Paeoniae Radix Alba effectively attenuates Polygonum multiflorum Thunb.-induced idiosyncratic liver injury by modulating M2 macrophage polarization

Ye Xiu, Zhixin Wu, Yichong Chen, Wenqing Mu, Xiaomei Zhao, Ming Dong, Yurong Li, Zhaofang Bai, Xiaohe Xiao

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Acupuncture and Herbal Medicine ›› 2024, Vol. 4 ›› Issue (2) : 209-221. DOI: 10.1097/HM9.0000000000000115
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Paeoniae Radix Alba effectively attenuates Polygonum multiflorum Thunb.-induced idiosyncratic liver injury by modulating M2 macrophage polarization

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Abstract

Objective: Polygonum multiflorum Thunb. (PM) is a commonly used tonic herb known to cause idiosyncratic drug-induced liver injury (IDILI). This study explored the detoxification effects and potential mechanisms of action of Paeoniae Radix Alba (PRA) on PM-induced IDILI.
Methods: Network pharmacology analysis was utilized to predict the related targets of “PRA-PM-innate immunity.” A non-hepatotoxic lipopolysaccharide (LPS) and PM-induced IDILI model was used to evaluate the detoxification effects of PRA by measuring liver function indicators, pathological examinations, and macrophage-related factors. Bone marrow-derived macrophages (BMDMs) were stimulated with IL-4 to differentiate into M2 macrophages, and the effects of PM and PRA on M2 macrophage polarization were explored.
Results: Target screening of “PRA-PM-innate immunity” identified 21 intersecting targets, most of which were closely associated with macrophage polarization. In rat models of IDILI induced by PM, the combined use of PRA significantly reduced the extent of liver damage and the levels of inflammatory factors, while promoting the expression of M2 macrophage-related factors such as interleukin (IL)-4, IL-10, arginase 1 (Arg1), and CD206. In vitro, PM dose-dependently inhibited the expression of the Arg1 protein and M2 macrophage-related genes, whereas PRA exhibited the opposite effect. When used in combination, PRA ameliorated the inhibitory effect of PM on M2 macrophage polarization.
Conclusions: Our results demonstrate that PRA has a therapeutic effect on PM-induced IDILI; its mechanism may involve alleviating liver injury by promoting M2 macrophage polarization, thus reducing the expression of inflammatory factors.

Keywords

IDILI / M2 macrophage polarization / Paeoniae Radix Alba / Polygonum multiflorum Thunb

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Ye Xiu, Zhixin Wu, Yichong Chen, Wenqing Mu, Xiaomei Zhao, Ming Dong, Yurong Li, Zhaofang Bai, Xiaohe Xiao. Paeoniae Radix Alba effectively attenuates Polygonum multiflorum Thunb.-induced idiosyncratic liver injury by modulating M2 macrophage polarization. Acupuncture and Herbal Medicine, 2024, 4(2): 209‒221 https://doi.org/10.1097/HM9.0000000000000115

References

[[1]]
Andrade RJ, Chalasani N, Björnsson ES, et al. Drug-induced liver injury. Nat Rev Dis Primers. 2019;5(1):58.
[[2]]
Björnsson HK, Björnsson ES. Drug-induced liver injury: pathogenesis, epidemiology, clinical features, and practical management. Eur J Intern Med. 2022;97:26-31.
[[3]]
Gao Y, Xu G, Ma L, et al. Icariside I specifically facilitates ATP or nigericin-induced NLRP3 inflammasome activation and causes idiosyncratic hepatotoxicity. Cell Commun Signal. 2021;19(1):13.
[[4]]
Uetrecht J. Mechanistic studies of idiosyncratic DILI: clinical implications. Front Pharmacol. 2019;10:837.
[[5]]
Segovia-Zafra A, Di Zeo-Sánchez DE, López-Gómez C, et al. Preclinical models of idiosyncratic drug-induced liver injury (iDILI): moving towards prediction. Acta Pharm Sin B. 2021;11(12):3685-3726.
[[6]]
Uetrecht J. Mechanisms of idiosyncratic drug-induced liver injury. Adv Pharmacol. 2019;85:133-163.
[[7]]
Jee A, Sernoskie SC, Uetrecht J. Idiosyncratic drug-induced liver injury: mechanistic and clinical challenges. Int J Mol Sci. 2021;22(6):2954.
[[8]]
Tu C, He Q, Li CY, et al. Susceptibility-related factor and biomarkers of dietary supplement polygonum multiflorum-induced liver injury in rats. Front Pharmacol. 2019;10:335.
[[9]]
Wang Z, Xu G, Wang H, et al. Icariside II, a main compound in Epimedii Folium, induces idiosyncratic hepatotoxicity by enhancing NLRP3 inflammasome activation. Acta Pharm Sin B. 2020;10(9):1619-1633.
[[10]]
Qin N, Xu G, Wang Y, et al. Bavachin enhances NLRP3 inflammasome activation induced by ATP or nigericin and causes idiosyncratic hepatotoxicity. Front Med. 2021;15(4):594-607.
[[11]]
Sun ML, Chen XY, Cao JJ, et al. Polygonum multiflorum Thunb extract extended the lifespan and healthspan of Caenorhabditis elegans via DAF-16/SIR-2.1/SKN-1. Food Funct. 2021;12(18):8774-8786.
[[12]]
Xue XY, Quan YY, Gong LH, et al. A review of the processed Polygonum multiflorum (Thunb.) for hepatoprotection: clinical use, pharmacology and toxicology. J Ethnopharmacol. 2020;261:113121.
[[13]]
Guilliams M, Scott CL. Liver macrophages in health and disease. Immunity. 2022;55(9):1515-1529.
[[14]]
Shapouri-Moghaddam A, Mohammadian S, Vazini H, et al. Macrophage plasticity, polarization, and function in health and disease. J Cell Physiol. 2018;233(9):6425-6440.
[[15]]
Chen YN, Hu MR, Wang L, et al. Macrophage M1/M2 polarization. Eur J Pharmacol. 2020;877:173090.
[[16]]
Locati M, Curtale G, Mantovani A. Diversity, mechanisms, and significance of macrophage plasticity. Annu Rev Pathol. 2020;15:123-147.
[[17]]
Chen S, Saeed A, Liu Q, et al. Macrophages in immunoregulation and therapeutics. Signal Transduct Target Ther. 2023;8(1):207.
[[18]]
Wang C, Ma C, Gong L, et al. Macrophage polarization and its role in liver disease. Front Immunol. 2021;12:803037.
[[19]]
Kazankov K, Jørgensen SMD, Thomsen KL, et al. The role of macrophages in nonalcoholic fatty liver disease and nonalcoholic steatohepatitis. Nat Rev Gastroenterol Hepatol. 2019;16(3):145-159.
[[20]]
Jiang HJ, Li J, Wang L, et al. Total glucosides of paeony: a review of its phytochemistry, role in autoimmune diseases, and mechanisms of action. J Ethnopharmacol. 2020;258:112913.
[[21]]
Shin MR, Lee SH, Roh SS. The potential hepatoprotective effect of paeoniae radix alba in thioacetamide-induced acute liver injury in rats. Evid Based Complement Alternat Med. 2022;2022:7904845.
[[22]]
Zhang YJ, Ren XL, Sun H, et al. Establishment of fingerprint and multivariate statistical analysis of compatible herb pairs with Polygonum multiflorum as the core. China Pharmacy. 2020;31(20):2486-2691 (in Chinese).
[[23]]
Zhang HJ, Ren XL, Sun H, et al. Study on change of ingredients content and DPPH free radical scavenging activity of drug pairs with Polygoni Multiflori Radix Praeparata based on semi-quantitative analysis. Chinese Traditional and Herbal Drugs. 2021;52(7):1924-1936 (in Chinese).
[[24]]
Jo GH, Kim SN, Kim MJ, et al. Protective effect of Paeoniae radix alba root extract on immune alterations in mice with atopic dermatitis. J Toxicol Environ Health A. 2018;81(12):502-511.
[[25]]
Li CY, Li XF, Tu C, et al. The idiosyncratic hepatotoxicity of Polygonum multiflorum based on endotoxin model. Yao Xue Xue Bao. 2015;50(1):28-33.
[[26]]
Du P, Xu JB, Jiang YF, et al. Saikosaponin-d attenuates Hashimoto’s thyroiditis by regulating macrophage polarization. J Immunol Res. 2022;2022:7455494.
[[27]]
Wang ST, Ji TS, Wang L, et al. Exploration of the mechanism by which Huangqi Guizhi Wuwu decoction inhibits LPS-induced inflammation by regulating macrophage polarization based on network pharmacology. BMC Complement Med Ther. 2023;23(1):8.
[[28]]
Zhao YS, Zhang Y, Kong H, et al. Carbon dots from paeoniae radix alba carbonisata: hepatoprotective effect. Int J Nanomedicine. 2020;15:9049-9059.
[[29]]
Vago JP, Galvão I, Negreiros-Lima GL, et al. Glucocorticoid-induced leucine zipper modulates macrophage polarization and apoptotic cell clearance. Pharmacol Res. 2020;158:104842.
[[30]]
Wang G, Liu Y, Hou XF, et al. Discussion on influence factors, mechanism and traditional Chinese medicine pathogenesis of idiosyncratic drug-induced liver injury. Zhongguo Zhong Yao Za Zhi. 2017;42(16):3036-3043.
[[31]]
Ali SE, Waddington JC, Park BK, et al. Definition of the chemical and immunological signals involved in drug-induced liver injury. Chem Res Toxicol. 2020;33(1):61-76.
[[32]]
Lin MM, Li YY, Cao B, et al. Bavachin combined with epimedin B induce idiosyncratic liver injury under immunological stress conditions. Chem Biol Interact. 2023;386:110774.
[[33]]
Li CY, Niu M, Liu YL, et al. Screening for susceptibility-related factors and biomarkers of Xianling Gubao capsule-induced liver injury. Front Pharmacol. 2020;11:810.
[[34]]
Gao Y, Wang Z, Tang J, et al. New incompatible pair of TCM: Epimedii Folium combined with Psoraleae Fructus induces idiosyncratic hepatotoxicity under immunological stress conditions. Front Med. 2020;14(1):68-80.
[[35]]
Li XY, Qu CH, He Q, et al. Acute hepatitis induced by a Chinese herbal product Qibao Meiran Wan: a case study. Int J Clin Exp Med. 2015;8(7):11624-11627.
[[36]]
Meng YK, Li CY, Li RY, et al. Cis-stilbene glucoside in Polygonum multiflorum induces immunological idiosyncratic hepatotoxicity in LPS-treated rats by suppressing PPAR-γ. Acta Pharmacol Sin. 2017;38(10):1340-1352.
[[37]]
He LZ, Yin P, Meng YK, et al. Immunological synergistic mechanisms of trans-/cis-stilbene glycosides in Heshouwu-related idiosyncratic liver injury. Sci Bull. 2017;62(11):748-751.
[[38]]
Gao D, Pang JY, Zhang CE, et al. Poria attenuates idiosyncratic liver injury induced by Polygoni Multiflori radix praeparata. Front Pharmacol. 2016;7:386.
[[39]]
Yan BF, Chen X, Chen YF, et al. Aqueous extract of Paeoniae Radix Alba (Paeonia lactiflora Pall.) ameliorates DSS-induced colitis in mice by tunning the intestinal physical barrier, immune responses, and microbiota. J Ethnopharmacol. 2022;294:115365.
[[40]]
Shan Z, Ju C. Hepatic macrophages in liver injury. Front Immunol. 2020;11:322.
[[41]]
Watanabe S, Alexander M, Misharin AV, et al. The role of macrophages in the resolution of inflammation. J Clin Invest. 2019;129(7):2619-2628.
[[42]]
Meng QL, Meng WT, Bian H, et al. Total glucosides of paeony protects THP-1 macrophages against monosodium urate-induced inflammation via MALAT1/miR-876-5p/NLRP3 signaling cascade in gouty arthritis. Biomed Pharmacother. 2021;138:111413.

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