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中药消水汤通过激活自噬抑制小鼠恶性胸腔积液并介导肿瘤相关巨噬细胞极化。

Chinese medicine Xiaoshui decoction inhibits malignant pleural effusion in mice and mediates tumor-associated macrophage polarization by activating autophagy.

机构信息

Institute of Basic Research in Clinical Medicine, China Academy of Chinese Medical Sciences, No. 16 Nanxiaojie, Dongzhimennei, Beijing, 100700, China; Jiangsu Province Hospital of Chinese Medicine, Affiliated Hospital of Nanjing University of Chinese Medicine, Nanjing, Jiangsu, 210029, China.

Changzhou TCM Hospital Affiliated to Nanjing University of Chinese Medicine, Changzhou, Jiangsu, 213003, China.

出版信息

J Ethnopharmacol. 2020 Mar 1;249:112412. doi: 10.1016/j.jep.2019.112412. Epub 2019 Nov 18.

Abstract

ETHNOPHARMACOLOGICAL RELEVANCE

Xiaoshui decoction (XSD) is a traditional Chinese medicine compound prescription that has been shown to reinforce the spleen and remove the fluid retention, while being widely used in the treatment of malignant pleural effusion (MPE). We previously reported that XSD alleviates symptoms and improves the quality of life in patients with MPE; however, the mechanism employed by XSD on MPE has not yet been elucidated.

AIM OF THE STUDY

To investigate the role and mechanism of XSD in inhibiting the development of MPE, and in regulating macrophage polarization in vitro and in vivo.

MATERIALS AND METHODS

A murine MPE model was used to study the effect of XSD on MPE. Mice with MPE were randomly allocated to a control group and XSD-low-dose (1.144 g/mL), XSD-middle-dose (2.288 g/mL), XSD-high-dose (4.576 g/mL), or cisplatin groups. RAW264.7 cells were induced to form tumor-associated macrophages (TAMs) as well as M1 and M2 macrophages using different conditioned media in vitro.

RESULTS

XSD effectively inhibited MPE formation, reduced pleural permeability and angiogenesis, and prolonged mice survival. Particularly, XSD treatment induced the polarization of TAMs to the M1 phenotype in MPE. Moreover, in-vitro XSD remarkably promoted the expansion of M1 macrophages and reduced M2 macrophages by enhancing autophagy.

CONCLUSIONS

XSD inhibits MPE development and regulates macrophage polarization by activating autophagy, indicating that XSD may serve as a novel option for integrative MPE therapies.

摘要

民族药理学相关性

消水汤(XSD)是一种中药复方,已被证明具有健脾利水的功效,广泛用于治疗恶性胸腔积液(MPE)。我们之前报道过 XSD 可缓解 MPE 患者的症状并提高其生活质量,但 XSD 对 MPE 的作用机制尚未阐明。

研究目的

研究 XSD 抑制 MPE 发展以及调节体外和体内巨噬细胞极化的作用和机制。

材料和方法

使用小鼠 MPE 模型研究 XSD 对 MPE 的影响。将患有 MPE 的小鼠随机分为对照组和 XSD 低剂量(1.144 g/mL)、XSD 中剂量(2.288 g/mL)、XSD 高剂量(4.576 g/mL)或顺铂组。体外使用不同的条件培养基诱导 RAW264.7 细胞形成肿瘤相关巨噬细胞(TAMs)以及 M1 和 M2 巨噬细胞。

结果

XSD 能有效抑制 MPE 的形成,降低胸腔通透性和血管生成,延长小鼠生存时间。特别是,XSD 治疗可诱导 MPE 中 TAMs 向 M1 表型极化。此外,XSD 可通过增强自噬作用,显著促进 M1 巨噬细胞的扩增和减少 M2 巨噬细胞。

结论

XSD 通过激活自噬抑制 MPE 的发展并调节巨噬细胞极化,表明 XSD 可能成为综合治疗 MPE 的一种新选择。

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