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抗新冠病毒中药方剂“克冠 1 号”对急性肺损伤的抑制作用及机制研究。

Inhibitory effects and mechanisms of the anti-covid-19 traditional Chinese prescription, Keguan-1, on acute lung injury.

机构信息

Senior Department of Hepatology, The Fifth Medical Center of PLA General Hospital, Beijing, 100039, China; China Military Institute of Chinese Medicine, The Fifth Medical Centre of PLA General Hospital, Beijing, 100039, China.

Medical Supplies Center of PLA General Hospital, Beijing, 100039, China.

出版信息

J Ethnopharmacol. 2022 Mar 1;285:114838. doi: 10.1016/j.jep.2021.114838. Epub 2021 Nov 14.

Abstract

ETHNOPHARMACOLOGICAL RELEVANCE

Keguan-1, a new traditional Chinese medicine (TCM) prescription contained seven Chinese herbs, is developed to treat coronavirus disease 19 (COVID-19). The first internationally registered COVID-19 randomised clinical trial on integrated therapy demonstrated that Keguan-1 significantly reduced the incidence of ARDS and inhibited the severe progression of COVID-19.

AIM OF THE STUDY

To investigate the protective mechanism of Keguan-1 on ARDS, a lipopolysaccharide (LPS)-induced acute lung injury (ALI) model was used to simulate the pathological state of ARDS in patients with COVID-19, focusing on its effect and mechanism on ALI.

MATERIALS AND METHODS

Mice were challenged with LPS (2 mg/kg) by intratracheal instillation (i.t.) and were orally administered Keguan-1 (low dose, 1.25 g/kg; medium dose, 2.5 g/kg; high dose, 5 g/kg) after 2 h. Bronchoalveolar lavage fluid (BALF) and lung tissue were collected 6 h and 24 h after i.t. administration of LPS. The levels of inflammatory factors tumour necrosis factor alpha (TNF-α), interleukin (IL)-6, IL-1β, keratinocyte-derived chemokine (KC or mCXCL1), macrophage inflammatory protein 2 (MIP2 or mCXCL2), angiotensin II (Ang II), and endothelial cell junction-associated proteins were analysed using ELISA or western blotting.

RESULTS

Keguan-1 improved the survival rate, respiratory condition, and pathological lung injury; decreased the production of proinflammatory factors (TNF-α, IL-6, IL-1β, KC, and MIP2) in BALF and the number of neutrophils in the lung tissues; and ameliorated inflammatory injury in the lung tissues of the mice with LPS-induced ALI. Keguan-1 also reduced the expression of Ang II and the adhesion molecule ICAM-1; increased tight junction proteins (JAM-1 and claudin-5) and VE-cadherin expression; and alleviated pulmonary vascular endothelial injury in LPS-induced ALI.

CONCLUSION

These results demonstrate that Keguan-1 can improve LPS-induced ALI by reducing inflammation and pulmonary vascular endothelial injury, providing scientific support for the clinical treatment of patients with COVID-19. Moreover, it also provides a theoretical basis and technical support for the scientific use of TCMs in emerging infectious diseases.

摘要

民族药理学相关性

冠一号,一种新的中药(TCM)处方,包含七种中草药,是为治疗 2019 年冠状病毒病(COVID-19)而开发的。第一个国际注册的 COVID-19 综合治疗随机临床试验表明,冠一号能显著降低 ARDS 的发生率,并抑制 COVID-19 的严重进展。

研究目的

为了研究冠一号对 ARDS 的保护机制,我们使用脂多糖(LPS)诱导的急性肺损伤(ALI)模型来模拟 COVID-19 患者的 ARDS 病理状态,重点研究其对 ALI 的作用和机制。

材料和方法

通过气管内滴注(i.t.)的方式用 LPS(2mg/kg)对小鼠进行攻击,在 i.t. 给药后 2 小时给予冠一号(低剂量,1.25g/kg;中剂量,2.5g/kg;高剂量,5g/kg)。在 LPS i.t. 给药后 6 小时和 24 小时收集支气管肺泡灌洗液(BALF)和肺组织。采用 ELISA 或 Western blot 法分析炎症因子肿瘤坏死因子-α(TNF-α)、白细胞介素(IL)-6、IL-1β、角质细胞衍生趋化因子(KC 或 mCXCL1)、巨噬细胞炎症蛋白 2(MIP2 或 mCXCL2)、血管紧张素 II(Ang II)和内皮细胞连接相关蛋白的水平。

结果

冠一号提高了 LPS 诱导的 ALI 小鼠的存活率、呼吸状况和肺损伤程度;降低了 BALF 中促炎因子(TNF-α、IL-6、IL-1β、KC 和 MIP2)的产生和肺组织中中性粒细胞的数量;改善了 LPS 诱导的 ALI 小鼠的肺组织炎症损伤。冠一号还降低了 Ang II 和黏附分子 ICAM-1 的表达;增加了紧密连接蛋白(JAM-1 和 Claudin-5)和 VE-钙粘蛋白的表达;减轻了 LPS 诱导的 ALI 中的肺血管内皮损伤。

结论

这些结果表明,冠一号通过减轻炎症和肺血管内皮损伤,可以改善 LPS 诱导的 ALI,为 COVID-19 患者的临床治疗提供科学依据。此外,它还为中医药在新发传染病中的科学应用提供了理论依据和技术支持。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f7df/8590745/467a79ad62f4/ga1_lrg.jpg

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