Kozlovsky Nitsan, Matar Michael A, Kaplan Zeev, Zohar Joseph, Cohen Hagit
State of Israel Ministry of Health, Anxiety and Stress Research Unit, Faculty of Health Sciences, Ben-Gurion University of the Negev, Beer-Sheva, Israel.
Biol Psychiatry. 2009 Mar 1;65(5):383-91. doi: 10.1016/j.biopsych.2008.10.034. Epub 2008 Dec 18.
Converging evidence implicates the regulatory neuropeptide galanin in anxiety- and depression-related behaviors, through modulation of neuroendocrine, serotonergic, and noradrenergic systems. This study examined the relationship between stress-induced posttraumatic stress disorder (PTSD)-like behavioral response patterns in rats and galanin mRNA levels in key brain areas and the effects of acute phase pharmacologic manipulation using an agonist (galnon) on behavioral, physiologic, and response patterns of brain-derived neurotrophic factor (BDNF) and 5-hydroxytryptamine-1A (5HT-1A).
Galanin mRNA expression was assessed in the frontal cortex and hippocampus in the short- and long-term (30 min and 7 days) after exposure to predator scent stress. The effects of intraperitoneal galnon .5 mg/kg versus saline 1 hour postexposure on behavioral tests (elevated plus maze and acoustic startle response) were evaluated 7 days later. Trauma-cue response, circulating corticosterone, and localized brain expression of 5HT-1A receptors and BDNF were subsequently assessed. All data were analyzed in relation to individual behavior patterns.
Whereas animals with minimal behavioral disruption displayed a lasting upregulation of galanin mRNA in the hippocampal CA1 area, those with extreme behavioral responses displayed downregulation in both CA1 and frontal cortex. Immediate postexposure treatment with galnon significantly reduced prevalence rates of extreme responders, reduced trauma-cue freezing responses, corrected the corticosterone response, and increased CA1 expression of 5HT-1A and BDNF mRNA compared with saline controls.
Galanin is actively involved in the neurobiological response to predator scent stress with resilience/recovery after stress exposure and thus warrants further study as a potential therapeutic avenue for the treatment of anxiety-related disorders.
越来越多的证据表明,调节性神经肽甘丙肽通过调节神经内分泌、血清素能和去甲肾上腺素能系统,参与与焦虑和抑郁相关的行为。本研究探讨了应激诱导的大鼠创伤后应激障碍(PTSD)样行为反应模式与关键脑区甘丙肽mRNA水平之间的关系,以及使用激动剂(galnon)进行急性期药物干预对行为、生理以及脑源性神经营养因子(BDNF)和5-羟色胺-1A(5HT-1A)反应模式的影响。
在暴露于捕食者气味应激后的短期和长期(30分钟和7天),评估额叶皮质和海马体中甘丙肽mRNA的表达。暴露1小时后,腹腔注射0.5mg/kg的galnon与生理盐水,7天后评估其对行为测试(高架十字迷宫和听觉惊吓反应)的影响。随后评估创伤线索反应、循环皮质酮以及5HT-1A受体和BDNF的局部脑表达。所有数据均根据个体行为模式进行分析。
行为干扰最小的动物海马CA1区甘丙肽mRNA持续上调,而行为反应极端的动物CA1区和额叶皮质均下调。与生理盐水对照组相比,暴露后立即用galnon治疗显著降低了极端反应者的患病率,减少了创伤线索冻结反应,纠正了皮质酮反应,并增加了CA1区5HT-1A和BDNF mRNA的表达。
甘丙肽积极参与对捕食者气味应激的神经生物学反应,并在应激暴露后具有恢复力/恢复能力,因此作为治疗焦虑相关疾病的潜在治疗途径值得进一步研究。