Long Ii Robert P, Aroniadou-Anderjaska Vassiliki, Prager Eric M, Pidoplichko Volodymyr I, Figueiredo Taiza H, Braga Maria F M
Department of Anatomy, Physiology, and Genetics, F. Edward Hébert School of Medicine, Uniformed Services University of the Health Sciences, 4301 Jones Bridge Road, Bethesda, MD 20814, USA; Program in Neuroscience, F. Edward Hébert School of Medicine, Uniformed Services University of the Health Sciences, 4301 Jones Bridge Road, Bethesda, MD 20814, USA.
Department of Anatomy, Physiology, and Genetics, F. Edward Hébert School of Medicine, Uniformed Services University of the Health Sciences, 4301 Jones Bridge Road, Bethesda, MD 20814, USA; Program in Neuroscience, F. Edward Hébert School of Medicine, Uniformed Services University of the Health Sciences, 4301 Jones Bridge Road, Bethesda, MD 20814, USA; Department of Psychiatry, F. Edward Hébert School of Medicine, Uniformed Services University of the Health Sciences, 4301 Jones Bridge Road, Bethesda, MD 20814, USA.
Neural Plast. 2016;2016:8524560. doi: 10.1155/2016/8524560. Epub 2016 May 23.
After surgery requiring general anesthesia, patients often experience emotional disturbances, but it is unclear if this is due to anesthetic exposure. In the present study, we examined whether isoflurane anesthesia produces long-term pathophysiological alterations in the basolateral amygdala (BLA), a brain region that plays a central role in emotional behavior. Ten-week-old, male rats were administered either a single, 1 h long isoflurane (1.5%) anesthesia or three, 1 h long isoflurane exposures, separated by 48 h. Long-term potentiation (LTP) and spontaneous GABAergic activity in the BLA were studied 1 day, 1 week, and 1 month later. Single isoflurane anesthesia had no significant effect on the magnitude of LTP. In contrast, after repeated isoflurane exposures, LTP was dramatically impaired at both 1 day and 1 week after the last exposure but was restored by 1 month after the exposures. Spontaneous GABAA receptor-mediated IPSCs were increased at 1 day and 1 week after repeated exposures but had returned to control levels by 1 month after exposure. Thus, repeated exposures to isoflurane cause a long-lasting-but not permanent-impairment of synaptic plasticity in the BLA, which could be due to increased basal GABAergic activity. These pathophysiological alterations may produce emotional disturbances and impaired fear-related learning.
在接受需要全身麻醉的手术后,患者常常会出现情绪障碍,但尚不清楚这是否是由于麻醉暴露所致。在本研究中,我们研究了异氟烷麻醉是否会在基底外侧杏仁核(BLA)产生长期的病理生理改变,该脑区在情绪行为中起核心作用。给10周龄的雄性大鼠单次给予1小时的异氟烷(1.5%)麻醉,或分三次给予,每次1小时,间隔48小时。在1天、1周和1个月后研究BLA中的长时程增强(LTP)和自发性GABA能活动。单次异氟烷麻醉对LTP的幅度没有显著影响。相比之下,反复暴露于异氟烷后,在最后一次暴露后的1天和1周时LTP显著受损,但在暴露后1个月恢复。反复暴露后1天和1周时,自发性GABAA受体介导的抑制性突触后电流(IPSCs)增加,但在暴露后1个月已恢复到对照水平。因此,反复暴露于异氟烷会导致BLA中突触可塑性出现长期但非永久性的损害,这可能是由于基础GABA能活动增加所致。这些病理生理改变可能会导致情绪障碍和与恐惧相关的学习受损。