Colman Ricki, Pierre Peter, Adriansjach Julie, Crosno Kristin, Noguchi Kevin K, Ikonomidou Chrysanthy
Wisconsin National Primate Research Center, Madison, WI, USA.
Department of Cell and Regenerative Biology, University of Wisconsin, School of Medicine, Madison, WI, USA.
Ann Neurol. 2023 Sep 14. doi: 10.1002/ana.26794.
Exposure of neonatal macaques to the antiseizure medications phenobarbital and midazolam (PbM) causes widespread apoptotic death of neurons and oligodendrocytes. We studied behavior and neurocognitive performance in 12 to 24 month-old macaques treated as neonates with PbM.
A total of 14 monkeys received phenobarbital and midazolam over 24 hours under normothermia (n = 8) or mild hypothermia (n = 6). Controls (n = 8) received no treatment. Animals underwent testing in the human intruder paradigm at ages 12 and 18 months, and a 3-step stimulus discrimination task at ages 12, 18, and 24 months.
Animals treated with PbM displayed lower scores for environmental exploration, and higher scores for locomotion and vocalizations compared with controls. Combined PbM and hypothermia resulted in lower scores for aggression and vigilance at 12 months compared with controls and normothermic PbM animals. A mixed-effects generalized linear model was used to test for differences in neurocognitive performance between the control and PbM groups in the first step of the stimulus discrimination task battery (shape center baited to shape center non-baited). The odds of passing this step differed by group (p = 0.044). At any given age, the odds of passing for a control animal were 9.53-fold (95% CI 1.06-85) the odds for a PbM animal. There was also evidence suggesting a higher learning rate in the shape center non-baited for the control relative to the PbM group (Cox model HR 2.13, 95% CI 1.02-4.43; p = 0.044).
These findings demonstrate that a 24-hour-long neonatal treatment with a clinically relevant combination of antiseizure medications can have long-lasting effects on behavior and cognition in nonhuman primates. ANN NEUROL 2023.
新生猕猴暴露于抗癫痫药物苯巴比妥和咪达唑仑(PbM)会导致神经元和少突胶质细胞广泛凋亡死亡。我们研究了在新生儿期接受PbM治疗的12至24个月大猕猴的行为和神经认知表现。
共有14只猴子在正常体温(n = 8)或轻度低温(n = 6)下24小时内接受苯巴比妥和咪达唑仑治疗。对照组(n = 8)未接受治疗。动物在12个月和18个月大时接受人类入侵者范式测试,并在12个月、18个月和24个月大时接受三步刺激辨别任务测试。
与对照组相比,接受PbM治疗的动物在环境探索方面得分较低,而在运动和发声方面得分较高。与对照组和正常体温的PbM动物相比,联合使用PbM和低温在12个月时导致攻击和警觉得分较低。在刺激辨别任务组的第一步(形状中心有诱饵与形状中心无诱饵)中,使用混合效应广义线性模型测试对照组和PbM组之间神经认知表现的差异。通过这一步的几率因组而异(p = 0.044)。在任何给定年龄,对照动物通过的几率是PbM动物的9.53倍(95% CI 1.06 - 85)。也有证据表明,相对于PbM组,对照组在形状中心无诱饵方面的学习率更高(Cox模型HR 2.13,95% CI 1.02 - 4.43;p = 0.044)。
这些发现表明,临床上相关的抗癫痫药物联合进行24小时的新生儿治疗可对非人灵长类动物的行为和认知产生长期影响。《神经病学年鉴》2023年。