Reduning Injection protects flu-infected mice by inhibiting infiltration of inflammatory cells in lung and down-regulating cytokine storm.
10.19540/j.cnki.cjcmm.20220427.402
- Author:
Xiao-Lan YE
1
;
Chen-Chen TANG
1
;
Hui LIU
1
;
You HU
1
;
Tian-Nan XIANG
1
;
Yue-Juan ZHENG
2
Author Information
1. Center for Traditional Chinese Medicine and Immunology Research, Shanghai University of Traditional Chinese Medicine Shanghai 201203, China.
2. Center for Traditional Chinese Medicine and Immunology Research, Shanghai University of Traditional Chinese Medicine Shanghai 201203, China the Research Center for Traditional Chinese Medicine, Shanghai Institute of Infectious Diseases and Biosecurity Shanghai 201203, China Shanghai Key Laboratory of Health Identification and Evaluation, Shanghai University of Traditional Chinese Medicine Shanghai 201203, China.
- Publication Type:Journal Article
- Keywords:
Reduning Injection;
cytokine storm;
influenza virus;
macrophages
- MeSH:
Animals;
Anti-Inflammatory Agents/pharmacology*;
Body Weight;
Chemokine CCL5/pharmacology*;
Chemokine CXCL10/pharmacology*;
Cytokine Release Syndrome;
Cytokines/genetics*;
Drugs, Chinese Herbal;
Female;
Imiquimod/pharmacology*;
Interleukin-10;
Interleukin-6;
Lung;
Mice;
Mice, Inbred C57BL;
Oseltamivir/pharmacology*;
Phosphates/pharmacology*;
RNA;
RNA, Messenger;
Sincalide/pharmacology*;
Tumor Necrosis Factor-alpha/genetics*;
Weight Loss
- From:
China Journal of Chinese Materia Medica
2022;47(17):4698-4706
- CountryChina
- Language:Chinese
-
Abstract:
This study aimed to explore the protective effect of Reduning Injection(RDN) on mice infected by influenza virus A/PR/8(PR8) and its immune regulatory roles during viral infection. In in vivo experiments, female C57 BL/6 mice were randomly divided into phosphate buffered saline(PBS) group, PR8-infected group, oseltamivir treatment group(OSV) and RDN treatment group. After 2 h of PR8 infection, mice in the oseltamivir group were gavaged with oseltamivir 30 mg·kg~(-1), and those in the RDN treatment group were injected intraperitoneally with RDN 1.5 mL·kg~(-1)once per day for seven consecutive days. The body weight of mice in each group was recorded at the same time every morning for 16 consecutive days. The line chart of body weight change was created to analyze the protective effect of RDN on flu-infected mice. The relative mRNA expression of different cytokines(IL-6, TNF-α, MCP-1, IL-1β, MIP-2, IP-10 and IL-10) in lung samples of flu-infected mice was detected by PCR. Flow cytometry was utilized to analyze the composition of immune cells of mouse BALF samples on day 5 after infection. Mouse macrophage cell line RAW264.7 was planted and treated by different concentrations of RDN(150, 300, 600 μg·mL~(-1)) for 24 h or 48 h, and cell proliferation was detected by CCK-8 assay. RAW264.7 cells and mouse primary peritoneal macrophages were stimulated with synthetic single stranded RNA(R837), which elicited the inflammatory response by mimicking the infection of single-stranded RNA viruses. The expression of cytokines and chemokines in the supernatants of above culture system was detected by ELISA and qPCR. On days 4, 5, 6, 7 and 15 after infection, the body weight loss of mice in the RDN treatment group was alleviated compared with that of PR8-infected mice(P<0.05). RDN treatment obviously reduced lung index and the production of IL-6, TNF-α, MCP-1 and MIP-2 in lung tissues of flu-infected mice(P<0.05). The proportions of macrophages, neutrophils and T cells in mouse BALF samples were analyzed by flow cytometry, and compared with PR8-infected mice, RDN decreased the proportion of macrophages in BALF of flu-infected mice(P<0.05), and the proportion of T cells was recovered dramatically(P<0.001). In CCK-8 assay, the concentrations of RDN(150, 300, 600 μg·mL~(-1)) failed to cause cytotoxicity to RAW264.7 cells. In addition, RDN lowered the expression of inflammatory cytokines such as IL-6, TNF-α,MCP-1, IL-1β, RANTES, and IP-10 and even anti-inflammatory cytokine IL-10 in R837-induced macrophages. RDN reduced the infiltration of inflammatory macrophages and the production of excessive inflammatory cytokines, alleviated the body weight loss of flu-infected mice. What's more, RDN restored the depletion of T cells, which might prevent secondary infection and deteriorative progression of the disease. Taken together, RDN may inhibit cytokine production and therefore down-regulate cytokine storm during the infection of influenza virus.
