Article(id=1322631285227499732, tenantId=1146029695717560320, journalId=1302319053441957962, issueId=1322631228000424183, articleNumber=null, orderNo=null, doi=10.7501/j.issn.0253-2670.2026.18.018, pmid=null, cstr=null, oa=null, hot=0, price=null, onlineType=0, articleFormat=0, articleType=null, articleTypeStr=null, receivedDate=1781193600000, receivedDateStr=2026-06-12, revisedDate=null, revisedDateStr=null, acceptedDate=null, acceptedDateStr=null, onlineDate=1793269471698, onlineDateStr=2026-10-29, pubDate=null, pubDateStr=null, doiRegisterDate=null, doiRegisterDateStr=null, onlineIssueDate=1793269471698, onlineIssueDateStr=2026-10-29, onlineJustAcceptDate=null, onlineJustAcceptDateStr=null, onlineFirstDate=null, onlineFirstDateStr=null, sourceXml=null, magXml=null, createTime=1793269471698, creator=13701087609, updateTime=1793269471698, updator=13701087609, issue=Issue{id=1322631228000424183, tenantId=1146029695717560320, journalId=1302319053441957962, year='2026', volume='57', issue='18', pageStart='7073', pageEnd='7500', issueExtLink='null', onlineDate='null', pubDate='1790524800000', pubDateStr='2026-09-28', beforeIssueId=null, nextIssueId=null, price=null, status=1, issueComplete=1, articleOrder=1, issueType=-1, specialIssue=null, createTime=1793269458054, creator='13701087609', updateTime=1793269548245, updator='13701087609', preIssue=null, nextIssue=null, articleTotal=null, ext={EN=IssueExt(id=1322631606339228314, tenantId=1146029695717560320, journalId=1302319053441957962, issueId=1322631228000424183, language=EN, specialIssueTitle=, coverIllustrator=null, specialIssueEditor=, specialIssueAbout=), CN=IssueExt(id=1322631606339228315, tenantId=1146029695717560320, journalId=1302319053441957962, issueId=1322631228000424183, language=CN, specialIssueTitle=, coverIllustrator=null, specialIssueEditor=, specialIssueAbout=)}, issueFiles=null, downloadFileDto=null}, startPage=7295, endPage=7308, ext={EN=ArticleExt(id=1322631285554655446, articleId=1322631285227499732, tenantId=1146029695717560320, journalId=1302319053441957962, language=EN, title=Analysis of key components in anti-browning process of medicine-food homology formula Wuzhiyin and its gastroprotective function, columnId=null, journalTitle=Chinese Traditional and Herbal Drugs, columnName=null, runingTitle=null, highlight=null, articleAbstract=Objective Given that the liquid formulation of the medicine-food homology formula Wuzhiyin is susceptible to non-enzymatic browning during storage, this study systematically investigates the underlying browning mechanism and evaluates the gastroprotective effect of Wuzhiyin prepared using an anti-browning processing technology against alcoholic gastric injury. Methods The differential metabolites and browning intermediates before and after browning of Wuzhiyin were analyzed by non-targeted ultra-performance liquid chromatography-mass spectrometry (UPLC-MS) and Spe-Pak microcolumn separation technology. The degree of browning was characterized by color changes, browning degree, and alterations in nutritional components. An anhydrous ethanol-induced acute gastric injury mouse model was established to evaluate the gastroprotective function of anti-browning prepared Wuzhiyin. Results Total sugars, total polyphenols, and total amino acids were significantly decreased by browning (P < 0.05). Nineteen key differential compounds were screened, among which fructose, sucrose, valine, isoleucine, tyrosine, and p -coumaric acid were identified as major driving factors. 2-Hydroxy-3-methyl-2-cyclopenten-1-one was identified as the core browning intermediate, and the browning mechanism was elucidated as a synergistic process involving the Maillard reaction, acid-promoted sugar degradation, and oxidative cross-linking of phenolic compounds. High-dose anti-browning prepared Wuzhiyin (43.72 g/kg) significantly reduced the gastric ulcer index (inhibition rate 72.42%) and alleviated pathological damage to the gastric mucosa. The underlying mechanisms include inhibiting nuclear factor-κB (NF-κB) pathway, reducing inflammatory cytokines [interleukin-1β (IL-1β), tumor necrosis factor-α (TNF-α), IL-6], regulating oxidative stress [elevation of superoxide dismutase (SOD)/malondialdehyde ratio], and protecting mucosal barrier [modulation of NO, prostaglandin E2 (PGE2 ), trefoil factor 2 (TFF2)]. Conclusion Fructose, sucrose, valine, isoleucine, tyrosine, and p -coumaric acid are the key drivers of browning in Wuzhiyin; the Maillard reaction, acid-catalyzed sugar degradation, and phenolic oxidative cross-linking constitute the major browning pathways; and Wuzhiyin prepared via the anti-browning processing technology exhibits a significant gastroprotective effect against alcoholic gastric injury., authors=YOU Yu1 , LI Juan1 , WU Jiaying1 , ZHOU Weiling1 , FAN Xinlu1 , YUAN Xingzhongyan1 , ZHOU Yanxi1 , DENG Hongdan1 , HU Huiling1 , FU Chaomei1 , authorsList=YOU Yu, LI Juan, WU Jiaying, ZHOU Weiling, FAN Xinlu, YUAN Xingzhongyan, ZHOU Yanxi, DENG Hongdan, HU Huiling, FU Chaomei, authorCompany=1 Sichuan Provincial Key Laboratory of Genetic Resources Innovation and Efficient Utilization of Chinese Medicinal Materials, Chengdu University of Traditional Chinese Medicine, Chengdu 611137, 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=1322631285479157973, articleId=1322631285227499732, tenantId=1146029695717560320, journalId=1302319053441957962, language=CN, title=药食同源五汁饮抗褐变工艺关键成分解析及其胃保护作用, columnId=1304140189132149234, journalTitle=中草药, columnName=药剂与工艺, runingTitle=null, highlight=null, articleAbstract=目的 针对药食同源复方五汁饮液体制剂储存期易发生的非酶褐变难题,系统解析其褐变机制,并评价抗褐变工艺制备的五汁饮对酒精性胃损伤的保护作用。方法 采用非靶向代谢组学超高效液相色谱-质谱联用(ultra-performance liquid chromatography-mass spectrometry,UPLC-MS)结合Spe-Pak微柱分离技术,分析五汁饮褐变前后差异代谢物及褐变中间体;以颜色、褐变度及营养成分变化表征褐变程度;建立无水乙醇诱导小鼠急性胃损伤模型,评价抗褐变工艺制备的五汁饮胃保护功能。结果 褐变导致总糖、总多酚及总氨基酸含量显著下降(P <0.05)。筛选出19种关键差异化合物,其中果糖、蔗糖、缬氨酸、异亮氨酸、酪氨酸及对香豆酸为主要驱动因子;鉴定出核心褐变中间体为2-羟基-3-甲基-2-环戊烯-1-酮,证实褐变由美拉德反应、酸催化糖降解及酚类氧化交联共同驱动;抗褐变工艺制备的五汁饮高剂量(43.72 g/kg)可显著降低小鼠胃溃疡指数(抑制率72.42%),减轻胃黏膜病理损伤,其机制与抑制核因子-κB(nuclear factor-κB,NF-κB)通路,降低炎症因子[白细胞介素-1β(interleukin-1β,IL-1β)、肿瘤坏死因子-α(tumor necrosis factor-α,TNF-α)、IL-6],调节氧化应激[升高超氧化物歧化酶(superoxide dismutase,SOD)/丙二醛比值]及保护黏膜屏障[(调节NO、前列腺素E₂(prostaglandin E₂,PGE₂)、三叶因子2(trefoil factor 2,TFF2)]相关。结论 果糖、蔗糖、缬氨酸、异亮氨酸、酪氨酸及对香豆酸是五汁饮褐变的关键驱动因子;美拉德反应、酸催化糖降解及酚类氧化交联是其主要褐变途径;抗褐变工艺制备的五汁饮对酒精性胃损伤具有显著保护功能。, authors=游宇1 , 李娟1 , 吴佳颖1 , 周玮玲1 , 樊馨璐1 , 袁兴钟滟1 , 周彦汐1 , 邓鸿丹1 , 胡慧玲1 , 傅超美1 , authorsList=游宇, 李娟, 吴佳颖, 周玮玲, 樊馨璐, 袁兴钟滟, 周彦汐, 邓鸿丹, 胡慧玲, 傅超美, authorCompany=1 成都中医药大学, 中药种质资源创新与高效利用四川省重点实验室, 四川 成都 611137, correspAuthors=胡慧玲, authorNote=游宇: 游宇(1986—),女,博士,副教授,硕士生导师,主要从事中药炮制与中药制剂研究。E-mail:yvonne@cdutcm.edu.cn, correspAuthorsNote=null, copyrightStatement=null, copyrightOwner=null, extLink=null, articleAbsUrl=null, sourceXml=null, magXml=null, pdfUrl=null, pdf=JSdkBYkBzwsrYNE8H4NxlA==, pdfFileSize=1868376, 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=国家自然科学基金青年基金资助项目 (81904088); 国家中医药管理局创新团队和人才培养计划 (ZYYCXTD-D-202209); 中国博士后科学基金第76批面上资助项目 (2024MD763926); 四川省科技厅青年基金项目 (2025ZNSFSC1804); 博士后科研项目特别资助 (TB2025092); 成都中医药大学2024-2025年度大学生科研实践创新项目 (ky-2025069))}, authors=null, keywords=[Keyword(id=1322634651433292439, tenantId=1146029695717560320, journalId=1302319053441957962, articleId=1322631285227499732, language=CN, orderNo=1, keyword=五汁饮), Keyword(id=1322634651508789912, tenantId=1146029695717560320, journalId=1302319053441957962, articleId=1322631285227499732, language=CN, orderNo=2, keyword=非酶褐变), Keyword(id=1322634651584287385, tenantId=1146029695717560320, journalId=1302319053441957962, articleId=1322631285227499732, language=CN, orderNo=3, keyword=褐变机制), 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中草药
|药剂与工艺
2026
, 57
(18) :
7295
-7308
药食同源五汁饮抗褐变工艺关键成分解析及其胃保护作用
全屏
游宇1 , 李娟1 , 吴佳颖1 , 周玮玲1 , 樊馨璐1 , 袁兴钟滟1 , 周彦汐1 , 邓鸿丹1 , 胡慧玲1 , 傅超美1
作者信息
1 成都中医药大学, 中药种质资源创新与高效利用四川省重点实验室, 四川 成都 611137
通讯作者:
胡慧玲
作者简介:
游宇: 游宇(1986—),女,博士,副教授,硕士生导师,主要从事中药炮制与中药制剂研究。E-mail:yvonne@cdutcm.edu.cn
Analysis of key components in anti-browning process of medicine-food homology formula Wuzhiyin and its gastroprotective function
YOU Yu1 , LI Juan1 , WU Jiaying1 , ZHOU Weiling1 , FAN Xinlu1 , YUAN Xingzhongyan1 , ZHOU Yanxi1 , DENG Hongdan1 , HU Huiling1 , FU Chaomei1
Affiliations
1 Sichuan Provincial Key Laboratory of Genetic Resources Innovation and Efficient Utilization of Chinese Medicinal Materials, Chengdu University of Traditional Chinese Medicine, Chengdu 611137, China
doi: 10.7501/j.issn.0253-2670.2026.18.018
文章导航
目的 针对药食同源复方五汁饮液体制剂储存期易发生的非酶褐变难题,系统解析其褐变机制,并评价抗褐变工艺制备的五汁饮对酒精性胃损伤的保护作用。方法 采用非靶向代谢组学超高效液相色谱-质谱联用(ultra-performance liquid chromatography-mass spectrometry,UPLC-MS)结合Spe-Pak微柱分离技术,分析五汁饮褐变前后差异代谢物及褐变中间体;以颜色、褐变度及营养成分变化表征褐变程度;建立无水乙醇诱导小鼠急性胃损伤模型,评价抗褐变工艺制备的五汁饮胃保护功能。结果 褐变导致总糖、总多酚及总氨基酸含量显著下降(P <0.05)。筛选出19种关键差异化合物,其中果糖、蔗糖、缬氨酸、异亮氨酸、酪氨酸及对香豆酸为主要驱动因子;鉴定出核心褐变中间体为2-羟基-3-甲基-2-环戊烯-1-酮,证实褐变由美拉德反应、酸催化糖降解及酚类氧化交联共同驱动;抗褐变工艺制备的五汁饮高剂量(43.72 g/kg)可显著降低小鼠胃溃疡指数(抑制率72.42%),减轻胃黏膜病理损伤,其机制与抑制核因子-κB(nuclear factor-κB,NF-κB)通路,降低炎症因子[白细胞介素-1β(interleukin-1β,IL-1β)、肿瘤坏死因子-α(tumor necrosis factor-α,TNF-α)、IL-6],调节氧化应激[升高超氧化物歧化酶(superoxide dismutase,SOD)/丙二醛比值]及保护黏膜屏障[(调节NO、前列腺素E₂(prostaglandin E₂,PGE₂)、三叶因子2(trefoil factor 2,TFF2)]相关。结论 果糖、蔗糖、缬氨酸、异亮氨酸、酪氨酸及对香豆酸是五汁饮褐变的关键驱动因子;美拉德反应、酸催化糖降解及酚类氧化交联是其主要褐变途径;抗褐变工艺制备的五汁饮对酒精性胃损伤具有显著保护功能。
五汁饮
/
非酶褐变
/
褐变机制
/
酒精性胃损伤
/
代谢组学
/
果糖
/
蔗糖
/
缬氨酸
/
异亮氨酸
/
酪氨酸
/
对香豆酸
/
2-羟基-3-甲基-2-环戊烯-1-酮
/
美拉德反应
Objective Given that the liquid formulation of the medicine-food homology formula Wuzhiyin is susceptible to non-enzymatic browning during storage, this study systematically investigates the underlying browning mechanism and evaluates the gastroprotective effect of Wuzhiyin prepared using an anti-browning processing technology against alcoholic gastric injury. Methods The differential metabolites and browning intermediates before and after browning of Wuzhiyin were analyzed by non-targeted ultra-performance liquid chromatography-mass spectrometry (UPLC-MS) and Spe-Pak microcolumn separation technology. The degree of browning was characterized by color changes, browning degree, and alterations in nutritional components. An anhydrous ethanol-induced acute gastric injury mouse model was established to evaluate the gastroprotective function of anti-browning prepared Wuzhiyin. Results Total sugars, total polyphenols, and total amino acids were significantly decreased by browning (P < 0.05). Nineteen key differential compounds were screened, among which fructose, sucrose, valine, isoleucine, tyrosine, and p -coumaric acid were identified as major driving factors. 2-Hydroxy-3-methyl-2-cyclopenten-1-one was identified as the core browning intermediate, and the browning mechanism was elucidated as a synergistic process involving the Maillard reaction, acid-promoted sugar degradation, and oxidative cross-linking of phenolic compounds. High-dose anti-browning prepared Wuzhiyin (43.72 g/kg) significantly reduced the gastric ulcer index (inhibition rate 72.42%) and alleviated pathological damage to the gastric mucosa. The underlying mechanisms include inhibiting nuclear factor-κB (NF-κB) pathway, reducing inflammatory cytokines [interleukin-1β (IL-1β), tumor necrosis factor-α (TNF-α), IL-6], regulating oxidative stress [elevation of superoxide dismutase (SOD)/malondialdehyde ratio], and protecting mucosal barrier [modulation of NO, prostaglandin E2 (PGE2 ), trefoil factor 2 (TFF2)]. Conclusion Fructose, sucrose, valine, isoleucine, tyrosine, and p -coumaric acid are the key drivers of browning in Wuzhiyin; the Maillard reaction, acid-catalyzed sugar degradation, and phenolic oxidative cross-linking constitute the major browning pathways; and Wuzhiyin prepared via the anti-browning processing technology exhibits a significant gastroprotective effect against alcoholic gastric injury.
Wuzhiyin
/
non-enzymatic browning
/
browning mechanism
/
alcoholic gastric injury
/
metabonomics
/
fructose
/
sucrose
/
valine
/
isoleucine
/
tyrosine
/
p -coumaric acid
/
2-hydroxy-3-methyl-2-cyclopenten-1-one
/
Maillard reaction
游宇, 李娟, 吴佳颖, 周玮玲, 樊馨璐, 袁兴钟滟, 周彦汐, 邓鸿丹, 胡慧玲, 傅超美.
药食同源五汁饮抗褐变工艺关键成分解析及其胃保护作用.
中草药,
2026
, 57
(18)
: 7295
-7308
.
DOI: 10.7501/j.issn.0253-2670.2026.18.018
YOU Yu, LI Juan, WU Jiaying, ZHOU Weiling, FAN Xinlu, YUAN Xingzhongyan, ZHOU Yanxi, DENG Hongdan, HU Huiling, FU Chaomei.
Analysis of key components in anti-browning process of medicine-food homology formula Wuzhiyin and its gastroprotective function[J].
Chinese Traditional and Herbal Drugs ,
2026
, 57
(18)
: 7295
-7308
.
DOI: 10.7501/j.issn.0253-2670.2026.18.018
国家自然科学基金青年基金资助项目 (81904088); 国家中医药管理局创新团队和人才培养计划 (ZYYCXTD-D-202209); 中国博士后科学基金第76批面上资助项目 (2024MD763926); 四川省科技厅青年基金项目 (2025ZNSFSC1804); 博士后科研项目特别资助 (TB2025092); 成都中医药大学2024-2025年度大学生科研实践创新项目 (ky-2025069)
参考文献
引证文献
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2026年第57卷第18期
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doi: 10.7501/j.issn.0253-2670.2026.18.018
接收时间:2026-06-12
首发时间:2026-10-29
https://castjournals.cast.org.cn/joweb/zcy/CN/10.7501/j.issn.0253-2670.2026.18.018
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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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