National Center for PTSD, VA Boston Healthcare System, United States; Boston University School of Medicine, United States.
Psychoneuroendocrinology. 2011 Aug;36(7):970-80. doi: 10.1016/j.psyneuen.2010.12.009. Epub 2011 Jan 26.
This study examined the effects of oral administration of 20mg hydrocortisone on baseline and fear-potentiated startle in 63 male veterans with or without PTSD. The procedure was based on a two-session, within-subject design in which acoustic startle eyeblink responses were recorded during intervals of threat or no threat of electric shock. Results showed that the magnitude of the difference between startle responses recorded during anticipation of imminent shock compared to "safe" periods was reduced after hydrocortisone administration relative to placebo. This effect did not vary as a function of PTSD group nor were there were any significant group differences in other indices startle amplitude. Findings suggest that the acute elevations in systemic cortisol produced by hydrocortisone administration may have fear-inhibiting effects. This finding may have implications for understanding the role of hypothalamic-pituitary-adrenal (HPA)-axis function in vulnerability and resilience to traumatic stress.
这项研究考察了口服 20 毫克氢可酮对有或没有创伤后应激障碍的 63 名男性退伍军人的基础惊吓和恐惧增强惊吓的影响。该程序基于双次、单次被试设计,在此设计中,在威胁或无电击威胁的间隔期间记录听觉惊吓眨眼反应。结果表明,与安慰剂相比,氢可酮给药后,记录到的对即将到来的电击的预期与“安全”期之间的惊吓反应差异幅度减小。这种影响与 PTSD 组无关,在其他惊吓幅度指标上也没有显著的组间差异。研究结果表明,氢可酮给药引起的全身皮质醇水平的急性升高可能具有抑制恐惧的作用。这一发现可能对理解下丘脑-垂体-肾上腺(HPA)轴功能在创伤性应激易感性和弹性中的作用具有重要意义。