Traditional Chinese Medicine Pien-Tze-Huang ameliorates LPS-induced sepsis through bile acid-mediated activation of TGR5-STAT3-A20 signaling

IF 6.1 1区 医学 Q1 PHARMACOLOGY & PHARMACY Journal of Pharmaceutical Analysis Pub Date : 2023-12-10 DOI:10.1016/j.jpha.2023.12.005
Bei Li, Yong Zhang, Xinyuan Liu, Ziyang Zhang, Shuqing Zhuang, Xiaoli Zhong, WenBo Chen, Yilin Hong, Pingli Mo, Shuhai Lin, Shicong Wang, Chundong Yu
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Abstract

Pien Tze Huang (PZH), a Class I nationally protected Traditional Chinese Medicine (TCM), has been used to treat liver diseases such as hepatitis; however, the effect of PZH on the progression of sepsis is unknown. Here, we reported that PZH attenuated lipopolysaccharide (LPS)-induced sepsis in mice and reduced LPS-induced production of proinflammatory cytokines in macrophages by inhibiting the activation of mitogen-activated protein kinase (MAPK) and nuclear factor-kappa B (NF-κB) signalling. Mechanistically, PZH stimulated signal transducer and activator of transcription 3 (STAT3) phosphorylation to induce the expression of A20, which could inhibit the activation of NF-κB and MAPK signalling. Knockdown of the bile acid (BA) receptor G protein-coupled bile acid receptor 1 (TGR5) in macrophages abolished the effects of PZH on STAT3 phosphorylation and A20 induction, as well as the LPS-induced inflammatory response, suggesting that BAs in PZH may mediate its anti-inflammatory effects by activating TGR5. Consistently, deprivation of BAs in PZH by cholestyramine resin reduced the effects of PZH on the expression of phosphorylated-STAT3 and A20, the activation of NF-κB and MAPK signalling, and the production of proinflammatory cytokines, whereas the addition of BAs to cholestyramine resin-treated PZH partially restored the inhibitory effects on the production of proinflammatory cytokines. Overall, our study identifies BAs as the effective components in PZH that activate TGR5-STAT3-A20 signalling to ameliorate LPS-induced sepsis.

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中药片仔癀通过胆汁酸介导的 TGR5-STAT3-A20 信号激活改善 LPS 诱导的败血症
国家一类保护中药--片仔癀(PZH)被用于治疗肝炎等肝脏疾病,但片仔癀对败血症进展的影响尚不清楚。在此,我们报告了 PZH 通过抑制丝裂原活化蛋白激酶(MAPK)和核因子-卡巴 B(NF-κB)信号的激活,减轻了脂多糖(LPS)诱导的小鼠败血症,并减少了 LPS 诱导的巨噬细胞促炎细胞因子的产生。从机制上讲,PZH 可刺激信号转导和转录激活因子 3(STAT3)磷酸化,诱导 A20 的表达,从而抑制 NF-κB 和 MAPK 信号的激活。巨噬细胞中胆汁酸(BA)受体G蛋白偶联胆汁酸受体1(TGR5)被敲除后,PZH对STAT3磷酸化和A20诱导的影响以及LPS诱导的炎症反应都消失了,这表明PZH中的BA可能是通过激活TGR5来介导其抗炎作用的。与此相一致的是,通过胆碱脂剥夺 PZH 中的 BAs 会降低 PZH 对磷酸化-STAT3 和 A20 的表达、NF-κB 和 MAPK 信号的激活以及促炎细胞因子的产生的影响,而在胆碱脂处理的 PZH 中添加 BAs 则会部分恢复对促炎细胞因子产生的抑制作用。总之,我们的研究发现 BAs 是 PZH 中激活 TGR5-STAT3-A20 信号以改善 LPS 诱导的败血症的有效成分。
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上海源叶 Cholestyramine resin
¥93.00~¥14994.00
来源期刊
Journal of Pharmaceutical Analysis
Journal of Pharmaceutical Analysis Chemistry-Electrochemistry
CiteScore
16.20
自引率
2.30%
发文量
674
审稿时长
22 weeks
期刊介绍: The Journal of Pharmaceutical Analysis (JPA), established in 2011, serves as the official publication of Xi'an Jiaotong University. JPA is a monthly, peer-reviewed, open-access journal dedicated to disseminating noteworthy original research articles, review papers, short communications, news, research highlights, and editorials in the realm of Pharmacy Analysis. Encompassing a wide spectrum of topics, including Pharmaceutical Analysis, Analytical Techniques and Methods, Pharmacology, Metabolism, Drug Delivery, Cellular Imaging & Analysis, Natural Products, and Biosensing, JPA provides a comprehensive platform for scholarly discourse and innovation in the field.
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