Smith C D, Lee R B, Moran A V, Sipos M L
US Army Medical Research Institute of Chemical Defense (USAMRICD), Aberdeen Proving Ground, MD 21010, United States..
US Army Medical Research Institute of Chemical Defense (USAMRICD), Aberdeen Proving Ground, MD 21010, United States.
Neurotoxicol Teratol. 2016 Mar-Apr;54:36-45. doi: 10.1016/j.ntt.2016.01.005. Epub 2016 Jan 29.
Chemical warfare nerve agents (CWNAs) are known to cause behavioral abnormalities in cases of human exposures and in animal models. The behavioral consequences of single exposures to CWNAs that cause observable toxic signs are particularly well characterized in animals; however, less is known regarding repeated smaller exposures that may or may not cause observable toxic signs. In the current study, guinea pigs were exposed to fractions (0.1, 0.2, or 0.4) of a medial lethal dose (LD50) of sarin, soman, or VX for two weeks. On each exposure day, and for a post-exposure period, acoustic startle response (ASR) was measured in each animal. Although relatively few studies use guinea pigs to measure behavior, this species is ideal for CWNA-related experiments because their levels of carboxylesterases closely mimic those of humans, unlike rats or mice. Results showed that the 0.4 LD50 doses of soman and VX transiently increased peak startle amplitude by the second week of injections, with amplitude returning to baseline by the second week post-exposure. Sarin also increased peak startle amplitude independent of week. Latencies to peak startle and PPI were affected by agent exposure but not consistently among the three agents. Most of the changes in startle responses returned to baseline following the cessation of exposures. These data suggest that doses of CWNAs not known to produce observable toxic signs in guinea pigs can affect behavior in the ASR paradigm. Further, these deficits are transient and usually return to baseline shortly after the end of a two-week exposure period.
众所周知,化学战神经毒剂(CWNAs)会在人体接触和动物模型中导致行为异常。单次接触能引起明显中毒症状的CWNAs对动物行为影响的研究较为充分;然而,对于反复低剂量接触(可能导致或不导致明显中毒症状)的情况,人们了解较少。在本研究中,豚鼠连续两周接触沙林、梭曼或VX的半数致死剂量(LD50)的几分之一(0.1、0.2或0.4)。在每次接触日以及接触后的一段时间内,测量每只动物的听觉惊吓反应(ASR)。尽管相对较少有研究使用豚鼠来测量行为,但该物种非常适合用于与CWNAs相关的实验,因为与大鼠或小鼠不同,它们的羧酸酯酶水平与人类非常相似。结果显示,在注射的第二周,梭曼和VX的0.4 LD50剂量会使惊吓峰值幅度短暂增加,接触后第二周幅度恢复到基线水平。沙林也会增加惊吓峰值幅度,且与周数无关。惊吓峰值潜伏期和预脉冲抑制受毒剂接触影响,但在三种毒剂中并不一致。接触停止后,大多数惊吓反应变化恢复到基线水平。这些数据表明,在豚鼠中未观察到明显中毒症状的CWNAs剂量可影响ASR范式中的行为。此外,这些缺陷是短暂的,通常在两周接触期结束后不久就会恢复到基线水平。