Proskocil Becky J, Bruun Donald A, Lorton Jesse K, Blensly Kirsten C, Jacoby David B, Lein Pamela J, Fryer Allison D
Department of Physiology and Pharmacology, Oregon Health & Science University, Portland, Oregon 97239, USA.
Environ Health Perspect. 2008 Mar;116(3):381-8. doi: 10.1289/ehp.10694.
Recent epidemiologic studies have identified organophosphorus pesticides (OPs) as environmental factors potentially contributing to the increase in asthma prevalence over the last 25 years. In support of this hypothesis, we have demonstrated that environmentally relevant concentrations of OPs induce airway hyperreactivity in guinea pigs.
Sensitization to allergen is a significant contributing factor in asthma, and we have shown that sensitization changes virus-induced airway hyperreactivity from an eosinophil-independent mechanism to one mediated by eosinophils. Here, we determine whether sensitization similarly influences OP-induced airway hyperreactivity.
Nonsensitized and ovalbumin-sensitized guinea pigs were injected subcutaneously with the OP parathion (0.001-1.0 mg/kg). Twenty-four hours later, animals were anesthetized and ventilated, and bronchoconstriction was measured in response to either vagal stimulation or intravenous acetylcholine. Inflammatory cells and acetylcholinesterase activity were assessed in tissues collected immediately after physiologic measurements.
Ovalbumin sensitization decreased the threshold dose for parathion-induced airway hyperreactivity and exacerbated parathion effects on vagally induced bronchoconstriction. Pretreatment with antibody to interleukin (IL)-5 prevented parathion-induced hyperreactivity in sensitized but not in nonsensitized guinea pigs. Parathion did not increase the number of eosinophils in airways or the number of eosinophils associated with airway nerves nor did it alter eosinophil activation as assessed by major basic protein deposition.
Antigen sensitization increases vulnerability to parathion-induced airway hyperreactivity and changes the mechanism to one that is dependent on IL-5. Because sensitization to allergens is characteristic of 50% of the general population and 80% of asthmatics (including children), these findings have significant implications for OP risk assessment, intervention, and treatment strategies.
近期的流行病学研究已确定有机磷农药(OPs)是过去25年中可能导致哮喘患病率上升的环境因素。为支持这一假说,我们已证明与环境相关浓度的OPs可诱导豚鼠气道高反应性。
对变应原致敏是哮喘的一个重要促成因素,并且我们已表明致敏会将病毒诱导的气道高反应性从一种不依赖嗜酸性粒细胞的机制转变为由嗜酸性粒细胞介导的机制。在此,我们确定致敏是否同样影响OP诱导的气道高反应性。
将未致敏和卵清蛋白致敏的豚鼠皮下注射有机磷农药对硫磷(0.001 - 1.0毫克/千克)。24小时后,将动物麻醉并进行通气,测量对迷走神经刺激或静脉注射乙酰胆碱的支气管收缩反应。在生理测量后立即收集的组织中评估炎症细胞和乙酰胆碱酯酶活性。
卵清蛋白致敏降低了对硫磷诱导气道高反应性的阈值剂量,并加剧了对硫磷对迷走神经诱导的支气管收缩的影响。用白细胞介素(IL)-5抗体预处理可预防致敏豚鼠而非未致敏豚鼠中对硫磷诱导的高反应性。对硫磷并未增加气道中嗜酸性粒细胞的数量或与气道神经相关的嗜酸性粒细胞数量,也未改变通过主要碱性蛋白沉积评估的嗜酸性粒细胞活化。
抗原致敏增加了对硫磷诱导的气道高反应性的易感性,并将机制转变为依赖IL - 5的机制。由于50%的普通人群和80%的哮喘患者(包括儿童)具有变应原致敏特征,这些发现对有机磷农药的风险评估、干预和治疗策略具有重要意义。