共 36 条
Andrographolide Protects against LPS-Induced Acute Lung Injury by Inactivation of NF-κB
被引:216
作者:
Zhu, Tao
[1
]
Wang, Dao-xin
[1
]
Zhang, Wei
[2
]
Liao, Xiu-qing
[3
]
Guan, Xian
[1
]
Bo, Hong
[4
]
Sun, Jia-yang
[5
]
Huang, Ni-wen
[5
]
He, Jing
[1
]
Zhang, Yun-kun
[1
]
Tong, Jing
[1
]
Li, Chang-yi
[1
]
机构:
[1] Chongqing Med Univ, Affiliated Hosp 2, Chongqing, Peoples R China
[2] Chengdu Med Coll, Affiliated Hosp 1, Chengdu, Peoples R China
[3] Chongqing Fuling Cent Hosp, Chongqing, Peoples R China
[4] Sichuan Univ, W China Hosp, Chengdu 610064, Peoples R China
[5] Guiyang Med Coll, Affiliated Hosp, Guiyang, Peoples R China
来源:
PLOS ONE
|
2013年
/
8卷
/
02期
基金:
中国国家自然科学基金;
关键词:
RESPIRATORY-DISTRESS-SYNDROME;
PI-3K/AKT-NF-KAPPA-B SIGNALING PATHWAY;
EPITHELIAL SODIUM-CHANNEL;
ALVEOLAR FLUID CLEARANCE;
INDUCED MITOGENIC FACTOR;
IN-VITRO;
EXPRESSION;
PANICULATA;
INHIBITION;
ACTIVATION;
D O I:
10.1371/journal.pone.0056407
中图分类号:
O [数理科学和化学];
P [天文学、地球科学];
Q [生物科学];
N [自然科学总论];
学科分类号:
07 ;
0710 ;
09 ;
摘要:
Background: Nuclear factor-kappa B (NF-kappa B) is a central transcriptional factor and a pleiotropic regulator of many genes involved in acute lung injury. Andrographolide is found in the plant of Andrographis paniculata and widely used in Traditional Chinese Medicine, exhibiting potently anti-inflammatory property by inhibiting NF-kappa B activity. The purpose of our investigation was designed to reveal the effect of andrographolide on various aspects of LPS induced inflammation in vivo and in vitro. Methods and Results: In vivo, BALB/C mice were subjected to LPS injection with or without andrographolide treatments to induce ALI model. In vitro, MLE-12 cells were stimulated with LPS in the presence and absence of andrographolide. In vivo, pulmonary inflammation, pulmonary edema, ultrastructure changes of type II alveolar epithelial cells, MPO activity, total cells, neutrophils, macrophages, TNF-alpha, IL-6 and IL-1 beta in BALF, along with the expression of VCAM-1 and VEGF were dose-dependently attenuated by andrographolide. Meanwhile, in vitro, the expression of VCAM-1 and VEGF was also reduced by andrographolide. Moreover, our data showed that andrographolide significantly inhibited the ratios of phospho-IKK beta/total IKK beta, phospho-I kappa B alpha/total I kappa B alpha and phospho-NF-kappa B p65/total NF-kappa B p65, and NF-kappa B p65 DNA binding activities, both in vivo and in vitro. Conclusions: These results indicate that andrographolide dose-dependently suppressed the severity of LPS-induced ALI, more likely by virtue of andrographolide-mediated NF-kappa B inhibition at the level of IKK beta activation. These results suggest andrographolide may be considered as an effective and safe drug for the potential treatment of ALI.
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