| Literature DB >> 25662753 |
Na-Rae Shin1, In-Sik Shin2, Hyuk-Hwan Song3, Ju-Mi Hong3, Ok-Kyoung Kwon3, Chan-Mi Jeon3, Jung-Hee Kim3, Sang-Woo Lee4, Joong-Ku Lee4, Hang Jin5, Wan Yi Li5, Sei-Ryang Oh3, Kyu-Woung Hahn6, Kyung-Seop Ahn7.
Abstract
Callicarpa japonica Thunb. (CJT) is traditionally used as an herbal remedy for the treatment of inflammatory diseases. This study aimed to investigate the anti-inflammatory response of CJT in lipopolysaccharide (LPS)-stimulated RAW264.7 cells and LPS-induced acute lung injury (ALI) in mice. The C57BL/6 mice were administered 30 mg/kg of CJT by oral gavage for 3 days. LPS is applied to animals by intranasal administration 1 h after final CJT treatment. LPS is applied to animals by intranasal administration 1h after final CJT treatment. LPS was delivered intranasally 1h after the final CJT treatment. In the LPS-stimulated RAW264.7 cells, CJT significantly decreased nitric oxide (NO) and interleukin (IL)-6 in a concentration-dependent manner by reducing inducible NO synthase (iNOS) and IL-6 mRNA levels. In the ALI model, CJT decreased the inflammatory cell count in the bronchoalveolar lavage fluid (BALF) while IL-6 levels were reduced in CJT-treated mice compared with the ALI control mice. CJT also inhibited airway inflammation by reducing iNOS expression in lung tissue. In conclusion, our results indicate that CJT inhibits inflammatory responses in LPS-stimulated RAW264.7 cells and in the LPS-induced ALI model. Therefore, we suggest that CJT has the potential to treat inflammatory diseases such as pneumonia.Entities:
Keywords: Acute lung injury; Callicarpa japonica Thunb.; Inducible nitric oxide synthase; Interleukin-6
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Year: 2015 PMID: 25662753 DOI: 10.1016/j.intimp.2015.01.025
Source DB: PubMed Journal: Int Immunopharmacol ISSN: 1567-5769 Impact factor: 4.932