Protective Effect of the Fruit Hull of Gleditsia sinensis on LPS-Induced Acute Lung Injury Is Associated with Nrf2 Activation

被引:20
作者
Choi, Jun-Young [1 ,2 ,3 ]
Kwun, Min Jung [4 ]
Kim, Kyun Ha [4 ]
Lyu, Ji Hyo [4 ]
Han, Chang Woo [2 ]
Jeong, Han-Sol [4 ]
Ha, Ki-Tae [4 ]
Jung, Hee-Jae [3 ]
Lee, Beom-Joon [5 ]
Sadikot, Ruxana T. [6 ,7 ]
Christman, John W. [6 ,7 ]
Jung, Sung-Ki [3 ]
Joo, Myungsoo [4 ,8 ]
机构
[1] Pusan Natl Univ, Sch Korean Med, Korean Med Hosp, Dept Korean Med Sci, Yangsan 626870, South Korea
[2] Pusan Natl Univ, Sch Korean Med, Korean Med Hosp, Dept Internal Med, Yangsan 626870, South Korea
[3] Kyung Hee Univ, Div Allergy Immune & Resp Syst, Dept Internal Med, Coll Oriental Med, Seoul 130701, South Korea
[4] Pusan Natl Univ, Sch Korean Med, Div Appl Med, Yangsan 626870, South Korea
[5] Kyung Hee Univ, Kangnam Korean Hosp, Dept Internal Med, Seoul 135501, South Korea
[6] Univ Illinois, Sect Pulm Crit Care & Sleep Med, Chicago, IL 60612 USA
[7] Jesse Brown Vet Affairs Med Ctr, Chicago, IL 60612 USA
[8] Vanderbilt Univ, Med Ctr, Div Allergy Pulm & Crit Care Med, Nashville, TN 37232 USA
关键词
FACTOR-KAPPA-B; RESPIRATORY-DISTRESS-SYNDROME; TRITERPENOIDAL SAPONINS; ENHANCES SUSCEPTIBILITY; TRANSCRIPTION FACTOR; OXIDATIVE STRESS; NITRIC-OXIDE; INDUCTION; INFLAMMATION; ROOTS;
D O I
10.1155/2012/974713
中图分类号
R [医药、卫生];
学科分类号
10 ;
摘要
The fruit hull of Gleditsia sinensis (FGS) has been prescribed as a traditional eastern Asian medicinal remedy for the treatment of various respiratory diseases, but the efficacy and underlying mechanisms remain poorly characterized. Here, we explored a potential usage of FGS for the treatment of acute lung injury (ALI), a highly fatal inflammatory lung disease that urgently needs effective therapeutics, and investigated a mechanism for the anti-inflammatory activity of FGS. Pretreatment of C57BL/6 mice with FGS significantly attenuated LPS-induced neutrophilic lung inflammation compared to sham-treated, inflamed mice. Reporter assays, semiquantitative RT-PCR, and Western blot analyses show that while not affecting NF-kappa B, FGS activated Nrf2 and expressed Nrf2-regulated genes including GCLC, NQO-1, and HO-1 in RAW 264.7 cells. Furthermore, pretreatment of mice with FGS enhanced the expression of GCLC and HO-1 but suppressed that of proinflammatory cytokines in including TNF-alpha and IL-1 beta in the inflamed lungs. These results suggest that FGS effectively suppresses neutrophilic lung inflammation, which can be associated with, at least in part, FGS-activating anti-inflammatory factor Nrf2. Our results suggest that FGS can be developed as a therapeutic option for the treatment of ALI.
引用
收藏
页数:11
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