Protective Effect of the Fruit Hull ofGleditsia sinensison LPS-Induced Acute Lung Injury Is Associated with Nrf2 Activation

Author:

Choi Jun-Young123,Kwun Min Jung4,Kim Kyun Ha4,Lyu Ji Hyo4,Han Chang Woo2,Jeong Han-Sol4,Ha Ki-Tae4,Jung Hee-Jae3,Lee Beom-Joon5,Sadikot Ruxana T.6,Christman John W.6,Jung Sung-Ki3,Joo Myungsoo47

Affiliation:

1. Department of Korean Medical Science, Korean Medicine Hospital, School of Korean Medicine, Pusan National University, Yangsan 626-870, Republic of Korea

2. Department of Internal Medicine, Korean Medicine Hospital, School of Korean Medicine, Pusan National University, Yangsan 626-870, Republic of Korea

3. Division of Allergy, Immune and Respiratory System, Department of Internal Medicine, College of Oriental Medicine, Kyung Hee University, Seoul 130-701, Republic of Korea

4. Division of Applied Medicine, School of Korean Medicine, Pusan National University, Yangsan 626-870, Republic of Korea

5. Department of Internal Medicine, Kangnam Korean Hospital, Kyung Hee University, Seoul 135-501, Republic of Korea

6. Section of Pulmonary, Critical Care and Sleep Medicine, University of Illinois and Jesse Brown Veterans Affairs Medical Center, Chicago, IL 60612, USA

7. Division of Allergy, Pulmonary and Critical Care Medicine, Vanderbilt University Medical Center, Nashville, TN 37232-2650, USA

Abstract

The fruit hull ofGleditsia 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-κB, 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-α and IL-1β 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.

Funder

Next-Generation BioGreen 21 Program

Publisher

Hindawi Limited

Subject

Complementary and alternative medicine

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