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Title

[A research on the influence of two herbal concoctions on Toll-like receptor signal pathways of influenza virus induced pneumonia in mice].

Authors

Liu Q, Wang J, Ma Y, Gu L.

Journal

Zhonghua Wei Zhong Bing Ji Jiu Yi Xue.

Year

2014

Vol (Issue)

26(5)

Page

321-4.

doi

10.3760/cma.j.issn.2095-4352.2014.05.007.

PMID

24809260

Url

http://www.ncbi.nlm.nih.gov/pubmed/24809260

MeSH

Animals
Drugs, Chinese Herbal/pharmacology*
Drugs, Chinese Herbal/therapeutic use
Influenzavirus A
Male
Mice
Mice, Inbred ICR
NF-kappa B/metabolism
Orthomyxoviridae Infections/drug therapy
Orthomyxoviridae Infections/metabolism*
Phytotherapy
Pneumonia, Viral/drug therapy
Pneumonia, Viral/metabolism*
Signal Transduction/drug effects*
Toll-Like Receptors/metabolism*

Keywords

Shufeng Xuanfei formula; Jiebiao Qingli formula; Pneumonia infected with influenza virus; Toll-like receptor; Gene chip; Mouse

한글 키워드

소풍선폐탕; 해표청리 처방; 인플루엔자 바이러스에 의한 감염; 톨유사수용체; 유전자 칩; 마우스

KMCRIC summary and commentary

없음

Korean Study

Abstract

OBJECTIVE:
To investigate the effect of Shufeng Xuanfei and Jiebiao Qingli concoctions on Toll-like receptor (TLR) signal pathway of pneumonia infected with influenza virus in mice.

METHODS:
The pneumonia model was reproduced by nasal dropping of influenza virus A in mice. The mice were randomly divided into nine groups: normal group (C), model group (M), tamiflu group (D), Shufeng Xuanfei low-dose (SL), medium-dose (SM) and high-dose (SH) groups, Jiebiao Qingli low-dose (JL), medium-dose (JM) and high-dose (JH) groups, each n=12. Two hours after model-reproduction, the mice in C group and M group received distilled water by gavage. The mice in D group received 2.5 g×mL(-1)×d(-1) oseltamivirphosphate. Shufeng Xuanfei formula in doses of 3.76, 1.88, 0.94 g×kg(-1)×d(-1) were respectively administered to SH, SM and SL groups by gavage, Jiebiao Qingli formula in doses of 4.37, 2.18, 1.09 g×kg(-1)×d(-1) was given to JH, JM and JL groups by gavage, respectively. Each group was in equal dose of 0.2 mL daily over a 4-day period. Total RNA was extracted in each group. Then gene chips were used to screen these RNA samples. Some genes that were involved in TLR signal pathways were selected. These candidate genes were verified by real-time reverse transcription-polymerase chain reaction (RT-PCR).

RESULTS:
TLR7, MYD88, CCL5, IFNB1, IL6, IL12a, NFKBIA and IKBKB were up-regulated in model group compared with control group. Compared with model group, down-regulated genes in medium-dose, low-dose Shufeng Xuanfei formula and medium-dose Jiebiao Qingli formula included TLR3, LR-3, TLR7, MYD88, CCL5, IFNB1, IL6, IL12a, NFKBIA and IKBKB (log2 signal intensity of SM/M in medium-dose Shufeng Xuanfei formula group were -1.24, -2.02, -1.36, -1.95, -0.63, -1.33, -3.50, -1.33, -1.33, log2 signal intensity of SL/M in low-dose Shufeng Xuanfei group were -1.07, -2.43, -2.63, -2.30, -5.09, -3.19, -3.53, -1.95, -1.95, log2 signal intensity of JM/M in medium-dose Jiebiao Qingli formula group were -1.78, -0.55, -1.35, -1.47, -1.65, -2.03, -3.02, -1.57, -1.57, respectively). The results suggested that the effect of Shufeng Xuanfei formula was better than that of Jiebiao Qingli formula. By RT-PCR, compared with model group, low-dose, medium-dose and high-dose groups of Shufeng Xuanfei formula, medium-dose and high-dose groups of Jiebiao Qingli formula, and tamiflu group, significant decrease in TLR7, nuclear factor-ΚB (NF-ΚB), myeloid differential protein-88 (MyD88) mRNA expression were found. Medium-dose and low-dose Shufeng Xuanfei formula group (TLR7 mRNA: 3.6±0.3, 3.5±1.2 vs. 7.4±1.6, NF-ΚB mRNA: 1.1±0.2, 1.0±0.2 vs. 2.2±0.4; MyD88 mRNA: 1.4±0.4, 1.0±0.3 vs. 3.4±0.9, all P<0.01) and medium-dose Jiebiao Qingli formula group (TLR7 mRNA: 4.9±0.3 vs. 7.4±1.6, NF-ΚB mRNA: 1.3±0.7 vs. 2.2±0.4, MyD88 mRNA: 1.6±0.8 vs. 3.4±0.9, P<0.05 or P<0.01) were shown statistically significant decreases compared with the model group.

CONCLUSIONS:
Medium-dose and low-dose Shufeng Xuanfei formula and medium-dose Jiebiao Qingli formula can inhibit the inflammatory reaction induced by influenza virus by down-regulating the NF-ΚB through TLR signal pathways dependent on MyD88. The regulation of Shufeng Xuanfei formula in TLR signal pathways was superior to that of Jiebiao Qingli formula.

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