| Literature DB >> 28011397 |
Hyung Won Ryu1, Su Ui Lee1, Seoghyun Lee2, Hyuk-Hwan Song3, Tae Hyun Son4, Yeah-Un Kim1, Heung Joo Yuk1, Hyunju Ro5, Chong-Kil Lee6, Sung-Tae Hong7, Sei-Ryang Oh8.
Abstract
Pseudolysimachion rotundum var. subintegrum is utilized as a traditional herbal remedy to treat cough, bronchitis, and asthma in Korea, Russia, China, and Europe. Here, we show that 3-methoxy-catalposide, a novel iridoide glycoside isolated from P. rotundum var. subintegrum has the anti-inflammatory activity in lipopolysaccharide (LPS)-stimulated macrophages. The chemical structure of 3-methoxy-catalposide was determined by NMR, optical rotation and HRESIMS. In in vitro experiment, RAW264.7 cells were treated with 3-methoxy-catalposide for 2h before exposure to LPS for different times. Inflammatory gene and protein expressions were assayed using RT-PCR and ELISA. Activities of signal proteins were examined using western analysis. Our results demonstrated that 3-methoxy-catalposide significantly inhibits the expression of cyclooxygenase (COX)-2 and inducible nitric oxide synthase (iNOS) in RAW264.7 cells stimulated by LPS, thereby suppressing the release of prostaglandin E2 (PGE2) and nitric oxide (NO). Moreover, 3-methoxy-catalposide markedly reduced the LPS-induced expression of pro-inflammatory genes, such as interleukin (IL)-6, IL-1β, and TNF-α. Further, 3-methoxy-catalposide inhibited both LPS-induced activation of three MAP kinases (ERK 1/2, JNK, and p38) and the nuclear translocation of NF-κB and AP-1. These results support that 3-methoxy-catalposide may be a promising candidate for inflammation treatment. Copyright ÂEntities:
Keywords: 3-Methoxy-catalposide; AP-1; MAP kinase; NF-κB; NO; PGE(2)
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Year: 2016 PMID: 28011397 DOI: 10.1016/j.cyto.2016.12.006
Source DB: PubMed Journal: Cytokine ISSN: 1043-4666 Impact factor: 3.861