Department of Emergency Medicine, The First Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou, People's Republic of China.
Emergency & Intensive Care Unit Center, Department of Emergency Medicine, Zhejiang Provincial People's Hospital, Affiliated People's Hospital, Hangzhou Medical College, Hangzhou, China.
Pharm Biol. 2022 Dec;60(1):1981-1993. doi: 10.1080/13880209.2022.2128824.
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.
Our study explores the therapeutic potential of Shenfu in ALI.
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 . Male C57BL/6 mice were divided into four groups: LPS, LPS + 3% dextran sulphate sodium (DSS), 3% DSS + Shenfu, and LPS + 3% DSS + Shenfu.
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 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.
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.
许多研究都探索了治疗急性肺损伤(ALI)的新方法,但都未能显著降低 ALI 的高死亡率。参附是一种中药,可能对 ALI 有效。
本研究旨在探讨参附注射液治疗 ALI 的潜力。
雄性 C57BL/6 小鼠被分为对照组、脂多糖(LPS)(500μg/100μL 每只小鼠)和 LPS+参附组。参附(10μL/mL)加入 LPS(10μg/mL)处理的 MLE-12 细胞中孵育 48 小时。雄性 C57BL/6 小鼠被分为四组:LPS 组、LPS+3%葡聚糖硫酸钠(DSS)组、3%DSS+参附组和 LPS+3%DSS+参附组。
与 ALI 组相比,参附降低了湿/干重比(19.8%,36.2%),降低了白细胞介素-2(IL-2)(40.9%,61.6%)、干扰素-γ(IFN-γ)(43.5%,53.3%)、肿瘤坏死因子-α(TNF-α)(54.1%,42.1%)、白细胞介素-6(IL-6)(54.8%,70%)和白细胞介素-1β(IL-1β)(39.9%,65.1%),降低了血清尿酸(18.8%,48.7%)和肌酐(17.4%,41.1%)。此外,参附通过上调紧密连接蛋白-4 的表达增强了 LPS 刺激的上皮细胞的活力(17.2%,59.9%)并抑制了细胞凋亡(63.0%)和 p38/ERK 磷酸化。机制上,参附通过上调紧密连接蛋白-4 的表达介导了其保护作用。此外,参附可预防急性胃肠损伤加重的 ALI 中的肺和肠道上皮损伤。
综上所述,该结果揭示了参附注射液在小鼠 ALI 模型中的治疗作用和潜在机制,表明其具有治疗 ALI 患者的临床潜力。