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清肠化湿颗粒通过激活 NLRP6 信号通路和调节 Th17/Treg 平衡来改善 DSS 诱导的结肠炎。

Qing-Chang-Hua-Shi granule ameliorates DSS-induced colitis by activating NLRP6 signaling and regulating Th17/Treg balance.

机构信息

Affiliated Hospital of Nanjing University of Chinese Medicine, Nanjing 210029, China; The First School of Clinical Medicine, Nanjing University of Chinese Medicine, Nanjing 210023, China.

Affiliated Hospital of Nanjing University of Chinese Medicine, Nanjing 210029, China.

出版信息

Phytomedicine. 2022 Dec;107:154452. doi: 10.1016/j.phymed.2022.154452. Epub 2022 Sep 13.

Abstract

BACKGROUND

Chinese herbal medicine Qing-Chang-Hua-Shi granule (QCHS) is widely used to treat ulcerative colitis in China. However, the molecular mechanisms of QCHS remains largely unknown.

PURPOSE

To assess the therapeutic effects of QCHS on colitis and to reveal its mechanisms of action.

METHODS

The main components of QCHS were identified using a UHPLC-QTOF-MS method and the efficacy of QCHS was evaluated using an DSS-induced mice model. The inflammatory responses and mucosal integrity in colon were comprehensively assessed. Flow cytometry was used to analysis the proportion of Th17 and Treg cells. Detect the signal transduction of the NOD-like receptor family pyrin domain containing 6 (NLRP6) both in vitro and in vivo. Furthermore, siNLRP6 transfection was used to validate the functional targets of QCHS.

RESULTS

QCHS treatment significantly alleviated colitis in mice by improving symptoms and pathological damage. Moreover, QCHS treatment suppressed the inflammatory response and preserved the integrity of colon tissue. Most importantly, QCHS balanced the Th17/Treg response of UC mice. Mechanistically, by activating NLRP6 inflammasome pathway, QCHS regulated the maturation of interleukin (IL)-1β and IL-18 to affect inflammation and drive Th17 cell differentiation.

CONCLUSIONS

The effect of QCHS on UC mice is dose-dependent, with high-dose QCHS being superior to 5-Aminosalicylic acid (200 mg/kg/day). QCHS acts through the NLRP6 signaling pathway to modulate Th17/Treg balance, resulting in the protective effects against colitis. This study investigated the relevant pharmacological mechanisms of QCHS, providing further evidence for the application of QCHS in UC treatment.

摘要

背景

中药清肠化湿颗粒(QCHS)在中国广泛用于治疗溃疡性结肠炎。然而,其分子机制仍知之甚少。

目的

评估 QCHS 对结肠炎的治疗作用,并揭示其作用机制。

方法

采用 UHPLC-QTOF-MS 法鉴定 QCHS 的主要成分,采用 DSS 诱导的小鼠模型评价 QCHS 的疗效。综合评估结肠的炎症反应和黏膜完整性。采用流式细胞术分析 Th17 和 Treg 细胞的比例。检测 NOD 样受体家族 pyrin 结构域包含 6(NLRP6)的信号转导,分别在体外和体内进行。此外,采用 siNLRP6 转染验证 QCHS 的功能靶点。

结果

QCHS 通过改善症状和病理损伤,显著缓解了小鼠的结肠炎。此外,QCHS 治疗抑制了炎症反应,保护了结肠组织的完整性。最重要的是,QCHS 平衡了 UC 小鼠的 Th17/Treg 反应。机制上,通过激活 NLRP6 炎性体途径,QCHS 调节白细胞介素(IL)-1β和 IL-18 的成熟,从而影响炎症和驱动 Th17 细胞分化。

结论

QCHS 对 UC 小鼠的作用呈剂量依赖性,高剂量 QCHS 优于 5-氨基水杨酸(200mg/kg/天)。QCHS 通过 NLRP6 信号通路调节 Th17/Treg 平衡,发挥对结肠炎的保护作用。本研究探讨了 QCHS 的相关药理机制,为 QCHS 在 UC 治疗中的应用提供了进一步的证据。

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