Ruland Tillmann, Domschke Katharina, Schütte Valerie, Zavorotnyy Maxim, Kugel Harald, Notzon Swantje, Vennewald Nadja, Ohrmann Patricia, Arolt Volker, Pfleiderer Bettina, Zwanzger Peter
Mood and Anxiety Disorders Research Unit, Department of Psychiatry and Psychotherapy, University of Muenster, Germany.
Department of Psychiatry, Psychosomatics and Psychotherapy, University of Wuerzburg, Germany.
Eur Neuropsychopharmacol. 2015 Oct;25(10):1677-82. doi: 10.1016/j.euroneuro.2015.07.011. Epub 2015 Jul 20.
An excitatory-inhibitory neurotransmitter dysbalance has been suggested in pathogenesis of panic disorder. The neuropeptide S (NPS) system has been implicated in modulating GABA and glutamate neurotransmission in animal models and to genetically drive altered fear circuit function and an increased risk of panic disorder in humans. Probing a multi-level imaging genetic risk model of panic, in the present magnetic resonance spectroscopy (MRS) study brain glutamate+glutamine (Glx) levels in the bilateral anterior cingulate cortex (ACC) during a pharmacological cholecystokinin tetrapeptide (CCK-4) panic challenge were assessed depending on the functional neuropeptide S receptor gene (NPSR1) rs324981 A/T variant in a final sample of 35 healthy male subjects. The subjective panic response (Panic Symptom Scale; PSS) as well as cortisol and ACTH levels were ascertained throughout the experiment. CCK-4 injection was followed by a strong panic response. A significant time×genotype interaction was detected (p=.008), with significantly lower ACC Glx/Cr levels in T allele carriers as compared to AA homozygotes 5min after injection (p=.003). CCK-4 induced significant HPA axis stimulation, but no effect of genotype was discerned. The present pilot data suggests NPSR1 gene variation to modulate Glx levels in the ACC during acute states of stress and anxiety, with blunted, i.e. possibly maladaptive ACC glutamatergic reactivity in T risk allele carriers. Our results underline the notion of a genetically driven rapid and dynamic response mechanism in the neural regulation of human anxiety and further strengthen the emerging role of the NPS system in anxiety.
惊恐障碍的发病机制中存在兴奋性-抑制性神经递质失衡的现象。动物模型研究表明,神经肽S(NPS)系统参与调节γ-氨基丁酸(GABA)和谷氨酸神经传递,且在人类中,该系统通过基因驱动改变恐惧回路功能,增加惊恐障碍风险。在本磁共振波谱(MRS)研究中,为探究惊恐障碍的多层次影像遗传学风险模型,对35名健康男性受试者的最终样本进行了研究,根据功能性神经肽S受体基因(NPSR1)rs324981 A/T变异,评估了在药理学胆囊收缩素四肽(CCK-4)诱发惊恐发作挑战期间双侧前扣带回皮质(ACC)中的脑谷氨酸+谷氨酰胺(Glx)水平。在整个实验过程中,测定了主观惊恐反应(惊恐症状量表;PSS)以及皮质醇和促肾上腺皮质激素水平。注射CCK-4后出现强烈的惊恐反应。检测到显著的时间×基因型交互作用(p = 0.008),与AA纯合子相比,注射后5分钟时,T等位基因携带者的ACC Glx/Cr水平显著降低(p = 0.003)。CCK-4诱导了显著的下丘脑-垂体-肾上腺(HPA)轴刺激,但未发现基因型的影响。本初步数据表明,NPSR1基因变异在应激和焦虑的急性状态下调节ACC中的Glx水平,T风险等位基因携带者的ACC谷氨酸能反应迟钝,即可能存在适应不良。我们的结果强调了在人类焦虑的神经调节中,由基因驱动的快速动态反应机制的概念,并进一步强化了NPS系统在焦虑中日益凸显的作用。