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자료유형
학술저널
저자정보
윤여환 (원광대학교 약학대학 한약학과, 원광 한약연구소, 원광대학교 한의학전문대학원 BK21 plus 사업팀) 김성배 (원광대학교 약학대학 한약학과, 원광 한약연구소, 원광대학교 한의학전문대학원 BK21 plus 사업팀) 강옥화 (원광대학교 약학대학 한약학과, 원광 한약연구소, 원광대학교 한의학전문대학원 BK21 plus 사업팀) 문수현 (원광대학교 약학대학 한약학과, 원광 한약연구소, 원광대학교 한의학전문대학원 BK21 plus 사업팀) 서윤수 (원광대학교 약학대학 한약학과, 원광 한약연구소, 원광대학교 한의학전문대학원 BK21 plus 사업팀) 양다운 (원광대학교 약학대학 한약학과, 원광 한약연구소, 원광대학교 한의학전문대학원 BK21 plus 사업팀) 강다혜 (원광대학교 약학대학 한약학과, 원광 한약연구소, 원광대학교 한의학전문대학원 BK21 plus 사업팀) 위경 (원광대학교 약학대학 한약학과, 원광 한약연구소, 원광대학교 한의) 임재수 (Dept. of Oriental Pharmacy, College of Pharmacy, Wonkwang Oriental Medicines Research Institute, and BK21 Plus Team, Professional Graduate School of Oriental Medicine, Wonkwang Univer) 김마룡 (Dept. of Oriental Pharmacy, College of Pharmacy, Wonkwang Oriental Medicines Research Institute, and BK21 Plus Team, Professional Graduate School of Oriental Medicine, Wonkwang Unive) 곽남원 (Dept. of Oriental Pharmacy, College of Pharmacy, Wonkwang Oriental Medicines Research Institute, and BK21 Plus Team, Professional Graduate School of Oriental Medicine, Wonkwang Unive) 공룡 (Dept. of Oriental Pharmacy, College of Pharmacy, Wonkwang Oriental Medicines Research Institute, and BK21 Plus Team, Professional Graduate School of Oriental Medicine, Wonkwang Universi) 권동렬 (Dept. of Oriental Pharmacy, College of Pharmacy, Wonkwang Oriental Medicines Research Institute, and BK21 Plus Team, Professional Graduate School of Oriental Medicine, Wonkwang Uni)
저널정보
대한본초학회 대한본초학회지(본초분과학회지) 대한본초학회지 제29권 제6호
발행연도
2014.1
수록면
125 - 132 (8page)

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Objectives : Suryeon-hwan (SRH) exhibits potent anti-inflammatory activity with an unknown mechanism. However, there has been a lack of studies regarding the effects of SRH on the inflammatory activities and effector inflammatory disease mechanism about macrophage before is not known. So, the investigation focused on whether SRH inhibited nitric oxide (NO) and prostaglandin $E_2$ ($PGE_2$) productions, as well as the expressions of inducible NO synthase (iNOS), cyclooxygenase-2 (COX-2), interleukin-6 (IL-6), and mitogen-activated protein kinases (MAPKs) in LPS-stimulated RAW 264.7 cells. Methods : Cells were treated with 200 ng/mL of LPS 30 min prior to the addition of SRH. Cell viability was measured by MTS assay. The production of nitric oxide (NO) was determined by reacting cultured medium with Griess reagent. The content of level of cytokines (PGE, IL-6) in media from LPS-stimulated Raw 264.7 cells was analyed by ELISA kit. The expression of COX-2, iNOS and MAPKs was investigated by Western blot, RT-PCR. Results : We found that SRH inhibited LPS-induced NO, $PGE_2$ and IL-6 productions as well as the expressions of iNOS and COX-2. Furthermore, SRH suppressed the LPS-induced phosphorylation of MAPK and extracellular signal-regulated kinase 1/2 (ERK 1/2) activation. Conclusions : These results suggest that SRH has inhibitory effects on LPS-induced $PGE_2$, NO, and IL-6 production, as well as the expressions of iNOS and COX-2 in the murine macrophage. These inhibitory effects occur through blockades on the phosphorylation of MAPKs following activation.

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