Eicosapentaenoic acid is more effective than docosahexaenoic acid in inhibiting proinflammatory mediator production and transcription from LPS-induced human asthmatic alveolar macrophage cells
Eicosapentaenoic acid is more effective than docosahexaenoic acid in inhibiting proinflammatory mediator production and transcription from LPS-induced human asthmatic alveolar macrophage cells
复制标题
DOI：
10.1016/j.clnu.2008.10.012
复制
发表时间：
2009-02-01
影响因子：
6.3
通讯作者：
Lindley, Martin R.
中科院分区：
文献类型：
--
作者：
Mickleborough, Timothy D.;Tecklenburg, Sandra L.;Lindley, Martin R.
Background & aims: The purpose of the study was to determine which of the active constituents of fish oil, eicosapentaenoic acid (EPA) or docosahexaenoic acid (DHA), is most effective in Suppressing Proinflammatory mediator generation and cytokine expression from LPS-stimulated human asthmatic alveolar macrophages (AM phi).Methods: The AM phi were obtained from twenty-one asthmatic adults using fiberoptic bronchoscopy. Cells were pretreated with DMEM, pure EPA, an EPA-rich media (45% EPA/10% DHA), pure DHA, a DHA-rich media (10% EPA/50% DHA) or Lipovenos (R) (n-6 PUFA), and then exposed to Dulbecco's Modified Eagle's Medium (DMEM) (-) or LPS (+). Supernatants were analyzed for leukotriene (LT)B-4, prostaglandin (PG)D-2, tumor necrosis factor (TNF)-alpha and interleukin (IL)-1 beta production. Detection of TNF-alpha and IL-1 beta mRNA expression levels was quantified by reverse transcriptase polymerase chain reaction.Results: 120 mu M pure EPA and EPA-rich media significantly (p < 0.05) Suppressed TNF-alpha. and IL-1 beta mRNA expression and the production of LTB4, PGD(2) and TNF-alpha and IL-1 beta in LPS-stimulated primary AM phi cells obtained from asthmatic patients to a Much greater extent than 120 mu M Pure DHA and DHA-rich media respectively.Conclusions: This study has shown for the first time that EPA is a more potent inhibitor than DHA of inflammatory responses in human asthmatic AM phi cells. (c) 2008 Elsevier Ltd and European Society for Clinical Nutrition and Metabolism. All rights reserved.
