Inflammatory responses to lipopolysaccharide are suppressed in 40% energy-restricted mice

被引:73
作者
Matsuzaki, J
Kuwamura, M
Yamaji, R
Inui, H [1 ]
Nakano, Y
机构
[1] Osaka Prefecture Univ, Dept Vet Sci, Osaka 5998531, Japan
[2] Osaka Prefecture Univ, Dept Appl Biol Chem, Osaka 5998531, Japan
关键词
energy-restricted mice; lipopolysaccharide; proinflammatory cytokines; inducible nitric oxide synthase; glucocorticoids;
D O I
10.1093/jn/131.8.2139
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
To elucidate the suppressive effects of energy restriction on the inflammatory responses to lipopoly-saccharicle (LPS), mice were divided into a control group (fed 5.0 g diet/d; 71 kJ/d) and a 40% energy-restricted group (fed 3.0 g diet/d; 43 kJ/d) at 8-wk of age. Four weeks later, 25 mug of LPS was intraperitoneally injected. After the LPS injection, interleukin-1 beta, interleukin-6 and tumor necrosis factor-a were elevated in serums in the 40% energy-restricted mice and in the controls, but the extent of the elevation was significantly lower in the restricted group. The LPS-induced expression of inducible nitric oxide synthase in the liver was significantly suppressed by the energy restriction. In addition, the LPS-induced elevations of serum aspartate and alanine aminotransferase activities, which are indexes of hepatic injury, were also significantly attenuated in the restricted group. Moreover, the extent of LPS-induced alterations in hepatic structure was less in the restricted mice than in controls. Serum corticosterone level in the restricted mice was higher than that in the controls before LIPS treatment (P < 0.05). Furthermore, after LIPS injection, the significantly higher level of corticosterone was maintained in the restricted mice, although the LPS treatment significantly enhanced the level even in the control group. These results suggest that the extreme inflammatory responses to endotoxin are prevented in the 40% energy-restricted mice, and corticosterone participates in the preventive effects.
引用
收藏
页码:2139 / 2144
页数:6
相关论文
共 41 条
  • [1] The role of nitric oxide in hepatic metabolism
    Alexander, B
    [J]. NUTRITION, 1998, 14 (04) : 376 - 390
  • [2] Aono K, 1997, J CELL BIOCHEM, V65, P349, DOI 10.1002/(SICI)1097-4644(19970601)65:3<349::AID-JCB5>3.3.CO
  • [3] 2-X
  • [4] CYTOKINES AS MODULATORS OF THE HYPOTHALAMUS PITUITARY-ADRENAL AXIS
    BESEDOVSKY, HO
    DELREY, A
    KLUSMAN, I
    FURUKAWA, H
    ARDITI, GM
    KABIERSCH, A
    [J]. JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY, 1991, 40 (4-6) : 613 - 618
  • [5] AN L-ARGININE-DEPENDENT MECHANISM MEDIATES KUPFFER CELL-INHIBITION OF HEPATOCYTE PROTEIN-SYNTHESIS INVITRO
    BILLIAR, TR
    CURRAN, RD
    STUEHR, DJ
    WEST, MA
    BENTZ, BG
    SIMMONS, RL
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 1989, 169 (04) : 1467 - 1472
  • [6] THE PATHOGENESIS OF SEPSIS
    BONE, RC
    [J]. ANNALS OF INTERNAL MEDICINE, 1991, 115 (06) : 457 - 469
  • [7] BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
  • [8] Suppression by dexamethasone of inducible nitric oxide synthase protein expression in vivo -: A possible role for lipocortin 1
    Bryant, CE
    Perretti, M
    Flower, RJ
    [J]. BIOCHEMICAL PHARMACOLOGY, 1998, 55 (03) : 279 - 285
  • [9] BUCKLIN SE, 1994, J ENDOTOXIN RES, V1, P45
  • [10] Melatonin inhibits expression of the inducible NO synthase II in liver and lung and prevents endotoxemia in lipopolysaccharide-induced multiple organ dysfunction syndrome in rats
    Crespo, E
    Macías, M
    Pozo, D
    Escames, G
    Martin, M
    Vives, F
    Guerrero, JM
    Acuña-Castroviejo, D
    [J]. FASEB JOURNAL, 1999, 13 (12) : 1537 - 1546