Article(id=1322926196048142836, tenantId=1146029695717560320, journalId=1255847919539208197, issueId=1322925862630339452, articleNumber=null, orderNo=null, doi=10.13193/j.issn.1673-7717.2025.07.049, 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=1793339783917, onlineDateStr=2026-10-30, pubDate=1752076800000, pubDateStr=2025-07-10, doiRegisterDate=null, doiRegisterDateStr=null, onlineIssueDate=1793339783917, onlineIssueDateStr=2026-10-30, onlineJustAcceptDate=null, onlineJustAcceptDateStr=null, onlineFirstDate=null, onlineFirstDateStr=null, sourceXml=null, magXml=null, createTime=1793339783917, creator=13701087609, updateTime=1793339783917, updator=13701087609, issue=Issue{id=1322925862630339452, tenantId=1146029695717560320, journalId=1255847919539208197, year='2025', volume='43', issue='7', pageStart='1', pageEnd='258', issueExtLink='null', onlineDate='null', pubDate='1752076800000', pubDateStr='2025-07-10', beforeIssueId=null, nextIssueId=null, price=null, status=1, issueComplete=1, articleOrder=1, issueType=-1, specialIssue=0, createTime=1793339704424, creator='13701087609', updateTime=1793340532184, updator='13701087609', preIssue=null, nextIssue=null, articleTotal=null, ext={EN=IssueExt(id=1322929334587105328, tenantId=1146029695717560320, journalId=1255847919539208197, issueId=1322925862630339452, language=EN, specialIssueTitle=, coverIllustrator=null, specialIssueEditor=, specialIssueAbout=), CN=IssueExt(id=1322929334587105329, tenantId=1146029695717560320, journalId=1255847919539208197, issueId=1322925862630339452, language=CN, specialIssueTitle=, coverIllustrator=null, specialIssueEditor=, specialIssueAbout=)}, issueFiles=null, downloadFileDto=null}, startPage=239, endPage=245, ext={EN=ArticleExt(id=1322926197780390389, articleId=1322926196048142836, tenantId=1146029695717560320, journalId=1255847919539208197, language=EN, title=Effects of Mongolian Medicine Sugemule-4 Decoction and Its Decomposed Formula and Single Drug on Gut-microbiota in Insomnia Model Rats, columnId=1256183365644968140, journalTitle=Chinese Archives of Traditional Chinese Medicine, columnName=Platform of Provincial Project, runingTitle=null, highlight=null, articleAbstract=
Objective

Based on gut microbiota,to explore the compatibility rules of Sugemule-4 Decoction.

Method

Seventy-two SPF grade male SD rats were randomly divided into control group(C),model group(M),Sugemule-4 Decoction group(S-4),lack of Suanzaoren(Ziziphi Spinosae Semen)formula group(QSZR),lack of Baidoukou(Amomum kravanh Pierre ex Gagnep)formula group(QBDK),lack of Xianghanqin(Cuminum cyminum L.)formula group(QXHQ),lack of Biba(Piperis Longi Fructus)formula group(QBB),Suanzaoren(Ziziphi Spinosae Semen)group(SZR),Baidoukou(Amomum kravanh Pierre ex Gagnep)group(BDK),Xianghanqin(Cuminum cyminum L.)group(XHQ),Biba(Piperis Longi Fructus)group(BB),Anshen Bunao Liquid(安神补脑液)group(Y). An insomnia rat model was established by using chronic unpredictable mild stress stimulation(CUMS)+parachlorophenylalanine(PCPA)method. After modeling,the corresponding drugs were administered for 7 days at a dose of 1.215 g/kg. Both group Cand group M were given the equal amounts of distilled water,while Group Y received a dose of 1.8 mL/kg. The general state and colon tissue morphology of rats in each group were compared after treatment,as well as the levels of 5-hydroxytryptamine(5-HT),γ-aminobutyric acid(GABA),acetylcholine(AChE),prostaglandin D2(PGD2),substance P(SP),vasoactive intestinal peptide(VIP)and gastrin(GAS)in serum,inducible nitric oxide synthase(INOS)content in colon and hypothalamic tissues,and 16SrDNA analysis of gut microbiota.

Results

After treatment,the circadian rhythm of the M group rats was disrupted or even disappeared,and their mental state deteriorated. The mental state of the other groups improved to varying degrees compared to those before treatment. Colon tissue HE staining showed that each treatment group could improve the pathological changes of the model rats to varying degrees. The serum levels of 5-HT,GABA,AChE,GASand VIP in group M rats were significantly altered(P<0.05),while the levels of INOSin the colon and hypothalamus were significantly increased(P<0.05). The S-4 group was able to significantly improve these changes(P<0.05). Baidoukou(Amomum kravanh Pierre ex Gagnep)had the strongest regulatory ability on insomnia related neurotransmitter levels,Xianghanqin(Cuminum cyminum L.)had the strongest regulatory ability on brain gut peptide levels,and Biba(Piperis Longi Fructus)had the strongest regulatory ability on INOSlevels in colon and hypothalamic tissues. The gut microbiota of each group at the level of gut microbiota genera was analyzed,linear discriminant effect analysis(LEfSe)was used to compare multiple groups,and 7 key differential bacterial genera were selected. Through analysis,it was found that each component in the formula can regulate the disorder of gut microbiota to varying degrees. Further exploring the relationship between the gut microbiota genus and the ELISA indicators detected in this article,it was found that the Coriobacteriaceae_UCG_002 showed a significant positive correlation with INOSin hypothalamic tissue,Anaerostipes showed a significant positive correlation with INOSin colon tissue and serum VIP,and Bifidobacterium showed a significant negative correlation with serum GAS.

Conclusion

Sugemule-4 Decoction and its split formula can improve the changes of insomnia related neurotransmitters,brain-gut peptide content and intestinal microbiota in the body of insomnia model rats to varying degrees.

, authors=Lina DU1, Dezhi YANG2, Lan WU1, Li MEI1, Sarula WU1, Yasula BA1, Yongchang BAO1, Rigugaqiqige SU1, Lin SONG1, authorsList=Lina DU, Dezhi YANG, Lan WU, Li MEI, Sarula WU, Yasula BA, Yongchang BAO, Rigugaqiqige SU, Lin SONG, authorCompany=null, correspAuthors=Lin SONG, 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=1322926210321359371, articleId=1322926196048142836, tenantId=1146029695717560320, journalId=1255847919539208197, language=CN, title=蒙药苏格木勒-4汤及其拆方与单药对失眠模型大鼠肠道菌群的影响, columnId=1256183369033965799, journalTitle=中华中医药学刊, columnName=省级项目平台, runingTitle=null, highlight=null, articleAbstract=
目的

基于肠道菌群,探讨苏格木勒-4汤的配伍规律。

方法

72只SPF级雄性SD大鼠,随机分为空白组(C)、模型组(M)、苏格木勒-4汤组(S-4)、缺酸枣仁方组(QSZR)、缺白豆蔻方组(QBDK)、缺香旱芹方组(QXHQ)、缺荜茇方组(QBB)、酸枣仁组(SZR)、白豆蔻组(BDK)、香旱芹组(XHQ)、荜茇组(BB)、安神补脑液组(Y)。使用慢性不可预知温和应激刺激(chronic unpredictable mild stimulation,CUMS)+对氯苯丙氨酸(parachlorophenylalanine,PCPA)法建立失眠大鼠模型。造模后分别给予相应药物治疗7 d,剂量为1.215 g/kg,C组和M组均给予等量蒸馏水,Y组剂量为1.8 mL/kg。比较治疗后各组大鼠一般状态与结肠组织形态,血清中5-羟色胺(5-hydroxytryptamine,5-HT)、γ-氨基丁酸(γ-aminobutyric acid,GABA)、乙酰胆碱(acetylcholine,AChE)、前列腺素D2(prostaglandin D2,PGD2)、P物质(substance P,SP)、血管活性肠肽(vasoactive intestinal peptide,VIP)、胃泌素(gastrin,GAS)含量,结肠组织与下丘脑组织中诱导型一氧化氮合酶(inducible nitric oxide synthase,iNOS)含量,以及肠道菌群16S核糖体DNA(16Sribosomal DNA identification,16SrDNA)。

结果

治疗结束后M组大鼠昼夜节律紊乱甚至消失,精神状态变差,其余各组精神状态较治疗前有不同程度好转。结肠组织HE染色显示治疗各组均可不同程度改善模型大鼠病理变化。M 组大鼠血清中5-HT、GABA、AChE、GAS、VIP水平显著改变(P<0.05),结肠与下丘脑INOS水平显著升高(P<0.05)。S-4组能显著改善这些变化(P<0.05)。方中白豆蔻对失眠相关神经递质水平调控能力最强,香旱芹对脑肠肽水平调控能力最强,荜茇对结肠与下丘脑组织中INOS水平调控能力最强。从肠道菌群属水平对各组肠道微生物群落进行分析,多个分组间比较采用线性判别效应量分析(LEfSe),筛选出关键差异菌属7种,并通过分析发现方中各个组分可不同程度调节肠道菌群的紊乱,进一步探讨肠道菌属与所检测ELISA指标之间的关系,得知红蝽菌UCG_002与下丘脑组织INOS呈显著正相关,丁酸弧菌与结肠组织INOS、血清VIP呈显著正相关,双歧杆菌与血清GAS呈显著负相关。

结论

苏格木勒-4汤及其拆方与单药可不同程度的改善失眠模型大鼠体内失眠相关神经递质、脑肠肽含量及肠道菌群的变化。

, authors=都丽娜1, 杨德志2, 乌兰1, 美丽1, 吴萨如拉1, 巴雅苏拉1, 包永昌1, 苏日古格其其格1, 松林1, authorsList=都丽娜, 杨德志, 乌兰, 美丽, 吴萨如拉, 巴雅苏拉, 包永昌, 苏日古格其其格, 松林, authorCompany=null, correspAuthors=松林, authorNote=

都丽娜(1996-),女(蒙古族),内蒙古赤峰人,博士在读,研究方向:蒙医方剂配伍规律。

, correspAuthorsNote=
松林(1972-),男(蒙古族),内蒙古通辽人,教授,博士研究生导师,博士,研究方向:蒙医药研究。E-mail:。
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都丽娜(1996-),女(蒙古族),内蒙古赤峰人,博士在读,研究方向:蒙医方剂配伍规律。

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都丽娜(1996-),女(蒙古族),内蒙古赤峰人,博士在读,研究方向:蒙医方剂配伍规律。

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Front Psychiatry,2019,10:34., articleTitle=Systematic review of gut microbiota and major depression, refAbstract=null)], funds=[Fund(id=1322926241766056546, tenantId=1146029695717560320, journalId=1255847919539208197, articleId=1322926196048142836, awardId=DC2100002252, language=CN, fundingSource=内蒙古自治区草原英才领军个人(乌兰)项目(DC2100002252), fundOrder=null, country=null), Fund(id=1322926242231624291, tenantId=1146029695717560320, journalId=1255847919539208197, articleId=1322926196048142836, awardId=2022—〔RC015〕, language=CN, fundingSource=内蒙古自治区中医药(蒙医药)中青年领军人才项目(2022—〔RC015〕), fundOrder=null, country=null)], companyList=[AuthorCompany(id=1322926210757566988, tenantId=1146029695717560320, journalId=1255847919539208197, articleId=1322926196048142836, xref=1., ext=[AuthorCompanyExt(id=1322926210765955597, tenantId=1146029695717560320, journalId=1255847919539208197, articleId=1322926196048142836, companyId=1322926210757566988, language=EN, country=null, province=null, city=null, postcode=null, companyName=null, departmentName=null, remark=1.Inner Mongolia Medical University,Hohhot 010110,Inner Mongolia,China), AuthorCompanyExt(id=1322926210778538510, tenantId=1146029695717560320, journalId=1255847919539208197, articleId=1322926196048142836, companyId=1322926210757566988, language=CN, country=null, province=null, city=null, postcode=null, companyName=null, departmentName=null, remark=1.内蒙古医科大学蒙医药学院,内蒙古 呼和浩特 010010)]), AuthorCompany(id=1322926210841453071, tenantId=1146029695717560320, journalId=1255847919539208197, articleId=1322926196048142836, xref=2., ext=[AuthorCompanyExt(id=1322926210849841680, tenantId=1146029695717560320, journalId=1255847919539208197, articleId=1322926196048142836, companyId=1322926210841453071, language=EN, country=null, province=null, city=null, postcode=null, companyName=null, departmentName=null, remark=2.Inner Mongolia International Mongolian Hospital,Hohhot 010065,Inner Mongolia,China), AuthorCompanyExt(id=1322926210858230289, tenantId=1146029695717560320, journalId=1255847919539208197, articleId=1322926196048142836, companyId=1322926210841453071, language=CN, country=null, province=null, city=null, postcode=null, companyName=null, departmentName=null, remark=2.内蒙古自治区国际蒙医医院,内蒙古 呼和浩特 010013)])], figs=[ArticleFig(id=1322926229694849616, tenantId=1146029695717560320, journalId=1255847919539208197, articleId=1322926196048142836, language=EN, label=null, caption=null, figureFileSmall=Wp+C+PyFfLsODo88gSsxWA==, figureFileBig=KodasUKmzvtdJSAIDynfKg==, tableContent=null), ArticleFig(id=1322926231682949713, tenantId=1146029695717560320, journalId=1255847919539208197, articleId=1322926196048142836, language=CN, label=图1, caption=各组大鼠结肠组织HE染色(×20), figureFileSmall=Wp+C+PyFfLsODo88gSsxWA==, figureFileBig=KodasUKmzvtdJSAIDynfKg==, tableContent=null), ArticleFig(id=1322926233008349778, tenantId=1146029695717560320, journalId=1255847919539208197, articleId=1322926196048142836, language=EN, label=null, caption=null, figureFileSmall=JXmH4PlkPArTbYyc6fVSCg==, figureFileBig=74cbaZxQHpJvhFtYn+YcgA==, tableContent=null), ArticleFig(id=1322926233121595987, tenantId=1146029695717560320, journalId=1255847919539208197, articleId=1322926196048142836, language=CN, label=图2, caption=各组大鼠肠道菌群Chao1指数稀释曲线(A),Shannon指数稀释曲线(B),PCA分析图(C)及PCoA分析图(D), figureFileSmall=JXmH4PlkPArTbYyc6fVSCg==, figureFileBig=74cbaZxQHpJvhFtYn+YcgA==, tableContent=null), ArticleFig(id=1322926233385837140, tenantId=1146029695717560320, journalId=1255847919539208197, articleId=1322926196048142836, language=EN, label=null, caption=null, figureFileSmall=ttllzSHyTXL1OTGSUjS6Mw==, figureFileBig=w5nha4w6YcfUHVWHIS5u4w==, tableContent=null), ArticleFig(id=1322926233478111829, tenantId=1146029695717560320, journalId=1255847919539208197, articleId=1322926196048142836, language=CN, label=图3, caption=各组大鼠肠道菌群属水平丰度排名前30的堆叠图(A),LEfSe分析图(B),组间非参数因子秩和检验筛选差异菌属图(C)及关键差异肠道菌属与Elisa指标相关性分析图(D), figureFileSmall=ttllzSHyTXL1OTGSUjS6Mw==, figureFileBig=w5nha4w6YcfUHVWHIS5u4w==, tableContent=null), ArticleFig(id=1322926233780101718, tenantId=1146029695717560320, journalId=1255847919539208197, articleId=1322926196048142836, language=EN, label=null, caption=null, figureFileSmall=null, figureFileBig=null, tableContent=
组别n5-HT/(ng/mL)GABA/(μmol/L)AChE/(nmol/L)PGD2/(pg/mL)
QSZR组62.68±0.13ab0.99±0.11ab37.42±4.67abc288.31±36.25
QBDK组62.81±0.21ab1.00±0.10ab35.94±4.77abc307.27±29.75
QXHQ组62.99±0.29ab1.19±0.11abc38.60±1.89abc265.79±16.92
QBB组63.10±0.32ab1.17±0.13ab37.74±2.86abc283.53±21.21
C组63.91±0.221.59±0.0646.00±2.73277.91±40.74
M组61.89±0.06a0.62±0.03a28.46±1.78b293.43±24.86
S-4组62.91±0.21ab1.06±0.10ab31.75±3.97a299.85±27.84
SZR组62.45±0.15abc0.87±0.11abc29.37±3.09a303.22±21.62
BDK组63.13±0.19ab1.18±0.12abc37.95±2.12abc264.80±29.81
XHQ组62.93±0.22ab1.01±0.03ab35.20±2.79ab296.48±30.90
BB组62.51±0.16abc0.89±0.10abc30.84±3.77a287.15±35.77
Y组63.66±0.23bc1.40±0.09abc39.06±1.79abc287.95±45.09
F值37.3439.5614.221.15
P值<0.001<0.001<0.0010.343
), ArticleFig(id=1322926235482989143, tenantId=1146029695717560320, journalId=1255847919539208197, articleId=1322926196048142836, language=CN, label=表1, caption=

各组大鼠血清5-HT、GABA、AChE、PGD2水平比较(±s)

, figureFileSmall=null, figureFileBig=null, tableContent=
组别n5-HT/(ng/mL)GABA/(μmol/L)AChE/(nmol/L)PGD2/(pg/mL)
QSZR组62.68±0.13ab0.99±0.11ab37.42±4.67abc288.31±36.25
QBDK组62.81±0.21ab1.00±0.10ab35.94±4.77abc307.27±29.75
QXHQ组62.99±0.29ab1.19±0.11abc38.60±1.89abc265.79±16.92
QBB组63.10±0.32ab1.17±0.13ab37.74±2.86abc283.53±21.21
C组63.91±0.221.59±0.0646.00±2.73277.91±40.74
M组61.89±0.06a0.62±0.03a28.46±1.78b293.43±24.86
S-4组62.91±0.21ab1.06±0.10ab31.75±3.97a299.85±27.84
SZR组62.45±0.15abc0.87±0.11abc29.37±3.09a303.22±21.62
BDK组63.13±0.19ab1.18±0.12abc37.95±2.12abc264.80±29.81
XHQ组62.93±0.22ab1.01±0.03ab35.20±2.79ab296.48±30.90
BB组62.51±0.16abc0.89±0.10abc30.84±3.77a287.15±35.77
Y组63.66±0.23bc1.40±0.09abc39.06±1.79abc287.95±45.09
F值37.3439.5614.221.15
P值<0.001<0.001<0.0010.343
), ArticleFig(id=1322926235889836632, tenantId=1146029695717560320, journalId=1255847919539208197, articleId=1322926196048142836, language=EN, label=null, caption=null, figureFileSmall=null, figureFileBig=null, tableContent=
组别nSP/(ng/mL)VIP/(pg/mL)GAS/(pg/mL)
QSZR组67.44±0.62150.42±29.09b218.81±36.89b
QBDK组66.84±0.89139.85±20.26b216.57±21.08b
QXHQ组66.86±1.23157.17±17.79201.95±38.91a
QBB组67.36±0.97156.90±31.52232.90±16.02b
C组67.44±0.69152.51±17.35228.46±13.48
M组67.65±0.71186.32±21.66a185.53±18.04a
S-4组67.08±0.74154.57±15.44b214.28±28.03b
SZR组66.88±0.60179.23±38.87219.39±18.33b
BDK组67.30±0.95180.37±31.38220.45±17.55b
XHQ组67.17±1.10150.79±36.49b231.05±9.71b
BB组66.86±0.98188.85±31.85ac243.09±16.14bc
Y组67.19±0.66150.79±24.15b202.59±18.14
F值0.592.17218.14
P值0.8260.0290.005
), ArticleFig(id=1322926235990499929, tenantId=1146029695717560320, journalId=1255847919539208197, articleId=1322926196048142836, language=CN, label=表2, caption=

各组大鼠血清SP、VIP、GAS水平比较(±s)

, figureFileSmall=null, figureFileBig=null, tableContent=
组别nSP/(ng/mL)VIP/(pg/mL)GAS/(pg/mL)
QSZR组67.44±0.62150.42±29.09b218.81±36.89b
QBDK组66.84±0.89139.85±20.26b216.57±21.08b
QXHQ组66.86±1.23157.17±17.79201.95±38.91a
QBB组67.36±0.97156.90±31.52232.90±16.02b
C组67.44±0.69152.51±17.35228.46±13.48
M组67.65±0.71186.32±21.66a185.53±18.04a
S-4组67.08±0.74154.57±15.44b214.28±28.03b
SZR组66.88±0.60179.23±38.87219.39±18.33b
BDK组67.30±0.95180.37±31.38220.45±17.55b
XHQ组67.17±1.10150.79±36.49b231.05±9.71b
BB组66.86±0.98188.85±31.85ac243.09±16.14bc
Y组67.19±0.66150.79±24.15b202.59±18.14
F值0.592.17218.14
P值0.8260.0290.005
), ArticleFig(id=1322926236317655642, tenantId=1146029695717560320, journalId=1255847919539208197, articleId=1322926196048142836, language=EN, label=null, caption=null, figureFileSmall=null, figureFileBig=null, tableContent=
组别n结肠INOS/(ng/g)下丘脑INOS/(ng/g)
QSZR组6115.46±34.79108.15±41.91
QBDK组6117.60±33.57103.59±36.45b
QXHQ组6128.95±39.97125.56±27.23a
QBB组6137.30±27.52117.76±35.61a
C组6109.74±25.5381.15±26.48
M组6147.67±22.53a141.64±21.77a
S-4组6109.77±23.13b99.23±33.34b
SZR组6145.99±36.11ac128.91±18.98a
BDK组6133.28±24.4294.35±25.28b
XHQ组6139.03±34.39132.46±25.19a
BB组6135.55±22.51110.93±38.36
Y组6130.79±41.63124.49±33.01a
F值1.091.93
P值0.3850.054
), ArticleFig(id=1322926236716114523, tenantId=1146029695717560320, journalId=1255847919539208197, articleId=1322926196048142836, language=CN, label=表3, caption=

各组大鼠结肠与下丘脑组织中INOS水平比较(±s)

, figureFileSmall=null, figureFileBig=null, tableContent=
组别n结肠INOS/(ng/g)下丘脑INOS/(ng/g)
QSZR组6115.46±34.79108.15±41.91
QBDK组6117.60±33.57103.59±36.45b
QXHQ组6128.95±39.97125.56±27.23a
QBB组6137.30±27.52117.76±35.61a
C组6109.74±25.5381.15±26.48
M组6147.67±22.53a141.64±21.77a
S-4组6109.77±23.13b99.23±33.34b
SZR组6145.99±36.11ac128.91±18.98a
BDK组6133.28±24.4294.35±25.28b
XHQ组6139.03±34.39132.46±25.19a
BB组6135.55±22.51110.93±38.36
Y组6130.79±41.63124.49±33.01a
F值1.091.93
P值0.3850.054
), ArticleFig(id=1322926236800000604, tenantId=1146029695717560320, journalId=1255847919539208197, articleId=1322926196048142836, language=EN, label=null, caption=null, figureFileSmall=null, figureFileBig=null, tableContent=
组别nChao1指数observed species指数Goods coverage指数
QSZR组6967.19±71.65b963.17±71.34b0.999 518±0.000 282b
QBDK组6854.50±142.89850.33±141.140.999 478±0.000 206b
QXHQ组6867.59±167.16863.83±169.130.999 547±0.000 236b
QBB组6834.83±113.64832.67±113.240.999 645±0.000 116
C组6718.82±95.31717.00±95.000.999 743±0.000 164
M组6775.33±98.15774.17±97.570.999 768±0.000 124
S-4组6798.63±139.46794.67±138.240.999 561±0.000 179
SZR组6775.05±95.01772.50±94.490.999 630±0.000 149
BDK组6753.27±77.25750.50±77.360.999 623±0.000 161
XHQ组6895.75±116.03889.67±115.990.999 333±0.000 164b
BB组6834.28±152.14830.17±151.850.999 460±0.000 084b
Y组6797.08±87.46793.17±85.630.999 561±0.000 248
F值2.0331.9942.582
P值0.0410.0450.009
), ArticleFig(id=1322926237173293661, tenantId=1146029695717560320, journalId=1255847919539208197, articleId=1322926196048142836, language=CN, label=表4, caption=

各组大鼠粪便菌群丰富度比较(±s)

, figureFileSmall=null, figureFileBig=null, tableContent=
组别nChao1指数observed species指数Goods coverage指数
QSZR组6967.19±71.65b963.17±71.34b0.999 518±0.000 282b
QBDK组6854.50±142.89850.33±141.140.999 478±0.000 206b
QXHQ组6867.59±167.16863.83±169.130.999 547±0.000 236b
QBB组6834.83±113.64832.67±113.240.999 645±0.000 116
C组6718.82±95.31717.00±95.000.999 743±0.000 164
M组6775.33±98.15774.17±97.570.999 768±0.000 124
S-4组6798.63±139.46794.67±138.240.999 561±0.000 179
SZR组6775.05±95.01772.50±94.490.999 630±0.000 149
BDK组6753.27±77.25750.50±77.360.999 623±0.000 161
XHQ组6895.75±116.03889.67±115.990.999 333±0.000 164b
BB组6834.28±152.14830.17±151.850.999 460±0.000 084b
Y组6797.08±87.46793.17±85.630.999 561±0.000 248
F值2.0331.9942.582
P值0.0410.0450.009
), ArticleFig(id=1322926237571752542, tenantId=1146029695717560320, journalId=1255847919539208197, articleId=1322926196048142836, language=EN, label=null, caption=null, figureFileSmall=null, figureFileBig=null, tableContent=
组别nShannon指数Simpson指数
QSZR组67.74±0.380.98±0.02
QBDK组67.03±0.980.96±0.03
QXHQ组66.95±0.940.95±0.06b
QBB组67.36±0.600.97±0.03
C组67.07±0.520.97±0.01
M组67.61±0.470.99±0.01
S-4组66.94±0.990.95±0.06
SZR组67.00±0.660.96±0.05
BDK组67.21±0.460.97±0.03
XHQ组67.72±0.440.98±0.01
BB组67.33±0.500.98±0.01
Y组67.25±0.450.97±0.03
F值1.1990.990
P值0.3070.466
), ArticleFig(id=1322926240079946335, tenantId=1146029695717560320, journalId=1255847919539208197, articleId=1322926196048142836, language=CN, label=表5, caption=

各组大鼠粪便菌群多样性指数比较(±s)

, figureFileSmall=null, figureFileBig=null, tableContent=
组别nShannon指数Simpson指数
QSZR组67.74±0.380.98±0.02
QBDK组67.03±0.980.96±0.03
QXHQ组66.95±0.940.95±0.06b
QBB组67.36±0.600.97±0.03
C组67.07±0.520.97±0.01
M组67.61±0.470.99±0.01
S-4组66.94±0.990.95±0.06
SZR组67.00±0.660.96±0.05
BDK组67.21±0.460.97±0.03
XHQ组67.72±0.440.98±0.01
BB组67.33±0.500.98±0.01
Y组67.25±0.450.97±0.03
F值1.1990.990
P值0.3070.466
), ArticleFig(id=1322926240541319776, tenantId=1146029695717560320, journalId=1255847919539208197, articleId=1322926196048142836, language=EN, label=null, caption=null, figureFileSmall=null, figureFileBig=null, tableContent=
组别n异杆菌梭状芽孢杆菌杜氏杆菌双歧杆菌
QSZR组62.024±1.084ab0.565±0.287b0.034±0.009b0.068±0.033b
QBDK组63.209±3.561b0.959±1.120b0.119±0.061b0.194±0.123b
QXHQ组63.091±1.510b0.980±1.038b0.162±0.139b0.355±0.226b
QBB组64.428±4.072b0.780±0.355b0.097±0.086b0.167±0.123b
C组65.853±3.9201.375±0.8470.149±0.1160.200±0.104
M组610.232±3.970a2.622±1.340a1.448±0.494a1.055±0.348a
S-4组61.352±0.972ab0.920±0.768b0.074±0.062b0.200±0.360b
SZR组62.660±1.736ab0.953±0.566b0.071±0.046b0.073±0.045b
BDK组61.660±1.338ab0.859±0.534b0.017±0.010b0.057±0.053b
XHQ组61.759±1.402ab0.608±0.578b0.066±0.046b0.058±0.041b
BB组60.787±0.552ab1.331±0.623b0.024±0.015b0.027±0.032b
Y组65.252±3.847bc1.135±0.584b0.077±0.067b0.189±0.168b
F值5.7582.88637.73414.716
P值<0.0010.004<0.001<0.001
组别n红蝽菌UCG_002丁酸弧菌副沙门氏菌
QSZR组60.005±0.005b0.127±0.183b0.285±0.142
QBDK组60.013±0.009b0.061±0.077b0.167±0.100b
QXHQ组60.064±0.055b0.207±0.323b0.247±0.301b
QBB组60.010±0.013b0.194±0.299b0.183±0.075b
C组60.005±0.0060.036±0.0250.142±0.090
M组60.357±0.166a1.385±1.324a0.591±0.492a
S-4组60.005±0.004b0.078±0.036b0.192±0.126b
SZR组60.022±0.026b1.623±1.549ac0.373±0.242
BDK组60.008±0.010b0.318±0.175b0.848±0.392ac
XHQ组60.026±0.025b0.119±0.244b0.767±0.438ac
BB组60.001±0.003b0.140±0.236b0.439±0.193
Y组60.023±0.021b0.228±0.505b0.759±0.416ac
F值21.7594.3034.872
P值<0.001<0.001<0.001
), ArticleFig(id=1322926241006887521, tenantId=1146029695717560320, journalId=1255847919539208197, articleId=1322926196048142836, language=CN, label=表6, caption=

各组大鼠粪便中关键差异菌属丰度比较(±s)

, figureFileSmall=null, figureFileBig=null, tableContent=
组别n异杆菌梭状芽孢杆菌杜氏杆菌双歧杆菌
QSZR组62.024±1.084ab0.565±0.287b0.034±0.009b0.068±0.033b
QBDK组63.209±3.561b0.959±1.120b0.119±0.061b0.194±0.123b
QXHQ组63.091±1.510b0.980±1.038b0.162±0.139b0.355±0.226b
QBB组64.428±4.072b0.780±0.355b0.097±0.086b0.167±0.123b
C组65.853±3.9201.375±0.8470.149±0.1160.200±0.104
M组610.232±3.970a2.622±1.340a1.448±0.494a1.055±0.348a
S-4组61.352±0.972ab0.920±0.768b0.074±0.062b0.200±0.360b
SZR组62.660±1.736ab0.953±0.566b0.071±0.046b0.073±0.045b
BDK组61.660±1.338ab0.859±0.534b0.017±0.010b0.057±0.053b
XHQ组61.759±1.402ab0.608±0.578b0.066±0.046b0.058±0.041b
BB组60.787±0.552ab1.331±0.623b0.024±0.015b0.027±0.032b
Y组65.252±3.847bc1.135±0.584b0.077±0.067b0.189±0.168b
F值5.7582.88637.73414.716
P值<0.0010.004<0.001<0.001
组别n红蝽菌UCG_002丁酸弧菌副沙门氏菌
QSZR组60.005±0.005b0.127±0.183b0.285±0.142
QBDK组60.013±0.009b0.061±0.077b0.167±0.100b
QXHQ组60.064±0.055b0.207±0.323b0.247±0.301b
QBB组60.010±0.013b0.194±0.299b0.183±0.075b
C组60.005±0.0060.036±0.0250.142±0.090
M组60.357±0.166a1.385±1.324a0.591±0.492a
S-4组60.005±0.004b0.078±0.036b0.192±0.126b
SZR组60.022±0.026b1.623±1.549ac0.373±0.242
BDK组60.008±0.010b0.318±0.175b0.848±0.392ac
XHQ组60.026±0.025b0.119±0.244b0.767±0.438ac
BB组60.001±0.003b0.140±0.236b0.439±0.193
Y组60.023±0.021b0.228±0.505b0.759±0.416ac
F值21.7594.3034.872
P值<0.001<0.001<0.001
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蒙药苏格木勒-4汤及其拆方与单药对失眠模型大鼠肠道菌群的影响
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都丽娜 1 , 杨德志 2 , 乌兰 1 , 美丽 1 , 吴萨如拉 1 , 巴雅苏拉 1 , 包永昌 1 , 苏日古格其其格 1 , 松林 1
中华中医药学刊 | 省级项目平台 2025,43(7): 239-245
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中华中医药学刊 |省级项目平台 2025 , 43 (7) : 239 -245
蒙药苏格木勒-4汤及其拆方与单药对失眠模型大鼠肠道菌群的影响
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都丽娜(1996-),女(蒙古族),内蒙古赤峰人,博士在读,研究方向:蒙医方剂配伍规律。

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都丽娜(1996-),女(蒙古族),内蒙古赤峰人,博士在读,研究方向:蒙医方剂配伍规律。

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都丽娜1, 杨德志2, 乌兰1, 美丽1, 吴萨如拉1, 巴雅苏拉1, 包永昌1, 苏日古格其其格1, 松林1
作者信息
  • 1.内蒙古医科大学蒙医药学院,内蒙古 呼和浩特 010010
  • 2.内蒙古自治区国际蒙医医院,内蒙古 呼和浩特 010013
通讯作者:
松林(1972-),男(蒙古族),内蒙古通辽人,教授,博士研究生导师,博士,研究方向:蒙医药研究。E-mail:。
作者简介:

都丽娜(1996-),女(蒙古族),内蒙古赤峰人,博士在读,研究方向:蒙医方剂配伍规律。

Effects of Mongolian Medicine Sugemule-4 Decoction and Its Decomposed Formula and Single Drug on Gut-microbiota in Insomnia Model Rats
Lina DU1, Dezhi YANG2, Lan WU1, Li MEI1, Sarula WU1, Yasula BA1, Yongchang BAO1, Rigugaqiqige SU1, Lin SONG1
Affiliations
  • 1.Inner Mongolia Medical University,Hohhot 010110,Inner Mongolia,China
  • 2.Inner Mongolia International Mongolian Hospital,Hohhot 010065,Inner Mongolia,China
出版时间: 2025-07-10 doi: 10.13193/j.issn.1673-7717.2025.07.049
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目的

基于肠道菌群,探讨苏格木勒-4汤的配伍规律。

方法

72只SPF级雄性SD大鼠,随机分为空白组(C)、模型组(M)、苏格木勒-4汤组(S-4)、缺酸枣仁方组(QSZR)、缺白豆蔻方组(QBDK)、缺香旱芹方组(QXHQ)、缺荜茇方组(QBB)、酸枣仁组(SZR)、白豆蔻组(BDK)、香旱芹组(XHQ)、荜茇组(BB)、安神补脑液组(Y)。使用慢性不可预知温和应激刺激(chronic unpredictable mild stimulation,CUMS)+对氯苯丙氨酸(parachlorophenylalanine,PCPA)法建立失眠大鼠模型。造模后分别给予相应药物治疗7 d,剂量为1.215 g/kg,C组和M组均给予等量蒸馏水,Y组剂量为1.8 mL/kg。比较治疗后各组大鼠一般状态与结肠组织形态,血清中5-羟色胺(5-hydroxytryptamine,5-HT)、γ-氨基丁酸(γ-aminobutyric acid,GABA)、乙酰胆碱(acetylcholine,AChE)、前列腺素D2(prostaglandin D2,PGD2)、P物质(substance P,SP)、血管活性肠肽(vasoactive intestinal peptide,VIP)、胃泌素(gastrin,GAS)含量,结肠组织与下丘脑组织中诱导型一氧化氮合酶(inducible nitric oxide synthase,iNOS)含量,以及肠道菌群16S核糖体DNA(16Sribosomal DNA identification,16SrDNA)。

结果

治疗结束后M组大鼠昼夜节律紊乱甚至消失,精神状态变差,其余各组精神状态较治疗前有不同程度好转。结肠组织HE染色显示治疗各组均可不同程度改善模型大鼠病理变化。M 组大鼠血清中5-HT、GABA、AChE、GAS、VIP水平显著改变(P<0.05),结肠与下丘脑INOS水平显著升高(P<0.05)。S-4组能显著改善这些变化(P<0.05)。方中白豆蔻对失眠相关神经递质水平调控能力最强,香旱芹对脑肠肽水平调控能力最强,荜茇对结肠与下丘脑组织中INOS水平调控能力最强。从肠道菌群属水平对各组肠道微生物群落进行分析,多个分组间比较采用线性判别效应量分析(LEfSe),筛选出关键差异菌属7种,并通过分析发现方中各个组分可不同程度调节肠道菌群的紊乱,进一步探讨肠道菌属与所检测ELISA指标之间的关系,得知红蝽菌UCG_002与下丘脑组织INOS呈显著正相关,丁酸弧菌与结肠组织INOS、血清VIP呈显著正相关,双歧杆菌与血清GAS呈显著负相关。

结论

苏格木勒-4汤及其拆方与单药可不同程度的改善失眠模型大鼠体内失眠相关神经递质、脑肠肽含量及肠道菌群的变化。

拆方  /  配伍规律  /  肠道菌群  /  失眠  /  苏格木勒-4汤
Objective

Based on gut microbiota,to explore the compatibility rules of Sugemule-4 Decoction.

Method

Seventy-two SPF grade male SD rats were randomly divided into control group(C),model group(M),Sugemule-4 Decoction group(S-4),lack of Suanzaoren(Ziziphi Spinosae Semen)formula group(QSZR),lack of Baidoukou(Amomum kravanh Pierre ex Gagnep)formula group(QBDK),lack of Xianghanqin(Cuminum cyminum L.)formula group(QXHQ),lack of Biba(Piperis Longi Fructus)formula group(QBB),Suanzaoren(Ziziphi Spinosae Semen)group(SZR),Baidoukou(Amomum kravanh Pierre ex Gagnep)group(BDK),Xianghanqin(Cuminum cyminum L.)group(XHQ),Biba(Piperis Longi Fructus)group(BB),Anshen Bunao Liquid(安神补脑液)group(Y). An insomnia rat model was established by using chronic unpredictable mild stress stimulation(CUMS)+parachlorophenylalanine(PCPA)method. After modeling,the corresponding drugs were administered for 7 days at a dose of 1.215 g/kg. Both group Cand group M were given the equal amounts of distilled water,while Group Y received a dose of 1.8 mL/kg. The general state and colon tissue morphology of rats in each group were compared after treatment,as well as the levels of 5-hydroxytryptamine(5-HT),γ-aminobutyric acid(GABA),acetylcholine(AChE),prostaglandin D2(PGD2),substance P(SP),vasoactive intestinal peptide(VIP)and gastrin(GAS)in serum,inducible nitric oxide synthase(INOS)content in colon and hypothalamic tissues,and 16SrDNA analysis of gut microbiota.

Results

After treatment,the circadian rhythm of the M group rats was disrupted or even disappeared,and their mental state deteriorated. The mental state of the other groups improved to varying degrees compared to those before treatment. Colon tissue HE staining showed that each treatment group could improve the pathological changes of the model rats to varying degrees. The serum levels of 5-HT,GABA,AChE,GASand VIP in group M rats were significantly altered(P<0.05),while the levels of INOSin the colon and hypothalamus were significantly increased(P<0.05). The S-4 group was able to significantly improve these changes(P<0.05). Baidoukou(Amomum kravanh Pierre ex Gagnep)had the strongest regulatory ability on insomnia related neurotransmitter levels,Xianghanqin(Cuminum cyminum L.)had the strongest regulatory ability on brain gut peptide levels,and Biba(Piperis Longi Fructus)had the strongest regulatory ability on INOSlevels in colon and hypothalamic tissues. The gut microbiota of each group at the level of gut microbiota genera was analyzed,linear discriminant effect analysis(LEfSe)was used to compare multiple groups,and 7 key differential bacterial genera were selected. Through analysis,it was found that each component in the formula can regulate the disorder of gut microbiota to varying degrees. Further exploring the relationship between the gut microbiota genus and the ELISA indicators detected in this article,it was found that the Coriobacteriaceae_UCG_002 showed a significant positive correlation with INOSin hypothalamic tissue,Anaerostipes showed a significant positive correlation with INOSin colon tissue and serum VIP,and Bifidobacterium showed a significant negative correlation with serum GAS.

Conclusion

Sugemule-4 Decoction and its split formula can improve the changes of insomnia related neurotransmitters,brain-gut peptide content and intestinal microbiota in the body of insomnia model rats to varying degrees.

decomposed formula  /  compatibility rules  /  gut microbiota  /  insomnia  /  Sugemule-4 Decoction
都丽娜, 杨德志, 乌兰, 美丽, 吴萨如拉, 巴雅苏拉, 包永昌, 苏日古格其其格, 松林. 蒙药苏格木勒-4汤及其拆方与单药对失眠模型大鼠肠道菌群的影响. 中华中医药学刊, 2025 , 43 (7) : 239 -245 . DOI: 10.13193/j.issn.1673-7717.2025.07.049
Lina DU, Dezhi YANG, Lan WU, Li MEI, Sarula WU, Yasula BA, Yongchang BAO, Rigugaqiqige SU, Lin SONG. Effects of Mongolian Medicine Sugemule-4 Decoction and Its Decomposed Formula and Single Drug on Gut-microbiota in Insomnia Model Rats[J]. Chinese Archives of Traditional Chinese Medicine, 2025 , 43 (7) : 239 -245 . DOI: 10.13193/j.issn.1673-7717.2025.07.049
失眠症是最常见的睡眠障碍,伴随着生活压力越来越大,失眠的发生率正在逐年上升[1],约三分之一的人受到失眠症状困扰[2],是对人体身心健康造成严重损害的病症[3]。越来越多的证据表明,菌群-肠-脑轴直接或间接地调节睡眠行为,并可能在睡眠障碍的病因和发病机制中发挥关键作用[4]。睡眠不足导致肠道菌群功能障碍,睡眠障碍常伴有肠道菌群组成的改变[5]。在脑肠互动过程中,脑肠肽既分布于神经系统,又分布于消化系统,而肠道菌群可间接参与中枢神经系统的调控,与大脑有双向通信功能[6],尤其在昼夜节律和睡眠中发挥着重要作用[7]。5-羟色胺(5-hydroxytryptamine,5-HT)、P物质(substance P,SP)、血管活性肠肽(vasoactive intestinal peptide,VIP)、胃泌素(gastrin,GAS)等脑肠肽与睡眠障碍直接有关[8]。5-HT、γ-氨基丁酸(γ-aminobutyric acid,GABA)、乙酰胆碱(acetylcholine,AChE)、前列腺素D2(prostaglandin D2,PGD2)等神经递质均是调节睡眠不可或缺神经递质[9-10],其中5-HT、GABA属于抑制性神经递质,可通过抑制神经元活动或神经传导而发挥镇静的作用[9]。诱导型一氧化氮合酶(inducible nitric oxide synthase,iNOS)是负责产生一氧化氮(nitric oxide,NO)的酶,在正常条件下不存在于大多数细胞中[11]。iNOS合成的NO 与包括炎症在内的各种病理生理过程有关[12],而炎症可以促进睡眠障碍的发生发展[13]。
苏格木勒-4汤是国医大师苏荣扎布教授的常用验方,由酸枣仁、白豆蔻、香旱芹和荜茇组成,主治赫依偏盛引起的失眠[14]。杨蕊、果佳霖等基于GC-MS技术鉴定了其挥发油成分并通过实验证实,苏格木勒-4汤可升高小鼠大脑皮层组织中5-HT、GABA、甘氨酸、去甲肾上腺素,降低多巴胺、谷氨酸含量,从而减缓失眠症状[15-16]。但他们所述的苏格木勒-4汤与本方有所差异(未使用香旱芹而是选择使用其替代药物白苣胜)。课题组前期研究表明苏格木勒-4汤能改善失眠模型大鼠的一般状态及行为学改变,升高血清与脑组织中AChE、5-HT及GABA含量,改善失眠[17]。蒙医学认为,失眠可能与赫依偏盛与血交搏,侵入心、主脉、神经、白脉等有关[18],此方中以镇赫依药为先导,治疗失眠的内因为主,且单味药材酸枣仁、白豆蔻、荜茇等都有治失眠、保护脑神经的作用[8,19-20]。而组方中单味药物在全方中的贡献作用尚不明确。因此,为进一步探讨组方药物的调控作用及其之间可能存在的协同作用,探讨这4种药物对神经递质、脑肠肽、结肠组织与下丘脑组织中INOS含量,以及肠道菌群的不同影响。现报道如下。
72只雄性SPF级SD大鼠,体质量为(200±20)g,3~8周龄,实验动物购自北京斯贝福动物有限责任公司,生产许可证号SCXK(京)2019-0010。饲养于温度(22±2)℃,相对湿度45%~65%的动物房中,光照条件设置为12 h的明/暗循环,大鼠可随意饮水和摄食。伦理审查编号:YKD202302055。
对氯苯丙氨酸(parachlorophenylalanine,PCPA)从SIGMA公司购得。无水乙醇(货号:100092683)、二甲苯(货号:10023418)、中性树胶(货号:10004160)从国药集团化学试剂有限公司购得,HE染液套装(货号:G1003)从Servicebio公司购得。AChE(货号:RX302125R)、5-HT(货号:RX303050R)、GABA(货号:RX303082R)、SP(货号:RX302949R)、VIP(货号:RX302215R)、GAS(货号:RX302271R)、PGD2(货号:RXJ302409R)及INOS(货号:RX301689R)ELISA试剂盒从睿信生物购得。
炒酸枣仁(批号:2109001)、白豆蔻(批号:C357210602)、香旱芹(批号:20220401)、荜茇(批号:2104001)药材饮片购于内蒙古天盛蒙中医药有限责任公司,由内蒙古医科大学蒙医药学院松林教授鉴定为真。安神补脑液从吉林敖东延边药业股份有限公司(批号:2111281)购得。取15倍处方量药材饮片(炒酸枣仁15 g,白豆蔻15 g,香旱芹10 g,荜茇5 g),粉碎过80目筛,加水450 mL,浸泡1 h,加盖煮沸30 min,煎煮后将药液于150目药典筛中过滤,冷却,置于-30℃速冻,再进行减压冷冻干燥。各缺方(缺炒酸枣仁、缺白豆蔻、缺香旱芹或缺荜茇)和各单味药材(炒酸枣仁,白豆蔻,香旱芹,荜茇)按上述煎煮方法,投料量与处方一致。
SD大鼠适应性饲养1周后,随机分为空白组(C)(n=6)和造模组(n=66),连续14 d对造模组大鼠给予慢性不可预知温和应激刺激(chronic unpredictable mild stimulation,CUMS),即实验第1天禁食禁水24 h、第2天铺垫湿垫料24 h、第3天强制在5℃冰水中游泳10 min、第4天强制在40℃热水中游泳10 min、第5天夹尾1 min、第6天使鼠笼倾斜45°角24 h、第7天持续光照24 h,循环两个周期,于最后2 d将PCPA制成45 mg/mL的浓度以每100 g给予1 mL的量连续腹腔注射。正常对照组大鼠前12 d不进行任何处理,最后2 d给予相同剂量的生理盐水腹腔注射。造模结束后进行一般状态观察,评估造模是否成功,体征观察包括于实验结束后观察各组大鼠皮毛、精神、活动、睡眠、饮食饮水、排泄等状态。当大鼠出现昼夜节律紊乱、白天活动不停、毛发杂乱、兴奋性增强、攻击性增强等显著的行为学改变表明大鼠失眠模型制备成功。
将造模组随机分为模型组(M)、苏格木勒-4汤组(S-4 1.215 g/kg)、缺酸枣仁方组(QSZR 1.215 g/kg)、缺白豆蔻方组(QBDK 1.215 g/kg)、缺香旱芹方组(QXHQ 1.215 g/kg)、缺荜茇方组(QBB 1.215 g/kg)、酸枣仁组(SZR 1.215 g/kg)、白豆蔻组(BDK 1.215 g/kg)、香旱芹组(XHQ 1.215 g/kg)、荜茇组(BB 1.215 g/kg)、安神补脑液组(Y 1.8 mL/kg)。C组和M组均给予等量蒸馏水。每日定时给药相应药物1次,连续给药7 d。
于最后一次给药前观察一般状态并收集新鲜粪便,用于检测肠道菌群,禁食不禁水12 h。最后一次给药2 h后,异氟烷麻醉,取血,置于低速离心机中20 min,分离血清,存放于-80℃冰箱,直至进行分析。解剖取一段结肠组织,于10%的多聚甲醛中固定,用于HE染色。
石蜡切片脱蜡至水:依次将切片放入二甲苯Ⅰ20 min→二甲苯Ⅱ20 min→无水乙醇Ⅰ5 min→无水乙醇Ⅱ5 min→75%酒精5 min,自来水洗;苏木素染色:切片入苏木素染液染3~5 min,自来水洗,分化液分化,自来水洗,返蓝液返蓝,流水冲洗;伊红染色:切片依次入85%、95%的梯度酒精脱水各5 min,入伊红染液中染色5 min;脱水封片:切片依次放入无水乙醇Ⅰ5 min→无水乙醇Ⅱ5 min→无水乙醇Ⅲ5 min→二甲Ⅰ5 min→二甲苯Ⅱ5 min透明,中性树胶封片;显微镜镜检,图像采集分析。
取出ELISA试剂盒,室温平衡30 min,从-80℃冰箱中取出待检测大鼠血清与脑组织样本,室温解冻。分别进行标准品的稀释、各孔加样、温育、配制洗涤液、洗涤、加酶、显色、终止,测定。详细步骤均按照说明书严谨进行。
采用16SrDNA基因测序技术进行检测。取样本,采用DNA提取试剂盒对样本总DNA进行抽提,采用超微量分光光度计对DNA进行定量,再通过琼脂糖凝胶电泳分析其质量。以341F(5'-CCTACGGGNGGCWGCAG-3')和805R(5'-GACTACHVGGGTATCTAATCC-3')为引物对V3-V4可变区进行PCR扩增,每个样品用特异性条形码标记引物的5'端,并对通用引物进行测序。PCR产物通过AMPure XT珠纯化,并通过Qubit定量。制备扩增子池用于测序,并分别在生物分析仪和Illumina文库定量试剂盒上评估扩增子文库的大小和数量。在NovaSeq PE250平台上对文库进行测序。对原始数据进行序列质控、去噪、拼接、去嵌合等处理后,得到有效数据。通过随机归一化到相同的序列,使用QIIME软件对α和β多样性、物种注释、菌群结构组成及差异进行分析。
实验数据均采用SPSS 26.0统计软件进行分析,采用表示,两独立样本比较采用t检验,多样本均数比较用单因素方差分析(OnewayANOVA)。如果实验数据为非正态性分布,则采用秩和检验(Kruskal-WallisH检验)。对4种缺方和单药进行加权排名赋分,例如4种单药组中对某一观测指标的排名为SZR>BDK>XHQ>BB,那就对酸枣仁、白豆蔻、香旱芹、荜茇依次赋分4、3、2、1;4种拆方组中对某一观测指标的排名为QSZR>QBDK>QXHQ>QBB,那就对酸枣仁、白豆蔻、香旱芹、荜茇依次赋分1、2、3、4,再将两组的相应分数相加,假设检测的一类指标有4个,而每个指标的权重都分别为25%(一类检测指标中,每个指标的权重相同,C组与M组无显著差异的指标不计入其内),酸枣仁在这4个指标中得分分别为8、6、4和4分。那么,酸枣仁的加权总分可以通过以下计算得出:总分=(8×0.25)+(6×0.25)+(4×0.25)+(4×0.25)=2+1.5+1+1=5.5分,并通过得分排名评价这味单药对整方的贡献。相关性采用Spearman相关系数分析。以P<0.05为差异具有统计学意义。
造模前各组大鼠精神状态良好,活泼好动,情绪平和,皮毛顺滑有光泽。造模后与C组对比,M组大鼠昼夜节律紊乱甚至消失,饮食、饮水量减少,皮毛晦暗易脱落,兴奋性增强,攻击性增强。给予药物治疗后精神状态较治疗前有不同程度好转,活动增多,反应迅速,饮食饮水量恢复,皮毛逐渐恢复光泽。
HE染色可见:C与QXHQ组未见明显病理变化,M组大鼠肠组织表面绒毛变少,肠组织可见少量黏膜上皮细胞脱落,固有层肠腺排列疏松,可见固有层有少量肠腺消失,伴有少量淋巴细胞浸润。QBB组肠组织可见少量黏膜上皮细胞脱落,其他各组均伴有少量淋巴细胞浸润。详见插页LⅧ图1。
ELISA检测分析各组大鼠血清失眠相关神经递质水平,发现造模后,5-HT、GABA、AChE水平显著降低(P<0.05),PGD2水平无显著改变,显示失眠模型大鼠神经递质水平失衡。给药干预后,S-4组5-HT、GABA明显升高(P<0.05),AChE有升高趋势,但差异无统计学意义(P>0.05),Y组5-HT、GABA、AChE明显升高(P<0.05),表明安神补脑液与苏格木勒-4汤能同时调节5-HT、GABA和AChE水平,具有改善神经递质失衡的作用;拆方及单药干预研究显示4种拆方及4种单药均能显著改善血清5-HT、GABA水平(P<0.05),4种拆方、BDK和XHQ组均能改善血清AChE水平(P<0.05),SZR组与BB组有升高AChE水平的趋势,但无统计学意义(P>0.05)。从表1可见,对5-HT的改善能力BDK>XHQ>BB>SZR及QBB>QXHQ>QBDK>QSZR,综合可知白豆蔻对5-HT改善能力最强,其次是酸枣仁与香旱芹,荜茇最弱;对GABA的改善能力BDK>XHQ>BB>SZR及QXHQ>QBB>QBDK>QSZR,综合可知白豆蔻对GABA改善能力最强,其次是酸枣仁、香旱芹与荜茇最弱;对AChE的改善能力BDK>XHQ>BB>SZR及QXHQ>QBB>QSZR>QBDK,综合可知白豆蔻对AChE改善能力最强,酸枣仁,香旱芹与荜茇改善能力相同。由此可见白豆蔻对失眠相关神经递质水平调控能力最强。
ELISA检测分析各组大鼠血清脑肠肽水平,发现造模后,VIP水平显著升高(P<0.05),GAS水平显著降低(P<0.05),SP水平有升高趋势,但差异无统计学意义(P>0.05),显示失眠模型大鼠脑肠肽水平失衡。给药干预后,S-4组VIP显著降低(P<0.05),GAS明显升高(P<0.05),SP有降低趋势,但差异无统计学意义(P>0.05),Y组VIP明显降低(P<0.05),GAS有升高趋势,SP有降低趋势,但差异无统计学意义(P>0.05),表明安神补脑液与苏格木勒-4汤能不同程度地调节SP、VIP、GAS水平,具有改善脑肠肽失衡的作用;拆方及单药干预研究显示XHQ、QSZR、QBDK组能改善血清VIP水平(P<0.05),BB组外其他各组有降低VIP水平的趋势,但无统计学意义(P>0.05);QXHQ组外其他各组均能明显改善血清GAS水平(P<0.05),QXHQ组有升高GAS水平的趋势,但无统计学意义(P>0.05);4种拆方与4种单药组均有降低SP水平的趋势,但无统计学意义(P>0.05)。从表2可见,对VIP的改善能力XHQ>SZR>BDK>BB及QBDK>QSZR>QBB>QXHQ,综合可知香旱芹对VIP的改善能力最强,其次是酸枣仁与荜茇,白豆蔻最弱;对GAS的改善能力BB>XHQ>BDK>SZR及QBB>QSZR>QBDK>QXHQ,综合可知香旱芹对GAS改善能力最强,其次是白豆蔻和荜茇,酸枣仁最弱。由此可见香旱芹对脑肠肽水平调控能力最强。
ELISA检测分析各组大鼠INOS水平,发现造模后,结肠组织与下丘脑组织中INOS水平显著升高(P<0.05),给药干预后,S-4组结肠组织与下丘脑组织中INOS水平显著降低(P<0.05),Y组下丘脑组织和结肠组织中INOS水平有降低趋势,但差异无统计学意义(P>0.05),表明安神补脑液与苏格木勒-4汤能不同程度地调节结肠组织与下丘脑组织中INOS水平,具有调节INOS的作用,但苏格木勒-4汤调节能力更强;拆方及单药干预研究显示4种拆方及4种单药均有改善结肠组织中INOS水平的趋势,但无统计学意义(P>0.05);BDK组与QBDK组能明显改善下丘脑INOS水平(P<0.05),其他各组有改善下丘脑INOS水平的趋势,但无统计学意义(P>0.05)。从表3可见,对结肠组织和下丘脑组织INOS水平改善能力BDK>BB>SZR>XHQ及QBDK>QSZR>QBB>QXHQ,综合可知荜茇对结肠组织INOS的改善能力最强,其次是白豆蔻与香旱芹,酸枣仁最弱。由此可见荜茇对INOS水平调控能力最强。
为了探讨MMS-4D对失眠大鼠肠道微生物群组成的调节中的潜在作用,我们对大鼠粪便进行了16SrDNA基因测序。经过质量控制后,从72个检测样本中生成了14 011个ASV特征序列,并用于以下分析。随后,通过Chao1和Shannon稀释曲线(插页LⅨ图2A、插页LⅨ图2B)和4个alpha多样性指数,即基于Chao1、Shannon和来评估细菌群落的丰度和多样性。当序列数增加到5000时,多样本稀疏曲线趋于平坦,说明所有样本群落丰富度、多样性、覆盖度、均匀度良好,测序数据量足够大,可充分反映各组大鼠粪便样本中绝大部分的肠道微生物多样性信息,能用于后续微生物组学分析。Chao1、observed species指数反映菌群丰富度,Shannon、Simpson反映菌群多样性,Goods coverage可以评估测序结果是否代表样本中微生物的真实情况,由表4、表5可知,均goods coverage>0.999,说明样本真实可信。与正常组比较,模型组大鼠粪便菌群Chao1、observed species、Shannon、Simpson呈上升趋势,差异无统计学意义;与模型组比较,SZR、BDK组大鼠粪便菌群observed species、Chao1指数呈下调趋势,剩余各组呈上升趋势。除QSZR组外剩余各组的Shannon指数呈下调趋势,所有治疗组Simpson指数呈下调趋势。
接下来,我们使用主成分分析(principal component analysis,PCA)、主坐标分析(principal coordinates analysis,PCoA)等方法来评估不同群体间肠道微生物群的beta多样性。PCA分析显示,各组大鼠的微生物群组成有明显的聚类(插页LⅨ图2C)。同时,PCoA分析显示,各组大鼠肠道微生物群组成有显著差异(插页LⅨ图2D),Anosim(Analysis of similarities)相似性分析结果显示-1<R=0.404 569<1,P=0.001<0.05,表明检验12组间的差异显著大于组内差异,说明12组大鼠的整体肠道微生物组成存在差异。
从肠道菌群属水平对各组肠道微生物群落进行分析,共获得648个细菌属分类物种,Romboutsia和UCG-005在所有12个组中均占优势,丰度排名前30的堆叠图见插页LⅨ图3A。相较于C组,M组大鼠肠道菌群构成中28种菌属发生了显著变化。与模型组比较,药物处理后可不同程度地逆转这种改变。
多个分组间比较采用线性判别效应量分析(LEfSe),结果见插页LⅩ图3B。各组中富集的差异菌属用不同颜色表示,根据线性判别分析值(LDAscore)大于3、组间非参数因子秩和检验筛选差异菌属,见插页LⅩ图3C。如表6所示,与C组比较,M组异杆菌(Allobaculum)、梭状芽孢杆菌(Clostridium_sensu_stricto_1)、杜氏杆菌(Dubosiella)、双歧杆菌(Bifidobacterium)、红蝽菌UCG_002(Coriobacteriaceae_UCG_002)、丁酸弧菌(Anaerostipes)、副沙门氏菌(Parasutterella)丰度升高(P<0.05)。与M组相比苏格木勒-4汤与安神补脑液均具有减少失眠模型大鼠肠道内有害菌的作用(P<0.05);拆方及单药干预研究显示4种拆方及4种单药均能改善肠道内异杆菌、梭状芽孢杆、杜氏杆菌、双歧杆菌、红蝽菌UCG_002的丰度(P<0.05);除SZR外其他各组均能改善丁酸弧菌丰度(P<0.05);QBDK、QXHQ、QBB组能显著改善副沙门氏菌丰度。从表6可见,对异杆菌的改善能力荜茇最强,酸枣仁最弱;对梭状芽孢杆菌的改善能力香旱芹最强,酸枣仁最弱;对杜氏杆菌的改善能力白豆蔻最强,酸枣仁最弱;对双歧杆菌的改善能力白豆蔻、香旱芹、荜茇相同,酸枣仁最弱;对红蝽菌UCG_002的改善能力白豆蔻最强,酸枣仁最弱;对丁酸弧菌的改善能力香旱芹与荜茇较强,白豆蔻与酸枣仁较弱;对副沙门氏菌的改善能力酸枣仁最强,白豆蔻最弱。
为进一步探讨肠道菌属与本文所检测ELISA指标之间的关系,采用spearman相关性分析考察了两者间的相关性。从插页LⅨ图3D可见红蝽菌UCG_002与下丘脑组织INOS呈显著正相关,丁酸弧菌与结肠组织INOS与血清VIP呈显著正相关。双歧杆菌与血清GAS呈显著负相关。上述菌属可能在苏格木勒-4汤改善失眠作用中具有较重要的介导作用,其作用有待进一步深入研究和验证。
肠道菌群作为神经递质的主要生产力,在肠道内能调节肠神经元细胞合成GABA、5-HT等神经递质,并影响中枢神经系统功能[21]。GABA作为一种主要的抑制性神经递质,有助于维持中枢神经系统神经元兴奋和抑制的整体平衡,在大脑发育和功能中起着核心作用之一[22]。研究证实大多数镇静催眠的草药共有的主要药理作用机制是通过神经递质GABA或通过刺激γ-氨基丁酸受体A起作用[23]。5-HT是一种血管收缩剂,在中枢神经系统中具有关键且明确的作用,包括调节情绪稳定性、疼痛耐受性或睡眠模式等[24]。也有研究表明失眠的发生常常伴随AChE含量的改变[25]。PGD2可诱导睡眠,并可能在睡眠和神经系统疾病中发挥作用[26]。所以本研究通过拆解苏格木勒-4汤,从血清神经递质GABA、5-HT、AChE、PGD2含量切入,探讨了苏格木勒-4汤中调节中枢神经递质的组分。发现苏格木勒-4汤能同时调节5-HT、GABA和AChE水平,具有改善神经递质失衡的作用,4种组分中白豆蔻对失眠相关神经递质水平调控能力最强。
肠道菌群-肠道肽相互作用在调节肠-脑信号传导中具有重要意义[27]。SP是中枢神经系统中分布最广泛的神经肽,它参与许多生理和病理生理过程,包括压力和焦虑相关行为[28]。VIP是一种28个氨基酸的神经肽,对神经元、上皮和内分泌细胞功能的发育、生长和控制具有多种生理和病理作用,进而调节离子分泌、营养吸收、肠道蠕动、血糖控制、致癌、免疫反应和昼夜节律[29-30]。胃泌素由黏膜G细胞合成和释放,作为经典的肠道激素和强效神经递质,存在于胃肠道、中枢神经系统和周围神经元中[31]。本研究通过拆解苏格木勒-4汤,发现苏格木勒-4汤能不同程度地调节血清脑肠肽SP、VIP、GAS含量,进一步探讨了苏格木勒-4汤中调节脑肠肽的组分。发现4种组分中香旱芹对脑肠肽调控能力最强。另外通过观察结肠组织HE染色发现,全方、4种拆方及4种单药均能改善失眠模型大鼠结肠组织的病理改变。
INOS和NO也是肠道中非常重要的递质,INOS含量升高会使NO含量增加,导致平滑肌松弛[32]。而大脑中INOS与NO的表达与睡眠与觉醒紧密相关[33]。我们的研究证实CUMS+PCPA造模后,模型大鼠结肠组织及下丘脑组织中INOS的含量的确会产生显著改变。苏格木勒-4汤能显著改善结肠组织与下丘脑组织中INOS水平。4种组分中香荜茇对INOS水平调控能力最强。
肠道菌群不仅可以影响肠道生理,还可以影响中枢神经系统。研究发现,肠道菌群可能是睡眠机制的关键调节者[34]。研究表明异杆菌,梭状芽孢杆菌,杜氏杆菌,红蝽菌UCG_002,副沙门氏菌与人类肠道炎症有关[35-38],丁酸弧菌与副沙门氏菌与重度抑郁症[39]有关。本研究中苏格木勒-4汤能有效减少失眠模型大鼠肠道内有害菌的丰度。这从侧面证实肠道菌群以及肠道功能的改变与失眠症的发生有关联,我们的相关性研究更加印证了这一点。4个组分对这些有害菌群都可发挥一定的抑制作用。
综上所述,苏格木勒-4汤及其拆方与单药可不同程度地改善失眠模型大鼠体内失眠相关神经递质、脑肠肽含量及肠道菌群的变化,从而改善肠道状态,缓解失眠。4个组分之间比较,白豆蔻对神经递质、香旱芹对脑肠肽、荜茇对INOS水平改善最强,4个组分对有害菌群都可发挥一定的抑制作用,各有各的优势。一起组成了对失眠有显著疗效的苏格木勒-4汤。
  • 内蒙古自治区草原英才领军个人(乌兰)项目(DC2100002252)
  • 内蒙古自治区中医药(蒙医药)中青年领军人才项目(2022—〔RC015〕)
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2025年第43卷第7期
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doi: 10.13193/j.issn.1673-7717.2025.07.049
  • 首发时间:2026-10-30
  • 出版时间:2025-07-10
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内蒙古自治区草原英才领军个人(乌兰)项目(DC2100002252)
内蒙古自治区中医药(蒙医药)中青年领军人才项目(2022—〔RC015〕)
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    1.内蒙古医科大学蒙医药学院,内蒙古 呼和浩特 010010
    2.内蒙古自治区国际蒙医医院,内蒙古 呼和浩特 010013

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松林(1972-),男(蒙古族),内蒙古通辽人,教授,博士研究生导师,博士,研究方向:蒙医药研究。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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