Kodavanti Urmila P
Environmental Public Health Division, National Health and Environmental Effects Research Laboratory, US Environmental Protection Agency, Research Triangle Park, NC, USA.
Toxicol Pathol. 2019 Dec;47(8):962-975. doi: 10.1177/0192623319878402. Epub 2019 Oct 8.
Diverse host factors/phenotypes may exacerbate or diminish biological responses induced by air pollutant exposure. We lack an understanding of biological indicators of environmental exposures that culminate in a physiological response versus those that lead to adversity. Variations in response phenotype might arise centrally and/or at the local tissue level. In addition to genetic differences, the current evidence supports the roles of preexisting cardiopulmonary diseases, diabetes, diet, adverse prenatal environments, neurobehavioral disorders, childhood infections, microbiome, sex, and psychosocial stressors in modifying the susceptibility to air pollutant exposures. Animal models of human diseases, obesity, nutritional inadequacies, and neurobehavioral conditions have been compared with healthy controls to understand the causes of variations in susceptibility. Although psychosocial stressors have been associated with increased susceptibility to air pollutant effects, the contribution of neuroendocrine stress pathways in mediating these effects is just emerging. The new findings of neuroendocrine activation leading to systemic metabolic and immunological effects of air pollutants, and the potential contribution to allostatic load, emphasize the consideration of these mechanisms into susceptibility. Variations in susceptibility to air pollution health effects are likely to underlie host genetic and physiological conditions in concert with disrupted neuroendocrine circuitry that alters physiological stability under the influence of stressors.
多种宿主因素/表型可能会加剧或减弱空气污染物暴露所引发的生物学反应。我们并不清楚环境暴露的生物学指标,哪些最终会导致生理反应,哪些又会导致不良后果。反应表型的差异可能出现在中枢和/或局部组织层面。除了基因差异外,目前的证据支持,既有的心肺疾病、糖尿病、饮食、不良的产前环境、神经行为障碍、儿童期感染、微生物群、性别以及心理社会压力源在改变对空气污染物暴露的易感性方面所起的作用。已将人类疾病、肥胖、营养不足和神经行为状况的动物模型与健康对照进行比较,以了解易感性差异的原因。虽然心理社会压力源与对空气污染物影响的易感性增加有关,但神经内分泌应激途径在介导这些影响方面的作用才刚刚显现。空气污染物导致神经内分泌激活进而产生全身代谢和免疫效应的新发现,以及对负荷应激的潜在影响,强调了在易感性研究中考虑这些机制的重要性。对空气污染健康影响的易感性差异,很可能是宿主遗传和生理状况与神经内分泌回路紊乱共同作用的结果,这种紊乱会在压力源的影响下改变生理稳定性。