Dept. of Physiology and Pharmacology, Sapienza University of Rome, 00185 Rome, Italy.
Dept. of Physiology and Pharmacology, Sapienza University of Rome, 00185 Rome, Italy; Neurobiology of Behavior Laboratory, Santa Lucia Foundation, 00143 Rome, Italy.
Neurobiol Learn Mem. 2021 Feb;178:107362. doi: 10.1016/j.nlm.2020.107362. Epub 2020 Dec 15.
Trauma patients treated with ketamine during emergency care present aggravated early post- traumatic stress reaction which is highly predictive of post-traumatic stress disorder (PTSD) development and severity. The use of ketamine in the acute trauma phase may directly or indirectly interfere with neural processes of memory consolidation of the traumatic event, thus leading to the formation of maladaptive memories, a hallmark symptom of PTSD. We have recently shown that ketamine anesthesia, immediately after a traumatic event, enhances memory consolidation and leads to long-lasting alterations of social behavior in rats. Based on the evidence that ketamine induces a robust central and peripheral adrenergic/noradrenergic potentiation and that activation of this system is essential for the formation of memory for stressful events, we explored the possibility that the strong sympathomimetic action of ketamine might underlie its memory enhancing effects. We found that rats given immediate, but not delayed, post-training ketamine anesthesia (125 mg/kg) presented enhanced 48-h memory retention in an inhibitory avoidance task and that these effects were blocked by adrenal medullectomy, lesions of the locus coeruleus, systemic or intra-basolateral amygdala ß-adrenergic receptor antagonism. Thus, the memory enhancing effects of ketamine anesthesia are time-dependent and mediated by a combined peripheral-central sympathomimetic action. We elucidated a mechanism by which ketamine exacerbates acute post-traumatic reaction, possibly leading to development of PTSD symptomatology later in life. These findings will help guide for a better management of sedation/anesthesia in emergency care to promote the prophylaxis and reduce the risk of developing trauma-related disorders in trauma victims.
在急救护理中接受氯胺酮治疗的创伤患者表现出加重的早期创伤后应激反应,这高度预测创伤后应激障碍(PTSD)的发展和严重程度。在急性创伤阶段使用氯胺酮可能直接或间接干扰创伤事件的记忆巩固的神经过程,从而导致适应不良记忆的形成,这是 PTSD 的一个标志性症状。我们最近表明,创伤事件后立即使用氯胺酮麻醉会增强记忆巩固,并导致大鼠的社交行为长期持久改变。基于氯胺酮诱导强烈的中枢和外周肾上腺素能/去甲肾上腺素能增强的证据,并且该系统的激活对于应激事件的记忆形成是必需的,我们探索了氯胺酮的强烈拟交感作用可能是其增强记忆作用的基础的可能性。我们发现,立即给予但不延迟给予术后氯胺酮麻醉(125mg/kg)的大鼠在抑制性回避任务中表现出增强的 48 小时记忆保留,并且这些作用被肾上腺髓质切除术、蓝斑核损伤、全身性或内侧基底杏仁核β-肾上腺素能受体拮抗剂阻断。因此,氯胺酮麻醉的增强记忆作用是时间依赖性的,并通过外周-中枢拟交感作用的组合介导。我们阐明了氯胺酮加剧急性创伤后反应的机制,这可能导致创伤后应激障碍症状在以后的生活中发展。这些发现将有助于指导急救护理中的镇静/麻醉管理,以促进预防和降低创伤受害者发生创伤相关障碍的风险。