Suppressive effects of coumarins from Mammea siamensis on inducible nitric oxide synthase expression in RAW264.7 cells

被引:28
|
作者
Morikawa, Toshio [1 ]
Sueyoshi, Mayumi [1 ]
Chaipech, Saowanee [1 ]
Matsuda, Hisashi [2 ]
Nomura, Yukiko [2 ]
Yabe, Mikuko [2 ]
Matsumoto, Tomoko [2 ]
Ninomiya, Kiyofumi [1 ]
Yoshikawa, Masayuki [1 ,2 ]
Pongpiriyadacha, Yutana [3 ]
Hayakawa, Takao [1 ]
Muraoka, Osamu [1 ]
机构
[1] Kinki Univ, Pharmaceut Res & Technol Inst, Higashiosaka, Osaka 5778502, Japan
[2] Kyoto Pharmaceut Univ, Yamashina Ku, Kyoto 6078412, Japan
[3] Rajamangala Univ Technol Srivijaya, Fac Sci & Technol, Thungsong 80110, Nakhonsithammar, Thailand
基金
日本学术振兴会;
关键词
Mammea siamensis; Mammeasin; Coumarin; NO production inhibitor; iNOS; LIPOPOLYSACCHARIDE-ACTIVATED MACROPHAGES; ABSOLUTE STEREOSTRUCTURES; MEDICINAL FOODSTUFFS; AMIDE CONSTITUENTS; ANTICANCER AGENTS; KAYEA-ASSAMICA; SURANGIN-B; TNF-ALPHA; INHIBITORS; XANTHONES;
D O I
10.1016/j.bmc.2012.06.031
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
A methanol extract of the flowers of Mammea siamensis (Calophyllaceae) was found to inhibit nitric oxide (NO) production in lipopolysaccharide-activated RAW264.7 cells. From the extract, two new geranylated coumarins, mammeasins A (1) and B (2), were isolated together with 17 known compounds including 15 coumarins. The structures of 1 and 2 were determined on the basis of their spectroscopic properties as well as of their chemical evidence. Among the isolates, 1 (IC50 = 1.8 mu M), 2 (6.4 mu M), surangins B (3, 5.0 mu M), C (4, 6.8 mu M), and D (5, 6.2 mu M), kayeassamins E (7, 6.1 mu M), F (8, 6.0 mu M), and G (9, 0.8 mu M), mammea A/AD (11, 1.3 mu M), and mammea E/BB (16, 7.9 mu M) showed NO production inhibitory activity. Compounds 1, 9, and 11 were found to inhibit induction of inducible nitric oxide synthase (iNOS). With regard to mechanism of action of these active constituents (1, 9, and 11), suppression of STAT1 activation is suggested to be mainly involved in their suppression of iNOS induction. (C) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:4968 / 4977
页数:10
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