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多酚对细胞因子和粒细胞对抗阻运动反应的影响。

The effect of polyphenols on cytokine and granulocyte response to resistance exercise.

作者信息

Jajtner Adam R, Hoffman Jay R, Townsend Jeremy R, Beyer Kyle S, Varanoske Alyssa N, Church David D, Oliveira Leonardo P, Herrlinger Kelli A, Radom-Aizik Shlomit, Fukuda David H, Stout Jeffrey R

机构信息

Institute of Exercise Physiology and Wellness, University of Central Florida, Orlando, Florida.

Department of Exercise Physiology, Kent State University, Kent, Ohio.

出版信息

Physiol Rep. 2016 Dec;4(24). doi: 10.14814/phy2.13058.

DOI:10.14814/phy2.13058
PMID:28039406
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5210375/
Abstract

This study examined the effect of resistance exercise on the production, recruitment, percentage, and adhesion characteristics of granulocytes with and without polyphenol (PPB) supplementation. Thirty-eight untrained men were randomized into three groups: PPB (n = 13, 21.8 ± 2.5 years, 171.2 ± 5.5 cm, 71.2 ± 8.2 kg), placebo (PL; n = 15, 21.6 ± 2.5 years, 176.5 ± 4.9 cm, 84.0 ± 15.7 kg), or control (CON; n = 10, 23.3 ± 4.3 years, 173.7 ± 12.6 cm, 77.3 ± 16.3 kg). Blood samples were obtained pre (PRE), immediately (IP), 1 h (1H), 5 h (5H), 24 h (24H), 48 h (48H), and 96 h (96H) postresistance exercise (PPB/PL) or rest (CON). Fine-needle biopsies were obtained from the vastus lateralis at PRE, 1H, 5H, and 48H. Plasma concentrations and intramuscular content of interleukin-8 (IL-8), granulocyte (G-CSF), and granulocyte-macrophage colony stimulating factor (GM-CSF) were analyzed via multiplex assays. Changes in relative number of circulating granulocytes and adhesion receptor (CD11b) were assessed using flow cytometry. Intramuscular IL-8 was significantly elevated at 1H, 5H, and 48H (P < 0.001). Area under the curve analysis indicated a greater intramuscular IL-8 content in PL than PPB (P = 0.011). Across groups, circulating G-CSF was elevated from PRE at IP (P < 0.001), 1H (P = 0.011), and 5H (P = 0.025), while GM-CSF was elevated at IP (P < 0.001) and 1H (P = 0.007). Relative number of granulocytes was elevated at 1H (P < 0.001), 5H (P < 0.001), and 24H (P = 0.005, P = 0.006) in PPB and PL, respectively. Across groups, granulocyte CD11b expression was upregulated from PRE to IP (P < 0.001) and 1H (P = 0.015). Results indicated an increase in circulating CD11b on granulocytes, and IL-8 within the muscle following intense resistance exercise. Polyphenol supplementation may attenuate the IL-8 response, however, did not affect granulocyte percentage and adhesion molecule expression in peripheral blood following resistance exercise.

摘要

本研究调查了阻力训练对补充和未补充多酚(PPB)情况下粒细胞的生成、募集、百分比及黏附特性的影响。38名未经训练的男性被随机分为三组:PPB组(n = 13,年龄21.8±2.5岁,身高171.2±5.5厘米,体重71.2±8.2千克)、安慰剂组(PL;n = 15,年龄21.6±2.5岁,身高176.5±4.9厘米,体重84.0±15.7千克)或对照组(CON;n = 10,年龄23.3±4.3岁,身高173.7±12.6厘米,体重77.3±16.3千克)。在进行阻力训练(PPB/PL)或休息(CON)前(PRE)、训练后即刻(IP)、1小时(1H)、5小时(5H)、24小时(24H)、48小时(48H)和96小时(96H)采集血样。在PRE、1H、5H和48H从股外侧肌获取细针活检样本。通过多重检测分析白细胞介素-8(IL-8)、粒细胞集落刺激因子(G-CSF)和粒细胞-巨噬细胞集落刺激因子(GM-CSF)的血浆浓度和肌肉内含量。使用流式细胞术评估循环粒细胞和黏附受体(CD11b)相对数量的变化。肌肉内IL-8在1H、5H和48H显著升高(P < 0.001)。曲线下面积分析表明PL组肌肉内IL-8含量高于PPB组(P = 0.011)。在所有组中,循环G-CSF在IP(P < 0.001)、1H(P = 0.011)和5H(P = 0.025)时较PRE升高,而GM-CSF在IP(P < 0.001)和1H(P = 0.007)时升高。PPB组和PL组中粒细胞相对数量分别在1H(P < 0.001)、5H(P < 0.001)和24H(P = 0.005,P = 0.006)时升高。在所有组中,粒细胞CD11b表达从PRE到IP(P < 0.001)和1H(P = 0.015)上调。结果表明,高强度阻力训练后粒细胞表面循环CD11b增加,肌肉内IL-8增加。补充多酚可能会减弱IL-8反应,然而,对阻力训练后外周血中粒细胞百分比和黏附分子表达没有影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eed0/5210375/9b0e4dfce0eb/PHY2-4-e13058-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eed0/5210375/96a510373125/PHY2-4-e13058-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eed0/5210375/3a229549ec01/PHY2-4-e13058-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eed0/5210375/63bc2abbc2ef/PHY2-4-e13058-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eed0/5210375/9b0e4dfce0eb/PHY2-4-e13058-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eed0/5210375/96a510373125/PHY2-4-e13058-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eed0/5210375/3a229549ec01/PHY2-4-e13058-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eed0/5210375/63bc2abbc2ef/PHY2-4-e13058-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eed0/5210375/9b0e4dfce0eb/PHY2-4-e13058-g004.jpg

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