Department of Emergency Medicine, University of Massachusetts, 55 Lake Ave North, Worcester, MA 01655, USA.
Neurotoxicology. 2011 Mar;32(2):206-14. doi: 10.1016/j.neuro.2011.01.005. Epub 2011 Jan 15.
The area of the brain responsible for organophosphate (OP)-induced central apnea is unknown. Automatic breathing is governed by circuits in the medulla and pons. Respiratory-related neurons in the brainstem are concentrated in a few areas, including ventral regions of the medulla, which contains a number of sites critical for respiratory rhythmogenesis, including the pre-Bötzinger complex (preBötC). The preBötC contains cholinergic receptors, making it a candidate site of action for the apnea-inducing effect of OP. We analyzed respiratory output during a series of experiments using both intact and reduced Wistar rat preparations exposed to dichlorvos (2,2-dichlorovinyl dimethyl phosphate). Exposure of the brainstem using a working heart-brainstem preparation resulted in a central apnea similar to that seen in intact animal models. In contrast, microdialysis of locally toxic doses of dichlorvos to the ventral region of the medulla resulted in delayed and mild respiratory depression in most animals and apnea in only 29% of the animals. We conclude that exposure of the entire brainstem to OP is sufficient to induce central apnea. Our microdialysis experiments suggest that the neural substrate for OP-induced central apnea involves a specific brainstem site other than the ventral region of the medulla, or apnea might result from a distributed effect involving cholinergic toxicities of multiple brainstem sites.
负责有机磷(OP)引起的中枢性呼吸暂停的脑区尚不清楚。自动呼吸由延髓和脑桥中的回路控制。脑干中的呼吸相关神经元集中在几个区域,包括延髓腹侧区域,其中包含许多对呼吸节律发生至关重要的部位,包括前 Bötzinger 复合体(preBötC)。preBötC 含有胆碱能受体,使其成为 OP 引起呼吸暂停作用的候选部位。我们使用完整和简化的 Wistar 大鼠制剂进行了一系列实验,分析了呼吸输出。使用工作心脏-脑干制剂暴露于敌敌畏(2,2-二氯乙烯基二甲磷酸酯)后,脑干暴露导致类似于完整动物模型中观察到的中枢性呼吸暂停。相比之下,向延髓腹侧区域局部给予有毒剂量的敌敌畏进行微透析,导致大多数动物出现延迟和轻度呼吸抑制,只有 29%的动物出现呼吸暂停。我们得出结论,暴露于整个脑干的 OP 足以引起中枢性呼吸暂停。我们的微透析实验表明,OP 引起的中枢性呼吸暂停的神经基础涉及特定的脑干部位,而不是延髓腹侧区域,或者呼吸暂停可能是由于涉及多个脑干部位的胆碱能毒性的分布效应所致。