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Effect of subanesthetic ketamine on intrinsic functional brain connectivity: A placebo-controlled functional magnetic resonance imaging study in healthy male volunteers

机译:亚麻醉氯胺酮对内在功能性大脑连通性的影响:安慰剂控制的功能性磁共振成像对健康男性志愿者的研究

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Background: The influence of psychoactive drugs on the central nervous system has been investigated with positron emission tomography and task-related functional magnetic resonance imaging. However, it is not known how these drugs affect the intrinsic large-scale interactions of the brain (resting-state functional magnetic resonance imaging connectivity). In this study, the effect of low-dose S(+)-ketamine on intrinsic brain connectivity was investigated. Methods: Twelve healthy, male volunteers received a 2-h intravenous S(+)-ketamine infusion (first hour 20 mg/70 kg, second hour 40 mg/70 kg). Before, during, and after S(+)-ketamine administration, resting-state brain connectivity was measured. In addition, heat pain tests were performed between imaging sessions to determine ketamine-induced analgesia. A mixed-effects general linear model was used to determine drug and pain effects on resting-state brain connectivity. Results: Ketamine increased the connectivity most importantly in the cerebellum and visual cortex in relation to the medial visual network. A decrease in connectivity was observed in the auditory and somatosensory network in relation to regions responsible for pain sensing and the affective processing of pain, which included the amygdala, insula, and anterior cingulate cortex. Connectivity variations related to fluctuations in pain scores were observed in the anterior cingulate cortex, insula, orbitofrontal cortex, and the brainstem, regions involved in descending inhibition of pain. Conclusions: Changes in connectivity were observed in the areas that explain ketamine's pharmacodynamic profile with respect to analgesia and psychedelic and other side effects. In addition, pain and ketamine changed brain connectivity in areas involved in endogenous pain modulation.
机译:背景:已通过正电子发射断层扫描和与任务相关的功能性磁共振成像研究了精神药物对中枢神经系统的影响。但是,尚不知道这些药物如何影响大脑的固有大规模相互作用(静止状态功能磁共振成像连接性)。在这项研究中,研究了低剂量S(+)-氯胺酮对内在大脑连通性的影响。方法:12名健康的男性志愿者接受2小时静脉内S(+)-氯胺酮输注(第一小时20 mg / 70 kg,第二小时40 mg / 70 kg)。在服用S(+)-氯胺酮之前,之中和之后,测量了静息状态的大脑连通性。另外,在成像期间之间进行热痛测试以确定氯胺酮诱导的镇痛作用。混合效应的一般线性模型用于确定药物和疼痛对静止状态大脑连接性的影响。结果:氯胺酮增加了相对于内侧视觉网络的小脑和视觉皮层的连接性。在听觉和体感网络中,与负责疼痛感测和疼痛的情感性处理的区域(包括杏仁核,岛突和扣带回皮层)相关的连接性下降。在前扣带回皮层,岛状,眶额皮层和脑干(与疼痛的下降抑制有关的区域)中观察到与疼痛评分波动相关的连通性变化。结论:在解释氯胺酮在镇痛和迷幻药及其他副作用方面的药效学特征的区域观察到连通性的变化。此外,疼痛和氯胺酮改变了内源性疼痛调节相关区域的大脑连通性。

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