Department of Radiology, University of Pittsburgh, Pittsburgh, Pennsylvania; Department of Psychiatry, University of Pittsburgh, Pittsburgh, Pennsylvania.
Department of Radiology, University of Pittsburgh, Pittsburgh, Pennsylvania.
Biol Psychiatry. 2019 Jun 15;85(12):1056-1064. doi: 10.1016/j.biopsych.2019.02.017. Epub 2019 Apr 4.
Posttraumatic stress disorder (PTSD) is a stress disorder that develops in only some individuals following a traumatic event. Data suggest that a substantial fraction of women recover after sexual violence. Thus, the investigation of stress and antistress neuropeptides in this sample has the potential to inform the neurochemistry of resilience following trauma. Nociceptin is an antistress neuropeptide in the brain that promotes resilience in animal models of PTSD.
[C]NOP-1A positron emission tomography was used to measure the in vivo binding to nociceptin receptors in 18 college women who had experienced sexual violence irrespective of whether they met DSM-5 diagnostic criteria for PTSD. [C]NOP-1A data from 18 healthy control subjects were also included to provide a contrast with the sexual violence group. [C]NOP-1A total distribution volume (V) in the regions of interest were measured with kinetic analysis using the arterial input function. The relationships between regional V and Clinician-Administered PTSD Scale for DSM-5 total symptom and subscale severity were examined using correlational analyses.
No differences in [C]NOP-1A V were noted between the sexual violence and control groups. V in the midbrain and cerebellum were positively correlated with PTSD total symptom severity in the past month before positron emission tomography. Intrusion/re-experiencing and avoidance subscale symptoms drove this relationship. Stratification of subjects by a DSM-5 PTSD diagnosis and contrasting their V with that in control subjects showed no group differences.
Decreased midbrain and cerebellum nociceptin receptors are associated with less severe PTSD symptoms. Medications that target nociceptin should be explored to prevent and treat PTSD.
创伤后应激障碍(PTSD)是一种应激障碍,仅在创伤事件后部分个体中发展。有数据表明,相当一部分女性在遭受性暴力后会康复。因此,对该样本中的应激和抗压神经肽进行研究,有可能为创伤后恢复的神经化学提供信息。孤啡肽是大脑中的一种抗压神经肽,可促进 PTSD 动物模型中的恢复能力。
使用[C]NOP-1A 正电子发射断层扫描来测量 18 名经历过性暴力的大学生女性体内的孤啡肽受体结合情况,无论她们是否符合 DSM-5 PTSD 诊断标准。还纳入了 18 名健康对照者的[C]NOP-1A 数据,以便与性暴力组进行对比。使用动脉输入函数的动力学分析测量感兴趣区域中的[C]NOP-1A 总分布容积(V)。使用相关分析检查区域 V 与临床医生管理的 DSM-5 PTSD 总症状和子量表严重程度之间的关系。
性暴力组和对照组之间的[C]NOP-1A V 没有差异。中脑和小脑的 V 与正电子发射断层扫描前一个月 PTSD 总症状严重程度呈正相关。侵入/再体验和回避子量表的症状驱动了这种关系。根据 DSM-5 PTSD 诊断对受试者进行分层,并将其 V 与对照组进行对比,并未显示出组间差异。
中脑和小脑孤啡肽受体减少与 PTSD 症状较轻有关。应探索靶向孤啡肽的药物,以预防和治疗 PTSD。