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二十碳五烯酸在抑制脂多糖诱导的人哮喘肺泡巨噬细胞产生促炎介质和转录方面比二十二碳六烯酸更有效。

Eicosapentaenoic acid is more effective than docosahexaenoic acid in inhibiting proinflammatory mediator production and transcription from LPS-induced human asthmatic alveolar macrophage cells.

作者信息

Mickleborough Timothy D, Tecklenburg Sandra L, Montgomery Gregory S, Lindley Martin R

机构信息

Exercise Biochemistry Laboratory, Department of Kinesiology, Indiana University, Bloomington, IN 47401, USA.

出版信息

Clin Nutr. 2009 Feb;28(1):71-7. doi: 10.1016/j.clnu.2008.10.012. Epub 2008 Dec 2.

Abstract

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 (AMphi).

METHODS

The AMphi 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 (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)-1beta production. Detection of TNF-alpha and IL-1beta mRNA expression levels was quantified by reverse transcriptase polymerase chain reaction.

RESULTS

120 microM pure EPA and EPA-rich media significantly (p<0.05) suppressed TNF-alpha and IL-1beta mRNA expression and the production of LTB(4), PGD(2) and TNF-alpha and IL-1beta in LPS-stimulated primary AMphi cells obtained from asthmatic patients to a much greater extent than 120 microM 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 AMphi cells.

摘要

背景与目的

本研究旨在确定鱼油中的活性成分二十碳五烯酸(EPA)或二十二碳六烯酸(DHA),哪一种在抑制脂多糖刺激的人哮喘肺泡巨噬细胞(AMphi)产生促炎介质和细胞因子表达方面最有效。

方法

使用纤维支气管镜从21名成年哮喘患者中获取AMphi。细胞先用DMEM、纯EPA、富含EPA的培养基(45% EPA/10% DHA)、纯DHA、富含DHA的培养基(10% EPA/50% DHA)或Lipovenos(n-6多不饱和脂肪酸)预处理,然后暴露于杜氏改良 Eagle培养基(DMEM)(-)或脂多糖(+)中。分析上清液中白三烯(LT)B4、前列腺素(PG)D2、肿瘤坏死因子(TNF)-α和白细胞介素(IL)-1β的产生。通过逆转录聚合酶链反应定量检测TNF-α和IL-1β mRNA表达水平。

结果

120 microM纯EPA和富含EPA的培养基分别比120 microM纯DHA和富含DHA的培养基更显著地(p<0.05)抑制了从哮喘患者获得的脂多糖刺激的原代AMphi细胞中TNF-α和IL-1β mRNA的表达以及LTB4、PGD2、TNF-α和IL-1β的产生。

结论

本研究首次表明,在人哮喘AMphi细胞中,EPA比DHA更有效地抑制炎症反应。

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