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Zanthoxylum rhetsa Stem bark extract inhibits LPS-induced COX-2 and iNOS expression in RAW 264.7 cells via the NF-κB inactivation

Thu N.B. College of Pharmacy, Chungnam National University, Daejeon 305-764, South Korea|
Bae K. | Phuong T.T. | Nam N.H. | Soulinho T. | Than N.V. College of Pharmacy, Thai Nguyen University, Thai Nguyen, Viet Nam| Khoi N.M. Hanoi University of Pharmacy, Hanoi, Viet Nam| Ha D.T. Vietnam Military Medical University, Hadong, Hanoi, Viet Nam| Trung T.N. National Institute of Medicinal Materials, 3B Quangtrung, Hoankiem, Hanoi, Viet Nam|

Natural Product Sciences Số 4, năm 2010 (Tập 16, trang 265-270)

ISSN: 12263907

ISSN: 12263907

DOI:

Tài liệu thuộc danh mục: Scopus

Article

English

Từ khóa: cyclooxygenase 2; herbaceous agent; immunoglobulin enhancer binding protein; inducible nitric oxide synthase; interleukin 1beta; lipopolysaccharide; messenger RNA; plant extract; prostaglandin E2; tumor necrosis factor alpha; unclassified drug; Zanthoxylum rhetsa extract; antiinflammatory activity; article; bark; concentration response; cytokine production; enzyme activity; enzyme inhibition; gene expression; macrophage; plant stem; protein expression; Zanthoxylum; Zanthoxylum rhetsa
Tóm tắt tiếng anh
The methanol extract of Zanthoxylum rhetsa (MZRR) were evaluated for its ability to suppress the formation of inducible nitric oxide synthase (iNOS) and cyclooxygenase-2 (COX-2) in lipopolysaccharide (LPS)- activated RAW 264.7 macrophages. MZRR presented an inhibition of LPS-induced production of nitric oxide (NO) and prostaglandin E2 (PGE2) in RAW 264.7 macrophages. Western blotting and RT-PCR analyses demonstrated that MZRR significantly inhibited the protein and mRNA expressions of iNOS and COX-2 in LPSactivated macrophages in a dose-dependent manner. LPS-induced COX-2, iNOS, and nuclear factor kappa beta (NF-κB) activity were also decreased in the presence of MZRR. The production of tumor necrosis factor-α (TNF- α), the mRNA expression levels of pro-inflammatory cytokines, including TNF-α and IL-1β, were reduced after MZRR administration in a dose dependent-manner. These results suggest that the MZRR extract involved in the inhibition of iNOS and COX-2 via the NF-κB pathway, revealing a partial molecular basis for anti-inflammatory properties of the MZRR extract.

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