Grimble Robert F, Howell W Martin, O'Reilly Gillian, Turner Stephen J, Markovic Olivera, Hirrell Sharon, East J Malcolm, Calder Philip C
Institute of Human Nutrition, School of Medicine, and the Biochemistry and Molecular Biology Division, School of Biological Sciences, University of Southampton, Southampton, United Kingdom.
Am J Clin Nutr. 2002 Aug;76(2):454-9. doi: 10.1093/ajcn/76.2.454.
Tumor necrosis factor alpha (TNF-alpha) mediates inflammation. High TNF-alpha production has adverse effects during disease. Polymorphisms in the TNF-alpha and lymphotoxin alpha genes influence TNF-alpha production. Fish oil suppresses TNF-alpha production and has variable antiinflammatory effects on disease.
We examined the relation between TNF-alpha and lymphotoxin alpha genotypes and the ability of dietary fish oil to suppress TNF-alpha production by peripheral blood mononuclear cells (PBMCs) in healthy men.
Polymorphisms in the TNF-alpha (TNF1 and TNF2) and lymphotoxin alpha (TNFB1 and TNFB2) genes were determined in 111 healthy young men. TNF-alpha production by endotoxin-stimulated PBMCs was measured before and 12 wk after dietary supplementation with fish oil (6 g/d).
Homozygosity for TNFB2 was 2.5 times more frequent in the highest than in the lowest tertile of inherent TNF-alpha production. The percentage of subjects in whom fish oil suppressed TNF-alpha production was lowest (22%) in the lowest tertile and doubled with each ascending tertile. In the highest and lowest tertiles, mean TNF-alpha production decreased by 43% (P < 0.05) and increased by 160% (P < 0.05), respectively. In the lowest tertile of TNF-alpha production, only TNFB1/TNFB*2 heterozygous subjects were responsive to the suppressive effect of fish oil. In the middle tertile, this genotype was 6 times more frequent than the other lymphotoxin alpha genotypes among responsive individuals. In the highest tertile, responsiveness to fish oil appeared unrelated to lymphotoxin alpha genotype.
The ability of fish oil to decrease TNF-alpha production is influenced by inherent TNF-alpha production and by polymorphisms in the TNF-alpha and lymphotoxin alpha genes.
肿瘤坏死因子α(TNF-α)介导炎症反应。疾病期间TNF-α的高产量具有不良影响。TNF-α和淋巴毒素α基因的多态性会影响TNF-α的产生。鱼油可抑制TNF-α的产生,并对疾病具有不同的抗炎作用。
我们研究了TNF-α和淋巴毒素α基因型之间的关系,以及膳食鱼油抑制健康男性外周血单核细胞(PBMC)产生TNF-α的能力。
在111名健康年轻男性中确定了TNF-α(TNF1和TNF2)和淋巴毒素α(TNFB1和TNFB2)基因的多态性。在膳食补充鱼油(6克/天)之前和之后12周,测量内毒素刺激的PBMC产生的TNF-α。
TNFB2的纯合性在固有TNF-α产生的最高三分位数中比最低三分位数中高2.5倍。鱼油抑制TNF-α产生的受试者百分比在最低三分位数中最低(22%),并随着每个上升的三分位数增加一倍。在最高和最低三分位数中,平均TNF-α产生分别下降了43%(P<0.05)和增加了160%(P<0.05)。在TNF-α产生的最低三分位数中,只有TNFB1/TNFB*2杂合受试者对鱼油的抑制作用有反应。在中间三分位数中,这种基因型在有反应的个体中比其他淋巴毒素α基因型频繁6倍。在最高三分位数中,对鱼油的反应性似乎与淋巴毒素α基因型无关。
鱼油降低TNF-α产生的能力受固有TNF-α产生以及TNF-α和淋巴毒素α基因多态性的影响。