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Stress and Proinflammatory Cytokines: Omega-3 Intervention

Stress and Proinflammatory Cytokines: Omega-3 Intervention
压力和促炎细胞因子:Omega-3 干预
批准号:
7846987
负责人:
JANICE KIECOLT-GLASER
金额:
$1.89万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2009
资助国家:
美国
项目状态:
已结题
起止时间:
2009-09-30 至 2010-07-31

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中文摘要
翻译
描述(由申请人提供):促炎细胞因子影响许多年龄相关疾病的发作和病程。压力和抑郁可以显著增加促炎细胞因子的产生。饮食也影响这些细胞因子的合成。花生四烯酸(AA)衍生的(ω-6或n-6)类二十烷酸(主要来自精制植物油,如玉米、向日葵和红花)增加这些细胞因子的产生。相比之下,在鱼、鱼油、核桃和亚麻籽产品中发现的ω-3(n-3)多不饱和脂肪酸(PUFA)可以抑制AA衍生的类二十烷酸的产生。因此,较高的n-6:n-3比率促进促炎细胞因子的产生。重要的是,高的n-6:n-3比率预测在压力时期细胞因子的更大增加,以及更高水平的抑郁症状。此外,NF-?B激活是上调促炎细胞因子产生的主要途径;心理应激促进NF-?B活化,而n-3 PUFAs可降低NF-?B激活。因此,我们将研究如何压力和饮食相互作用,影响免疫功能和情绪的60名医学生。该设计将是一项为期3个月的双盲、安慰剂对照、随机临床试验。将在较低压力或非检查基线(时间1)和检查早晨(时间2)采集血样,以监测脂肪酸变化以及免疫学和心理学数据。接下来的四个时间点将提供一个机会,看看补充剂将如何影响随后较低和较高压力时期的反应。时间4样本将在补充开始后约6周收集,而时间6样本将在补充后3个月收集,提供有关变化动力学的数据。具体目的:(1)确定补充n-3 PUFA是否会降低NF-?B激活以及促炎细胞因子产生;评估补充后这些变化的时间过程;(2)确定情绪是否有可靠的变化与安慰剂条件相比,在n-3 PUFA补充后的抑郁和焦虑症状以及愤怒;(3)评估补充n-3 PUFA在学术考试期间调节细胞因子产生和情绪的典型应激相关增加的程度;和(4)比较使用外周血单核细胞(PBMC)n-3 PUFA含量变化作为连续测量的统计分析与简单使用n-3 PUFA补充剂与安慰剂的统计分析的效用。虽然行为对免疫功能的影响被广泛认可,但对饮食影响下压力和免疫功能如何相互作用知之甚少。作为心理神经免疫学和营养神经科学领域的桥梁,这项研究将通过强调饮食增强或抑制应激相关免疫变化的方式,为有关应激、脂肪酸和免疫功能的文献做出贡献。 公共卫生相关性:虽然行为对免疫功能的影响被广泛认可,但对饮食影响下压力和免疫功能如何相互作用知之甚少。这个安慰剂对照,随机临床试验将填补几个显着的空白,在文献中解决的方式,压力和n-3多不饱和脂肪酸补充相互作用,影响NF-?B激活、促炎细胞因子水平、对应激的急性炎症反应和情绪。
英文摘要
DESCRIPTION (provided by applicant): Proinflammatory cytokines influence the onset and course of a number of age-associated diseases. Stress and depression can substantially enhance the production of proinflammatory cytokines. Diet also influences the synthesis of these cytokines. Arachidonic acid (AA) derived (omega-6 or n-6) eicosanoids (primarily from refined vegetable oils such as corn, sunflower, and safflower) increase the production of these cytokines. In contrast, the omega-3 (n-3) polyunsaturated fatty acids (PUFAs), found in fish, fish oil, walnuts, and flax seed products, can curb the production of AA-derived eicosanoids. Thus, higher n-6:n-3 ratios promote proinflammatory cytokine production. Importantly, high n-6:n-3 ratios predict greater increases in cytokines during stressful periods, as well as higher levels of depressive symptoms. Furthermore, NF-?B activation is a prime pathway for up-regulating proinflammatory cytokine production; psychological stress promotes NF-?B activation, while n-3 PUFAs can decrease NF-?B activation. Accordingly, we will examine how stress and diet interact to influence immune function and mood in 60 medical students. The design will be a double-blind, placebo-controlled, randomized clinical trial with supplementation over a 3-month period. Blood samples to monitor changes in fatty acids as well as immunological and psychological data will be collected at a lower- stress or non-exam baseline (time 1) and again on the morning of an exam (time 2). The next four time points will provide an opportunity to see how supplementation will affect responses during subsequent lower and higher stress periods. The time 4 sample will be collected approximately 6 weeks after supplementation has been initiated, while the time 6 sample will be collected 3 months after supplementation, providing data on the kinetics of change. Specific aims: (1) To determine if n-3 PUFA supplementation will decrease NF-?B activation, as well as proinflammatory cytokine production; to evaluate the time course for these changes following supplementation; (2) to determine if there are reliable changes in mood (depressive and anxiety symptoms, and anger) following n-3 PUFA supplementation compared to the placebo condition; (3) to assess the extent to which n-3 PUFA supplementation modulates typical stress-related increases in cytokine production and mood during academic examinations; and (4) to compare the utility of statistical analyses that use changes in peripheral blood mononuclear cell (PBMC) n-3 PUFA content as continuous measures with those that simply use n-3 PUFA supplementation vs. placebo. Although behavioral influences on immune function are widely recognized, very little is known about how stress and immune function interact in the context of dietary influences. Bridging the fields of psychoneuroimmunology and nutritional neuroscience, the proposed study would contribute to the literatures on stress, fatty acids, and immune function by highlighting the ways in which diet enhances or inhibits stress-related immune change. Public health relevance: Although behavioral influences on immune function are widely recognized, very little is known about how stress and immune function interact in the context of dietary influences. This placebo-controlled, randomized clinical trial will fill several significant gaps in the literature by addressing the ways in which stress and n-3 PUFA supplementation interact to influence NF-?B activation, proinflammatory cytokine levels, acute inflammatory responses to stress, and mood.
期刊论文(1)
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会议论文
DOI: 10.1016/j.bbi.2011.07.229
发表时间: 2011-11
期刊: BRAIN BEHAVIOR AND IMMUNITY
影响因子: 15.1
作者: [Kiecolt-Glaser, Janice K., Belury, Martha A., Andridge, Rebecca, Malarkey, William B., Glaser, Ronald]
通讯作者: Glaser, Ronald
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  • 财政年份:
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  • 负责人:
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  • 依托单位:
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  • 负责人:
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海外基金