Insights Into the Mechanisms and Mediators of the Effects of Air Pollution Exposure on Blood Pressure and Vascular Function in Healthy Humans

被引:409
作者
Brook, Robert D. [1 ]
Urch, Bruce [5 ,8 ]
Dvonch, J. Timothy [2 ]
Bard, Robert L. [1 ]
Speck, Mary [8 ]
Keeler, Gerald [2 ]
Morishita, Masako [2 ]
Marsik, Frank J. [2 ]
Kamal, Ali S. [2 ]
Kaciroti, Niko [3 ,4 ]
Harkema, Jack [9 ]
Corey, Paul [6 ,8 ]
Silverman, Frances [5 ,6 ,7 ,8 ]
Gold, Diane R. [13 ]
Wellenius, Greg [10 ]
Mittleman, Murray A. [10 ]
Rajagopalan, Sanjay [11 ]
Brook, Jeffrey R. [8 ,12 ]
机构
[1] Univ Michigan, Div Cardiovasc Med, Ann Arbor, MI 48106 USA
[2] Univ Michigan, Sch Publ Hlth, Ann Arbor, MI 48106 USA
[3] Univ Michigan, Ctr Human Growth & Dev, Ann Arbor, MI 48106 USA
[4] Univ Michigan, Dept Biostat, Ann Arbor, MI 48106 USA
[5] Univ Toronto, Inst Med Sci, Toronto, ON M5S 1A1, Canada
[6] Univ Toronto, Dalla Lana Sch Publ Hlth, Toronto, ON, Canada
[7] Univ Toronto, Dept Med, Toronto, ON, Canada
[8] Gage Occupat & Environm Hlth Unit, Toronto, ON, Canada
[9] Michigan State Univ, Sch Vet Med, E Lansing, MI 48824 USA
[10] Beth Israel Deaconess Med Ctr, Dept Med, Cardiovasc Epidemiol Res Unit, Boston, MA 02215 USA
[11] Ohio State Univ, Coll Med, Davis Heart Lung Res Inst, Columbus, OH 43210 USA
[12] Environm Canada, Toronto, ON, Canada
[13] Harvard Univ, Brigham & Womens Hosp, Sch Med, Boston, MA 02115 USA
基金
美国国家卫生研究院;
关键词
hypertension; endothelium; sympathetic nervous system; inflammation; oxidative stress; DIESEL-EXHAUST INHALATION; ACUTE ARTERIAL VASOCONSTRICTION; PARTICULATE MATTER; CARDIOVASCULAR-DISEASE; AMBIENT PARTICLES; DYSFUNCTION; OZONE; ATHEROSCLEROSIS; ASSOCIATIONS; INFLAMMATION;
D O I
10.1161/HYPERTENSIONAHA.109.130237
中图分类号
R6 [外科学];
学科分类号
1002 ; 100210 ;
摘要
Fine particulate matter air pollution plus ozone impairs vascular function and raises diastolic blood pressure. We aimed to determine the mechanism and air pollutant responsible. The effects of pollution on heart rate variability, blood pressure, biomarkers, and brachial flow-mediated dilatation were determined in 2 randomized, double-blind, crossover studies. In Ann Arbor, 50 subjects were exposed to fine particles (150 mu g/m(3)) plus ozone (120 parts per billion) for 2 hours on 3 occasions with pretreatments of an endothelin antagonist (Bosentan, 250 mg), antioxidant (Vitamin C, 2 g), or placebo. In Toronto, 31 subjects were exposed to 4 different conditions (particles plus ozone, particles, ozone, and filtered air). In Toronto, diastolic blood pressure significantly increased (2.9 and 3.6 mm Hg) only during particle-containing exposures in association with particulate matter concentration and reductions in heart rate variability. Flow-mediated dilatation significantly decreased (2.0% and 2.9%) only 24 hours after particle-containing exposures in association with particulate matter concentration and increases in blood tumor necrosis factor alpha. In Ann Arbor, diastolic blood pressure significantly similarly increased during all of the exposures (2.5 to 4.0 mm Hg), a response not mitigated by pretreatments. Flow-mediated dilatation remained unaltered. Particulate matter, not ozone, was responsible for increasing diastolic blood pressure during air pollution inhalation, most plausibly by instigating acute autonomic imbalance. Only particles from urban Toronto additionally impaired endothelial function, likely via slower proinflammatory pathways. Our findings demonstrate credible mechanisms whereby fine particulate matter could trigger acute cardiovascular events and that aspects of exposure location may be an important determinant of the health consequences. (Hypertension. 2009;54:659-667.)
引用
收藏
页码:659 / 667
页数:9
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