Article(id=1304388181445603517, tenantId=1146029695717560320, journalId=1302319053441957962, issueId=1304388108988997783, articleNumber=null, orderNo=null, doi=10.7501/j.issn.0253-2670.2026.12.005, pmid=null, cstr=null, oa=null, hot=0, price=null, onlineType=0, articleFormat=0, articleType=null, articleTypeStr=null, receivedDate=1770912000000, receivedDateStr=2026-02-13, revisedDate=null, revisedDateStr=null, acceptedDate=null, acceptedDateStr=null, onlineDate=1788919976816, onlineDateStr=2026-09-09, pubDate=null, pubDateStr=null, doiRegisterDate=null, doiRegisterDateStr=null, onlineIssueDate=1788919976816, onlineIssueDateStr=2026-09-09, onlineJustAcceptDate=null, onlineJustAcceptDateStr=null, onlineFirstDate=null, onlineFirstDateStr=null, sourceXml=null, magXml=null, createTime=1788919976816, creator=13701087609, updateTime=1788919976816, updator=13701087609, issue=Issue{id=1304388108988997783, tenantId=1146029695717560320, journalId=1302319053441957962, year='2026', volume='57', issue='12', pageStart='4509', pageEnd='4948', issueExtLink='null', onlineDate='null', pubDate='1782576000000', pubDateStr='2026-06-28', beforeIssueId=null, nextIssueId=null, price=null, status=1, issueComplete=1, articleOrder=1, issueType=-1, specialIssue=null, createTime=1788919959542, creator='13701087609', updateTime=1788923461082, updator='13701087609', preIssue=null, nextIssue=null, articleTotal=null, ext={EN=IssueExt(id=1304402795579330582, tenantId=1146029695717560320, journalId=1302319053441957962, issueId=1304388108988997783, language=EN, specialIssueTitle=, coverIllustrator=null, specialIssueEditor=, specialIssueAbout=), CN=IssueExt(id=1304402795579330583, tenantId=1146029695717560320, journalId=1302319053441957962, issueId=1304388108988997783, language=CN, specialIssueTitle=, coverIllustrator=null, specialIssueEditor=, specialIssueAbout=)}, issueFiles=null, downloadFileDto=null}, startPage=4553, endPage=4569, ext={EN=ArticleExt(id=1304388183249154239, articleId=1304388181445603517, tenantId=1146029695717560320, journalId=1302319053441957962, language=EN, title=Analysis of blood-absorbed and brain-absorbed components of Kaixin San in normal and depressive model rats, columnId=null, journalTitle=Chinese Traditional and Herbal Drugs, columnName=null, runingTitle=null, highlight=null, articleAbstract=Objective To systematically analyze the blood-absorbed and brain-absorbed components of the classical formula Kaixin San (KXS) in normal and depression model rats, and preliminarily elucidate the pharmacological material basis of its antidepressant effect. Methods A depression model rat was established using the chronic unpredictable mild stress (CUMS) method, and behavioral verification was performed through open field test, novel object recognition test, sucrose preference test, and forced swimming test. The components in the serum and brain tissue from normal and model rats after intragastric administration of KXS were comprehensively analyzed by UPLC-Q-Exactive Orbitrap MS/MS. Results In the control rats, 143 (including 47 prototypes and 96 metabolites) and 11 components were identified in serum and brain tissue, respectively. In contrast, the overall number in the depression model rats significantly decreased, with only 83 (including 28 prototypes and 55 metabolites) and 4 components detected in serum and brain tissue, respectively. Among them, four prototype components were confirmed to cross the brain in serum and brain tissue samples of the CUMS model rats, including β-asarone, ginsenoside Rg1 , ginsenoside Rb1 , and polygalaxanthone III. Conclusion This study identified four key active components from the blood-absorbed and brain-absorbed components of KXS in normal and depression model rats, providing experimental evidence for screening quality markers of KXS and in-depth analysis its antidepressant mechanism., authors=ZHANG Xiaoqian, YANG Xuan, GAO Yu, ZHAN Ting, Xing Chengjie, XIE Pengfei, ZENG Hanrui, MO Zhangchenyu, SHI Wenjin, ZHANG Caiyun, authorsList=ZHANG Xiaoqian, YANG Xuan, GAO Yu, ZHAN Ting, Xing Chengjie, XIE Pengfei, ZENG Hanrui, MO Zhangchenyu, SHI Wenjin, ZHANG Caiyun, authorCompany=null, 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=1304388183161073854, articleId=1304388181445603517, tenantId=1146029695717560320, journalId=1302319053441957962, language=CN, title=开心散在正常与抑郁模型大鼠体内的入血与入脑成分分析, columnId=1304140187169214944, journalTitle=中草药, columnName=化学成分, runingTitle=null, highlight=null, articleAbstract=目的 系统分析经典名方开心散在正常与抑郁模型大鼠体内的入血及入脑成分,初步揭示其抗抑郁作用的药效物质基础。方法 采用慢性不可预知温和应激(chronic unpredicted mild stress,CUMS)法构建抑郁模型大鼠,并通过旷场实验、新物体识别实验、糖水偏好实验和强迫游泳实验进行行为学验证;随后,运用UPLC-Q-Exactive Orbitrap MS/MS技术,对正常组与模型组大鼠ig开心散后血清及脑组织样本进行系统检测与分析。结果 在正常组大鼠血清和脑组织中分别鉴定出143个(47个原型+96个代谢物)和11个成分;而在抑郁模型组中整体数量显著减少,仅分别鉴定出83个(28个原型+55个代谢物)和4个成分。其中,在CUMS模型组血清和脑组织样本中均检测到β-细辛醚、人参皂苷Rg₁、人参皂苷Rb₁和远志𠮿酮Ⅲ能直接透过血脑屏障的原型成分。结论 初步明确了开心散在正常和抑郁模型大鼠体内的入血及入脑成分,鉴定出4个关键活性成分,为后续开心散的质量标志物筛选和深入抗抑郁作用机制解析提供了科学实验基础。, authors=张晓倩1,2,3,4 , 杨璇1,2,3,4 , 高裕1,2,3,4 , 詹婷1,2,3,4 , 邢承洁1,2,3,4 , 谢鹏飞1,2,3,4 , 曾韩睿1,2,3,4 , 莫张晨雨1,2,3,4 , 施文锦1,2,3,4 , 张彩云1,2,3,4 , authorsList=张晓倩, 杨璇, 高裕, 詹婷, 邢承洁, 谢鹏飞, 曾韩睿, 莫张晨雨, 施文锦, 张彩云, authorCompany=1 安徽中医药大学药学院,新安医学与中医药现代化研究所,安徽合肥 230012; 2 药物制剂技术与应用安徽省重点实验室,安徽省教育厅现代药物制剂工程技术研究中心,安徽合肥 230012; 3 安徽省道地中药材品质提升创新协同中心,安徽省中医药科学院药物制剂研究所,安徽合肥 230012; 4 中药复方安徽省重点实验室,安徽合肥 230012, correspAuthors=张彩云, authorNote=张晓倩: 张晓倩,女,博士研究生,研究方向为中药制剂。E-mail:zhangxq@stu.ahtcm.edu.cn, correspAuthorsNote=null, copyrightStatement=null, copyrightOwner=null, extLink=null, articleAbsUrl=null, sourceXml=null, magXml=null, pdfUrl=null, pdf=YMPk15rWDe3BAbDkvSvZPQ==, pdfFileSize=2486865, 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=合肥综合性国家科学中心大健康研究院新安医学与中医药现代化研究所“揭榜挂帅”项目 (2023CXMMTCM014); 安徽省科技厅自然基金项目 (2408085MH229); 安徽省科技重大专项项目 (202203a07020031))}, authors=null, keywords=[Keyword(id=1304401912112116609, tenantId=1146029695717560320, journalId=1302319053441957962, articleId=1304388181445603517, language=CN, orderNo=1, keyword=开心散), 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Advances in the treatment of depression [J]. Int Clin Psychopharmacol, 2022, 37(5): 183-184. Chao S. Overview of depression [J]. Emerg Med Clin North Am, 2024, 42(1): 105-113. Agerbo E, Trabjerg B B, Børglum A D, et al. Risk of early-onset depression associated with polygenic liability, parental psychiatric history, and socioeconomic status [J]. JAMA Psychiatry, 2021, 78(4): 387-397. Sampogna G, Toni C, Catapano P, et al. New trends in personalized treatment of depression [J]. Curr Opin Psychiatry, 2024, 37(1): 3-8. 雷舒扬, 王丽颖, 朱爱松. 从“因虚致郁, 因郁化毒, 因毒损心”探讨冠心病伴发抑郁状态的病机及治疗[J]. 北京中医药大学学报, 2023, 46(11): 1605-1610. 冯彩玲, 邓慧芳, 张六燕, 等. 疏肝护心汤联合氟哌噻吨美利曲辛治疗冠心病术后伴焦虑抑郁的疗效分析[J]. 广州中医药大学学报, 2023, 40(7): 1615-1620. 乔怡倩. 慢性应激对肠道屏障及结直肠癌肝转移的影响[D]. 石家庄: 河北医科大学, 2023. Terao I, Tsuge T, Endo K, et al. Comparative efficacy, tolerability and acceptability of intravenous racemic ketamine with intranasal esketamine, aripiprazole and lithium as augmentative treatments for treatment-resistant unipolar depression: A systematic review and network Meta-analysis [J]. J Affect Disord, 2024, 346: 49-56. 姚莉, 高可平. 清心疏肝方联合子午流注针法治疗脑卒中后肝气郁结型抑郁的效果[J]. 河南医学研究, 2024, 33(1): 156-159. Zhuang W, Liu S L, Xi S Y, et al. Traditional Chinese medicine decoctions and Chinese patent medicines for the treatment of depression: Efficacies and mechanisms [J]. J Ethnopharmacol, 2023, 307: 116272. Qu W, Liu S, Zhang W J, et al. Impact of traditional Chinese medicine treatment on chronic unpredictable mild stress-induced depression-like behaviors: Intestinal microbiota and gut microbiome function [J]. Food Funct, 2019, 10(9): 5886-5897. Sun C Y, Gao M Z, Qiao M Q. Research progress of traditional Chinese medicine compound “Xiaochaihu Decoction” in the treatment of depression [J]. Biomed Pharmacother, 2023, 159: 114249. Zhao W D, Ji C, Zheng J, et al. Effects of Xiaoyao San on exercise capacity and liver mitochondrial metabolomics in rat depression model [J]. Chin Herb Med, 2024, 16(1): 132-142. 国家中医药管理局. 国家中医药管理局关于发布《古代经典名方目录(第一批)》的通知[EB/OL]. (2018-04-13) [2019-05-20]. https://www.gov.cn/zhengce/zhengceku/ 2018-12/31/content_5429153.htm. 孙永康, 孙田烨, 李明远, 等. 开心散现代药理作用及作用机制研究[J]. 中国中医基础医学杂志, 2021, 27(4): 650-654. 易腾达, 李玉丽, 牛林强, 等. 经典名方开心散及类方的古代文献考证[J]. 中国实验方剂学杂志, 2021, 27(5): 8-15. B Shekhawat P, B Pokharkar V. Understanding peroral absorption: Regulatory aspects and contemporary approaches to tackling solubility and permeability hurdles [J]. Acta Pharm Sin B, 2017, 7(3): 260-280. 刘文静. 应用超高效液相色谱串联质谱法分析清热凉血方的成分[D]. 北京: 北京中医药大学, 2018. 马聪玉, 生宁, 李元元, 等. 中药成分质谱分析新技术和新策略进展[J]. 质谱学报, 2021, 42(5): 709-717. 易可可, 谢洁, 龚晓云, 等. 液相色谱-串联质谱应用研究进展[J]. 计量科学与技术, 2021, 65(2): 7-15. Kumar A, Saini G, Nair A, et al. UPLC: A preeminent technique in pharmaceutical analysis [J]. Acta Pol Pharm, 2012, 69(3): 371-380. 杨青, 田冶, 江志钦, 等. 液质联用技术在抗生素分析中的应用[J]. 中国药物评价, 2022, 39(2): 113-118. 熊陈思慧, 定天明, 刘杰, 等. 超高效液相色谱-线性离子阱/静电场轨道阱高分辨质谱法快速检测化妆品中22种功效成分[J]. 色谱, 2022, 40(9): 817-824. 张定堃, 林俊芝, 秦春凤, 等. 微粉化对穿心莲内酯粉体学性质和溶出度的影响[J]. 中国医药工业杂志, 2014, 45(4): 325-329. Chen J J, Li T, Huang D H, et al. Integrating UHPLC-MS/MS quantitative analysis and exogenous purine supplementation to elucidate the antidepressant mechanism of Chaigui Granules by regulating purine metabolism [J]. J Pharm Anal, 2023, 13(12): 1562-1576. Wen J X, Yang Y, Hao J J. Acori Tatarinowii Rhizoma: A comprehensive review of its chemical composition, pharmacology, pharmacokinetics and toxicity [J]. Front Pharmacol, 2023, 14: 1090526. Zhao X, Cui Y L, Wu P, et al. Polygalae Radix: A review of its traditional uses, phytochemistry, pharmacology, toxicology, and pharmacokinetics [J]. Fitoterapia, 2020, 147: 104759. Liu X L, Zhong C, Xie J, et al. Geographical region traceability of Poria cocos and correlation between environmental factors and biomarkers based on a metabolomic approach [J]. Food Chem, 2023, 417: 135817. 李浩然, 董萍萍, 李华健, 等. 基于UHPLC-Q-Exactive Orbitrap MS/MS快速分析开心散物质基准中的化学成分[J]. 中国中药杂志, 2022, 47(4): 938-950. 杨璇, 李俊莹, 单晓晓, 等. 开心散化学成分、药理作用的研究进展及质量标志物的预测分析[J]. 中国中药杂志, 2023, 48(8): 2077-2085. Wang H Q, Zheng R F, Ai Q D, et al. Ginsenoside Rg1 alleviates chronic stress-induced depression in rats by targeting Cx43-YAP axis [J]. Acta Pharmacol Sin, 2025, 46(7): 1877-1891. Hermes L, Römermann J, Cramer B, et al. Phase II metabolism of asarone isomers in vitro and in humans using HPLC-MS/MS and HPLC-QTOF/MS [J]. Foods, 2021, 10(9): 2032. Zhao G D, Ma Y F, Wang X, et al. Configurational alteration results in change in hepatotoxicity of asarone [J]. J Agric Food Chem, 2023, 71(1): 884-894. Dong H Y, Gao Z Y, Rong H, et al. β-Asarone reverses chronic unpredictable mild stress-induced depression-like behavior and promotes hippocampal neurogenesis in rats [J]. Molecules, 2014, 19(5): 5634-5649. Wang Z F, Huang P G, Wang N B, et al. β-Asarone inhibits autophagy by activating the PI3K/Akt/mTOR pathway in a rat model of depression in Parkinson’s disease [J]. Behav Brain Res, 2024, 465: 114966. Yu S Q, Yin Z, Ling M, et al. Ginsenoside Rg1 enriches gut microbial indole-3-acetic acid to alleviate depression-like behavior in mice via oxytocin signaling [J]. Phytomedicine, 2024, 135: 156186. Jia K K, Pan S M, Wu W Y, et al. Ginsenoside Rg1 exerts antidepressant effect by regulating hepatic kynurenine metabolism through promoting the interaction between HNF4α and PGC1α [J]. J Ginseng Res, 2025, 49(2): 179-188. Li C F, Zhang Q P, Cheng J, et al. Role of ginsenoside Rb1 in attenuating depression-like symptoms through astrocytic and microglial complement C3 pathway [J]. Metab Brain Dis, 2024, 39(6): 1039-1050. Wang G L, An T Y, Lei C, et al. Antidepressant-like effect of ginsenoside Rb1 on potentiating synaptic plasticity via the miR-134-mediated BDNF signaling pathway in a mouse model of chronic stress-induced depression [J]. J Ginseng Res, 2022, 46(3): 376-386.)
中草药
|化学成分
2026
, 57
(12) :
4553
-4569
开心散在正常与抑郁模型大鼠体内的入血与入脑成分分析
全屏
张晓倩1,2,3,4 , 杨璇1,2,3,4 , 高裕1,2,3,4 , 詹婷1,2,3,4 , 邢承洁1,2,3,4 , 谢鹏飞1,2,3,4 , 曾韩睿1,2,3,4 , 莫张晨雨1,2,3,4 , 施文锦1,2,3,4 , 张彩云1,2,3,4
作者信息
1 安徽中医药大学药学院,新安医学与中医药现代化研究所,安徽合肥 230012; 2 药物制剂技术与应用安徽省重点实验室,安徽省教育厅现代药物制剂工程技术研究中心,安徽合肥 230012; 3 安徽省道地中药材品质提升创新协同中心,安徽省中医药科学院药物制剂研究所,安徽合肥 230012; 4 中药复方安徽省重点实验室,安徽合肥 230012
通讯作者:
张彩云
作者简介:
张晓倩: 张晓倩,女,博士研究生,研究方向为中药制剂。E-mail:zhangxq@stu.ahtcm.edu.cn
Analysis of blood-absorbed and brain-absorbed components of Kaixin San in normal and depressive model rats
ZHANG Xiaoqian, YANG Xuan, GAO Yu, ZHAN Ting, Xing Chengjie, XIE Pengfei, ZENG Hanrui, MO Zhangchenyu, SHI Wenjin, ZHANG Caiyun
Affiliations
doi: 10.7501/j.issn.0253-2670.2026.12.005
文章导航
目的 系统分析经典名方开心散在正常与抑郁模型大鼠体内的入血及入脑成分,初步揭示其抗抑郁作用的药效物质基础。方法 采用慢性不可预知温和应激(chronic unpredicted mild stress,CUMS)法构建抑郁模型大鼠,并通过旷场实验、新物体识别实验、糖水偏好实验和强迫游泳实验进行行为学验证;随后,运用UPLC-Q-Exactive Orbitrap MS/MS技术,对正常组与模型组大鼠ig开心散后血清及脑组织样本进行系统检测与分析。结果 在正常组大鼠血清和脑组织中分别鉴定出143个(47个原型+96个代谢物)和11个成分;而在抑郁模型组中整体数量显著减少,仅分别鉴定出83个(28个原型+55个代谢物)和4个成分。其中,在CUMS模型组血清和脑组织样本中均检测到β-细辛醚、人参皂苷Rg₁、人参皂苷Rb₁和远志𠮿酮Ⅲ能直接透过血脑屏障的原型成分。结论 初步明确了开心散在正常和抑郁模型大鼠体内的入血及入脑成分,鉴定出4个关键活性成分,为后续开心散的质量标志物筛选和深入抗抑郁作用机制解析提供了科学实验基础。
开心散
/
UPLC-Q-Exactive Orbitrap MS/MS
/
抑郁症
/
入血成分
/
入脑成分
Objective To systematically analyze the blood-absorbed and brain-absorbed components of the classical formula Kaixin San (KXS) in normal and depression model rats, and preliminarily elucidate the pharmacological material basis of its antidepressant effect. Methods A depression model rat was established using the chronic unpredictable mild stress (CUMS) method, and behavioral verification was performed through open field test, novel object recognition test, sucrose preference test, and forced swimming test. The components in the serum and brain tissue from normal and model rats after intragastric administration of KXS were comprehensively analyzed by UPLC-Q-Exactive Orbitrap MS/MS. Results In the control rats, 143 (including 47 prototypes and 96 metabolites) and 11 components were identified in serum and brain tissue, respectively. In contrast, the overall number in the depression model rats significantly decreased, with only 83 (including 28 prototypes and 55 metabolites) and 4 components detected in serum and brain tissue, respectively. Among them, four prototype components were confirmed to cross the brain in serum and brain tissue samples of the CUMS model rats, including β-asarone, ginsenoside Rg1 , ginsenoside Rb1 , and polygalaxanthone III. Conclusion This study identified four key active components from the blood-absorbed and brain-absorbed components of KXS in normal and depression model rats, providing experimental evidence for screening quality markers of KXS and in-depth analysis its antidepressant mechanism.
Kaixin San
/
UPLC-Q-Exactive Orbitrap MS/MS
/
depression
/
blood-absorbed components
/
brain-absorbed components
张晓倩, 杨璇, 高裕, 詹婷, 邢承洁, 谢鹏飞, 曾韩睿, 莫张晨雨, 施文锦, 张彩云.
开心散在正常与抑郁模型大鼠体内的入血与入脑成分分析.
中草药,
2026
, 57
(12)
: 4553
-4569
.
DOI: 10.7501/j.issn.0253-2670.2026.12.005
ZHANG Xiaoqian, YANG Xuan, GAO Yu, ZHAN Ting, Xing Chengjie, XIE Pengfei, ZENG Hanrui, MO Zhangchenyu, SHI Wenjin, ZHANG Caiyun.
Analysis of blood-absorbed and brain-absorbed components of Kaixin San in normal and depressive model rats[J].
Chinese Traditional and Herbal Drugs ,
2026
, 57
(12)
: 4553
-4569
.
DOI: 10.7501/j.issn.0253-2670.2026.12.005
合肥综合性国家科学中心大健康研究院新安医学与中医药现代化研究所“揭榜挂帅”项目 (2023CXMMTCM014); 安徽省科技厅自然基金项目 (2408085MH229); 安徽省科技重大专项项目 (202203a07020031)
参考文献
引证文献
Serretti A. Advances in the treatment of depression [J]. Int Clin Psychopharmacol, 2022, 37(5): 183-184. Chao S. Overview of depression [J]. Emerg Med Clin North Am, 2024, 42(1): 105-113. Agerbo E, Trabjerg B B, Børglum A D, et al. Risk of early-onset depression associated with polygenic liability, parental psychiatric history, and socioeconomic status [J]. JAMA Psychiatry, 2021, 78(4): 387-397. Sampogna G, Toni C, Catapano P, et al. New trends in personalized treatment of depression [J]. Curr Opin Psychiatry, 2024, 37(1): 3-8. 雷舒扬, 王丽颖, 朱爱松. 从“因虚致郁, 因郁化毒, 因毒损心”探讨冠心病伴发抑郁状态的病机及治疗[J]. 北京中医药大学学报, 2023, 46(11): 1605-1610. 冯彩玲, 邓慧芳, 张六燕, 等. 疏肝护心汤联合氟哌噻吨美利曲辛治疗冠心病术后伴焦虑抑郁的疗效分析[J]. 广州中医药大学学报, 2023, 40(7): 1615-1620. 乔怡倩. 慢性应激对肠道屏障及结直肠癌肝转移的影响[D]. 石家庄: 河北医科大学, 2023. Terao I, Tsuge T, Endo K, et al. Comparative efficacy, tolerability and acceptability of intravenous racemic ketamine with intranasal esketamine, aripiprazole and lithium as augmentative treatments for treatment-resistant unipolar depression: A systematic review and network Meta-analysis [J]. J Affect Disord, 2024, 346: 49-56. 姚莉, 高可平. 清心疏肝方联合子午流注针法治疗脑卒中后肝气郁结型抑郁的效果[J]. 河南医学研究, 2024, 33(1): 156-159. Zhuang W, Liu S L, Xi S Y, et al. Traditional Chinese medicine decoctions and Chinese patent medicines for the treatment of depression: Efficacies and mechanisms [J]. J Ethnopharmacol, 2023, 307: 116272. Qu W, Liu S, Zhang W J, et al. Impact of traditional Chinese medicine treatment on chronic unpredictable mild stress-induced depression-like behaviors: Intestinal microbiota and gut microbiome function [J]. Food Funct, 2019, 10(9): 5886-5897. Sun C Y, Gao M Z, Qiao M Q. Research progress of traditional Chinese medicine compound “Xiaochaihu Decoction” in the treatment of depression [J]. Biomed Pharmacother, 2023, 159: 114249. Zhao W D, Ji C, Zheng J, et al. Effects of Xiaoyao San on exercise capacity and liver mitochondrial metabolomics in rat depression model [J]. Chin Herb Med, 2024, 16(1): 132-142. 国家中医药管理局. 国家中医药管理局关于发布《古代经典名方目录(第一批)》的通知[EB/OL]. (2018-04-13) [2019-05-20]. https://www.gov.cn/zhengce/zhengceku/ 2018-12/31/content_5429153.htm. 孙永康, 孙田烨, 李明远, 等. 开心散现代药理作用及作用机制研究[J]. 中国中医基础医学杂志, 2021, 27(4): 650-654. 易腾达, 李玉丽, 牛林强, 等. 经典名方开心散及类方的古代文献考证[J]. 中国实验方剂学杂志, 2021, 27(5): 8-15. B Shekhawat P, B Pokharkar V. Understanding peroral absorption: Regulatory aspects and contemporary approaches to tackling solubility and permeability hurdles [J]. Acta Pharm Sin B, 2017, 7(3): 260-280. 刘文静. 应用超高效液相色谱串联质谱法分析清热凉血方的成分[D]. 北京: 北京中医药大学, 2018. 马聪玉, 生宁, 李元元, 等. 中药成分质谱分析新技术和新策略进展[J]. 质谱学报, 2021, 42(5): 709-717. 易可可, 谢洁, 龚晓云, 等. 液相色谱-串联质谱应用研究进展[J]. 计量科学与技术, 2021, 65(2): 7-15. Kumar A, Saini G, Nair A, et al. UPLC: A preeminent technique in pharmaceutical analysis [J]. Acta Pol Pharm, 2012, 69(3): 371-380. 杨青, 田冶, 江志钦, 等. 液质联用技术在抗生素分析中的应用[J]. 中国药物评价, 2022, 39(2): 113-118. 熊陈思慧, 定天明, 刘杰, 等. 超高效液相色谱-线性离子阱/静电场轨道阱高分辨质谱法快速检测化妆品中22种功效成分[J]. 色谱, 2022, 40(9): 817-824. 张定堃, 林俊芝, 秦春凤, 等. 微粉化对穿心莲内酯粉体学性质和溶出度的影响[J]. 中国医药工业杂志, 2014, 45(4): 325-329. Chen J J, Li T, Huang D H, et al. Integrating UHPLC-MS/MS quantitative analysis and exogenous purine supplementation to elucidate the antidepressant mechanism of Chaigui Granules by regulating purine metabolism [J]. J Pharm Anal, 2023, 13(12): 1562-1576. Wen J X, Yang Y, Hao J J. Acori Tatarinowii Rhizoma: A comprehensive review of its chemical composition, pharmacology, pharmacokinetics and toxicity [J]. Front Pharmacol, 2023, 14: 1090526. Zhao X, Cui Y L, Wu P, et al. Polygalae Radix: A review of its traditional uses, phytochemistry, pharmacology, toxicology, and pharmacokinetics [J]. Fitoterapia, 2020, 147: 104759. Liu X L, Zhong C, Xie J, et al. Geographical region traceability of Poria cocos and correlation between environmental factors and biomarkers based on a metabolomic approach [J]. Food Chem, 2023, 417: 135817. 李浩然, 董萍萍, 李华健, 等. 基于UHPLC-Q-Exactive Orbitrap MS/MS快速分析开心散物质基准中的化学成分[J]. 中国中药杂志, 2022, 47(4): 938-950. 杨璇, 李俊莹, 单晓晓, 等. 开心散化学成分、药理作用的研究进展及质量标志物的预测分析[J]. 中国中药杂志, 2023, 48(8): 2077-2085. Wang H Q, Zheng R F, Ai Q D, et al. Ginsenoside Rg1 alleviates chronic stress-induced depression in rats by targeting Cx43-YAP axis [J]. Acta Pharmacol Sin, 2025, 46(7): 1877-1891. Hermes L, Römermann J, Cramer B, et al. Phase II metabolism of asarone isomers in vitro and in humans using HPLC-MS/MS and HPLC-QTOF/MS [J]. Foods, 2021, 10(9): 2032. Zhao G D, Ma Y F, Wang X, et al. Configurational alteration results in change in hepatotoxicity of asarone [J]. J Agric Food Chem, 2023, 71(1): 884-894. Dong H Y, Gao Z Y, Rong H, et al. β-Asarone reverses chronic unpredictable mild stress-induced depression-like behavior and promotes hippocampal neurogenesis in rats [J]. Molecules, 2014, 19(5): 5634-5649. Wang Z F, Huang P G, Wang N B, et al. β-Asarone inhibits autophagy by activating the PI3K/Akt/mTOR pathway in a rat model of depression in Parkinson’s disease [J]. Behav Brain Res, 2024, 465: 114966. Yu S Q, Yin Z, Ling M, et al. Ginsenoside Rg1 enriches gut microbial indole-3-acetic acid to alleviate depression-like behavior in mice via oxytocin signaling [J]. Phytomedicine, 2024, 135: 156186. Jia K K, Pan S M, Wu W Y, et al. Ginsenoside Rg1 exerts antidepressant effect by regulating hepatic kynurenine metabolism through promoting the interaction between HNF4α and PGC1α [J]. J Ginseng Res, 2025, 49(2): 179-188. Li C F, Zhang Q P, Cheng J, et al. Role of ginsenoside Rb1 in attenuating depression-like symptoms through astrocytic and microglial complement C3 pathway [J]. Metab Brain Dis, 2024, 39(6): 1039-1050. Wang G L, An T Y, Lei C, et al. Antidepressant-like effect of ginsenoside Rb1 on potentiating synaptic plasticity via the miR-134-mediated BDNF signaling pathway in a mouse model of chronic stress-induced depression [J]. J Ginseng Res, 2022, 46(3): 376-386.
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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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