Proskocil Becky J, Bruun Donald A, Garg Jasmine A, Villagomez Chloe C, Jacoby David B, Lein Pamela J, Fryer Allison D
1 Pulmonary and Critical Care Medicine, Oregon Health and Science University, Portland, Oregon; and.
2 Department of Molecular Biosciences, University of California School of Veterinary Medicine, Davis, California.
Am J Respir Cell Mol Biol. 2015 Nov;53(5):738-47. doi: 10.1165/rcmb.2014-0444OC.
We previously demonstrated that antigen sensitization increases vulnerability to airway hyperreactivity induced by the organophosphorus pesticide (OP) parathion. Sensitization also changes the mechanism of parathion-induced airway hyperreactivity to one that is dependent on IL-5. To determine whether this effect can be generalized to other OPs, and to other classes of pesticides, we measured airway responsiveness to vagal stimulation or intravenous acetylcholine in nonsensitized and ovalbumin-sensitized guinea pigs 24 hours after a single subcutaneous injection of the OPs diazinon or chlorpyrifos, or the pyrethroid permethrin. Sensitization exacerbated the effects of chlorpyrifos on bronchoconstriction in response to vagal stimulation or intravenous acetylcholine. Pretreatment with function-blocking IL-5 antibody prevented chlorpyrifos-induced airway hyperreactivity in sensitized, but not in nonsensitized, guinea pigs. In sensitized guinea pigs, blocking IL-5 decreased eosinophil activation, as measured by decreased eosinophil major basic protein in the trachea. In contrast, sensitization did not alter diazinon-induced airway hyperreactivity, and permethrin did not cause airway hyperreactivity in either nonsensitized or sensitized guinea pigs. None of the pesticides affected inflammatory cells in the bronchoalveolar lavage fluid or blood. We have previously shown that three different OPs cause airway hyperreactivity via loss of neuronal M2 muscarinic receptor function. Similar to parathion, but unlike diazinon, the mechanism of chlorpyrifos-induced airway hyperreactivity is changed by sensitization. Thus, OP-induced airway hyperreactivity is dependent on sensitization status and on the OP used, which may influence therapeutic approaches.
我们之前证明,抗原致敏会增加对有机磷农药(OP)对硫磷诱导的气道高反应性的易感性。致敏还会将对硫磷诱导的气道高反应性机制转变为依赖白细胞介素-5(IL-5)的机制。为了确定这种效应是否可推广到其他有机磷农药以及其他类别的农药,我们在单次皮下注射有机磷农药二嗪农或毒死蜱,或拟除虫菊酯氯菊酯24小时后,测量了未致敏和卵清蛋白致敏的豚鼠对迷走神经刺激或静脉注射乙酰胆碱的气道反应性。致敏加剧了毒死蜱对迷走神经刺激或静脉注射乙酰胆碱引起的支气管收缩的影响。用功能阻断性IL-5抗体预处理可预防致敏豚鼠而非未致敏豚鼠中由毒死蜱诱导的气道高反应性。在致敏豚鼠中,通过测量气管中嗜酸性粒细胞主要碱性蛋白的减少来评估,阻断IL-5可降低嗜酸性粒细胞的活化。相比之下,致敏并未改变二嗪农诱导的气道高反应性,并且氯菊酯在未致敏或致敏的豚鼠中均未引起气道高反应性。这些农药均未影响支气管肺泡灌洗液或血液中的炎性细胞。我们之前已经表明,三种不同的有机磷农药通过神经元M2毒蕈碱受体功能丧失引起气道高反应性。与对硫磷类似,但与二嗪农不同,致敏会改变毒死蜱诱导的气道高反应性机制。因此,有机磷农药诱导的气道高反应性取决于致敏状态和所使用的有机磷农药,这可能会影响治疗方法。