Liquiritigenin, isoliquiritigenin rich extract of glycyrrhiza glabra roots attenuates inflammation in macrophages and collagen-induced arthritis in rats

被引:12
作者
Babu, Vineet [1 ]
Kapkoti, Deepak Singh [2 ]
Binwal, Monika [1 ,7 ]
Bhakuni, Rajendra S. [2 ]
Shanker, Karuna [3 ]
Singh, Manju [3 ]
Tandon, Sudeep [4 ]
Mugale, Madhav N. [5 ]
Kumar, Narendra [6 ]
Bawankule, Dnyaneshwar U. [1 ,7 ]
机构
[1] CSIR Cent Inst Med & Aromat Plants, Bioprospect & Prod Dev Div, PO CIMAP,Near Kukrail Picn Spot, Lucknow 226015, Uttar Pradesh, India
[2] Cent Inst Med & Aromat Plants CSIR, Phytochem Div, Lucknow 226015, India
[3] CSIR Cent Inst Med & Aromat Plants CIMAP, Phytochem Div, Analyt Chem Lab, Lucknow 226015, India
[4] Council Sci & Ind Res CSIR, Cent Inst Med & Aromat Plants CIMAP, Proc Chem & Chem Engn Dept, PO CIMAP,Near Kukrail Picn Spot, Lucknow 226015, India
[5] CSIR Cent Drug Res Inst CDRI, Dept Toxicol & Expt Med, Lucknow 226031, Uttar Pradesh, India
[6] CSIR Cent Inst Med & Aromat Plants CIMAP, Bot & Pharmacognosy, Lucknow, Uttar Pradesh, India
[7] Acad Sci & Innovat Res AcSIR, Ghaziabad, Uttar Pradesh, India
关键词
Glycyrrhiza glabra; Root; Isoliquiritigenin; Liquiritigenin; Anti-inflammatory arthritis; RHEUMATOID-ARTHRITIS; PHENOLIC-COMPOUNDS; LICORICE; CYTOKINES; PREVENTION; PLANTS; MODEL;
D O I
10.1007/s10787-023-01152-w
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Liquiritigenin (LTG) and its bioprecursor isoliquiritigenin(ISL), the main bioactives from roots of Glycyrrhiza genus are progressively documented as a potential pharmacological agent for the management of chronic diseases. The aim of this study was to evaluate the pharmacological potential of liquiritigenin, isoliquiritigenin rich extract of Glycyrrhiza glabra roots (IVT-21) against the production of pro-inflammatory cytokines from activated macrophages as well as further validated the efficacy in collagen-induced arthritis model in rats. We also performed the safety profile of IVT-21 using standard in-vitro and in-vivo assays. Results of this study revealed that the treatment of IVT-21 and its major bioactives (LTG, ISL) was able to reduce the production of pro-inflammatory cytokines (TNF-alpha, IL-6) in LPS-activated primary peritoneal macrophages in a dose-dependent manner compared with vehicle-alone treated cells without any cytotoxic effect on macrophages. In-vivo efficacy profile against collagen-induced arthritis in Rats revealed that oral administration of IVT-21 significantly reduced the arthritis index, arthritis score, inflammatory mediators level in serum. IVT-21 oral treatment is also able to reduce the NF kappa B-p65 expression as evidence of immunohistochemistry in knee joint tissue and mRNA level of pro-inflammatory cytokines in paw tissue in a dose-dependent manner when compared with vehicle treated rats. Acute oral toxicity profile of IVT-21 demonstrated that it is safe up to 2000 mg/kg body weight in experimental mice. This result suggests the suitability of IVT-21 for further study in the management of arthritis and related complications.
引用
收藏
页码:983 / 996
页数:14
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