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青黛对甲型流感病毒诱导的急性肺损伤的有益作用。

Beneficial effect of Indigo Naturalis on acute lung injury induced by influenza A virus.

作者信息

Tu Peng, Tian Rong, Lu Yan, Zhang Yunyi, Zhu Haiyan, Ling Lijun, Li Hong, Chen Daofeng

机构信息

Department of Natural Medicine, School of Pharmacy, Fudan University, No. 826, Zhangheng Road, Shanghai, 201203, People's Republic of China.

Department of Pharmacology, School of Pharmacy, Fudan University, No. 826, Zhangheng Road, Shanghai, 201203, People's Republic of China.

出版信息

Chin Med. 2020 Dec 21;15(1):128. doi: 10.1186/s13020-020-00415-w.

Abstract

BACKGROUND

Infections induced by influenza viruses, as well as coronavirus disease 19 (COVID-19) pandemic induced by severe acute respiratory coronavirus 2 (SARS-CoV-2) led to acute lung injury (ALI) and multi organ failure, during which traditional Chinese medicine (TCM) played an important role in treatment of the pandemic. The study aimed to investigate the effect of Indigo Naturalis on ALI induced by influenza A virus (IAV) in mice.

METHOD

The anti-influenza and anti-inflammatory properties of aqueous extract of Indigo Naturalis (INAE) were evaluated in vitro. BALB/c mice inoculated intranasally with IAV (H1N1) were treated intragastrically with INAE (40, 80 and 160 mg/kg/day) 2 h later for 4 or 7 days. Animal lifespan and mortality were recorded. Expression of high mobility group box-1 protein (HMGB-1) and toll-like receptor 4 (TLR4) were evaluated through immunohistological staining. Inflammatory cytokines were also monitored by ELISA.

RESULT

INAE inhibited virus replication on Madin-Darby canine kidney (MDCK) cells and decreased nitric oxide (NO) production from lipopolysaccharide (LPS)-stimulated peritoneal macrophages in vitro. The results showed that oral administration of 160 mg/kg of INAE significantly improved the lifespan (P < 0.01) and survival rate of IAV infected mice, improved lung injury and lowered viral replication in lung tissue (P < 0.01). Treatment with INAE (40, 80 and 160 mg/kg) significantly increased liver weight and liver index (P < 0.05), as well as weight and organ index of thymus and spleen at 160 mg/kg (P < 0.05). Serum alanine transaminase (ALT) and aspartate aminotransferase (AST) levels were reduced by INAE administration (P < 0.05). The expression of HMGB-1 and TLR4 in lung tissue were also suppressed. The increased production of myeloperoxidase (MPO) and methylene dioxyamphetamine (MDA) in lung tissue were inhibited by INAE treatment (P < 0.05). Treatment with INAE reduced the high levels of interferon α (IFN-α), interferon β (IFN-β), monocyte chemoattractant protein-1 (MCP-1), regulated upon activation normal T cell expressed and secreted factor (RANTES), interferon induced protein-10 (IP-10), tumor necrosis factor-α (TNF-α), interleukin-6 (IL-6) (P < 0.05), with increased production of interferon γ (IFN-γ) and interleukin-10 (IL-10) (P < 0.05).

CONCLUSION

The results showed that INAE alleviated IAV induced ALI in mice. The mechanisms of INAE were associated with its anti-influenza, anti-inflammatory and anti-oxidation properties. Indigo Naturalis might have clinical potential to treat ALI induced by IAV.

摘要

背景

流感病毒引起的感染以及严重急性呼吸综合征冠状病毒2(SARS-CoV-2)引发的2019冠状病毒病(COVID-19)大流行导致急性肺损伤(ALI)和多器官功能衰竭,在此期间,中药在该大流行疾病的治疗中发挥了重要作用。本研究旨在探讨青黛对甲型流感病毒(IAV)诱导的小鼠ALI的影响。

方法

体外评估青黛水提取物(INAE)的抗流感和抗炎特性。用IAV(H1N1)鼻内接种BALB/c小鼠,2小时后分别以40、80和160mg/kg/天的剂量灌胃给予INAE,持续4或7天。记录动物寿命和死亡率。通过免疫组织化学染色评估高迁移率族蛋白B1(HMGB-1)和Toll样受体4(TLR4)的表达。还通过酶联免疫吸附测定法监测炎性细胞因子。

结果

INAE在体外抑制了Madin-Darby犬肾(MDCK)细胞上的病毒复制,并降低了脂多糖(LPS)刺激的腹腔巨噬细胞中一氧化氮(NO)的产生。结果显示,口服160mg/kg的INAE可显著提高IAV感染小鼠的寿命(P<0.01)和存活率,改善肺损伤并降低肺组织中的病毒复制(P<0.01)。用INAE(40、80和160mg/kg)治疗可显著增加肝脏重量和肝脏指数(P<0.05),以及160mg/kg剂量时胸腺和脾脏的重量及器官指数(P<0.05)。给予INAE可降低血清丙氨酸转氨酶(ALT)和天冬氨酸转氨酶(AST)水平(P<0.05)。肺组织中HMGB-1和TLR4的表达也受到抑制。INAE治疗可抑制肺组织中髓过氧化物酶(MPO)和亚甲基二氧安非他明(MDA)的增加(P<0.05)。用INAE治疗可降低高水平的干扰素α(IFN-α)、干扰素β(IFN-β)、单核细胞趋化蛋白-1(MCP-1)、活化正常T细胞表达和分泌因子(RANTES)、干扰素诱导蛋白10(IP-10)、肿瘤坏死因子-α(TNF-α)、白细胞介素-6(IL-6)(P<0.05),同时增加干扰素γ(IFN-γ)和白细胞介素-10(IL-10)的产生(P<0.05)。

结论

结果表明,INAE可减轻IAV诱导的小鼠ALI。INAE的作用机制与其抗流感、抗炎和抗氧化特性有关。青黛可能具有治疗IAV诱导的ALI的临床潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9ef0/7751115/141360d68e5d/13020_2020_415_Fig1_HTML.jpg

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