Suppr超能文献

在超长链饱和脂肪酸积累的巨噬细胞中一氧化氮、活性氧和促炎细胞因子的产生增加。

Enhanced production of nitric oxide, reactive oxygen species, and pro-inflammatory cytokines in very long chain saturated fatty acid-accumulated macrophages.

作者信息

Yanagisawa Naotake, Shimada Kazunori, Miyazaki Tetsuro, Kume Atsumi, Kitamura Yohei, Sumiyoshi Katsuhiko, Kiyanagi Takashi, Iesaki Takafumi, Inoue Nao, Daida Hiroyuki

机构信息

Department of Cardiovascular Medicine, Juntendo University School of Medicine, Tokyo, Japan.

出版信息

Lipids Health Dis. 2008 Nov 28;7:48. doi: 10.1186/1476-511X-7-48.

Abstract

BACKGROUND

Deterioration of peroxisomal beta-oxidation activity causes an accumulation of very long chain saturated fatty acids (VLCSFA) in various organs. We have recently reported that the levels of VLCSFA in the plasma and/or membranes of blood cells were significantly higher in patients with metabolic syndrome and in patients with coronary artery disease than the controls. The aim of the present study is to investigate the effect of VLCSFA accumulation on inflammatory and oxidative responses in VLCSFA-accumulated macrophages derived from X-linked adrenoleukodystrophy (X-ALD) protein (ALDP)-deficient mice.

RESULTS

Elevated levels of VLCSFA were confirmed in macrophages from ALDP-deficient mice. The levels of nitric oxide (NO) production stimulated by lipopolysaccharide (LPS) and interferon-gamma (IFN-gamma), intracellular reactive oxygen species (ROS), and pro-inflammatory cytokines, including tumor necrosis factor-alpha (TNF-alpha), interluekin-6 (IL-6), and interleukin-12p70 (IL-12p70), were significantly higher in macrophages from ALDP-deficient mice than in those from wild-type mice. The inducible NO synthase (iNOS) mRNA expression also showed an increase in macrophages from ALDP-deficient mice.

CONCLUSION

These results suggested that VLCSFA accumulation in macrophages may contribute to the pathogenesis of inflammatory diseases through the enhancement of inflammatory and oxidative responses.

摘要

背景

过氧化物酶体β-氧化活性的降低会导致各器官中极长链饱和脂肪酸(VLCSFA)的积累。我们最近报道,代谢综合征患者和冠状动脉疾病患者血浆和/或血细胞细胞膜中的VLCSFA水平显著高于对照组。本研究的目的是探讨VLCSFA积累对源自X连锁肾上腺脑白质营养不良(X-ALD)蛋白(ALDP)缺陷小鼠的VLCSFA积累巨噬细胞中炎症和氧化反应的影响。

结果

在ALDP缺陷小鼠的巨噬细胞中证实了VLCSFA水平升高。脂多糖(LPS)和干扰素-γ(IFN-γ)刺激产生的一氧化氮(NO)水平、细胞内活性氧(ROS)以及包括肿瘤坏死因子-α(TNF-α)、白细胞介素-6(IL-6)和白细胞介素-12p70(IL-12p70)在内的促炎细胞因子水平,在ALDP缺陷小鼠的巨噬细胞中显著高于野生型小鼠。诱导型一氧化氮合酶(iNOS)mRNA表达在ALDP缺陷小鼠的巨噬细胞中也有所增加。

结论

这些结果表明,巨噬细胞中VLCSFA的积累可能通过增强炎症和氧化反应而促进炎症性疾病的发病机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2052/2613382/58d3ebb6368a/1476-511X-7-48-1.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验