Bauman Richard Alexander, Widholm John J
Walter Reed Army Institute of Research, United States.
Pharmacol Biochem Behav. 2007 Oct;87(4):444-52. doi: 10.1016/j.pbb.2007.05.021. Epub 2007 Jun 7.
Cyanide is a potent toxin that binds to cytochrome oxidase blocking electron transfer and the synthesis of adenosine triphosphate (ATP). Many antidotes to cyanide poisoning oxidize hemoglobin to methemoglobin (metHb), which serves as a scavenger of the cyanide anion. However, sufficiently high levels of metHb can be toxic because metHb cannot bind O(2) until it is reduced. The purpose of the proposed study was twofold: (1) Characterize the time course of metHb formation for different doses of p-aminopropiophenone (PAPP), a drug that oxidizes hemoglobin and can be used as an antidote to cyanide intoxication; and (2) Determine whether the effort of an operant response affects the behavioral toxicity of metHb, since more effortful responses presumably are more energetically demanding. In Experiment I, the oral metHb kinetics of p-aminopropiophenone (PAPP) were studied; four doses of PAPP (1, 5, 10, and 20 mg/kg) or the vehicle, polyethylene glycol 200 (PEG200), were delivered via a gavage tube to separate groups of rats. In Experiment II, rats were trained to press a lever or run in an activity wheel at any time during a 12-hour light/dark cycle for their entire daily food intake; five presses or turns were required for the delivery of each food pellet. The same doses of PAPP were delivered p.o. shortly before the onset of darkness, 2100 h. Results from Exp I showed that PAPP induced a dose-dependent rapid increase and relatively slower exponential-like decline in metHb concentration. In Exp. II, the same doses of PAPP induced a dose-dependent reduction in hourly outputs of leverpresses and wheelturns however; wheelturns were reduced significantly more than leverpresses. When the best-fitting metHb curves from Experiment I were superimposed on the time scale for outputs of wheelturns and leverpresses, reduction of output was inversely related to the kinetics of metHb formation. These findings are consistent with the conclusion that PAPP-induced metHb formation reduced the output of wheelrunning more than leverpressing because the more energetically demanding response of wheelrunning was more affected by metHb induced hypoxemia. Furthermore, these data suggest that although certain longacting metHb formers might be useful prophylactics for warfighters, it will be critical to determine the energetic loads of required battlefield activities because even low (10%) therapeutic metHb levels might impair the performance of those activities.
氰化物是一种强效毒素,它与细胞色素氧化酶结合,阻断电子传递和三磷酸腺苷(ATP)的合成。许多氰化物中毒的解毒剂会将血红蛋白氧化为高铁血红蛋白(metHb),高铁血红蛋白可作为氰化物阴离子的清除剂。然而,高铁血红蛋白水平过高可能有毒,因为高铁血红蛋白在被还原之前无法结合氧气。本研究的目的有两个:(1)描述不同剂量对氨基苯丙酮(PAPP)形成高铁血红蛋白的时间进程,PAPP是一种能氧化血红蛋白且可作为氰化物中毒解毒剂的药物;(2)确定操作性反应的努力程度是否会影响高铁血红蛋白的行为毒性,因为据推测,更费力的反应在能量需求上更高。在实验一中,研究了对氨基苯丙酮(PAPP)的口服高铁血红蛋白动力学;将四剂PAPP(1、5、10和20毫克/千克)或赋形剂聚乙二醇200(PEG200)通过灌胃管给予不同组的大鼠。在实验二中,训练大鼠在12小时明/暗周期的任何时间按压杠杆或在活动轮中奔跑以获取全天的食物;每次输送一粒食物丸需要按压五次或转动五次。在接近黑暗开始的2100时口服相同剂量的PAPP。实验一的结果表明,PAPP诱导高铁血红蛋白浓度呈剂量依赖性快速升高和相对较慢的指数式下降。在实验二中,相同剂量的PAPP导致杠杆按压和轮转的每小时输出量呈剂量依赖性减少;然而,轮转的减少比杠杆按压明显更多。当将实验一中拟合度最佳的高铁血红蛋白曲线叠加在轮转和杠杆按压输出的时间尺度上时,输出的减少与高铁血红蛋白形成的动力学呈负相关。这些发现与以下结论一致:PAPP诱导的高铁血红蛋白形成对轮转输出的降低比对杠杆按压的降低更大,因为能量需求更高的轮转反应受高铁血红蛋白诱导的低氧血症影响更大。此外,这些数据表明,尽管某些长效高铁血红蛋白形成剂可能对战地人员是有用的预防药物,但确定所需战场活动的能量负荷至关重要,因为即使是低水平(10%)的治疗性高铁血红蛋白也可能损害这些活动的表现。