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三黄泻心汤通过调节炎症和胆汁酸代谢改善 DSS 诱导的结肠炎继发肝损伤。

Sanhuang xiexin decoction ameliorates secondary liver injury in DSS-induced colitis involve regulating inflammation and bile acid metabolism.

机构信息

Department of Pharmacy, Sichuan Agricultural University, Chengdu, 611130, China.

Chengdu Agricultural College, Chengdu, 611130, China.

出版信息

J Ethnopharmacol. 2022 Dec 5;299:115682. doi: 10.1016/j.jep.2022.115682. Epub 2022 Sep 1.

Abstract

ETHNOPHARMACOLOGICAL RELEVANCE

SanHuang XieXin decoction (SXD) is a widely applicated traditional Chinese medicine (TCM) with a significant gut-liver axis regulation effect.

AIM OF THE STUDY

To evaluate the therapeutic effect and elucidate the possible underlying molecular mechanisms of SXD on liver damage secondary to ulcerative colitis (UC) in mice.

MATERIALS AND METHODS

A model of liver damage secondary to UC was induced by drinking 5% dextran sodium sulfate (DSS) in mice. These mice were treated with one of three doses of SXD or sulfasalazine (SASP), then liver samples were collected and tested.

RESULTS

The results reveal that SXD treatment reduced liver cells swelling, and inhibited the accumulation of the hepatic-pro-inflammatory cytokines IL-1β and tumor necrosis factor-α (TNF-α) in mice with colitis. In addition, SXD reduced the production of nitric oxide (NO) and malondialdehyde (MDA), and increased the activities of superoxide dismutase (SOD). In inflammation regulating, SXD significantly down regulated the protein expression of MyD88 and p-Iκα, but upregulated Iκα. In bile acid metabolism regulating, SXD significantly down regulated the protein expression of FXR, MRP, BESP and SHP. Therefore, SXD treatment can regulate the TLR4-NF-κB and bile acid metabolism pathways to alleviate liver inflammation and cholestasis.

CONCLUSIONS

These results demonstrate that SXD is a potential alternative therapeutic medicine for the treatment of liver damage secondary to colitis.

摘要

民族药理学相关性

三黄泻心汤(SXD)是一种广泛应用的中药,具有显著的肠道-肝脏轴调节作用。

研究目的

评估 SXD 对溃疡性结肠炎(UC)继发肝损伤的治疗效果,并阐明其可能的潜在分子机制。

材料与方法

通过给小鼠饮用 5%葡聚糖硫酸钠(DSS)来诱导 UC 继发肝损伤模型。用 SXD 或柳氮磺胺吡啶(SASP)三种剂量中的一种对这些小鼠进行治疗,然后收集肝脏样本进行测试。

结果

结果表明,SXD 治疗可减轻结肠炎小鼠肝细胞肿胀,抑制肝促炎细胞因子白细胞介素-1β和肿瘤坏死因子-α(TNF-α)的积累。此外,SXD 降低了一氧化氮(NO)和丙二醛(MDA)的产生,并增加了超氧化物歧化酶(SOD)的活性。在炎症调节方面,SXD 显著下调了 TLR4-NF-κB 信号通路中的 MyD88 和 p-IκB 蛋白表达,而上调了 IκB 蛋白表达。在胆汁酸代谢调节方面,SXD 显著下调了 FXR、MRP、BESP 和 SHP 的蛋白表达。因此,SXD 治疗可以调节 TLR4-NF-κB 和胆汁酸代谢途径,从而减轻肝脏炎症和胆汁淤积。

结论

这些结果表明,SXD 是治疗结肠炎继发肝损伤的一种有潜力的替代治疗药物。

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