中药参附上调claudin - 4可减轻急性肺损伤加重急性胃肠损伤引起的肺组织损伤。

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC
Yueliang Zheng, Mian Zheng, Jing Shao, Chengxing Jiang, Jian Shen, Rujia Tao, Yuqin Deng, Yingge Xu, Yuanqiang Lu
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引用次数: 2

摘要

背景:许多研究探索了治疗急性肺损伤(ALI)的新方法;然而,这些方法都不能显著改变ALI的高死亡率。参附是一种可能对ALI有效的中药。目的:探讨参附对急性心绞痛的治疗作用。材料与方法:雄性C57BL/6小鼠分为对照组、脂多糖(LPS)组(500µg/100 μL /只)和脂多糖+参附组(30 mL/kg)。将参附(10µL/mL)加入到LPS(10µg/mL)处理的MLE-12细胞中,作用48 h。雄性C57BL/6小鼠分为LPS、LPS + 3%葡聚糖硫酸钠(DSS)、3% DSS +参附、LPS + 3% DSS +参附4组。结果:与ALI组比较,参复降低了湿/干重比(19.8%,36.2%),降低了IL-2(40.9%, 61.6%)、IFN-γ(43.5%, 53.3%)、TNF-α(54.1%, 42.1%)、IL-6(54.8%,70%)、IL-1β(39.9%, 65.1%),降低了血清尿酸(18.8%,48.7%)、肌酐(17.4%,41.1%)。此外,参附可提高体外培养的LPS刺激上皮细胞的细胞活力(17.2%,59.9%),抑制细胞凋亡(63.0%)和p38/ERK磷酸化。在机制上,参附通过上调claudin-4的表达介导了保护作用。此外,参附对急性胃肠损伤加重型ALI的肺和肠上皮均有保护作用。讨论与结论:综上所述,研究结果揭示了参附注射液对小鼠ALI模型的治疗效果及作用机制,提示参附注射液治疗ALI患者的临床潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Upregulation of claudin‑4 by Chinese traditional medicine Shenfu attenuates lung tissue damage by acute lung injury aggravated by acute gastrointestinal injury.

Upregulation of claudin‑4 by Chinese traditional medicine Shenfu attenuates lung tissue damage by acute lung injury aggravated by acute gastrointestinal injury.

Upregulation of claudin‑4 by Chinese traditional medicine Shenfu attenuates lung tissue damage by acute lung injury aggravated by acute gastrointestinal injury.

Upregulation of claudin‑4 by Chinese traditional medicine Shenfu attenuates lung tissue damage by acute lung injury aggravated by acute gastrointestinal injury.

Context: Many studies have explored new methods to cure acute lung injury (ALI); however, none of those methods could significantly change the high mortality rate of ALI. Shenfu is a Chinese traditional medicine that might be effective against ALI.

Objective: Our study explores the therapeutic potential of Shenfu in ALI.

Materials and methods: Male C57BL/6 mice were assigned to control, lipopolysaccharide (LPS) (500 µg/100 μL per mouse), and LPS + Shenfu (30 mL/kg) groups. Shenfu (10 µL/mL) was added to LPS (10 µg/mL) treated MLE-12 cells for 48 h in vitro. Male C57BL/6 mice were divided into four groups: LPS, LPS + 3% dextran sulphate sodium (DSS), 3% DSS + Shenfu, and LPS + 3% DSS + Shenfu.

Results: Compared with the ALI group, Shenfu reduced wet/dry weight ratio (19.8%, 36.2%), and reduced the IL-2 (40.9%, 61.6%), IFN-γ (43.5%, 53.3%) TNF-α (54.1%, 42.1%), IL-6 (54.8%,70%), and IL-1β (39.9%, 65.1%), reduced serum uric acid (18.8%, 48.7%) and creatinine (17.4%, 41.1%). Moreover, Shenfu enhanced cell viability (17.2%, 59.9%) and inhibited cell apoptosis (63.0%) and p38/ERK phosphorylation in in vitro cultured epithelial cells with LPS stimulation. Mechanistically, Shenfu mediated the protective effect by upregulating claudin-4 expression. In addition, Shenfu could protect against both lung and intestinal epithelial damage in acute gastrointestinal injury-exacerbated ALI.

Discussion and conclusions: Taken together, the results revealed the therapeutic effect and the underlying mechanism of Shenfu injection in an ALI in mouse model, indicating its clinical potential to treat patients with ALI.

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CiteScore
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