高,肝脏出现大量空泡及脂滴,小肠绒毛变短,肝脏TG升高,回肠HDL3、ABCA1和apoA-I水平降低,肝脏CD86与TLR4呈现共定位,肝脏LBP、NF-κB、IκBα、IL-6、TNF-α及IL-1β mRNA表达升高,肝脏LBP、p-NF-κB、p-IκBα、IL-6、TNF-α及IL-1β蛋白表达显著升高(P<0.05);与Abcalfl/fl +HFD组比,Abcalfl/fl +HFD+M-XS组血脂水平降低,肝脏空泡及脂滴减少,小肠绒毛长度增加,肝脏TG降低,回肠HDL3、ABCA1和apoA-I水平升高,肝脏CD86与TLR4共定位程度减弱,LBP、NF-κB、IκBα、IL-6、TNF-α及IL-1β mRNA表达降低,LBP、p-NF-κB、p-IκBα、IL-6、TNF-α及IL-1β蛋白表达显著降低(P<0.05);与Abcalfl/fl +HFD组比,Abcal△Vill+HFD组血脂水平升高,肝脏空泡及脂滴增多,肝脏TG升高,肝脏CD86与TLR4共定位程度增强,LBP、NF-κB、IκBα、IL-6、TNF-α及IL-1β mRNA表达升高,LBP、p-NF-κB、p-IκBα、TNF-α及IL-1β蛋白表达显著升高(P<0.05);与Abcalfl/fl+HFD+M-XS组比,Abcal△Vill +HFD+M-XS组血脂水平升高,肝脏空泡及脂滴增多,肝脏TG升高,肝脏CD86与TLR4共定位增强,LBP、NF-κB、IκBα、IL-6、TNF-α及IL-1β mRNA表达升高,LBP、p-NF-κB、p-IκBα、IL-6、TNF-α及IL-1β蛋白表达显著升高(P<0.05)。结果表明,加味香砂六君子汤通过调节肠道HDL3水平,改善肝脏炎症反应,纠正血脂异常。

, authors=

车梦竹,博士研究生,主要从事中西医结合防治心脑血管疾病研究,E-mail:

, authorsList=车梦竹, 张琦, 隋国媛, 闵冬雨, 贾连群, 杨关林, authorCompany=null, correspAuthors=贾连群, 杨关林, authorNote=null, correspAuthorsNote=

*

杨关林,教授,主要从事中西医结合防治心脑血管疾病研究,E-mail:

*

贾连群,教授,博士生导师,主要从事中西医结合防治心血管疾病研究,E-mail:
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2.National and Local Joint Engineering Laboratory of Integrated Traditional Chinese and Western Medicine for Prevention and Treatment of Cardio-Cerebral Diseases, Liaoning University of Traditional Chinese Medicine, Shenyang 110847, China
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2.辽宁中医药大学 心脑合病中西医结合防治技术国家地方联合工程实验室,辽宁 沈阳 110847
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车梦竹,博士研究生,主要从事中西医结合防治心脑血管疾病研究,E-mail:

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车梦竹,博士研究生,主要从事中西医结合防治心脑血管疾病研究,E-mail:

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加味香砂六君子汤调控高脂血症小鼠肠源性HDL3改善肝脏炎症反应的机制研究
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车梦竹 1, 2, 3 , 张琦 1, 2, 3 , 隋国媛 1 , 闵冬雨 4 , 贾连群 1, * , 杨关林 1, *
中国中药杂志 | 药理 2026,51(1): 232-240
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中国中药杂志 |药理 2026 , 51 (1) : 232 -240
加味香砂六君子汤调控高脂血症小鼠肠源性HDL3改善肝脏炎症反应的机制研究
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车梦竹1, 2, 3 , 张琦1, 2, 3, 隋国媛1, 闵冬雨4, 贾连群1, * , 杨关林1, *
作者信息
  • 1.辽宁中医药大学,辽宁 沈阳 110847
  • 2.辽宁中医药大学 心脑合病中西医结合防治技术国家地方联合工程实验室,辽宁 沈阳 110847
  • 3.辽宁中医药大学 中医脏象理论及应用教育部重点实验室,辽宁 沈阳 110847
  • 4.辽宁中医药大学附属医院,辽宁 沈阳 110032
通讯作者:

*

杨关林,教授,主要从事中西医结合防治心脑血管疾病研究,E-mail:

*

贾连群,教授,博士生导师,主要从事中西医结合防治心血管疾病研究,E-mail:
Mechanism study of modified Xiangsha Liujunzi Decoction in regulating intestinal HDL3 to ameliorate hepatic inflammation in hyperlipidemic mice
Meng-zhu CHE1, 2, 3 , Qi ZHANG1, 2, 3, Guo-yuan SUI1, Dong-yu MIN4, Lian-qun JIA1, * , Guan-lin YANG1, *
Affiliations
  • 1.Liaoning University of Traditional Chinese Medicine, Shenyang 110847, China
  • 2.National and Local Joint Engineering Laboratory of Integrated Traditional Chinese and Western Medicine for Prevention and Treatment of Cardio-Cerebral Diseases, Liaoning University of Traditional Chinese Medicine, Shenyang 110847, China
  • 3.Key Laboratory of Traditional Chinese Medicine Visceral Theory and Applications, Ministry of Education, Liaoning University of Traditional Chinese Medicine, Shenyang 110847, China
  • 4.Affiliated Hospital of Liaoning University of Traditional Chinese Medicine, Shenyang 110032, China
出版时间: 2026-01-01 doi: 10.19540/j.cnki.cjcmm.20250925.801
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探讨加味香砂六君子汤调控肠道高密度脂蛋白3(high-density lipoprotein 3, HDL3)水平改善高脂血症小鼠肝脏炎症的作用机制。将肠特异性ATP结合盒转运体A1(ATP-binding cassette transporter A1, ABCA1)基因敲除小鼠(Abcal-Villin-cre-Tg)随机分为3组,每组8只:肠特异性敲除组(Abcal△Vill组),肠特异性敲除高脂组(Abcal△Vill+HFD组),肠特异性敲除中药干预组(Abcal△Vill +HFD+M-XS组);同窝对照小鼠随机分为3组,每组8只:空白组(Abcalfl/fl组),高脂组(Abcalfl/fl +HFD组),中药干预组(Abcalfl/fl +HFD+M-XS组)。除Abcalfl/fl组和Abcal△Vill组外,其余组给予高脂饲料饲养10周。连续给药6周,给药剂量23.66 g·kg-1·d-1。检测各组小鼠血脂四项;肝脏HE、油红O染色及回肠HE染色观察病理情况;酶联免疫吸附测定法(ELISA)检测小鼠回肠HDL3水平;GPO-PAP法检测肝脏甘油三酯(triacylglycerol, TG)水平;免疫荧光检测肝脏组织CD86与Toll样受体4(Toll-like receptor 4, TLR4)共定位情况;real-time PCR检测肝脏脂多糖结合蛋白(lipopolysaccharide-binding protein, LBP)、核转录因子-κB p65(nuclear factor kappa-light-chain-enhancer of activated B cells p65, NF-κB p65)、核因子-κBα抑制蛋白(inhibitor of nuclear factor kappa-B alpha, IκBα)、白细胞介素6(interleukin-6, IL-6)、肿瘤坏死因子-α(tumor necrosis factor alpha, TNF-α)、白细胞介素-1β(interleukin-1 beta, IL-1β)mRNA表达;Western blot检测回肠ABCA1、载脂蛋白A-I(apolipoprotein A-I, apoA-I)及肝脏LBP、p-NF-κB、p-IκBα、IL-6、TNF-α和IL-1β蛋白表达。结果显示,与Abcalfl/fl组比,Abcalfl/fl +HFD组血脂水平升高,肝脏出现大量空泡及脂滴,小肠绒毛变短,肝脏TG升高,回肠HDL3、ABCA1和apoA-I水平降低,肝脏CD86与TLR4呈现共定位,肝脏LBP、NF-κB、IκBα、IL-6、TNF-α及IL-1β mRNA表达升高,肝脏LBP、p-NF-κB、p-IκBα、IL-6、TNF-α及IL-1β蛋白表达显著升高(P<0.05);与Abcalfl/fl +HFD组比,Abcalfl/fl +HFD+M-XS组血脂水平降低,肝脏空泡及脂滴减少,小肠绒毛长度增加,肝脏TG降低,回肠HDL3、ABCA1和apoA-I水平升高,肝脏CD86与TLR4共定位程度减弱,LBP、NF-κB、IκBα、IL-6、TNF-α及IL-1β mRNA表达降低,LBP、p-NF-κB、p-IκBα、IL-6、TNF-α及IL-1β蛋白表达显著降低(P<0.05);与Abcalfl/fl +HFD组比,Abcal△Vill+HFD组血脂水平升高,肝脏空泡及脂滴增多,肝脏TG升高,肝脏CD86与TLR4共定位程度增强,LBP、NF-κB、IκBα、IL-6、TNF-α及IL-1β mRNA表达升高,LBP、p-NF-κB、p-IκBα、TNF-α及IL-1β蛋白表达显著升高(P<0.05);与Abcalfl/fl+HFD+M-XS组比,Abcal△Vill +HFD+M-XS组血脂水平升高,肝脏空泡及脂滴增多,肝脏TG升高,肝脏CD86与TLR4共定位增强,LBP、NF-κB、IκBα、IL-6、TNF-α及IL-1β mRNA表达升高,LBP、p-NF-κB、p-IκBα、IL-6、TNF-α及IL-1β蛋白表达显著升高(P<0.05)。结果表明,加味香砂六君子汤通过调节肠道HDL3水平,改善肝脏炎症反应,纠正血脂异常。

加味香砂六君子汤  /  小鼠  /  回肠  /  高密度脂蛋白3  /  血脂

This study aims to investigate the mechanism by which modified Xiangsha Liujunzi Decoction (M-XS) ameliorates hepatic inflammation in hyperlipidemic mice by regulating the intestinal high-density lipoprotein 3 (HDL3) level. Intestine-specific ATP-binding cassette transporter A1 (ABCA1) knockout mice (Abcal-Villin-cre-Tg) were randomized into 3 groups (n = 8): intestine-specific knockout group (Abcal△Vill), intestine-specific knockout mice fed a high-fat diet group (Abcal△Vill + HFD), and intestine-specific knockout with Chinese herbal medicine intervention group (Abcal△Vill + HFD + M-XS). Littermate control mice were randomly allocated into 3 groups (n = 8): blank group (Abcalfl/fl), high-fat diet group (Abcalfl/fl+HFD), and Chinese herbal medicine intervention group (Abcalfl/fl +HFD+M-XS). Except the Abcalfl/fl and Abcal△Vill groups, the other groups were fed a HFD for 10 weeks. Drug administration lasted for 6 weeks at a dose of 23.66 g·kg-1·d-1. Serum lipid profiles (four items), hepatic histopathology (HE and oil red O staining), and ileal histopathology (HE staining) were assessed. Ileal HDL3 levels were measured by ELISA, hepatic triacylglycerol (TG) levels by the GPO-PAP method, and co-localization of CD86 and Toll-like receptor 4 (TLR4) in the liver tissue by immunofluorescence. The mRNA levels of hepatic lipopolysaccharide-binding protein (LBP), nuclear factor kappa-light-chain-enhancer of activated B cells p65 (NF-κB p65), inhibitor of nuclear factor kappa-B alpha (IκBα), interleukin-6 (IL-6), tumor necrosis factor-alpha (TNF-α), and interleukin-1 beta (IL-1β) were determined by real-time PCR. The protein levels of ABCA1 and apolipoprotein A-I (apoA-I) in the ileum, as well as LBP, p-NF-κB, p-IκBα, IL-6, TNF-α, and IL-1β in the liver, were assessed by Western blot. Compared with the Abcalfl/fl group, the Abcalfl/fl +HFD group showed increased blood lipid levels, numerous vacuoles and lipid droplets in the liver, shortened intestinal villi, elevated hepatic TG level, reduced levels of HDL3, ABCA1, and apoA-I in the ileum, co-localization of CD86 and TLR4 in the liver, and up-regulated mRNA levels of LBP, NF-κB, IκBα, IL-6, TNF-α, and IL-1β as well as protein levels of LBP, p-NF-κB, p-IκBα, IL-6, TNF-α, and IL-1β in the liver (P<0.05). Compared with the Abcalfl/fl +HFD group, the Abcalfl/fl +HFD+M-XS group showed decreased blood lipid levels, reduced vacuoles and lipid droplets in the liver, increased intestinal villus length, decreased hepatic TG level, elevated levels of HDL3, ABCA1, and apoA-I in the ileum, weakened co-localization of CD86 and TLR4 in the liver, and down-regulated mRNA levels of LBP, NF-κB, IκBα, IL-6, TNF-α, and IL-1β and protein levels of LBP, p-NF-κB, p-IκBα, IL-6, TNF-α, and IL-1β (P<0.05). Compared with the Abcalfl/fl+HFD group, the AbcalVill+HFD group showed raised blood lipid levels, increased vacuoles and lipid droplets in the liver, elevated hepatic TG level, enhanced co-localization of CD86 and TLR4 in the liver, and up-regulated mRNA levels of LBP, NF-κB, IκBα, IL-6, TNF-α, and IL-1β and protein levels of LBP, p-NF-κB, p-IκBα, TNF-α, and IL-1β (P<0.05). Compared with the Abcalfl/fl+HFD+M-XS group, the Abcal△Vill+HFD+M-XS group showed raised blood lipid levels, increased vacuoles and lipid droplets in the liver, elevated hepatic TG level, enhanced co-localization of CD86 and TLR4 in the liver, and up-regulated mRNA levels of LBP, NF-κB, IκBα, IL-6, TNF-α, and IL-1β and protein levels of LBP, p-NF-κB, p-IκBα, IL-6, TNF-α, and IL-1β (P<0.05). In conclusion, modified Xiangsha Liujunzi Decoction ameliorates hepatic inflammation and corrects dyslipidemia by modulating intestinal HDL3 levels.

modified Xiangsha Liujunzi Decoction  /  mice  /  ileum  /  high-density lipoprotein 3  /  blood lipid
车梦竹, 张琦, 隋国媛, 闵冬雨, 贾连群, 杨关林. 加味香砂六君子汤调控高脂血症小鼠肠源性HDL3改善肝脏炎症反应的机制研究. 中国中药杂志, 2026 , 51 (1) : 232 -240 . DOI: 10.19540/j.cnki.cjcmm.20250925.801
Meng-zhu CHE, Qi ZHANG, Guo-yuan SUI, Dong-yu MIN, Lian-qun JIA, Guan-lin YANG. Mechanism study of modified Xiangsha Liujunzi Decoction in regulating intestinal HDL3 to ameliorate hepatic inflammation in hyperlipidemic mice[J]. Chinese Journal of Traditional Chinese Medicine, 2026 , 51 (1) : 232 -240 . DOI: 10.19540/j.cnki.cjcmm.20250925.801
  • 国家自然科学基金面上项目(82374423; 82474221)
  • 辽宁省科技计划联合计划项目(2024JH2/102600194)
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doi: 10.19540/j.cnki.cjcmm.20250925.801
  • 接收时间:2025-07-11
  • 首发时间:2026-06-25
  • 出版时间:2026-01-01
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  • 收稿日期:2025-07-11
基金
国家自然科学基金面上项目(82374423; 82474221)
辽宁省科技计划联合计划项目(2024JH2/102600194)
作者信息
    1.辽宁中医药大学,辽宁 沈阳 110847
    2.辽宁中医药大学 心脑合病中西医结合防治技术国家地方联合工程实验室,辽宁 沈阳 110847
    3.辽宁中医药大学 中医脏象理论及应用教育部重点实验室,辽宁 沈阳 110847
    4.辽宁中医药大学附属医院,辽宁 沈阳 110032

通讯作者:

*

杨关林,教授,主要从事中西医结合防治心脑血管疾病研究,E-mail:

*

贾连群,教授,博士生导师,主要从事中西医结合防治心血管疾病研究,E-mail:
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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
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