Article(id=1304414955458027617, tenantId=1146029695717560320, journalId=1302319053441957962, issueId=1304414955046985824, articleNumber=null, orderNo=null, doi=10.7501/j.issn.0253-2670.2026.07.001, pmid=null, cstr=null, oa=null, hot=0, price=null, onlineType=0, articleFormat=0, articleType=null, articleTypeStr=null, receivedDate=1768233600000, receivedDateStr=2026-01-13, revisedDate=null, revisedDateStr=null, acceptedDate=null, acceptedDateStr=null, onlineDate=1788926360238, onlineDateStr=2026-09-09, pubDate=null, pubDateStr=null, doiRegisterDate=null, doiRegisterDateStr=null, onlineIssueDate=1788926360238, onlineIssueDateStr=2026-09-09, onlineJustAcceptDate=null, onlineJustAcceptDateStr=null, onlineFirstDate=null, onlineFirstDateStr=null, sourceXml=null, magXml=null, createTime=1788926360238, creator=13701087609, updateTime=1788926360238, updator=13701087609, issue=Issue{id=1304414955046985824, tenantId=1146029695717560320, journalId=1302319053441957962, year='2026', volume='57', issue='7', pageStart='2445', pageEnd='2876', issueExtLink='null', onlineDate='null', pubDate='1775923200000', pubDateStr='2026-04-12', beforeIssueId=null, nextIssueId=null, price=null, status=1, issueComplete=1, articleOrder=1, issueType=-1, specialIssue=null, createTime=1788926360140, creator='13701087609', updateTime=1788926711174, updator='13701087609', preIssue=null, nextIssue=null, articleTotal=null, ext={EN=IssueExt(id=1304416427457409395, tenantId=1146029695717560320, journalId=1302319053441957962, issueId=1304414955046985824, language=EN, specialIssueTitle=, coverIllustrator=null, specialIssueEditor=, specialIssueAbout=), CN=IssueExt(id=1304416427457409396, tenantId=1146029695717560320, journalId=1302319053441957962, issueId=1304414955046985824, language=CN, specialIssueTitle=, coverIllustrator=null, specialIssueEditor=, specialIssueAbout=)}, issueFiles=null, downloadFileDto=null}, startPage=2445, endPage=2455, ext={EN=ArticleExt(id=1304414955818737763, articleId=1304414955458027617, tenantId=1146029695717560320, journalId=1302319053441957962, language=EN, title=Chemical components of intestinal bacterial transformation products from total saponins of Platycodonis Radix and their anti-drug-induced liver injury activity, columnId=null, journalTitle=Chinese Traditional and Herbal Drugs, columnName=null, runingTitle=null, highlight=null, articleAbstract=Objective To investigate the chemical constituents of the intestinal bacteria transformation products of total saponins from Platycodon grandiflorus and their anti-drug-induced liver injury activity. Methods The compounds were isolated and purified by column chromatography techniques including AB-8 macroporous resin, normal phase silica gel, Sephadex LH-20 gel chromatography, and semi-preparative high-performance liquid chromatography. Their structures were identified based on physicochemical properties, mass spectrometry and nuclear magnetic resonance spectral data. The anti-drug-induced liver injury activities of the isolated compounds were evaluated using an acetaminophen-induced AML12 cell hepatic injury model. Results A total of 16 compounds were isolated from the intestinal bacteria transformation products of total saponins from P. grandifloras and identified as 3-O -β-D -glucopyranosyloxy-2β,3β,16α,23- tetrahydroxyolean-12-en-28-oic acid-28-O -α-L -rhamnopyranosyl-(1→2)-α-L -arabinopyranoside (1 ), polygalacin D (2 ), 3-O- β-D -glucopyranosyl platycodigenin (3 ), platycodin D3 (4 ), platycoside F (5 ), platycodin D (6 ), deapio-platycodin D (7 ), platycodonoid B (8 ), 3-O- β-D -glucopyranosyl polygalacic acid (9 ), leiyemudanoside A (10 ), linoleic acid (11 ), (6Z ,9Z )- 6,9-hexadecadienoic acid (12 ), glyceryl linoleate (13 ), (2S )-1-O -(9Z ,12Z -octadecandienyl)-3-O- β-galactosyl glycerol (14 ), dibutyl phthalate (15 ), and triallyl isocyanurate (16 ). Anti-drug-induced liver injury activity study showed that compounds 1 —3 , 5 —7 , 9 , and 14 significantly inhibited the levels of alanine aminotransferase and aspartate aminotransferase in acetaminophen-induced AML12 cell supernatants (P < 0.05,0.01). Conclusion A total of 16 compounds were successfully isolated and identified from the intestinal bacterial transformation products from total saponins of P. grandiflorus . Compound 1 is a new compound named des-apio-xylosyl polygalacin D. Compounds 1 —3 , 5 —7 , 9 , and 14 exhibit significant anti-drug-induced liver injury activities, showing potential hepatoprotective effects., authors=PENG Yu, ZHONG Yuanhan, WAN Tonglin, LIU Guangpeng, WEN Liyun, RAO Jianbo, LIANG Jian, QIN Qian, ZHANG Shouwen, ZHONG Guoyue, ZENG Jinxiang, LIANG Yonghong, authorsList=PENG Yu, ZHONG Yuanhan, WAN Tonglin, LIU Guangpeng, WEN Liyun, RAO Jianbo, LIANG Jian, QIN Qian, ZHANG Shouwen, ZHONG Guoyue, ZENG Jinxiang, LIANG Yonghong, 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=1304414955705491554, articleId=1304414955458027617, tenantId=1146029695717560320, journalId=1302319053441957962, language=CN, title=桔梗总皂苷肠道菌转化产物的化学成分及其抗药物性肝损伤活性研究, columnId=1304140187169214944, journalTitle=中草药, columnName=化学成分, runingTitle=null, highlight=null, articleAbstract=目的 研究桔梗总皂苷肠道菌转化产物的化学成分及其抗肝损伤活性。方法 采用AB-8大孔吸附树脂、正相硅胶、Sephadex LH-20凝胶柱色谱和半制备高效液相色谱等柱色谱技术进行分离纯化,根据所分化合物理化性质及质谱、核磁共振波谱数据鉴定化合物结构。采用对乙酰氨基酚诱导AML12细胞肝损伤模型评价所分离化合物的抗肝损伤活性。结果 从桔梗总皂苷肠道菌转化产物中分离得到16个化合物,分别鉴定为3-O -β-D -吡喃葡萄糖氧基-2β,3β,16α,23- 四羟基齐墩果烷-12-烯-28-酸-28-O -α-L -吡喃鼠李糖基-(1→2)-α-L -吡喃阿拉伯糖苷(1 )、远志皂苷D(2 )、3-O- β-D- 吡喃葡萄糖基桔梗皂苷元(3 )、桔梗皂苷D₃(4 )、桔梗皂苷F(5 )、桔梗皂苷D(6 )、去芹糖桔梗皂苷D(7 )、桔梗皂苷元B(8 )、3-O- β-D- 吡喃葡萄糖基远志酸(9 )、雷叶木皂苷A(10 )、亚油酸(11 )、(6Z ,9Z )- 6,9- 十六碳二烯酸(12 )、亚油酸甘油酯(13 )、(2S )- 1-O- (9Z ,12Z- 十八烷二烯基)-3-O- β-半乳糖基甘油(14 )、邻苯二甲酸二丁酯(15 )、三烯丙基异氰脲酸酯(16 )。抗药物性肝损伤活性研究表明,化合物1 ~3 、5 ~7 、9 、14 能显著抑制对乙酰氨基酚诱导的AML12细胞上清液中丙氨酸氨基转移酶、天门冬氨酸氨基转移酶水平(P <0.05、0.01)。结论 从桔梗总皂苷肠道菌转化产物中成功分离并鉴定了16个化合物,其中化合物1 为新化合物,命名为去芹糖木糖基远志皂苷D;化合物1 ~3 、5 ~7 、9 、14 表现出显著的抗药物性肝损伤活性,具有抗肝损伤潜力。, authors=彭昱1 , 钟渊涵1 , 万同林1 , 刘光鹏1 , 文丽云1 , 饶建波1 , 梁健1 , 秦倩1 , 张寿文1 , 钟国跃1 , 曾金祥1 , 梁永红2 , authorsList=彭昱, 钟渊涵, 万同林, 刘光鹏, 文丽云, 饶建波, 梁健, 秦倩, 张寿文, 钟国跃, 曾金祥, 梁永红, authorCompany=1 江西中医药大学中药资源与民族药研究中心, 江西 南昌 330004; 2 江西中医药大学现代中药制剂教育部重点实验室, 江西 南昌 330004, correspAuthors=曾金祥, authorNote=彭昱: 彭昱,硕士研究生,研究方向为中药与民族药资源。E-mail:2660266234@qq.com, correspAuthorsNote=null, copyrightStatement=null, copyrightOwner=null, extLink=null, articleAbsUrl=null, sourceXml=null, magXml=null, pdfUrl=null, pdf=CQh5aHfayqSTnp7FQjDZjw==, pdfFileSize=1408618, 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=国家自然科学基金项目 (82160736); 江西中医药大学科技创新团队项目 (CXTD22002))}, authors=null, keywords=[Keyword(id=1304414955973927012, tenantId=1146029695717560320, journalId=1302319053441957962, articleId=1304414955458027617, language=CN, 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Platycodon grandiflorum(Jacq.)A. DC.:A review of phytochemistry,pharmacology, toxicology and traditional use[J].Phytomedicine, 2022, 106:154422. 赵雨芯,谢龙,李小芳,等.桔梗皂苷的药理作用研究进展[J].中药与临床, 2022, 13(2):94-98. 沈漫,吴宇娟,李医明,等.桔梗皂苷药理学及临床应用研究进展[J].上海中医药大学学报, 2018, 32(5):86-91. Zhang C, Wang X H, Zhong Y H, et al. Active microbial metabolites study on antitussive and expectorant effects and metabolic mechanisms of platycosides fraction of Platycodonis Radix[J]. J Chromatogr B Analyt Technol Biomed Life Sci, 2022, 1195:123171. Yau L F, Huang H, Tong T T, et al. Characterization of deglycosylated metabolites of platycosides reveals their biotransformation after oral administration[J]. Food Chem, 2022, 393:133383. Zhang W, Qian S H, Qian D W, et al. Screening of intestinal bacterial metabolites of platycodin D using ultraperformance liquid chromatography/quadrupole time-offlight mass spectrometry[J]. Am J Chin Med, 2016, 44(4):817-833. Shin, Kyung C, Deok K O. Biotransformation of platycosides, saponins from balloon flower root, into bioactive deglycosylated platycosides[J]. Antioxidants,2023, 12(2):327. Kang S H, Kim T H, Shin K C, et al. Biotransformation of food-derived saponins, platycosides, into deglucosylated saponins including deglucosylated platycodin D and their anti-inflammatory activities[J]. J Agric Food Chem, 2019,67(5):1470-1477. Hosack T, Damry D, Biswas S. Drug-induced liver injury:A comprehensive review[J]. Therap Adv Gastroenterol,2023, 16:1-13. Deng X Y, Li Y B, Chen Y, et al. Paeoniflorin protects hepatocytes from APAP-induced damage through launching autophagy via the MAPK/mTOR signaling pathway[J]. Cell Mol Biol Lett, 2024, 29(1):119. 杨必乾,何慧明,殷亭湄,等. N-乙酰半胱氨酸缓解顺铂肝损伤的作用机制研究[J].重庆医科大学学报,2025, 50(6):815-820 孙志运,孙梦迪,王克婧,等.桔梗的化学成分、药理作用研究进展及质量标志物(Q-Marker)预测[J].药物评价研究, 2026, 49(1):327-342. 刘艳平,余自成,陈红君.基于肠道菌群代谢的知母皂苷BII体外代谢转化研究[J].中国中医药信息杂志,2018, 25(5):66-70. Karachaliou E, Pertuit D, Bruguière A, et al. Three new triterpene glycosides from the roots of Deutzia x hybrida“strawberry fields”(Hydrangeaceae)[J]. Molecules, 2024,29(23):5781. 范万翠. O-糖链的非还原性解离及同时PMP衍生化的方法研究[D].西安:西北大学, 2010. Fu W W, Dou D Q, Zhao C J, et al. Triterpenoid saponins from Platycodon grandiflurum[J]. J Asian Nat Prod Res,2007, 9(1):35-40. 付文卫,窦德强,侯文彬,等.桔梗中三萜皂苷的分离与结构鉴定[J].中国药物化学杂志, 2005, 15(5):297-301. Wei L, Lan X, Jing Z, et al. A new triterpenoid saponin from the roots of Platycodon grandiflorum[J]. Chin Chem Lett, 2007, 18(3):306-308. Zhan Q, Zhang F, Sun L N, et al. Two new oleanane-type triterpenoids from Platycodi Radix and anti-proliferative activity in HSC-T6 cells[J]. Molecules, 2012, 17(12):14899-14907. Fu W W, Dou D Q, Shimizu N, et al. Studies on the chemical constituents from the roots of Platycodon grandiflorum[J]. J Nat Med, 2006, 60(1):68-72. Li G Y, Zhang Y H, Yang B Y, et al. Leiyemudanosides AC, three new bidesmosidic triterpenoid saponins from the roots of Caulophyllum robustum[J]. Fitoterapia, 2010,81(3):200-204. 李雯岐,罗汉,张虹,等.湘黄精中高异黄酮类化学成分研究[J].安徽中医药大学学报, 2024, 43(2):102-108. 周洁,王雨曦,魏玉莲,等.高山猴头菌的化学成分及抑制α-葡萄糖苷酶活性研究[J].中草药, 2024, 55(16):5407-5417. 范升,陆盛胜,吴秋艺,等.广东红冬蛇菰及其内生真菌Penicillium coprophilum Mzz9的化学成分研究[J].天然产物研究与开发, 2020, 32(9):1539-1544. 谢安琪,池军,张伟进,等.半夏乙酸乙酯部位化学成分及抗炎活性研究[J].天然产物研究与开发, 2024,36(8):1339-1349. 何红霞,王钰,刘华,等.无花果叶二氯甲烷部位化学成分研究[J].中药材, 2025, 48(12):3055-3060. 付继勇,王静宜,余俊东,等.健脑宁合剂化学成分及其抗氧化活性研究[J].中成药, 2024, 46(12):4020-4028. 许伟辰,罗子宸,谢彤,等.中药桔梗研究进展及其质量标志物预测初步分析[J].南京中医药大学学报,2021, 37(2):294-302. Zhong Y H, Wu X W, Zhang X Y, et al. Intestinal microbiota-mediated serum pharmacochemistry reveals hepatoprotective metabolites of Platycodonis Radix against APAP-induced liver injury[J]. J Chromatogr B Analyt Technol Biomed Life Sci, 2025, 1251:124395. 宫勋,王建刚.桔梗中脂肪酸成分的GC-MS分析[J].安徽农业科学, 2010, 38(22):11780-11782. Ma X T, Shao S, Xiao F Q, et al. Platycodon grandiflorum extract:Chemical composition and whitening, antioxidant,and anti-inflammatory effects[J]. RSC Adv, 2021, 11(18):10814-10826. 张若冰,王士杰,沈琼,等.桔梗皂苷D改善对乙酰氨基酚致L02细胞损伤的作用及分子机制[J].吉林农业大学学报, 2024, 46(4):667-672. Fu C L, Liu Y, Leng J, et al. Platycodin D protects acetaminophen-induced hepatotoxicity by inhibiting hepatocyte MAPK pathway and apoptosis in C57BL/6J mice[J]. Biomed Pharmacother, 2018, 107:867-877.)
中草药
|化学成分
2026
, 57
(7) :
2445
-2455
桔梗总皂苷肠道菌转化产物的化学成分及其抗药物性肝损伤活性研究
全屏
彭昱1 , 钟渊涵1 , 万同林1 , 刘光鹏1 , 文丽云1 , 饶建波1 , 梁健1 , 秦倩1 , 张寿文1 , 钟国跃1 , 曾金祥1 , 梁永红2
作者信息
1 江西中医药大学中药资源与民族药研究中心, 江西 南昌 330004; 2 江西中医药大学现代中药制剂教育部重点实验室, 江西 南昌 330004
通讯作者:
曾金祥
作者简介:
彭昱: 彭昱,硕士研究生,研究方向为中药与民族药资源。E-mail:2660266234@qq.com
Chemical components of intestinal bacterial transformation products from total saponins of Platycodonis Radix and their anti-drug-induced liver injury activity
PENG Yu, ZHONG Yuanhan, WAN Tonglin, LIU Guangpeng, WEN Liyun, RAO Jianbo, LIANG Jian, QIN Qian, ZHANG Shouwen, ZHONG Guoyue, ZENG Jinxiang, LIANG Yonghong
Affiliations
doi: 10.7501/j.issn.0253-2670.2026.07.001
文章导航
目的 研究桔梗总皂苷肠道菌转化产物的化学成分及其抗肝损伤活性。方法 采用AB-8大孔吸附树脂、正相硅胶、Sephadex LH-20凝胶柱色谱和半制备高效液相色谱等柱色谱技术进行分离纯化,根据所分化合物理化性质及质谱、核磁共振波谱数据鉴定化合物结构。采用对乙酰氨基酚诱导AML12细胞肝损伤模型评价所分离化合物的抗肝损伤活性。结果 从桔梗总皂苷肠道菌转化产物中分离得到16个化合物,分别鉴定为3-O -β-D -吡喃葡萄糖氧基-2β,3β,16α,23- 四羟基齐墩果烷-12-烯-28-酸-28-O -α-L -吡喃鼠李糖基-(1→2)-α-L -吡喃阿拉伯糖苷(1 )、远志皂苷D(2 )、3-O- β-D- 吡喃葡萄糖基桔梗皂苷元(3 )、桔梗皂苷D₃(4 )、桔梗皂苷F(5 )、桔梗皂苷D(6 )、去芹糖桔梗皂苷D(7 )、桔梗皂苷元B(8 )、3-O- β-D- 吡喃葡萄糖基远志酸(9 )、雷叶木皂苷A(10 )、亚油酸(11 )、(6Z ,9Z )- 6,9- 十六碳二烯酸(12 )、亚油酸甘油酯(13 )、(2S )- 1-O- (9Z ,12Z- 十八烷二烯基)-3-O- β-半乳糖基甘油(14 )、邻苯二甲酸二丁酯(15 )、三烯丙基异氰脲酸酯(16 )。抗药物性肝损伤活性研究表明,化合物1 ~3 、5 ~7 、9 、14 能显著抑制对乙酰氨基酚诱导的AML12细胞上清液中丙氨酸氨基转移酶、天门冬氨酸氨基转移酶水平(P <0.05、0.01)。结论 从桔梗总皂苷肠道菌转化产物中成功分离并鉴定了16个化合物,其中化合物1 为新化合物,命名为去芹糖木糖基远志皂苷D;化合物1 ~3 、5 ~7 、9 、14 表现出显著的抗药物性肝损伤活性,具有抗肝损伤潜力。
桔梗总皂苷
/
肠道菌
/
转化产物
/
药物性肝损伤
/
去芹糖木糖基远志皂苷D
/
远志皂苷D
/
桔梗皂苷D3
Objective To investigate the chemical constituents of the intestinal bacteria transformation products of total saponins from Platycodon grandiflorus and their anti-drug-induced liver injury activity. Methods The compounds were isolated and purified by column chromatography techniques including AB-8 macroporous resin, normal phase silica gel, Sephadex LH-20 gel chromatography, and semi-preparative high-performance liquid chromatography. Their structures were identified based on physicochemical properties, mass spectrometry and nuclear magnetic resonance spectral data. The anti-drug-induced liver injury activities of the isolated compounds were evaluated using an acetaminophen-induced AML12 cell hepatic injury model. Results A total of 16 compounds were isolated from the intestinal bacteria transformation products of total saponins from P. grandifloras and identified as 3-O -β-D -glucopyranosyloxy-2β,3β,16α,23- tetrahydroxyolean-12-en-28-oic acid-28-O -α-L -rhamnopyranosyl-(1→2)-α-L -arabinopyranoside (1 ), polygalacin D (2 ), 3-O- β-D -glucopyranosyl platycodigenin (3 ), platycodin D3 (4 ), platycoside F (5 ), platycodin D (6 ), deapio-platycodin D (7 ), platycodonoid B (8 ), 3-O- β-D -glucopyranosyl polygalacic acid (9 ), leiyemudanoside A (10 ), linoleic acid (11 ), (6Z ,9Z )- 6,9-hexadecadienoic acid (12 ), glyceryl linoleate (13 ), (2S )-1-O -(9Z ,12Z -octadecandienyl)-3-O- β-galactosyl glycerol (14 ), dibutyl phthalate (15 ), and triallyl isocyanurate (16 ). Anti-drug-induced liver injury activity study showed that compounds 1 —3 , 5 —7 , 9 , and 14 significantly inhibited the levels of alanine aminotransferase and aspartate aminotransferase in acetaminophen-induced AML12 cell supernatants (P < 0.05,0.01). Conclusion A total of 16 compounds were successfully isolated and identified from the intestinal bacterial transformation products from total saponins of P. grandiflorus . Compound 1 is a new compound named des-apio-xylosyl polygalacin D. Compounds 1 —3 , 5 —7 , 9 , and 14 exhibit significant anti-drug-induced liver injury activities, showing potential hepatoprotective effects.
total saponins of Platycodonis Radix
/
intestinal bacterial
/
transformation product
/
drug-induced liver injury
/
des-apio-xylosyl polygalacin D
/
polygalacin D
/
platycodin D3
彭昱, 钟渊涵, 万同林, 刘光鹏, 文丽云, 饶建波, 梁健, 秦倩, 张寿文, 钟国跃, 曾金祥, 梁永红.
桔梗总皂苷肠道菌转化产物的化学成分及其抗药物性肝损伤活性研究.
中草药,
2026
, 57
(7)
: 2445
-2455
.
DOI: 10.7501/j.issn.0253-2670.2026.07.001
PENG Yu, ZHONG Yuanhan, WAN Tonglin, LIU Guangpeng, WEN Liyun, RAO Jianbo, LIANG Jian, QIN Qian, ZHANG Shouwen, ZHONG Guoyue, ZENG Jinxiang, LIANG Yonghong.
Chemical components of intestinal bacterial transformation products from total saponins of Platycodonis Radix and their anti-drug-induced liver injury activity[J].
Chinese Traditional and Herbal Drugs ,
2026
, 57
(7)
: 2445
-2455
.
DOI: 10.7501/j.issn.0253-2670.2026.07.001
参考文献
引证文献
Zhang S N, Chai X Y, Hou G G, et al. Platycodon grandiflorum(Jacq.)A. DC.:A review of phytochemistry,pharmacology, toxicology and traditional use[J].Phytomedicine, 2022, 106:154422. 赵雨芯,谢龙,李小芳,等.桔梗皂苷的药理作用研究进展[J].中药与临床, 2022, 13(2):94-98. 沈漫,吴宇娟,李医明,等.桔梗皂苷药理学及临床应用研究进展[J].上海中医药大学学报, 2018, 32(5):86-91. Zhang C, Wang X H, Zhong Y H, et al. Active microbial metabolites study on antitussive and expectorant effects and metabolic mechanisms of platycosides fraction of Platycodonis Radix[J]. J Chromatogr B Analyt Technol Biomed Life Sci, 2022, 1195:123171. Yau L F, Huang H, Tong T T, et al. Characterization of deglycosylated metabolites of platycosides reveals their biotransformation after oral administration[J]. Food Chem, 2022, 393:133383. Zhang W, Qian S H, Qian D W, et al. Screening of intestinal bacterial metabolites of platycodin D using ultraperformance liquid chromatography/quadrupole time-offlight mass spectrometry[J]. Am J Chin Med, 2016, 44(4):817-833. Shin, Kyung C, Deok K O. Biotransformation of platycosides, saponins from balloon flower root, into bioactive deglycosylated platycosides[J]. Antioxidants,2023, 12(2):327. Kang S H, Kim T H, Shin K C, et al. Biotransformation of food-derived saponins, platycosides, into deglucosylated saponins including deglucosylated platycodin D and their anti-inflammatory activities[J]. J Agric Food Chem, 2019,67(5):1470-1477. Hosack T, Damry D, Biswas S. Drug-induced liver injury:A comprehensive review[J]. Therap Adv Gastroenterol,2023, 16:1-13. Deng X Y, Li Y B, Chen Y, et al. Paeoniflorin protects hepatocytes from APAP-induced damage through launching autophagy via the MAPK/mTOR signaling pathway[J]. Cell Mol Biol Lett, 2024, 29(1):119. 杨必乾,何慧明,殷亭湄,等. N-乙酰半胱氨酸缓解顺铂肝损伤的作用机制研究[J].重庆医科大学学报,2025, 50(6):815-820 孙志运,孙梦迪,王克婧,等.桔梗的化学成分、药理作用研究进展及质量标志物(Q-Marker)预测[J].药物评价研究, 2026, 49(1):327-342. 刘艳平,余自成,陈红君.基于肠道菌群代谢的知母皂苷BII体外代谢转化研究[J].中国中医药信息杂志,2018, 25(5):66-70. Karachaliou E, Pertuit D, Bruguière A, et al. Three new triterpene glycosides from the roots of Deutzia x hybrida“strawberry fields”(Hydrangeaceae)[J]. Molecules, 2024,29(23):5781. 范万翠. O-糖链的非还原性解离及同时PMP衍生化的方法研究[D].西安:西北大学, 2010. Fu W W, Dou D Q, Zhao C J, et al. Triterpenoid saponins from Platycodon grandiflurum[J]. J Asian Nat Prod Res,2007, 9(1):35-40. 付文卫,窦德强,侯文彬,等.桔梗中三萜皂苷的分离与结构鉴定[J].中国药物化学杂志, 2005, 15(5):297-301. Wei L, Lan X, Jing Z, et al. A new triterpenoid saponin from the roots of Platycodon grandiflorum[J]. Chin Chem Lett, 2007, 18(3):306-308. Zhan Q, Zhang F, Sun L N, et al. Two new oleanane-type triterpenoids from Platycodi Radix and anti-proliferative activity in HSC-T6 cells[J]. Molecules, 2012, 17(12):14899-14907. Fu W W, Dou D Q, Shimizu N, et al. Studies on the chemical constituents from the roots of Platycodon grandiflorum[J]. J Nat Med, 2006, 60(1):68-72. Li G Y, Zhang Y H, Yang B Y, et al. Leiyemudanosides AC, three new bidesmosidic triterpenoid saponins from the roots of Caulophyllum robustum[J]. Fitoterapia, 2010,81(3):200-204. 李雯岐,罗汉,张虹,等.湘黄精中高异黄酮类化学成分研究[J].安徽中医药大学学报, 2024, 43(2):102-108. 周洁,王雨曦,魏玉莲,等.高山猴头菌的化学成分及抑制α-葡萄糖苷酶活性研究[J].中草药, 2024, 55(16):5407-5417. 范升,陆盛胜,吴秋艺,等.广东红冬蛇菰及其内生真菌Penicillium coprophilum Mzz9的化学成分研究[J].天然产物研究与开发, 2020, 32(9):1539-1544. 谢安琪,池军,张伟进,等.半夏乙酸乙酯部位化学成分及抗炎活性研究[J].天然产物研究与开发, 2024,36(8):1339-1349. 何红霞,王钰,刘华,等.无花果叶二氯甲烷部位化学成分研究[J].中药材, 2025, 48(12):3055-3060. 付继勇,王静宜,余俊东,等.健脑宁合剂化学成分及其抗氧化活性研究[J].中成药, 2024, 46(12):4020-4028. 许伟辰,罗子宸,谢彤,等.中药桔梗研究进展及其质量标志物预测初步分析[J].南京中医药大学学报,2021, 37(2):294-302. Zhong Y H, Wu X W, Zhang X Y, et al. Intestinal microbiota-mediated serum pharmacochemistry reveals hepatoprotective metabolites of Platycodonis Radix against APAP-induced liver injury[J]. J Chromatogr B Analyt Technol Biomed Life Sci, 2025, 1251:124395. 宫勋,王建刚.桔梗中脂肪酸成分的GC-MS分析[J].安徽农业科学, 2010, 38(22):11780-11782. Ma X T, Shao S, Xiao F Q, et al. Platycodon grandiflorum extract:Chemical composition and whitening, antioxidant,and anti-inflammatory effects[J]. RSC Adv, 2021, 11(18):10814-10826. 张若冰,王士杰,沈琼,等.桔梗皂苷D改善对乙酰氨基酚致L02细胞损伤的作用及分子机制[J].吉林农业大学学报, 2024, 46(4):667-672. Fu C L, Liu Y, Leng J, et al. Platycodin D protects acetaminophen-induced hepatotoxicity by inhibiting hepatocyte MAPK pathway and apoptosis in C57BL/6J mice[J]. Biomed Pharmacother, 2018, 107:867-877.
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doi: 10.7501/j.issn.0253-2670.2026.07.001
接收时间:2026-01-13
首发时间:2026-09-09
https://castjournals.cast.org.cn/joweb/zcy/CN/10.7501/j.issn.0253-2670.2026.07.001
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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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