Whiskey Congeners Suppress LPS/IFNγ-Induced NO Production in Murine Macrophage RAW 264 Cells by Inducing Heme Oxygenase-1 Expression

被引:7
作者
Itoh, Tomohiro [1 ]
Ando, Masashi [1 ]
Tsukamasa, Yasuyuki [1 ]
Wakimoto, Toshiyuki [2 ]
Nukaya, Haruo [3 ]
机构
[1] Kinki Univ, Fac Agr, Dept Fisheries, Lab Aquat Food Sci, Nara 6318505, Japan
[2] Univ Tokyo, Fac Pharmaceut Sci, Grad Sch Pharmaceut Sci, Bunkyo Ku, Tokyo 1130033, Japan
[3] Univ Shizuoka, Suruga Ku, Shizuoka 4228526, Japan
关键词
whiskey congeners; nitric oxide; heme oxygenase-1; Nrf2/ARE signaling; intracellular ROS; NITRIC-OXIDE; ACTIVATION; INDUCTION; PATHWAY; DERIVATIVES; ENDOTOXIN; PROTEINS; GENE; NRF2;
D O I
10.1021/jf3040385
中图分类号
S [农业科学];
学科分类号
09 ;
摘要
Whiskey includes many nonvolatile substances (whiskey congeners; Whc) that seep from the oak cask during the maturation process. To date, many functions of Whc have reported, such as antiallergy and antimelanogenesis. This study examined the effect of Whc on LPS/IFN gamma-induced nitric oxide (NO) production in murine macrophage RAW 264 cells. Whc suppressed LPS/IFN gamma-induced NO production in a concentration-dependent manner. To determine the active compounds in Whc, the effect of 10 major compounds isolated from Whc on LPS/IFN gamma-induced NO production was examined. Coniferylaldehyde (CA) and sinapylaldehyde (SiA) strongly suppressed LPS/IFN gamma-induced NO production. Pretreatment with Whc, CA, and SiA induced heme oxygenase-1 (HO-1) expression. The expression of HO-1 by Whc, CA, and SiA pretreatment was due to activation of Nrf2/ARE signaling via the elevation of intracellular reactive oxygen species. To investigate the in vivo effects of Whc, Whc was administered to mice with antitype II collagen antibody-induced arthritis, and we the arthritis score and hind paw volume were measured. Administration of Whc remarkably suppressed the arthritis score and hind paw volume. Taken together, these findings suggest that Whc is beneficial for the treatment of inflammatory disease.
引用
收藏
页码:12491 / 12500
页数:10
相关论文
共 44 条
  • [1] The role of nitric oxide in tissue destruction
    Abramson, SB
    Amin, AR
    Clancy, RM
    Attur, M
    [J]. BEST PRACTICE & RESEARCH IN CLINICAL RHEUMATOLOGY, 2001, 15 (05): : 831 - 845
  • [2] Adfa M, 2012, BIOL PHARM BULL, V35, P963
  • [3] Transcriptional regulation of the heme oxygenase-1 gene via the stress response element pathway
    Alam, J
    Cook, JL
    [J]. CURRENT PHARMACEUTICAL DESIGN, 2003, 9 (30) : 2499 - 2511
  • [4] The NOX family of ROS-generating NADPH oxidases: Physiology and pathophysiology
    Bedard, Karen
    Krause, Karl-Heinz
    [J]. PHYSIOLOGICAL REVIEWS, 2007, 87 (01) : 245 - 313
  • [5] Nitric oxide and the regulation of gene expression
    Bogdan, C
    [J]. TRENDS IN CELL BIOLOGY, 2001, 11 (02) : 66 - 75
  • [6] Nitric oxide and the immune response
    Bogdan, C
    [J]. NATURE IMMUNOLOGY, 2001, 2 (10) : 907 - 916
  • [7] Induction of inducible nitric oxide synthase-NO• by lipoarabinomannan of Mycobacterium tuberculosis is mediated by MEK1-ERK, MKK7-JNK, and NF-κB signaling pathways
    Chan, ED
    Morris, KR
    Belisle, JT
    Hill, P
    Remigio, LK
    Brennan, PJ
    Riches, DWH
    [J]. INFECTION AND IMMUNITY, 2001, 69 (04) : 2001 - 2010
  • [8] IFN-γ + LPS induction of iNOS is modulated by ERK, JNK/SAPK, and p38mapk in a mouse macrophage cell line
    Chan, ED
    Riches, DWH
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 2001, 280 (03): : C441 - C450
  • [9] Ethanol alters cellular activation and CD14 partitioning in lipid rafts
    Dai, Q
    Zhang, J
    Pruett, SB
    [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2005, 332 (01) : 37 - 42
  • [10] DING AH, 1988, J IMMUNOL, V141, P2407