Effect of short term calorie restriction on pro-inflammatory NF-kB and AP-1 in aged rat kidney

被引:107
作者
Jung, K. J. [1 ]
Lee, E. K. [1 ]
Kim, J. Y. [1 ]
Zou, Y. [1 ]
Sung, B. [1 ]
Heo, H. S. [1 ]
Kim, M. K. [2 ,3 ]
Lee, J. [1 ,2 ,3 ]
Kim, N. D. [1 ,2 ,3 ]
Yu, B. Pal [2 ,3 ,4 ]
Chung, H. Y. [1 ,2 ,3 ]
机构
[1] Pusan Natl Univ, Coll Pharm, Dept Pharm, Pusan 609735, South Korea
[2] Pusan Natl Univ, Longev Life Sci Inst, Pusan 609735, South Korea
[3] Pusan Natl Univ, Inst Technol, Pusan 609735, South Korea
[4] Univ Texas Hlth Sci Ctr San Antonio, Dept Physiol, San Antonio, TX 78229 USA
关键词
Aging; Short term calorie restriction; Molecular inflammation; NF-kappa B; AP-1; OXIDATIVE STRESS; MODULATION; PROTEIN; THIOREDOXIN; LONGEVITY; RESPONSES; BRAIN;
D O I
10.1007/s00011-008-7227-2
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
To compare the effect of short-term calorie restriction (CR) on aging with that of already known long-term CR, the anti-inflammatory efficacy of 10-day CR was explored in aged rat kidney. Two different age groups, 6 months (young) and 24 months (old) were used. In the old group, one sub-group was control, fed ad libitum (AL) and the other was fed CR for 10 days with 40 % of the food intake of the AL subgroup (n = 5). Reactive species (RS), lipid peroxides and COX-2 activity were measured. The activities of proinflammatory transcription factors NF-kB and AP-1 were measured by electro-mobility shift assay (EMSA). Upstream signaling cascades of NF-kB and AP-1 as well as proinflammatory gene expression were detected by Western blot. 10-day CR suppressed RS, lipid peroxides, and COX-2 activity in aged rat kidney. CR also inhibited upstream signaling cascades and DNA binding activity of NF-kB and AP-1, and thioredoxin/Ref-1 pathway. CR blocked expression of NF-kB-and AP-1-responsive gene COX-2, iNOS, VCAM-1 and ICAM-1. We report for the first time that 10-day CR can attenuate the altered signaling transduction for inflammatory processes which is mediated through RS-induced NF-kB and AP-1 in aged kidney.
引用
收藏
页码:143 / 150
页数:8
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