Yinchenhao Decoction Combined with Praziquantel Ameliorates Inflammation and Hepatic Fibrosis in Schistosoma japonicum-Infected Mice

Jia-hua Liu , Mei Peng , Fang Chen , Qiu-yue Song , Li-chao Zhang , Yao Liao , Lan-gui Song , Zhong-dao Wu

Current Medical Science ›› 2025, Vol. 45 ›› Issue (4) : 944 -956.

PDF
Current Medical Science ›› 2025, Vol. 45 ›› Issue (4) : 944 -956. DOI: 10.1007/s11596-025-00089-1
Original Article
research-article

Yinchenhao Decoction Combined with Praziquantel Ameliorates Inflammation and Hepatic Fibrosis in Schistosoma japonicum-Infected Mice

Author information +
History +
PDF

Abstract

Objective

This study aimed to investigate the therapeutic effects and underlying mechanisms of the combination of Yinchenhao decoction (YCHD) and praziquantel (PZQ) in a Schistosoma japonicum (S. japonicum)-induced mouse model of schistosomiasis.

Methods

Six-week-old male BALB/c mice were randomly divided into five groups: control group, infected group, infected-PZQ group (I-PZQ), infected-YCHD group (I-YCHD), and infected-PZQ + YCHD group (I-PZQ + YCHD). The mice were infected with S. japonicum cercariae in infected group, I-PZQ group, I-YCHD group, and I-PZQ + YCHD group (n = 6 per group) and maintained for 63 days. From day 43 to day 63 postinfection, the mice received PZQ (150 mg/kg, intragastric gavage), YCHD (10 mL/kg, intragastric gavage), or a combination of both. The control and infected groups received equal amounts of sterile double-distilled water for the same period. At the end of the experiment, the mice were anesthetized with pentobarbital sodium and sacrificed. Serum alanine transaminase (ALT) and aspartate transaminase (AST) levels were measured. Network pharmacology analysis was used to predict the targets of YCHD in the treatment of schistosomiasis. Histopathological analysis, Western blotting, immunofluorescence, quantitative polymerase chain reaction and flow cytometry were employed to evaluate liver pathology and molecular changes.

Results

Compared with the other groups, the I-PZQ + YCHD group presented significantly decreased serum ALT and AST levels (P < 0.001). The I-PZQ + YCHD group exhibited improved pathological changes in the liver, as evidenced by reduced area of single granuloma (P < 0.01), granuloma area (P < 0.01), and Ishak score of liver fibrosis (P < 0.01). Network pharmacology analysis suggested that YCHD may alleviate schistosomiasis-related liver injury through the modulation of the endoplasmic reticulum stress (ERS) pathway. Western blot analysis revealed that ERS-related markers, including glucose-regulated protein 78 (GRP78), inositol-requiring enzyme 1 alpha (IRE1α), X-box binding protein 1 (XBP-1), and C/EBP homologous protein (CHOP), were significantly downregulated in the I-PZQ + YCHD group (P < 0.05). Furthermore, the I-PZQ + YCHD group presented reduced hepatocyte apoptosis (P < 0.05), diminished hepatic macrophage infiltration (P < 0.05) and downregulated expression of proinflammatory cytokines (TNF-α, IL-1β and IL-6) (P < 0.05).

Conclusion

YCHD combined with PZQ reduced schistosomiasis-associated hepatic granulomatous inflammation and fibrosis by inhibiting hepatic apoptosis and ERS.

Keywords

Schistosomiasis / Praziquantel / Yinchenhao decoction / Endoplasmic reticulum stress / Granuloma / Fibrosis

Cite this article

Download citation ▾
Jia-hua Liu, Mei Peng, Fang Chen, Qiu-yue Song, Li-chao Zhang, Yao Liao, Lan-gui Song, Zhong-dao Wu. Yinchenhao Decoction Combined with Praziquantel Ameliorates Inflammation and Hepatic Fibrosis in Schistosoma japonicum-Infected Mice. Current Medical Science, 2025, 45(4): 944-956 DOI:10.1007/s11596-025-00089-1

登录浏览全文

4963

注册一个新账户 忘记密码

References

[1]

Lackey EK, Horrall S. Schistosomiasis. StatPearls. Treasure Island (FL), 2021.

[2]

WangJ, PazC, PadalinoG, et al.. Large-scale RNAi screening uncovers therapeutic targets in the parasite Schistosoma mansoni. Science., 2020, 369(6511): 1649-1653.

[3]

KS W. The pathogenesis of “clay-pipe stem cirrhosis” in mice with chronic schistosomiasis mansoni, with a note on the longevity of the schistosomes. Am J Pathol. 1966;Sep;49(3):477–489.

[4]

ColleyDG, BustinduyAL, SecorWE, et al.. Human schistosomiasis. Lancet., 2014, 383(9936): 2253-2264.

[5]

MaiersJL, MalhiH. Endoplasmic Reticulum Stress in Metabolic Liver Diseases and Hepatic Fibrosis. Semin Liver Dis., 2019, 39(2): 235-248.

[6]

DuanM, YangY, PengS, et al.. C/EBP Homologous Protein (CHOP) Activates Macrophages and Promotes Liver Fibrosis in Schistosoma japonicum-Infected Mice. J Immunol Res., 2019, 20195148575.

[7]

LiJ, CaiX, YangY, et al.. Macrophage MST1 protects against schistosomiasis-induced liver fibrosis by promoting the PPARgamma-CD36 pathway and suppressing NF-kappaB signaling. PLoS Pathog., 2024, 2012. e1012790

[8]

GieseckRL3rd, WilsonMS, WynnTA. Type 2 immunity in tissue repair and fibrosis. Nat Rev Immunol., 2018, 18(1): 62-76.

[9]

StadeckerMJ, AsahiH, FingerE, et al.. The immunobiology of Th1 polarization in high-pathology schistosomiasis. Immunol Rev., 2004, 201: 168-179.

[10]

CrellenT, WalkerM, LambertonPH, et al.. Reduced Efficacy of Praziquantel Against Schistosoma mansoni Is Associated With Multiple Rounds of Mass Drug Administration. Clin Infect Dis., 2016, 63(9): 1151-1159.

[11]

MoAX, ColleyDG. Workshop report: Schistosomiasis vaccine clinical development and product characteristics. Vaccine., 2016, 34(8): 995-1001.

[12]

GrayDJ, McManusDP, LiY, et al.. Schistosomiasis elimination: lessons from the past guide the future. Lancet Infect Dis., 2010, 10(10): 733-736.

[13]

RossAG, OlvedaRM, LiY. An audacious goal: the elimination of schistosomiasis in our lifetime through mass drug administration. Lancet., 2015, 385(9983): 2220-2221.

[14]

SongL, ZhangB, LiuJ, et al.. Reversal of liver fibrosis after splenectomy in a patient with advanced schistosomiasis japonica: A case report with 4-year follow-up. PLoS Negl Trop Dis., 2019, 134. e0007174

[15]

EasthamG, FausnachtD, BeckerMH, et al.. Praziquantel resistance in schistosomes: a brief report. Front Parasitol., 2024, 31471451.

[16]

AlwanSN, TaylorAB, RhodesJ, et al.. Oxamniquine derivatives overcome Praziquantel treatment limitations for Schistosomiasis. PLoS Pathog., 2023, 197. e1011018

[17]

MirandaVHS, GomesTR, EllerDE, et al.. Liver damage in schistosomiasis is reduced by adipose tissue-derived stem cell therapy after praziquantel treatment. PLoS Negl Trop Dis., 2020, 148. e0008635

[18]

XiangF, ZhangZ, LiY, et al.. Research progress in the treatment of schistosomiasis with traditional Chinese medicine. J Ethnopharmacol., 2024, 333. 118501

[19]

ZhangA, SunH, QiuS, et al.. Advancing drug discovery and development from active constituents of yinchenhao tang, a famous traditional Chinese medicine formula. Evid Based Complement Alternat Med., 2013, 2013. 257909

[20]

LuoS, HuangM, LuX, et al.. Optimized therapeutic potential of Yinchenhao decoction for cholestatic hepatitis by combined network meta-analysis and network pharmacology. Phytomedicine., 2024, 129. 155573

[21]

GuoY, LiJX, WangYL, et al.. Yinchen Linggui Zhugan Decoction Ameliorates Nonalcoholic Fatty Liver Disease in Rats by Regulating the Nrf2/ARE Signaling Pathway. Evid Based Complement Alternat Med., 2017, 20176178358.

[22]

YiYX, DingY, ZhangY, et al.. Yinchenhao Decoction Ameliorates Alpha-Naphthylisothiocyanate Induced Intrahepatic Cholestasis in Rats by Regulating Phase II Metabolic Enzymes and Transporters. Front Pharmacol., 2018, 9510.

[23]

CaiY, ZhengQ, SunR, et al.. Recent progress in the study of Artemisiae Scopariae Herba (Yin Chen), a promising medicinal herb for liver diseases. Biomed Pharmacother., 2020, 130. 110513

[24]

LiJY, CaoHY, SunL, et al.. Therapeutic mechanism of Yin-Chen-Hao decoction in hepatic diseases. World J Gastroenterol., 2017, 23(7): 1125-1138.

[25]

Yang R, Jiang D, Xu H, et al. Network Pharmacology and Molecular Docking Integrated with Molecular Dynamics Simulations Investigate the Pharmacological Mechanism of Yinchenhao Decoction in the Treatment of Non-alcoholic Fatty Liver Disease. Curr Comput Aided Drug Des. 2024.

[26]

WuYL, LiZL, ZhangXB, et al.. Yinchenhao decoction attenuates obstructive jaundice-induced liver injury and hepatocyte apoptosis by suppressing protein kinase RNA-like endoplasmic reticulum kinase-induced pathway. World J Gastroenterol., 2019, 25(41): 6205-6221.

[27]

ChenZ, LinT, LiaoX, et al.. Network pharmacology based research into the effect and mechanism of Yinchenhao Decoction against Cholangiocarcinoma. Chin Med., 2021, 16113.

[28]

LiuJJ, XuY, ChenS, et al.. The mechanism of Yinchenhao decoction in treating obstructive-jaundice-induced liver injury based on Nrf2 signaling pathway. World J Gastroenterol., 2022, 28(32): 4635-4648.

[29]

ZhaoX, WuX, HuQ, et al.. Yinchenhao Decoction Protects Against Acute Liver Injury in Mice With Biliary Acute Pancreatitis by Regulating the Gut Microflora-Bile Acids-Liver Axis. Gastroenterol Res Pract., 2024, 20248882667.

[30]

WangX, SunH, ZhangA, et al.. Pharmacokinetics screening for multi-components absorbed in the rat plasma after oral administration traditional Chinese medicine formula Yin-Chen-Hao-Tang by ultra performance liquid chromatography-electrospray ionization/quadrupole-time-of-flight mass spectrometry combined with pattern recognition methods. Analyst., 2011, 136(23): 5068-5076.

[31]

IshakK, BaptistaA, BianchiL, et al.. Histological grading and staging of chronic hepatitis. J Hepatol., 1995, 22(6): 696-699.

[32]

RuJ, LiP, WangJ, et al.. TCMSP: a database of systems pharmacology for drug discovery from herbal medicines. J Cheminform., 2014, 613.

[33]

Wang P, Wang S, Chen H, et al. TCMIP v2.0 Powers the Identification of Chemical Constituents Available in Xinglou Chengqi Decoction and the Exploration of Pharmacological Mechanisms Acting on Stroke Complicated With Tanre Fushi Syndrome. Front Pharmacol. 2021;12:598200.

[34]

McManusDP, DunneDW, SackoM, et al.. Schistosomiasis. Nat Rev Dis Primers., 2018, 4113.

[35]

LuY, TangW, ZhangH, et al.. Effect of hepatocyte damage in hepatic fibrogenesis of patients infected with Schistosoma japonicum. Infect Immun., 2024, 926. e0002624

[36]

NingA, WuX, LiH, et al.. Abnormal liver function in different patients with Schistosoma japonicum. Parasitol Res., 2015, 114(1): 85-90.

[37]

HuangY, LuJ, XuY, et al.. Xiaochaihu decorction relieves liver fibrosis caused by Schistosoma japonicum infection via the HSP47/TGF-beta pathway. Parasit Vectors., 2020, 131254.

[38]

AtwaMTM, Abd-ElrazekAM, SalemNIS. Dandelion (Taraxacum officinale) Improves the Therapeutic Efficiency of Praziquantel in Experimental Schistosomiasis. Acta Parasitol., 2022, 67(2): 773-783.

[39]

LuoS, YangB, XuH, et al.. Lithospermic acid improves liver fibrosis through Piezo1-mediated oxidative stress and inflammation. Phytomedicine., 2024, 134. 155974

[40]

CarsonJP, RammGA, RobinsonMW, et al.. Schistosome-Induced Fibrotic Disease: The Role of Hepatic Stellate Cells. Trends Parasitol., 2018, 34(6): 524-540.

[41]

YanJ, XieG, LiangC, et al.. Herbal medicine Yinchenhaotang protects against alpha-naphthylisothiocyanate-induced cholestasis in rats. Sci Rep., 2017, 714211.

[42]

CaiFF, WuR, SongYN, et al.. Yinchenhao Decoction Alleviates Liver Fibrosis by Regulating Bile Acid Metabolism and TGF-beta/Smad/ERK Signalling Pathway. Sci Rep., 2018, 8115367.

[43]

ZhaoM, YinY, YangB, et al.. Ameliorative effects of Modified Huangqi Chifeng decoction on podocyte injury via autophagy mediated by PI3K/AKT/mTOR and AMPK/mTOR pathways. J Ethnopharmacol., 2024, 321. 117520

[44]

ChenC, WuH, YeH, et al.. Activation of the Unfolded Protein Response (UPR) Is Associated with Cholangiocellular Injury, Fibrosis and Carcinogenesis in an Experimental Model of Fibropolycystic Liver Disease. Cancers (Basel)., 2021, 14178.

[45]

YuYR, NiXQ, HuangJ, et al.. Taurine drinking ameliorates hepatic granuloma and fibrosis in mice infected with Schistosoma japonicum. Int J Parasitol Drugs Drug Resist., 2016, 6(1): 35-43.

[46]

YanH, HuY, LiangJ, et al.. Yinchenhao Decoction mitigates intestinal impairment induced by high carbohydrate diet in largemouth bass (Micropterus salmoides): insights from inflammation, apoptosis, oxidative stress, tight junctions, and microbiota homeostasis. Fish Physiol Biochem., 2024, 50(6): 2207-2223.

[47]

CaiFF, BianYQ, WuR, et al.. Yinchenhao decoction suppresses rat liver fibrosis involved in an apoptosis regulation mechanism based on network pharmacology and transcriptomic analysis. Biomed Pharmacother., 2019, 114. 108863

[48]

BarronL, WynnTA. Macrophage activation governs schistosomiasis-induced inflammation and fibrosis. Eur J Immunol., 2011, 41(9): 2509-2514.

[49]

RenC, LiuF, XingC, et al.. IL-37 alleviates liver granuloma caused by Schistosoma japonicum infection by inducing alternative macrophage activation. Parasit Vectors., 2022, 151300.

[50]

BustinduyAL, SutherlandLJ, Chang-CojulunA, et al.. Age-Stratified Profiles of Serum IL-6, IL-10, and TNF-alpha Cytokines Among Kenyan Children with Schistosoma haematobium, Plasmodium falciparum, and Other Chronic Parasitic Co-Infections. Am J Trop Med Hyg., 2015, 92(5): 945-951.

[51]

HouY, ChenC, LiZ, et al.. Protective effect of quercetin against macrophage-mediated hepatocyte injury via anti-inflammation, anti-apoptosis and inhibition of ferroptosis. Autoimmunity., 2024, 5712350202.

Funding

National Natural Science Foundation of China(81802036)

RIGHTS & PERMISSIONS

The Author(s), under exclusive licence to Huazhong University of Science and Technology

AI Summary AI Mindmap
PDF

100

Accesses

0

Citation

Detail

Sections
Recommended

AI思维导图

/