McFarlin Brian K, Flynn Michael G, Campbell Wayne W, Craig Bruce A, Robinson J Paul, Stewart Laura K, Timmerman Kyle L, Coen Paul M
Department of Health and Human Performance, University of Houston, 3855 Holman St., Houston, Texas 77204, USA.
J Gerontol A Biol Sci Med Sci. 2006 Apr;61(4):388-93. doi: 10.1093/gerona/61.4.388.
Chronic inflammation has been implicated in the development of cardiovascular disease, diabetes mellitus, cachexia, and osteoporosis. Regular physical activity has been purported to possess "anti-inflammatory" properties which may limit chronic inflammation. Recently, we hypothesized that toll-like receptor 4 (TLR4) may play a role in activity-induced modulation of inflammation. Therefore, the purpose of this study was to determine the association between age, physical activity status, biomarkers of inflammation, and TLR4.
Male and female participants (n = 84) were recruited to fill one of the following groups: young (18-30 years), active; young, inactive; old (60-80 years), active; or old, inactive. To assess physical activity status, participants completed a Paffenbarger Physical Activity Questionnaire and a modified Balke submaximal treadmill test. After grouping and screening, participants were given a standard mixed diet to consume 24 hours prior to arriving at the laboratory. Participants were instructed to consume all food by 10 pm the night prior to blood sampling (8-hour fast). Following 30 minutes of seated rest in a quiet room, venous blood samples were collected. Lipopolysaccharide-stimulated inflammatory cytokine production and plasma high-sensitivity C-reactive protein (hsCRP) were determined by enzyme-linked immunosorbent assay, and TLR4 expression was determined by flow cytometry.
Lipopolysaccharide-stimulated interleukin-6, interleukin-1beta, and tumor necrosis factor-alpha production, TLR4 expression, and hsCRP were significantly lower in active compared to inactive participants (p <.05). Also, older participants had significantly higher hsCRP than young participants had (p <.05).
The findings of the present study support previous reports which infer that acute exercise or a physically active lifestyle may possess anti-inflammatory properties. Also this study, along with previous work from our laboratory, suggests that TLR4 may play a role in regulating the link between inflammatory cytokine production and a physically active lifestyle.
慢性炎症与心血管疾病、糖尿病、恶病质和骨质疏松症的发生有关。经常进行体育活动据称具有“抗炎”特性,可能会限制慢性炎症。最近,我们推测Toll样受体4(TLR4)可能在活动诱导的炎症调节中起作用。因此,本研究的目的是确定年龄、身体活动状态、炎症生物标志物和TLR4之间的关联。
招募了男性和女性参与者(n = 84),分为以下几组:年轻(18 - 30岁)、活跃组;年轻、不活跃组;老年(60 - 80岁)、活跃组;或老年、不活跃组。为了评估身体活动状态,参与者完成了帕芬巴格体力活动问卷和改良的巴尔克次极量跑步机测试。分组和筛选后,参与者在到达实验室前24小时食用标准混合饮食。参与者被要求在采血前一晚晚上10点前吃完所有食物(禁食8小时)。在安静房间静坐休息30分钟后,采集静脉血样。通过酶联免疫吸附测定法测定脂多糖刺激的炎性细胞因子产生和血浆高敏C反应蛋白(hsCRP),通过流式细胞术测定TLR4表达。
与不活跃参与者相比,活跃参与者中脂多糖刺激的白细胞介素-6、白细胞介素-1β和肿瘤坏死因子-α产生、TLR4表达和hsCRP显著降低(p <.05)。此外,老年参与者的hsCRP显著高于年轻参与者(p <.05)。
本研究结果支持先前的报告,这些报告推断急性运动或积极的生活方式可能具有抗炎特性。此外,本研究以及我们实验室之前的工作表明,TLR4可能在调节炎性细胞因子产生与积极的生活方式之间的联系中起作用。