Docosahexaenoic diet supplementation, exercise and temperature affect cytokine production by lipopolysaccharide-stimulated mononuclear cells

被引:0
|
作者
Xavier Capó
Miquel Martorell
Antoni Sureda
Juan Miguel Batle
Josep Antoni Tur
Antoni Pons
机构
[1] University of Balearic Islands,Research Group on Community Nutrition and Oxidative Stress, Science Laboratory of Physical Activity, Department of Fundamental Biology and Health Sciences
[2] CIBER: CB12/03/30038 Fisiopatología de la Obesidad y la Nutrición,Nutrition and Dietetics Department, School of Pharmacy
[3] CIBEROBN,undefined
[4] Instituto de Salud Carlos III (ISCIII),undefined
[5] University of Concepción,undefined
来源
关键词
Cytokine; Inflammation; Docosahexaenoic acid; Temperature; Exercise;
D O I
暂无
中图分类号
学科分类号
摘要
Acute exercise induces changes in peripheral mononuclear cells’ (PBMCs) capabilities to produce cytokines. The aim was to investigate the effect of docosahexaenoic acid (DHA) diet supplementation on cytokine production, by lipopolysaccharide (LPS)-stimulated PBMCs after exercise, and the in vitro influence of temperature. Fifteen male soccer players were randomly assigned to a placebo or an experimental group. The experimental group consumed an almond-based beverage enriched with DHA (1.16 g DHA/day) for 8 weeks, whereas the placebo group consumed a similar non-enriched beverage. Blood samples were taken before and after the nutritional intervention in basal conditions and 2 h after acute exercise. Nutritional intervention significantly increased the DHA content in erythrocytes only in experimental group (from 34 ± 3.6 to 43 ± 3.6 nmols DHA/109 erythrocytes). Exercise significantly increased Toll-like receptor 4 (TLR4) in PBMCs but only in the placebo group (203 %). Exercise also significantly increased IL6, IL8, VEGF, INFγ, TNFα, IL1α, IL1β, MCP1, and EGG production rates by LPS-stimulated PBMCs, and this response was attenuated by DHA supplementation. Temperature but not DHA also affected the pattern of cytokine production increasing IL6, IL8, IL1β, and MCP1 synthesis. The higher change was evidenced in IL1β increasing the production rate at 39.5 °C from 3.19 ± 0.77 to 22.4 ± 6.1 pg/h 106 PBMC in placebo and from 2.36 ± 0.11 to 10.6 ± 0.38 pg/h 106 PBMC in the supplemented group. The profile of affected cytokines differs between temperature and exercise, suggesting a different PBMC activation pathway. DHA diet supplementation only attenuated cytokine production after exercise and not that induced by temperature.
引用
收藏
页码:421 / 434
页数:13
相关论文
共 50 条
  • [21] Heparin-like polymers modulate proinflammatory cytokine production by lipopolysaccharide-stimulated human monocytes
    Anastase-Ravion, S
    Carreno, MP
    Blondin, C
    Ravion, O
    Champion, J
    Chaubet, F
    Haeffner-Cavaillon, N
    Letourneur, D
    JOURNAL OF BIOMEDICAL MATERIALS RESEARCH, 2002, 60 (03): : 375 - 383
  • [22] Anti-Inflammatory Effect of Columbianetin on Lipopolysaccharide-Stimulated Human Peripheral Blood Mononuclear Cells
    Lu, Junying
    Fang, Keyong
    Wang, Shiji
    Xiong, Lingxin
    Zhang, Chao
    Liu, Zhongmin
    Guan, Xuewa
    Zheng, Ruipeng
    Wang, Guoqiang
    Zheng, Jingtong
    Wang, Fang
    MEDIATORS OF INFLAMMATION, 2018, 2018
  • [23] Effect of inositol hexaphosphate on lipopolysaccharide-stimulated release of TNF-α from human mononuclear cells
    Weglarz, L.
    Parfiniewicz, B.
    Mertas, A.
    Kondera-Anasz, Z.
    Jaworska-Kik, M.
    Dzierzewicz, Z.
    POLISH JOURNAL OF ENVIRONMENTAL STUDIES, 2008, 17 (02): : 283 - 290
  • [24] RETINOIDS ENHANCE IGA PRODUCTION BY LIPOPOLYSACCHARIDE-STIMULATED MURINE SPLEEN-CELLS
    TOKUYAMA, H
    TOKUYAMA, Y
    CELLULAR IMMUNOLOGY, 1993, 150 (02) : 353 - 363
  • [25] Mechanism that regulates nitric oxide production by lipopolysaccharide-stimulated rat Kupffer cells
    Ikeda, K
    Kubo, S
    Hirohashi, K
    Kinoshita, H
    Kaneda, K
    Kawada, N
    Sato, EF
    Inoue, M
    PHYSIOLOGICAL CHEMISTRY AND PHYSICS AND MEDICAL NMR, 1996, 28 (04) : 239 - 253
  • [26] Minocycline reduces cytokine and chemokine production in lipopolysaccharide-stimulated THP-1 monocytic cells by inhibition of IκB kinase α/β
    Tai, K.
    Iwasaki, H.
    Ikegaya, S.
    Ueda, T.
    INTERNATIONAL JOURNAL OF ANTIMICROBIAL AGENTS, 2013, 42 : S88 - S89
  • [27] Cardiopulmonary bypass decreases cytokine production in lipopolysaccharide-stimulated whole blood cells:: Roles of interleukin-10 and the extracorporeal circuit
    Dehoux, MS
    Hernot, S
    Asehnoune, K
    Boutten, A
    Paquin, S
    Leçon-Malas, V
    Toueg, ML
    Desmonts, JM
    Durand, G
    Philip, I
    CRITICAL CARE MEDICINE, 2000, 28 (06) : 1721 - 1727
  • [28] GRANULOCYTE-ACTIVATING MEDIATORS (GRAM) .1. GENERATION BY LIPOPOLYSACCHARIDE-STIMULATED MONONUCLEAR-CELLS
    KAPP, A
    LUGER, TA
    MALY, FE
    SCHOPF, E
    JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1986, 86 (05) : 523 - 528
  • [29] EXPRESSION OF INTERLEUKIN-8 BY LIPOPOLYSACCHARIDE-STIMULATED BONE MARROW-DERIVED MONONUCLEAR-CELLS
    DIBB, CR
    STRIETER, RM
    BURDICK, M
    KUNKEL, SL
    INFECTION AND IMMUNITY, 1992, 60 (08) : 3052 - 3058
  • [30] Curcumin does not add to the quercetin-induced decrease in TNF-α production from lipopolysaccharide-stimulated peripheral blood mononuclear cells
    Meaney, Mary Pat
    Neiman, David C.
    FASEB JOURNAL, 2013, 27