Ghrelin is a persistent biomarker for chronic stress exposure in adolescent rats and humans

被引:55
作者
Yousufzai, Muhammad I. ul Akbar [1 ]
Harmatz, Elia S. [2 ,3 ]
Shah, Mohsin [1 ]
Malik, Muhammad O. [1 ]
Goosens, Ki A. [4 ]
机构
[1] Khyber Med Univ, Inst Basic Med Sci, Dept Physiol, Peshawar, Pakistan
[2] McGovern Inst Brain Res, 77 Massachusetts Ave, Cambridge, MA 02139 USA
[3] Dept Brain & Cognit Sci, 77 Massachusetts Ave, Cambridge, MA 02139 USA
[4] Massachusetts Gen Hosp, Dept Neurol, 114 16th St, Charlestown, MA 02129 USA
来源
TRANSLATIONAL PSYCHIATRY | 2018年 / 8卷
关键词
HORMONE-RELEASING PEPTIDE; POSTTRAUMATIC-STRESS; BODY-WEIGHT; FOOD-INTAKE; GHS-R; DISORDER; RECEPTOR; FEAR; REINFORCEMENT; MALTREATMENT;
D O I
10.1038/s41398-018-0135-5
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
Prolonged stressor exposure in adolescence enhances the risk of developing stress-sensitive mental illnesses, including posttraumatic stress disorder (PTSD), for many years following exposure cessation, but the biological underpinnings of this long-term vulnerability are unknown. We show that severe stressor exposure increased circulating levels of the hormone acyl-ghrelin in adolescent rats for at least 130 days and in adolescent humans for at least 4.5 years. Using a rodent model of longitudinal PTSD vulnerability in which rodents with a history of stressor exposure during adolescence display enhanced fear in response to fear conditioning administered weeks after stressor exposure ends, we show that systemic delivery of a ghrelin receptor antagonist for 4 weeks surrounding stressor exposure (2 weeks during and 2 weeks following) prevented stress-enhanced fear memory. These data suggest that protracted exposure to elevated acyl-ghrelin levels mediates a persistent vulnerability to stress-enhanced fear after stressor exposure ends.
引用
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页数:11
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