Chlorogenic acid protects mice against lipopolysaccharide-induced acute lung injury
被引:173
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Zhang, Xu
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Huang, Huang
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Yang, Tingting
[1
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Ye, Yin
[1
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Shan, Jianhua
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Nanjing Normal Univ, Coll Life Sci, Jiangsu Prov Key Lab Mol, Nanjing 210046, Peoples R ChinaNanjing Univ, Sch Life Sci, State Key Lab Pharmaceut Biotechnol, Nanjing 210093, Jiangsu, Peoples R China
Shan, Jianhua
[2
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Yin, Zhimin
[2
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Luo, Lan
[1
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[1] Nanjing Univ, Sch Life Sci, State Key Lab Pharmaceut Biotechnol, Nanjing 210093, Jiangsu, Peoples R China
[2] Nanjing Normal Univ, Coll Life Sci, Jiangsu Prov Key Lab Mol, Nanjing 210046, Peoples R China
来源:
INJURY-INTERNATIONAL JOURNAL OF THE CARE OF THE INJURED
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2010年
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41卷
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07期
Chlorogenic acid (CGA) is one of the most abundant polyphenol compounds in human diet. Our previous in vitro study demonstrates that CGA presents anti-inflammatory activities in RAW 264.7 cells. Here we show that CGA protects mice against lipopolysaccharide (LPS)-induced acute lung injury (ALI). We treated mice with CGA (5, 20 and 50 mg/kg body weight) 30 min or 3 h after intratracheal administration of LPS. The histological results showed that CGA, at dose of 50 mg/kg, protected mice from LPS-induced ALI which displayed by edema, haemorrhage, blood vessel and alveolar structural damage. CGA inhibited LPS-increased pulmonary MPO activity and migration of polymorphonuclear neutrophils (PMNs) into bronchoalveolar lavage fluid (BALF). Furthermore, CGA markedly decreased the activity of inducible nitric oxide synthase (iNOS) in lung tissues and thus prevented nitric oxide (NO) release in response to LPS challenge. In conclusion, these results indicated that CGA was greatly effective in inhibiting ALI and might act as a potential therapeutic reagent for treating ALI in the future. (C) 2010 Elsevier Ltd. All rights reserved.