Magnolia kobus DC leaf ethanol extract alleviated lipopolysaccharide-induced acute lung inflammation by suppressing NF-κB and Nrf2 signaling

Author:

Kim Yeyoung1ORCID,Lee Soyoung2ORCID,Choi Young-Ae1ORCID,Chung Jae-Min3ORCID,Kim Eun-Nam4ORCID,Lee Byungheon5ORCID,Kim Sang-Yong6ORCID,Jeong Gil-Saeng4ORCID,Kim Sang-Hyun1ORCID

Affiliation:

1. Department of Pharmacology, School of Medicine, Kyungpook National University, Daegu 41944, South Korea

2. Immunoregulatory Materials Research Center, Korea Research Institute of Bioscience and Biotechnology, Jeongeup 56212, South Korea

3. Department of Gardens Education, Korea National Arboretum, Pocheon 11186, South Korea

4. College of Pharmacy, Chungnam National University, Daejeon 34134, South Korea

5. Department of Biochemistry and Cell Biology, School of Medicine, Kyungpook National University, Daegu 41944, South Korea

6. DMZ Botanic Garden, Korea National Arboretum, Yanggu 24564, South Korea

Abstract

Introduction: Magnolia kobus DC has been used as herbal medicine to treat coughs and is known to exert biological effects such as anti-inflammatory, antioxidant, and antibacterial properties. We aimed to define the pharmacological effects of M. kobus leaf ethanol extract (MLEE) on acute lung inflammation and explore the underlying mechanisms of action. Methods: For in vitro investigations, RAW 264.7 cells were pretreated with MLEE (1, 10, and 100 μg/mL) and stimulated with lipopolysaccharide (LPS). For in vivo investigations, BALB/c mice were intratracheally administered with LPS for 24 hours after injection of MLEE (0.3, 3, and 30 mg/kg). Hematoxylin and eosin staining was used for histopathology analysis of lung tissue. The phytochemical constituents of MLEE were analyzed using high-performance liquid chromatography. Results: In RAW 264.7 cells, MLEE reduced the activation of the inflammatory mediators (inducible nitric oxide synthase and cyclooxygenase-2) and the nuclear translocation of nuclear factor (NF)-κB and nuclear factor erythroid-2-related factor 2 (Nrf2). The intraperitoneal injection of MLEE (30 mg/kg) attenuated interstitial edema and immune cell infiltration in LPS-induced acute lung inflammation. MLEE also inhibited the activation of cyclooxygenase-2, NF-κB, and Nrf2 in the lung tissue. Conclusion: Taken together, MLEE exerted an anti-inflammatory effect by inhibiting inflammatory and oxidative mediators on acute lung inflammation suggesting that it might be used as a natural drug for treating acute lung inflammatory diseases.

Publisher

Maad Rayan Publishing Company

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