Innovative analysis and future prospects of Bupleuri Radix’s pharmacology and toxicity based on the gut–liver axis

Jie Ma , Qian Lu , Suoyan Tian , Zhiyuan Huang , Xinyu He , Xinyu Dai , Tongyan Jiao , Shenshen Yang , Yubo Li

MedScience ››

PDF (5327KB)
MedScience ›› DOI: 10.1007/s11684-026-1213-3
REVIEW
Innovative analysis and future prospects of Bupleuri Radix’s pharmacology and toxicity based on the gut–liver axis
Author information +
History +
PDF (5327KB)

Abstract

Bupleuri Radix (BR) is a traditional Chinese medicine, which has a significant protective effect on hepatic and intestinal diseases, but its potential hepatotoxicity is still worrying. The bi-directional effects of BR are systematically summarized in this review, with a primary focus on the gut–liver axis. Saikosaponins, as the main bioactive components of BR, are converted by the gut microbiota into metabolites with enhanced bioavailability, thereby regulating the intestinal flora, strengthening the intestinal barrier, and alleviating inflammation through pathways such as NFB, PI3K/Akt/mTOR, and STAT3. Concurrently, BR and its components exert hepatoprotective effects through antioxidant, anti-inflammatory, and metabolic regulation mechanisms. However, saikosaponin and volatile oil may induce hepatotoxicity via oxidative stress and apoptosis. Critical evidence gaps persist regarding the systematic interplay between BR’s multi-component actions and the gut–liver axis, the toxicity of metabolites, and clinical hepatotoxicity risk. Future research should prioritize these areas to optimize the safe and effective application of BR.

Keywords

Bupleuri Radix / pharmacokinetics / gut–liver axis / intestinal disease / liver disease / toxicity

Cite this article

Download citation ▾
Jie Ma, Qian Lu, Suoyan Tian, Zhiyuan Huang, Xinyu He, Xinyu Dai, Tongyan Jiao, Shenshen Yang, Yubo Li. Innovative analysis and future prospects of Bupleuri Radix’s pharmacology and toxicity based on the gut–liver axis. MedScience DOI:10.1007/s11684-026-1213-3

登录浏览全文

4963

注册一个新账户 忘记密码

References

[1]

Zhao JC , Weng QQ , Zhang Y , Zhang W , Peng HS , Yang HJ , Zhan ZL . Textual research on Bupleuri Radix in Chinese classical prescriptions. China J Chin Mater Med (Zhongguo Zhong Yao Za Zhi) 2020; 45(3): 697–703

[2]

Sun P , Li Y , Wei S , Zhao T , Wang Y , Son C , Xue L , Wang F , Xiao L , Wu J , Qiao M . Pharmacological effects and chemical constituents of Bupleurum. Mini Rev Med Chem 2019; 19(1): 34–55

[3]

Shi LX , Li K , Qin XM , Li CY , Cui LJ , Li SY , Cao YX , Wang SJ . Identification of different Bupleurum varieties based on carbohydrate-specific chromatograms. Acta Pharmaceutica Sinica (Yao Xue Xue Bao) 2020; 55(12): 2968–2975

[4]

Yuan B , Yang R , Ma Y , Zhou S , Zhang X , Liu Y . A systematic review of the active saikosaponins and extracts isolated from Radix Bupleuri and their applications. Pharm Biol 2017; 55(1): 620–635

[5]

Dai HY , Huang GY , Li Y , Xu WC , Shen Y . Application of minor Bupleurum decoction to the treatment of liver diseases. Henan Tradit Chin Med (Henan Zhong Yi) 2022; 42(6): 837–841

[6]

Wang YT , Wang XL , Wang ZZ , Lei L , Hu D , Zhang Y . Antidepressant effects of the traditional Chinese herbal formula Xiao-Yao-San and its bioactive ingredients. Phytomedicine 2023; 109: 154558

[7]

Hu J , Teng J , Wang W , Yang N , Tian H , Zhang W , Peng X , Zhang J . Clinical efficacy and safety of traditional Chinese medicine Xiao Yao San in insomnia combined with anxiety. Medicine (Baltimore) 2021; 100(43): e27608

[8]

Gong YL . Application of Chaihu Guizhi Decoction in the treatment of pediatric diseases. Guangxi J Tradit Chin Med (Guangxi Zhong Yi Yao) 2022; 45(6): 68–71

[9]

Chen WL , Peng XY , Yu JX , Gao B , Xu ZH , Pan YF . Composition analysis and quality standard discussion of Bupleurum Injection with different preparation techniques. Chin Tradit Pat Med (Zhong Cheng Yao) 2019; 41(4): 895–901

[10]

Jiao Y , Liu J , Jiang L , Liu Q , Li X , Zhang S , Zhao B , Wang T . Guidelines on common cold for traditional Chinese medicine based on pattern differentiation. J Tradit Chin Med 2013; 33(4): 417–422

[11]

Tian Y , Guo J , Jiang X , Lu H , Xie J , Zhang F , Du Z , Hao E . Exploring the therapeutic potential of Bupleurum in medical treatment: a comprehensive overview. Pharmaceuticals (Basel) 2025; 18(9): 1331

[12]

Jiang H , Yang L , Hou A , Zhang J , Wang S , Man W , Zheng S , Yu H , Wang X , Yang B , Wang Q , Kuang H . Botany, traditional uses, phytochemistry, analytical methods, processing, pharmacology and pharmacokinetics of Bupleuri Radix: a systematic review. Biomed Pharmacother 2020; 131: 110679

[13]

Yang F , Dong X , Yin X , Wang W , You L , Ni J . Radix Bupleuri: a review of traditional uses, botany, phytochemistry, pharmacology, and toxicology. BioMed Res Int 2017; 2017(1): 7597596

[14]

Xie GZ , Huang LL , Zhang SH , Tan ZJ . Advances in metabolism of glycosides by gut microbiota. Nat Prod Res Dev (Tian Ran Chan Wu Yan Jiu Yu Kai Fa) 2022; 34(7): 1261–1271

[15]

Lemos FO , Florentino RM , Lima Filho ACM , Dos Santos ML , Leite MF . Inositol 1, 4, 5-trisphosphate receptor in the liver: expression and function. World J Gastroenterol 2019; 25(44): 6483–6494

[16]

Huang E , Kim S , Park H , Park S , Ji Y , Todorov SD , Lim SD , Holzapfel WH . Modulation of the gut microbiome and obesity biomarkers by Lactobacillus plantarum KC28 in a diet-induced obesity murine model. Probiotics Antimicrob Proteins 2021; 13(3): 677–697

[17]

Tilg H , Adolph TE , Trauner M . Gut–liver axis: pathophysiological concepts and clinical implications. Cell Metab 2022; 34(11): 1700–1718

[18]

Marshall JC . The gut as a potential trigger of exercise-induced inflammatory responses. Can J Physiol Pharmacol 1998; 76(5): 479–484

[19]

Ticho AL , Malhotra P , Dudeja PK , Gill RK , Alrefai WA . Intestinal absorption of bile acids in health and disease. Compr Physiol 2019; 10(1): 21–56

[20]

Safari Z , Gérard P . The links between the gut microbiome and non-alcoholic fatty liver disease (NAFLD). Cell Mol Life Sci 2019; 76(8): 1541–1558

[21]

Li S , Xu Z , Guo J , Zheng J , Sun X , Yu J . Farnesoid X receptor activation induces antitumour activity in colorectal cancer by suppressing JAK2/STAT3 signalling via transactivation of SOCS3 gene. J Cell Mol Med 2020; 24(24): 14549–14560

[22]

Bajaj JS . Alcohol, liver disease and the gut microbiota. Nat Rev Gastroenterol Hepatol 2019; 16(4): 235–246

[23]

Milosevic I , Vujovic A , Barac A , Djelic M , Korac M , Radovanovic Spurnic A , Gmizic I , Stevanovic O , Djordjevic V , Lekic N , Russo E , Amedei A . Gut–liver axis, gut microbiota, and its modulation in the management of liver diseases: a review of the literature. Int J Mol Sci 2019; 20(2): 395

[24]

Demir M , Lang S , Hartmann P , Duan Y , Martin A , Miyamoto Y , Bondareva M , Zhang X , Wang Y , Kasper P , Bang C , Roderburg C , Tacke F , Steffen HM , Goeser T , Kruglov A , Eckmann L , Stärkel P , Fouts DE , Schnabl B . The fecal mycobiome in non-alcoholic fatty liver disease. J Hepatol 2022; 76(4): 788–799

[25]

Frumento D , Țălu Ș . Interaction between human microbiota, immune system, and hepatitis C virus infection: a narrative review. Appl Sci (Basel) 2025; 15(6): 3157

[26]

Feng W , Ao H , Peng C , Yan D . Gut microbiota, a new frontier to understand traditional Chinese medicines. Pharmacol Res 2019; 142: 176–191

[27]

Zhang F , He F , Li L , Guo L , Zhang B , Yu S , Zhao W . Bioavailability based on the gut microbiota: a new perspective. Microbiol Mol Biol Rev 2020; 84(2): e00072–19

[28]

Li HF , Yuan TJ , Jiang S . Research progress of bioavailability of oral drugs based on the gut microbiota. Chin J Pharm (Zhongguo Yi Yao Gong Ye Za Zhi) 2022; 53(9): 1262–1269

[29]

Gong X , Li X , Bo A , Shi RY , Li QY , Lei LJ , Zhang L , Li MH . The interactions between gut microbiota and bioactive ingredients of traditional Chinese medicines: a review. Pharmacol Res 2020; 157: 104824

[30]

Wang YZ , Wang XN , Zhang Y , Duan CC , Zhang JY . Study on metabolic profiling of total saponins of Bupleurum chinense DC in rats. J Zunyi Med Univ 2023; 46(1): 21–29

[31]

Li P , Wu M , Xiong W , Li J , An Y , Ren J , Xie Y , Xue H , Yan D , Li M , Zhong G . Saikosaponin-d ameliorates dextran sulfate sodium-induced colitis by suppressing NF-κB activation and modulating the gut microbiota in mice. Int Immunopharmacol 2020; 81: 106288

[32]

Zheng Q , Li X , Huang N , Li F , Ge J , Wang D , Sun R , Liu R . Saikosaponins ameliorate hyperlipidemia in rats by enhancing hepatic lipid and cholesterol metabolism. J Ethnopharmacol 2023; 305: 116110

[33]

Liu Q , Xue Y , Liu J , Ren S , Xu J , Yang J , Xing Y , Zhang Z , Song R . Saikosaponins and the deglycosylated metabolites exert liver meridian guiding effect through PXR/CYP3A4 inhibition. J Ethnopharmacol 2021; 279: 114344

[34]

Chen C , Gong W , Tian J , Gao X , Qin X , Du G , Zhou Y . Radix Paeoniae Alba attenuates Radix Bupleuri-induced hepatotoxicity by modulating gut microbiota to alleviate the inhibition of saikosaponins on glutathione synthetase. J Pharm Anal 2023; 13(6): 640–659

[35]

Zhang QQ , Huang WQ , Gao YQ , Han ZD , Zhang W , Zhang ZJ , Xu FG . Metabolomics reveals the efficacy of caspase inhibition for Saikosaponin D-induced hepatotoxicity. Front Pharmacol 2018; 9: 732

[36]

Xu L , Song R , Tian JX , Tian Y , Liu GQ , Zhang ZJ . Analysis of saikosaponins in rat plasma by anionic adducts-based liquid chromatography tandem mass spectrometry method. Biomed Chromatogr 2012; 26(7): 808–815

[37]

Chen Y , Wang J , Yuan L , Zhou L , Jia X , Tan X . Interaction of the main components from the traditional Chinese drug pair Chaihu-Shaoyao based on rat intestinal absorption. Molecules 2011; 16(11): 9600–9610

[38]

Kida H , Akao T , Meselhy MR , Hattori M . Metabolism and pharmacokinetics of orally administered saikosaponin b1 in conventional, germ-free and Eubacterium sp. A-44-infected gnotobiote rats. Biol Pharm Bull 1998; 21(6): 588–593

[39]

Ren S , Liu J , Xue Y , Zhang M , Liu Q , Xu J , Zhang Z , Song R . Comparative permeability of three saikosaponins and corresponding saikogenins in Caco-2 model by a validated UHPLC-MS/MS method. J Pharm Anal 2021; 11(4): 435–443

[40]

Liu J , Xue Y , Sun J , Fu R , Ren S , Zhang Z , Song R . Pharmacokinetics and oral bioavailability studies of three saikogenins in rats using a validated UFLC-MS/MS method. J Chromatogr B Analyt Technol Biomed Life Sci 2019; 1124: 265–272

[41]

Fu RJ , Song R . Effect of Saikosaponin b2 on liver distribution of Saikosaponin a in rats. Guangzhou Chem Ind (Guangzhou Hua Gong) 2019; 47(11): 56–59

[42]

Yu BB , Wang L , Yin LS , Sun R . Research on biotransformation of saikosaponin A in vitro based on HPLC-DAD-MSn. Chin Tradit Herbal Drugs (Zhong Cao Yao) 2017; 48(2): 333–338

[43]

Shimizu K , Amagaya S , Ogihara Y . Structural transformation of saikosaponins by gastric juice and intestinal flora. J Pharmacobiodyn 1985; 8(9): 718–725

[44]

Tang C , Fu Q , Chen X , Hu Y , Renaud H , Ma C , Rao T , Chen Y , Tan Z , Klaassen CD , Shi S , Guo Y . The biotransformation of Bupleuri Radix by human gut microbiota. Xenobiotica 2020; 50(9): 1011–1022

[45]

Yu KU , Jang IS , Kang KH , Sung CK , Kim DH . Metabolism of saikosaponin c and naringin by human intestinal bacteria. Arch Pharm Res 1997; 20(5): 420–424

[46]

He Y , Hu Z , Li A , Zhu Z , Yang N , Ying Z , He J , Wang C , Yin S , Cheng S . Recent advances in biotransformation of saponins. Molecules 2019; 24(13): 2365

[47]

Zhou P , Shi W , He XY , Du QY , Wang F , Guo J . Saikosaponin D: review on the antitumour effects, toxicity and pharmacokinetics. Pharm Biol 2021; 59(1): 1478–1489

[48]

Yu P , Qiu H , Wang M , Tian Y , Zhang Z , Song R . In vitro metabolism study of saikosaponin d and its derivatives in rat liver microsomes. Xenobiotica 2017; 47(1): 11–19

[49]

Liu G , Tian Y , Li G , Xu L , Song R , Zhang Z . Metabolism of saikosaponin a in rats: diverse oxidations on the aglycone moiety in liver and intestine in addition to hydrolysis of glycosidic bonds. Drug Metab Dispos 2013; 41(3): 622–633

[50]

Fujiwara K , Ogihara Y . Pharmacological effects of oral saikosaponin a may differ depending on conditions of the gastrointestinal tract. Life Sci 1986; 39(4): 297–301

[51]

Liu LJ , Li JF , Chen GW , Yang CN , Wei JX , Li LQ , Weng XX , Xie S . Research progress on the relationship between “gut–liver axis” and cirrhosis. CJITWMD 2021; 29(3): 222–226

[52]

Balmer ML , Slack E , de Gottardi A , Lawson MA , Hapfelmeier S , Miele L , Grieco A , Van Vlierberghe H , Fahrner R , Patuto N , Bernsmeier C , Ronchi F , Wyss M , Stroka D , Dickgreber N , Heim MH , McCoy KD , Macpherson AJ . The liver may act as a firewall mediating mutualism between the host and its gut commensal microbiota. Sci Transl Med 2014; 6(237): 237ra66

[53]

Panzitt K , Wagner M . FXR in liver physiology: multiple faces to regulate liver metabolism. Biochim Biophys Acta Mol Basis Dis 2021; 1867(7): 166133

[54]

Xue R , Su L , Lai S , Wang Y , Zhao D , Fan J , Chen W , Hylemon PB , Zhou H . Bile acid receptors and the gut–liver axis in nonalcoholic fatty liver disease. Cells 2021; 10(11): 2806

[55]

Chen MJ , Liu C , Wan Y , Yang L , Jiang S , Qian DW , Duan JA . Enterohepatic circulation of bile acids and their emerging roles on glucolipid metabolism. Steroids 2021; 165: 108757

[56]

Hall B , Levy S , Dufault-Thompson K , Arp G , Zhong A , Ndjite GM , Weiss A , Braccia D , Jenkins C , Grant MR , Abeysinghe S , Yang Y , Jermain MD , Wu CH , Ma B , Jiang X . BilR is a gut microbial enzyme that reduces bilirubin to urobilinogen. Nat Microbiol 2024; 9(1): 173–184

[57]

Kipp ZA , Badmus OO , Stec DE , Hall B , Hinds TD Jr . Bilirubin bioconversion to urobilin in the gut–liver-kidney axis: a biomarker for insulin resistance in the Cardiovascular-Kidney-Metabolic (CKM) Syndrome. Metabolism 2025; 163: 156081

[58]

Vítek L , Tiribelli C . Gut microbiota and bilirubin metabolism: unveiling new pathways in health and disease. Trends Mol Med 2025; 31(7): 591–594

[59]

Kipp ZA , Pauss SN , Martinez GJ , Hinds TD Jr , Lee WH . Bilirubin hepatic and intestinal transport and catabolism: physiology, pathophysiology, and benefits. Antioxidants (Basel) 2025; 14(11): 1326

[60]

Hamoud AR , Weaver L , Stec DE , Hinds TD Jr . Bilirubin in the liver–gut signaling axis. Trends Endocrinol Metab 2018; 29(3): 140–150

[61]

Hu Q , Zhang W , Wu Z , Tian X , Xiang J , Li L , Li Z , Peng X , Wei S , Ma X , Zhao Y . Baicalin and the liver–gut system: pharmacological bases explaining its therapeutic effects. Pharmacol Res 2021; 165: 105444

[62]

Sun L , Cai J , Gonzalez FJ . The role of farnesoid X receptor in metabolic diseases, and gastrointestinal and liver cancer. Nat Rev Gastroenterol Hepatol 2021; 18(5): 335–347

[63]

Portincasa P , Bonfrate L , Vacca M , De Angelis M , Farella I , Lanza E , Khalil M , Wang DQ , Sperandio M , Di Ciaula A . Gut microbiota and short chain fatty acids: implications in glucose homeostasis. Int J Mol Sci 2022; 23(3): 1105

[64]

Liu W , Yang G , Liu P , Jiang X , Xin Y . Modulation of adipose tissue metabolism by microbial-derived metabolites. Front Microbiol 2022; 13: 1031498

[65]

Chen J , Vitetta L . Gut microbiota metabolites in NAFLD pathogenesis and therapeutic implications. Int J Mol Sci 2020; 21(15): 5214

[66]

Ji Y , Yin Y , Li Z , Zhang W . Gut microbiota-derived components and metabolites in the progression of non-alcoholic fatty liver disease (NAFLD). Nutrients 2019; 11(8): 1712

[67]

Philips CA , Schnabl B , Bajaj JS . Gut microbiome and alcohol-associated liver disease. J Clin Exp Hepatol 2022; 12(5): 1349–1359

[68]

Grander C , Adolph TE , Wieser V , Lowe P , Wrzosek L , Gyongyosi B , Ward DV , Grabherr F , Gerner RR , Pfister A , Enrich B , Ciocan D , Macheiner S , Mayr L , Drach M , Moser P , Moschen AR , Perlemuter G , Szabo G , Cassard AM , Tilg H . Recovery of ethanol-induced Akkermansia muciniphila depletion ameliorates alcoholic liver disease. Gut 2018; 67(5): 891–901

[69]

Lang S , Fairfied B , Gao B , Duan Y , Zhang X , Fouts DE , Schnabl B . Changes in the fecal bacterial microbiota associated with disease severity in alcoholic hepatitis patients. Gut Microbes 2020; 12(1): 1785251

[70]

Duan Y , Llorente C , Lang S , Brandl K , Chu H , Jiang L , White RC , Clarke TH , Nguyen K , Torralba M , Shao Y , Liu J , Hernandez-Morales A , Lessor L , Rahman IR , Miyamoto Y , Ly M , Gao B , Sun W , Kiesel R , Hutmacher F , Lee S , Ventura-Cots M , Bosques-Padilla F , Verna EC , Abraldes JG , Brown RS Jr , Vargas V , Altamirano J , Caballería J , Shawcross DL , Ho SB , Louvet A , Lucey MR , Mathurin P , Garcia-Tsao G , Bataller R , Tu XM , Eckmann L , van der Donk WA , Young R , Lawley TD , Stärkel P , Pride D , Fouts DE , Schnabl B . Bacteriophage targeting of gut bacterium attenuates alcoholic liver disease. Nature 2019; 575(7783): 505–511

[71]

Wandrer F , Liebig S , Marhenke S , Vogel A , John K , Manns MP , Teufel A , Itzel T , Longerich T , Maier O , Fischer R , Kontermann RE , Pfizenmaier K , Schulze-Osthoff K , Bantel H . TNF-Receptor-1 inhibition reduces liver steatosis, hepatocellular injury and fibrosis in NAFLD mice. Cell Death Dis 2020; 11(3): 212

[72]

Wang WM , Xu XS , Miao CM . Kupffer cell-derived TNF-α triggers the apoptosis of hepatic stellate cells through TNF-R1/caspase 8 due to ER stress. BioMed Res Int 2020; 2020(1): 8035671

[73]

Radziszewska M , Smarkusz-Zarzecka J , Ostrowska L , Pogodziński D . Nutrition and supplementation in ulcerative colitis. Nutrients 2022; 14(12): 2469

[74]

Ţălu Ş , Frumento D . A linkage between inflammatory bowel diseases and type 2 diabetes. Suranaree J Sci Technol 2023; 30(6): 070067(1–7)

[75]

Yao D , Dai W , Dong M , Dai C , Wu S . MUC2 and related bacterial factors: therapeutic targets for ulcerative colitis. EBioMedicine 2021; 74: 103751

[76]

Wu M , Wu Y , Li J , Bao Y , Guo Y , Yang W . The dynamic changes of gut microbiota in Muc2 deficient mice. Int J Mol Sci 2018; 19(9): 2809

[77]

Gao F , Xu Q , Lin Y , Zhang JW . Effect of saikosaponin A on IKK/IKB/NF-κB signaling pathway and apoptosis of intestinal epithelial cells in rats with ulcerative colitis. Chin J Gerontol (Zhongguo Lao Nian Xue Za zhi) 2022; 42(17): 4289–4294

[78]

Zhou F , Wang N , Yang L , Zhang LC , Meng LJ , Xia YC . Saikosaponin A protects against dextran sulfate sodium-induced colitis in mice. Int Immunopharmacol 2019; 72: 454–458

[79]

Ndrepepa G . Myeloperoxidase—a bridge linking inflammation and oxidative stress with cardiovascular disease. Clin Chim Acta 2019; 493: 36–51

[80]

Zhao L , Lei W , Deng C , Wu Z , Sun M , Jin Z , Song Y , Yang Z , Jiang S , Shen M , Yang Y . The roles of liver X receptor α in inflammation and inflammation-associated diseases. J Cell Physiol 2021; 236(7): 4807–4828

[81]

Mu HX , Liu J , Fatima S , Lin CY , Shi XK , Du B , Xiao HT , Fan BM , Bian ZX . Anti-inflammatory actions of (+)-3′α-angeloxy-4′-keto-3′,4′-dihydroseselin (Pd-Ib) against dextran sulfate sodium-induced colitis in C57BL/6 mice. J Nat Prod 2016; 79(4): 1056–1062

[82]

Shinji S , Yamada T , Matsuda A , Sonoda H , Ohta R , Iwai T , Takeda K , Yonaga K , Masuda Y , Yoshida H . Recent advances in the treatment of colorectal cancer: a review. J Nippon Med Sch 2022; 89(3): 246–254

[83]

Xiao LX , Zhou HN , Jiao ZY . Present and future prospects of the anti-cancer activities of saikosaponins. Curr Cancer Drug Targets 2023; 23(1): 2–14

[84]

Zhang X , Liu Z , Chen S , Li H , Dong L , Fu X . A new discovery: total Bupleurum saponin extracts can inhibit the proliferation and induce apoptosis of colon cancer cells by regulating the PI3K/Akt/mTOR pathway. J Ethnopharmacol 2022; 283: 114742

[85]

Kim BM , Hong SH . Sequential caspase-2 and caspase-8 activation is essential for saikosaponin a-induced apoptosis of human colon carcinoma cell lines. Apoptosis 2011; 16(2): 184–197

[86]

Yang KR , Wang JS . Saikosaponin-D inhibits the proliferation of colorectal cancer SW480 cell by inducing G2-M cell cycle arrest. J Mod Oncol (Xian Dai Zhong Liu Yi Xue) 2016; 24(9): 1353–1357

[87]

Dang F , Yang KR , Liu F , Han XP . The molecular mechanism disscussion on saikosaponin-D inhibits proliferation of colorectal cancer cell line SW480. J Mod Oncol (Xian Dai Zhong Liu Yi Xue) 2018; 26(14): 2159–2162

[88]

Dang F , Yang KR , Liu WP , Li F , Han XP . Saikosaponin-D inhibits the proliferation of colorectal cancer cell line SW480 by inducing autophagy: an experimental study. J Mod Oncol (Xian Dai Zhong Liu Yi Xue) 2020; 28(8): 1272–1276

[89]

Lu M , Sunlu HR , Yang J , Wang L . Effects of Saikosaponin D on apoptosis genes expression profile of the colon cancer cells HT-29. Afr J Pharm Pharmacol 2013; 7(24): 1640–1644

[90]

Dang F , Yang KR , Liu WP , Li F , Han XP . Saikosaponin-D inhibits cell migration and invasion via EMT and stemness suppression in colorectal cancer cell line SW480. JMod Oncol (Xian Dai Zhong Liu Yi Xue) 2020; 28(7): 1091–1096

[91]

Zhang Y , Lin L , Wang Y , Liu Z , Xia W , Sui H , Fu X . Saikosaponin B4 suppression cancer progression by inhibiting SW480 and SW620 cells proliferation via the PI3K/AKT/mTOR pathway in colon cancer. Curr Cancer Drug Targets 2022; 22(11): 889–903

[92]

Wu G , Win S , Than TA , Chen P , Kaplowitz N . Gut microbiota and liver injury (I)-acute liver injury. Adv Exp Med Biol 2020; 1238: 23–37

[93]

Jayalakshmi VT , Bernal W . Update on the management of acute liver failure. Curr Opin Crit Care 2020; 26(2): 163–170

[94]

Bak SB , Song YR , Bae SJ , Lee WY , Kim YW . Integrative approach to uncover antioxidant properties of Bupleuri Radix and its active compounds: multiscale interactome-level analysis with experimental validation. Free Radic Biol Med 2023; 199: 141–153

[95]

Zou C , Tan X , Ye H , Sun Z , Chen S , Liu Q , Xu M , Ye C , Wang A . The hepatoprotective effects of Radix Bupleuri extracts against D-galactosamine/lipopolysaccharide induced liver injury in hybrid grouper (Epinephelus lanceolatus♂ × Epinephelus fuscoguttatus♀). Fish Shellfish Immunol 2018; 83: 8–17

[96]

Lin L , Que R , Shen Y , Chen Y , Yan N , Li Y . Saikosaponin-d alleviates carbon-tetrachloride induced acute hepatocellular injury by inhibiting oxidative stress and NLRP3 inflammasome activation in the HL-7702 cell line. Mol Med Rep 2018; 17(6): 7939–7946

[97]

Liu A , Tanaka N , Sun L , Guo B , Kim JH , Krausz KW , Fang Z , Jiang C , Yang J , Gonzalez FJ . Saikosaponin d protects against acetaminophen-induced hepatotoxicity by inhibiting NF-κB and STAT3 signaling. Chem Biol Interact 2014; 223: 80–86

[98]

Chen Y , Que R , Lin L , Shen Y , Liu J , Li Y . Inhibition of oxidative stress and NLRP3 inflammasome by Saikosaponin-d alleviates acute liver injury in carbon tetrachloride-induced hepatitis in mice. Int J Immunopathol Pharmacol 2020; 34: 1–11

[99]

Chang GR , Lin WL , Lin TC , Liao HJ , Lu YW . The ameliorative effects of Saikosaponin in thioacetamide-induced liver injury and non-alcoholic fatty liver disease in mice. Int J Mol Sci 2021; 22(21): 11383

[100]

Lin LB , Que RY , Li YP , Shen YT , Chen YR , Li Y . Effect of saikosaponin-d on the expression of high mobility group protein B1 in mice with acute liver injury. J Li-Shizhen Tradit Chin Med (Shizhen Guo Yi Guo Yao) 2019; 30(3): 527–531

[101]

You M , Li RF , Gao ZH , Li YY , Liu WY , Wang JG , Wang HW , Li SQ . Effects of saikosaponin b_2 on inflammation and energy metabolism in mice with acute liver injury induced by LPS/GalN. China J Chin Mater Med (Zhongguo Zhong Yao Za Zhi) 2019; 44(14): 2966–2971

[102]

Lv XZ , Li RF , Gao ZH , Wang HW , Li SQ , Wang JG . Saikosaponin-b2 inhibits endoplasmic reticulum stress signaling pathway to alleviate acute liver injury induced by carbon tetrachloride in mice. Chin J Pharmacol Toxicol (Zhongguo Yao Li Xue Yu Du Li Xue Za Zhi) 2019; 33(2): 109–115

[103]

Zhao W , Li JJ , Yue SQ , Zhang LY , Dou KF . Antioxidant activity and hepatoprotective effect of a polysaccharide from Bei Chaihu (Bupleurum chinense DC). Carbohydr Polym 2012; 89(2): 448–452

[104]

Nassir F . NAFLD: mechanisms, treatments, and biomarkers. Biomolecules 2022; 12(6): 824

[105]

Xu R , Pan J , Zhou W , Ji G , Dang Y . Recent advances in lean NAFLD. Biomed Pharmacother 2022; 153: 113331

[106]

Flessa CM , Kyrou I , Nasiri-Ansari N , Kaltsas G , Kassi E , Randeva HS . Endoplasmic reticulum stress in nonalcoholic (metabolic associated) fatty liver disease (NAFLD/MAFLD). J Cell Biochem 2022; 123(10): 1585–1606

[107]

Gu M , Zhao P , Zhang S , Fan S , Yang L , Tong Q , Ji G , Huang C . Betulinic acid alleviates endoplasmic reticulum stress-mediated nonalcoholic fatty liver disease through activation of farnesoid X receptors in mice. Br J Pharmacol 2019; 176(7): 847–863

[108]

Wu L , Guo T , Deng R , Liu L , Yu Y . Apigenin ameliorates insulin resistance and lipid accumulation by endoplasmic reticulum stress and SREBP-1c/SREBP-2 pathway in Palmitate-induced HepG2 cells and high-fat diet-fed mice. J Pharmacol Exp Ther 2021; 377(1): 146–156

[109]

Yeh KY , Lai CY , Lin CY , Hsu CC , Lo CP , Her GM . ATF4 overexpression induces early onset of hyperlipidaemia and hepatic steatosis and enhances adipogenesis in zebrafish. Sci Rep 2017; 7(1): 16362

[110]

Hu H , Tian M , Ding C , Yu S . The C/EBP homologous protein (CHOP) transcription factor functions in endoplasmic reticulum stress-induced apoptosis and microbial infection. Front Immunol 2019; 9: 3083

[111]

Nasiri-Ansari N , Nikolopoulou C , Papoutsi K , Kyrou I , Mantzoros CS , Kyriakopoulos G , Chatzigeorgiou A , Kalotychou V , Randeva MS , Chatha K , Kontzoglou K , Kaltsas G , Papavassiliou AG , Randeva HS , Kassi E . Empagliflozin attenuates non-alcoholic fatty liver disease (NAFLD) in high fat diet fed ApoE–/– mice by activating autophagy and reducing ER stress and apoptosis. Int J Mol Sci 2021; 22(2): 818

[112]

Gu Y , Duan S , Ding M , Zheng Q , Fan G , Li X , Li Y , Liu C , Sun R , Liu R . Saikosaponin D attenuates metabolic associated fatty liver disease by coordinately tuning PPARα and INSIG/SREBP1c pathway. Phytomedicine 2022; 103: 154219

[113]

Li X , Ge J , Li Y , Cai Y , Zheng Q , Huang N , Gu Y , Han Q , Li Y , Sun R , Liu R . Integrative lipidomic and transcriptomic study unravels the therapeutic effects of saikosaponins A and D on non-alcoholic fatty liver disease. Acta Pharm Sin B 2021; 11(11): 3527–3541

[114]

Liu XC , Wu JJ , Zhang W , Hu J , Lai RY . Effect of saikosaponin A on insulin resistance in nonalcoholic fatty liver disease mice induced by high fat. Chin J Clin Pharmacol (Zhongguo Lin Chuang Yao Li Xue Za Zhi) 2020; 36(7): 772–774

[115]

Chen H , Sun Y , Zhao H , Qi X , Cui H , Li Q , Ma Y . α-Lactalbumin peptide Asp-Gln-Trp alleviates hepatic insulin resistance and modulates gut microbiota dysbiosis in high-fat diet-induced NAFLD mice. Food Funct 2022; 13(19): 9878–9892

[116]

Kong LZ , Chandimali N , Han YH , Lee DH , Kim JS , Kim SU , Kim TD , Jeong DK , Sun HN , Lee DS , Kwon T . Pathogenesis, early diagnosis, and therapeutic management of alcoholic liver disease. Int J Mol Sci 2019; 20(11): 2712

[117]

Fu K , Wang C , Ma C , Zhou H , Li Y . The potential application of Chinese medicine in liver diseases: a new opportunity. Front Pharmacol 2021; 12: 771459

[118]

Liu SY , Tsai IT , Hsu YC . Alcohol-related liver disease: basic mechanisms and clinical perspectives. Int J Mol Sci 2021; 22(10): 5170

[119]

Gupta P , Venugopal SK . Augmenter of liver regeneration: a key protein in liver regeneration and pathophysiology. Hepatol Res 2018; 48(8): 587–596

[120]

Verma AK , Sharma A , Subramaniyam N , Gandhi CR . Augmenter of liver regeneration: mitochondrial function and steatohepatitis. J Hepatol 2022; 77(5): 1410–1421

[121]

Ge HY , Chen B , Liu HL . Effect of saikosaponin on the expression of augmenter of liver regeneration in rats with alcoholic liver disease. Chin J Gerontol (Zhongguo Lao Nian Xue Za Zhi) 2013; 33(16): 3923–3924

[122]

Ge HY , Chen B , Li YT . Protective effects of saikoside on rats with alcoholic liver disease. J Clin Hepatol (Lin Chuang Gan Dan Bing Za Zhi) 2012; 28(12): 945–947

[123]

Huang XF , Liu ZG , Lei P , Meng ZJ , Wang LB , Du SM . Protective effect of saikosaponin-d on H2O2-induced hepatocellular injury and its mechanism. Chin J Pharmacol Toxicol (Zhongguo Yao Li Xue Yu Du Li Xue Za Zhi) 2021; 35(03): 169–175

[124]

Wu X , Fan X , Miyata T , Kim A , Cajigas-Du Ross CK , Ray S , Huang E , Taiwo M , Arya R , Wu J , Nagy LE . Recent advances in understanding of pathogenesis of alcohol-associated liver disease. Annu Rev Pathol 2023; 18(1): 411–438

[125]

Taniai M . Alcohol and hepatocarcinogenesis. Clin Mol Hepatol 2020; 26(4): 736–741

[126]

Chuang YC , Tsai KN , Ou JJ . Pathogenicity and virulence of Hepatitis B virus. Virulence 2022; 13(1): 258–296

[127]

Fanning GC , Zoulim F , Hou J , Bertoletti A . Therapeutic strategies for hepatitis B virus infection: towards a cure. Nat Rev Drug Discov 2019; 18(11): 827–844

[128]

Zhao Q , Ren X , Chen M , Yue SJ , Zhang MQ , Chen KX , Guo YW , Shao CL , Wang CY . Effects of traditional Chinese medicine formula Le-Cao-Shi on hepatitis B: in vivo and in vitro studies. J Ethnopharmacol 2019; 244: 112132

[129]

Chiang LC , Ng LT , Liu LT , Shieh DE , Lin CC . Cytotoxicity and anti-hepatitis B virus activities of saikosaponins from Bupleurum species. Planta Med 2003; 69(8): 705–709

[130]

Pan Y , Ke Z , Ye H , Sun L , Ding X , Shen Y , Zhang R , Yuan J . Saikosaponin C exerts anti-HBV effects by attenuating HNF1α and HNF4α expression to suppress HBV pgRNA synthesis. Inflamm Res 2019; 68(12): 1025–1034

[131]

Yang L , Wang H , Yan H , Wang K , Wu S , Li Y . (−)-Lariciresinol isolated from the roots of Isatis indigotica Fortune ex Lindl. Inhibits Hepatitis B virus by regulating viral transcription. Molecules 2022; 27(10): 3223

[132]

Park S , Ha YN , Dezhbord M , Lee AR , Park ES , Park YK , Won J , Kim NY , Choo SY , Shin JJ , Ahn CH , Kim KH . Suppression of hepatocyte nuclear factor 4 α by long-term infection of hepatitis B virus contributes to tumor cell proliferation. Int J Mol Sci 2020; 21(3): 948

[133]

Sato A , Ono C , Tamura T , Mori H , Izumi T , Torii S , Fauzyah Y , Yamamoto T , Morioka Y , Okuzaki D , Fukuhara T , Matsuura Y . Rimonabant suppresses RNA transcription of hepatitis B virus by inhibiting hepatocyte nuclear factor 4α. Microbiol Immunol 2020; 64(5): 345–355

[134]

Li X , Ke Z , Lian D , Yuan J , Pan Y . Combination of saikosaponin c and telbivudine synergistically enhances the anti-HBV activity. Inflamm Res 2020; 69(6): 545–547

[135]

Sucher E , Sucher R , Gradistanac T , Brandacher G , Schneeberger S , Berg T . Autoimmune hepatitis-immunologically triggered liver pathogenesis-diagnostic and therapeutic strategies. J Immunol Res 2019; 2019: 1–19

[136]

Olivas I , Rodríguez-Tajes S , Londoño MC . Autoimmune hepatitis: challenges and novelties. Med Clin (Barc) 2022; 159(6): 289–298

[137]

Dalekos GN , Samakidou A , Lyberopoulou A , Banakou E , Gatselis NK . Recent advances in the diagnosis and management of autoimmune hepatitis. Pol Arch Intern Med 2022; 132(9): 16334

[138]

Chen H , Hao JT , Li ZC , Xu HC , Gao Y , Miao YC , Hao HQ , Liu Y . Screening for differentially expressed genes in mice with autoimmune hepatitis and effect of saikosaponin-d on the expression of several differentially expressed genes. J Clin Hepatol (Lin Chuang Gan Dan Bing Za Zhi) 2020; 36(4): 840–846

[139]

Hao JT , Chen H , Gao Y , Xu HC , Gao YT , Miao YC , Hao HQ , Liu Y . Effects of Saikosaponin d on differentially expressed genes CTLA-4, IL-10 and IL-17 in mice with autoimmune hepatitis. J Shanghai Jiaotong Univ (Med Sci) (Shanghai Jiao Tong Da Xue Xue Bao (Yi Xue Ban)) 2020; 40(3): 303–309

[140]

Ding H , Wang G , Yu Z , Sun H , Wang L . Role of interferon-gamma (IFN-γ) and IFN-γ receptor 1/2 (IFNγR1/2) in regulation of immunity, infection, and cancer development: IFN-γ-dependent or independent pathway. Biomed Pharmacother 2022; 155: 113683

[141]

Hosseini A , Gharibi T , Marofi F , Babaloo Z , Baradaran B . CTLA-4: From mechanism to autoimmune therapy. Int Immunopharmacol 2020; 80: 106221

[142]

Leung CY , Liu L , Wong RN , Zeng YY , Li M , Zhou H . Saikosaponin-d inhibits T cell activation through the modulation of PKCtheta, JNK, and NF-kappaB transcription factor. Biochem Biophys Res Commun 2005; 338(4): 1920–1927

[143]

Wong VK , Zhou H , Cheung SS , Li T , Liu L . Mechanistic study of saikosaponin-d (Ssd) on suppression of murine T lymphocyte activation. J Cell Biochem 2009; 107(2): 303–315

[144]

Wang W , Wang LN , Xu Z , Jia TZ . Comparative study on the anti- immunological hepatic fibrosis effects of Bupleurum chinense and vinegar Bupleurum chinense in rats. Chin Tradit Pat Med (Zhong Cheng Yao) 2014; 36(4): 828–830

[145]

Dhar D , Baglieri J , Kisseleva T , Brenner DA . Mechanisms of liver fibrosis and its role in liver cancer. Exp Biol Med (Maywood) 2020; 245(2): 96–108

[146]

Ren LL , Li XJ , Duan TT , Li ZH , Yang JZ , Zhang YM , Zou L , Miao H , Zhao YY . Transforming growth factor-β signaling: From tissue fibrosis to therapeutic opportunities. Chem Biol Interact 2023; 369: 110289

[147]

Yang Z , Zhang H , Yin M , Cheng Z , Jiang P , Feng M , Liu Z , Liao B . TGF-β1/Smad3 upregulates UCA1 to promote liver fibrosis through DKK1 and miR18a. J Mol Med (Berl) 2022; 100(10): 1465–1478

[148]

Wu SJ , Tam KW , Tsai YH , Chang CC , Chao JC . Curcumin and saikosaponin a inhibit chemical-induced liver inflammation and fibrosis in rats. Am J Chin Med 2010; 38(1): 99–111

[149]

Zhang K , Lin L , Zhu Y , Zhang N , Zhou M , Li Y . Saikosaponin d alleviates liver fibrosis by negatively regulating the ROS/NLRP3 inflammasome through activating the ERβ pathway. Front Pharmacol 2022; 13: 1–15

[150]

Hu CH , He Y . Effect of saikosaponin D on TGF-β/Smad signaling pathway in regulating high glucose induced fibrosis of HK-2 cells. J Shenyang Pharm Univ (Shenyang Yao Ke Da Xue Xue Bao) 2022; 39(12): 1471–1477

[151]

Chen YR , Que RY , Liu JK , Lin LB , Li Y . Influence of Saikosaponins-d on the Expressions of TGFβ-Smad Signal Path mRNA in Rat Hepatic Stellate Cells. West J Tradit Chin Med (Xi Bu Zhong Yi Yao) 2022; 35(8): 15–19

[152]

Li ST , Wang BY , Yang HM , Qi JM , Wang R . Effect of saikosaponin on the expression of transforming growth factor-β1 and α-smooth muscle actin in liver of rats with alcoholic liver disease. Chin J Gerontol (Zhongguo Lao Nian Xue Za Zhi) 2011; 31(22): 4389–4391

[153]

Zhangdi HJ , Su SB , Wang F , Liang ZY , Yan YD , Qin SY , Jiang HX . Crosstalk network among multiple inflammatory mediators in liver fibrosis. World J Gastroenterol 2019; 25(33): 4835–4849

[154]

Lin L , Zhou M , Que R , Chen Y , Liu X , Zhang K , Shi Z , Li Y . Saikosaponin-d protects against liver fibrosis by regulating the estrogen receptor-β/NLRP3 inflammasome pathway. Biochem Cell Biol 2021; 99(5): 666–674

[155]

Huang Y , Xia L , Lei QS , Zhang CJ , Liu HB , Li L . Protective effects and mechanism of saikosaponin D on immune hepatic fibrosis in rats. J Army Med Univ (Lu Jun Jun Yi Da Xue Xue Bao) 2022; 44(14): 1410–1420

[156]

Zhang N , Li Y . Study on protective effect of Bupleurin D on human hepatocyte injury and mechanism of anti-liver fibrosis. Chin Arch Tradit Chin Med (Zhong Hua Zhong Yi Yao Xue Kan) 2021; 39(12): 21–27+275

[157]

Chen Y , Que R , Zhang N , Lin L , Zhou M , Li Y . Saikosaponin-d alleviates hepatic fibrosis through regulating GPER1/autophagy signaling. Mol Biol Rep 2021; 48(12): 7853–7863

[158]

Li J , Zeng C , Zheng B , Liu C , Tang M , Jiang Y , Chang Y , Song W , Wang Y , Yang C . HMGB1-induced autophagy facilitates hepatic stellate cells activation: a new pathway in liver fibrosis. Clin Sci (Lond) 2018; 132(15): 1645–1667

[159]

Ginès P , Krag A , Abraldes JG , Solà E , Fabrellas N , Kamath PS . Liver cirrhosis. Lancet 2021; 398(10308): 1359–1376

[160]

Engelmann C , Clària J , Szabo G , Bosch J , Bernardi M . Pathophysiology of decompensated cirrhosis: portal hypertension, circulatory dysfunction, inflammation, metabolism and mitochondrial dysfunction. J Hepatol 2021; 75(Suppl 1): S49–S66

[161]

Zhang F , Wang F , He J , Lian N , Wang Z , Shao J , Ding H , Tan S , Chen A , Zhang Z , Wang S , Zheng S . Regulation of hepatic stellate cell contraction and cirrhotic portal hypertension by Wnt/β-catenin signalling via interaction with Gli1. Br J Pharmacol 2021; 178(11): 2246–2265

[162]

Wang Y , Pang X , Zhang BC , Yu CY , Wang L . Effects of saikosaponin d on hepatic stellate cells. J Beijing Univ Chem Technol (Nat Sci Ed) (Beijing Hua Gong Da Xue Xue Bao (Zi Ran Ke Xue Ban)) 2020; 47(5): 76–82

[163]

Lin LB , Que RY , Liu JK , Shen YT , Tao ZH , Li Y . Effect of saikosaponin-d on expression of matrix metalloproteinase-1 and tissue inhibitor of metalloproteinase-1 in activated HSC-T6 cells: underlying mechanism. World Chin J Digestology 2016; 24(8): 1159–1165

[164]

Que R , Shen Y , Ren J , Tao Z , Zhu X , Li Y . Estrogen receptor-β-dependent effects of saikosaponin-d on the suppression of oxidative stress-induced rat hepatic stellate cell activation. Int J Mol Med 2018; 41(3): 1357–1364

[165]

Jiang H , Liu J , Zhang K , Zeng Q . Saikosaponin D inhibits the proliferation and promotes the apoptosis of rat hepatic stellate cells by inducing autophagosome formation. Evid Based Complement Alternat Med 2021; 2021: 1–10

[166]

Chen MF , Huang CC , Liu PS , Chen CH , Shiu LY . Saikosaponin a and saikosaponin d inhibit proliferation and migratory activity of rat HSC-T6 cells. J Med Food 2013; 16(9): 793–800

[167]

Kong M , Chen X , Lv F , Ren H , Fan Z , Qin H , Yu L , Shi X , Xu Y . Serum response factor (SRF) promotes ROS generation and hepatic stellate cell activation by epigenetically stimulating NCF1/2 transcription. Redox Biol 2019; 26: 101302

[168]

Du Z , Lin Z , Wang Z , Liu D , Tian D , Xia L . SPOCK1 overexpression induced by platelet-derived growth factor-BB promotes hepatic stellate cell activation and liver fibrosis through the integrin α5β1/PI3K/Akt signaling pathway. Lab Invest 2020; 100(8): 1042–1056

[169]

Muscella A , Vetrugno C , Cossa LG , Marsigliante S . TGF-β1 activates RSC96 Schwann cells migration and invasion through MMP-2 and MMP-9 activities. J Neurochem 2020; 153(4): 525–538

[170]

Yu ZQ , Wang LM , Yang WX . How vitamin E and its derivatives regulate tumour cells via the MAPK signalling pathway. Gene 2022; 808: 145998

[171]

Cai S , Wu L , Yuan S , Liu G , Wang Y , Fang L , Xu D . Carvacrol alleviates liver fibrosis by inhibiting TRPM7 and modulating the MAPK signaling pathway. Eur J Pharmacol 2021; 898: 173982

[172]

Wang W , Wei C . Advances in the early diagnosis of hepatocellular carcinoma. Genes Dis 2020; 7(3): 308–319

[173]

Vogel A , Meyer T , Sapisochin G , Salem R , Saborowski A . Hepatocellular carcinoma. Lancet 2022; 400(10360): 1345–1362

[174]

Liu C , Yang S , Wang K , Bao X , Liu Y , Zhou S , Liu H , Qiu Y , Wang T , Yu H . Alkaloids from traditional Chinese medicine against hepatocellular carcinoma. Biomed Pharmacother 2019; 120: 109543

[175]

Jia W , Wang L . Using traditional Chinese medicine to treat hepatocellular carcinoma by targeting tumor immunity. Evid Based Complement Alternat Med 2020; 2020(1): 9843486

[176]

Zhang Z , Li JW , Zeng PH , Gao WH , Tian XF . Data mining and systems pharmacology to elucidate effectiveness and mechanisms of Chinese medicine in treating primary liver cancer. Chin J Integr Med 2022; 28(7): 636–643

[177]

Ren M , McGowan E , Li Y , Zhu X , Lu X , Zhu Z , Lin Y , He S . Saikosaponin-d suppresses COX2 through p-STAT3/C/EBPβ signaling pathway in liver cancer: a novel mechanism of action. Front Pharmacol 2019; 10: 623

[178]

Hsu YL , Kuo PL , Chiang LC , Lin CC . Involvement of p53, nuclear factor kappaB and Fas/Fas ligand in induction of apoptosis and cell cycle arrest by saikosaponin d in human hepatoma cell lines. Cancer Lett 2004; 213(2): 213–221

[179]

Wu QX , Li HC , Qiao ZQ , Jia TY . Inhibition of saikosaponin D on cell proliferation of HepG2 cells and tumor growth of liver cancer. Chin J Immunol (Zhongguo Mian Yi Xue Za Zhi) 2018; 34(11): 1664–1668

[180]

Lu XL , Lu CH , Cao Y , Zhang X , Wang X , Li YR , Guo D , He SX . Saikosaponin-d simultaneously apoptotic and paraptosis-like cell death in hepatoma cells. J Xi’an Jiaotong Univ (Med Sci) (Xi’an Jiaotong Da Xue Xue Bao (Yi Xue Ban)) 2020; 41(06): 966–971

[181]

Wang ZM , Wang M , Xiao HZ . Effect and mechanism of Saikosaponin D on autophagy by regulating mTORC pathway in human hepatocellular carcinoma cells. Chin Pharm J (Zhongguo Yao Xue Za Zhi) 2018; 53(19): 1652–1657

[182]

Ji MF , Xu HC . Effect of saponin D on autophagy of human hepatocellular carcinoma cells and its molecular mechanism. J North Pharm (Bei Fang Yao Xue) 2021; 18(11): 1–4

[183]

Wang B , Min W , Lin S , Song L , Yang P , Ma Q , Guo J . Saikosaponin-d increases radiation-induced apoptosis of hepatoma cells by promoting autophagy via inhibiting mTOR phosphorylation. Int J Med Sci 2021; 18(6): 1465–1473

[184]

Xiao Y , Ren MD , Lu GF , Zhao Y , Zhang D , Liu YP , Lu XL , He SX . The effects of saikosaponin-d on the expression of human hepatocellular carcinoma cell BECN1 and autophagy function. J Xi’an Jiaotong Univ (Med Sci) (Xi’an Jiao Tong Da Xue Xue Bao (Yi Xue Ban)) 2017; 38(1): 127–130+150

[185]

Tian YD , Lin S , Yang PT , Bai MH , Jin YY , Min WL , Ma HB , Wang BF . Saikosaponin-d increases the radiosensitivity of hepatoma cells by adjusting cell autophagy. J Cancer 2019; 10(20): 4947–4953

[186]

Ma R , Gao ZH , Bai X , Li RF , Wang HW , Wang JG . Effect of Saikosaponin-b2 on angiogenesis in primary liver cancer mice. Chin J Clin Pharmacol (Zhongguo Lin Chuang Yao Li Xue Za Zhi) 2020; 36(14): 2063–2065

[187]

Wu L , Yan Q , Chen F , Cao C , Wang S . Bupleuri radix extract ameliorates impaired lipid metabolism in high-fat diet-induced obese mice via gut microbia-mediated regulation of FGF21 signaling pathway. Biomed Pharmacother 2021; 135: 1–17

[188]

Li XY , He C , Zhu Y , Lu NH . Role of gut microbiota on intestinal barrier function in acute pancreatitis. World J Gastroenterol 2020; 26(18): 2187–2193

[189]

Zhou CH , Meng YT , Xu JJ , Fang X , Zhao JL , Zhou W , Zhao J , Han JC , Zhang L , Wang KX , Hu LH , Liao Z , Zou WB , Li ZS , Zou DW . Altered diversity and composition of gut microbiota in Chinese patients with chronic pancreatitis. Pancreatology 2020; 20(1): 16–24

[190]

Hong J , Fu Y , Chen X , Zhang Y , Li X , Li T , Liu Y , Fan M , Lin R . Gut microbiome changes associated with chronic pancreatitis and pancreatic cancer: a systematic review and meta-analysis. Int J Surg 2024; 110(9): 5781–5794

[191]

Hou S , Tang X , Cui H , Liu C , Bai X , Shi L , Shi Y . Fatty liver disease is associated with the severity of acute pancreatitis: a systematic review and meta-analysis. Int J Surg 2019; 65: 147–153

[192]

Li J , Han J , Lv J , Wang S , Qu L , Jiang Y . Saikosaponin A-induced gut microbiota changes attenuate severe acute pancreatitis through the activation of Keap1/Nrf2-ARE antioxidant signaling. Oxid Med Cell Longev 2020; 2020: 1–19

[193]

Li C , Cui L , Zhang L , Yang L , Zhuo Y , Cui J , Cui N , Zhang S . Saikosaponin D attenuates pancreatic injury through suppressing the apoptosis of acinar cell via modulation of the MAPK signaling pathway. Front Pharmacol 2021; 12: 735079

[194]

Cui LH , Li CX , Zhuo YZ , Yang L , Cui NQ , Zhang SK . Saikosaponin d ameliorates pancreatic fibrosis by inhibiting autophagy of pancreatic stellate cells via PI3K/Akt/mTOR pathway. Chem Biol Interact 2019; 300: 18–26

[195]

Wang CZ , Liu C , Chen XB , Wang XR , Ma XJ . Analysis of 531 cases of adverse drug reactions/events of Bupleurum Injection. Strait Pharm J (Hai Xia Yao Xue) 2018; 30(08): 279–281

[196]

Zhou AQ . Study on the types and causes of common clinical adverse reactions of Bupleurum Injection and intervention measures. J China Prescription Drug (Zhongguo Chu Fang Yao) 2022; 20(12): 96–98

[197]

Awshima Y . The truth of accident-some patient died from side effects of Xiao Chai Hu Tang. J Tianjin Univ Tradit Chin Med (Tianjin Zhong Yi Yao Da Xue Xue Bao) 2002; 21(1): 47–48

[198]

Hou L , Wang L , Liu RP , Sun R . Study on basis of liver toxicity of decoction Bupleurum chinense based on integrated model of spectrum toxicity relationship and liver toxicity network. Chin Tradit Herb Drugs (Zhong Cao Yao) 2020; 51(10): 2798–2806

[199]

Yang Y , Chen H , Sun J , Chen Y , Bai D , Wang S , Zhang J , Song J , Sun Z , Dai L . Research progress on extraction, purification, biotransformation, pharmacological effects, toxicity, combined therapy and new dosage forms of saikosaponins. J Ethnopharmacol 2025; 352: 120274

[200]

Huang W , Sun R . Study on hepatotoxicity on rats caused by crude extracts of total saikosaponins and correlation with oxidative damage mechanism. China J Chin Mater Med (Zhongguo Zhongyao Zazhi) 2010; 35(13): 1745–1749

[201]

Sun R , Yang Q . Experimental study on the “dosage-time-toxicity” relationship of chronic hepatotoxicity induced by volatile oil from Bupleurum chinense in rats. Pharmacol Clin Chin Mater Med (Zhong Yao Yao Li Yu Lin Chuang) 2011; 27(03): 49–51

[202]

Lin M , Zhang W , Su J . Toxic polyacetylenes in the genus Bupleurum (Apiaceae)—distribution, toxicity, molecular mechanism and analysis. J Ethnopharmacol 2016; 193: 566–573

[203]

Li X , Li X , Lu J , Huang Y , Lv L , Luan Y , Liu R , Sun R . Saikosaponins induced hepatotoxicity in mice via lipid metabolism dysregulation and oxidative stress: a proteomic study. BMC Complement Altern Med 2017; 17(1): 219

[204]

Li XY , Li XJY , Sun R . “Dose-time-toxicity” relationship and its mechanism of Saikosdponin d on the human liver L-02 cells in vitro. Pharmacol Clin Chin Mater Med (Zhong Yao Yao Li Yu Lin Chuang) 2016; 32(2): 87–90

[205]

Chen L , Zhang F , Kong D , Zhu X , Chen W , Wang A , Zheng S . Saikosaponin D disrupts platelet-derived growth factor-β receptor/p38 pathway leading to mitochondrial apoptosis in human LO2 hepatocyte cells: a potential mechanism of hepatotoxicity. Chem Biol Interact 2013; 206(1): 76–82

[206]

Zhang F , Chen L , Jin H , Shao J , Wu L , Lu Y , Zheng S . Activation of Fas death receptor pathway and Bid in hepatocytes is involved in saikosaponin D induction of hepatotoxicity. Environ Toxicol Pharmacol 2016; 41: 8–13

[207]

Wang YF , Ma RX , Zou B , Li J , Yao Y , Li J . Endoplasmic reticulum stress regulates autophagic response that is involved in Saikosaponin a-induced liver cell damage. Toxicol In Vitro 2023; 88: 105534

[208]

Wang RM , Lv LL , Huang W , Huang YY , Sun R . Research on mechanism of energy metabolism disorders of rat’s hepatoxicity induced by saikosaponins. China J Chin Mater Med (Zhongguo Zhong Yao Za Zhi) 2011; 36(18): 2557–2561

[209]

Sun R , Huang YY , Huang W , Lv LL , Qian XL , Lu JX , Wang Y . The research on dose-time-toxicity relationship of hepatotoxicity based on abnormal energy metabolism of mice livers caused by exracts of saikosaponins. Pharmacol Clin Chin Mater Med (Zhong Yao Yao Li Yu Lin Chuang) 2012; 28(4): 60–62

[210]

Yang Q , Sun R . Experimental study on mechanisms of hepar-toxical oxidative damage in rats caused by essential oil from Bupleurum chinense. Pharmacol Clin Chin Mater Med (Zhong Yao Yao Li Yu Lin Chuang) 2010; 26(5): 59–61

[211]

Yang Q , Sun R . Study on mechanism of cytokine and no injury in the Hepatotoxical injury in rats caused by volatile oil from Bupleurum chinense. Chin J Pharmacovigilance (Zhongguo Yao Wu Jing Jie) 2011; 8(8): 459–461

[212]

Sun R , Yang Q . Effect of volatile oil from Bupleurum chinense on energy metabolism of the liver in rats. Chin J Pharmacol Toxicol (Zhongguo Yaolixue Yu Dulixue Zazhi) 2011; 25(3): 310–313

[213]

Yuan C , Fan J , Jiang L , Ye W , Chen Z , Wu W , Huang Q , Qian L . Integrated analysis of gut microbiome and liver metabolome to evaluate the effects of fecal microbiota transplantation on lipopolysaccharide/D-galactosamine-induced acute liver injury in mice. Nutrients 2023; 15(5): 1149

[214]

Huang XH , Zhou TT . Investigation on the mechanism of anti-drug-induced liver injury and related effector substances of traditional Chinese medicine from the perspective of metabolism. Acta Pharm Sin B (Yao Xue Xue Bao) 2023; 58(3): 646–658

[215]

Zeng Q , Feng J , T , Xu L , Min C , Xie H . Influence of chromatogram baseline shifts and exogenous metabolite signals on metabolic profiles of traditional Chinese medicine Chaihu and its liver toxicity metabonomics. Chem Res Chin Univ 2017; 33(1): 17–23

[216]

Zhang XY , Li CJ , Hu Y , Sun LJ . Theoretical connotation and extended application of “the principle that if there is enough reason, a toxic medicine can also be used without harm”. Henan Tradit Chin Med (Henan Zhong Yi) 2021; 41(8): 1142–1146

RIGHTS & PERMISSIONS

Higher Education Press

PDF (5327KB)

211

Accesses

0

Citation

Detail

Sections
Recommended

/