Sleep deprivation affects fear memory consolidation: bi-stable amygdala connectivity with insula and ventromedial prefrontal cortex

被引:25
|
作者
Feng, Pan [1 ,2 ]
Becker, Benjamin [3 ]
Zheng, Yong [1 ,2 ]
Feng, Tingyong [1 ,2 ]
机构
[1] Southwest Univ, Fac Psychol, 1 Tian Sheng RD, Chongqing 400715, Peoples R China
[2] Southwest Univ, Key Lab Cognit & Personal, Minist Educ, Chongqing 400715, Peoples R China
[3] Univ Elect Sci & Technol China, Chengdu Brain Sci Inst, Key Lab NeuroInformat, Clin Hosp,Minist Educ, Chengdu 611731, Sichuan, Peoples R China
基金
中国博士后科学基金; 中国国家自然科学基金;
关键词
sleep deprivation; fear consolidation; amygdala; insula; vmPFC; POSTTRAUMATIC-STRESS-DISORDER; STATE FUNCTIONAL CONNECTIVITY; RESTING-STATE; REM-SLEEP; STRUCTURAL CONNECTIVITY; ANTERIOR CINGULATE; EMOTIONAL BRAIN; EXTINCTION; ANXIETY; PTSD;
D O I
10.1093/scan/nsx148
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Sleep plays an important role for successful fear memory consolidation. Growing evidence suggests that sleep disturbances might contribute to the development and the maintenance of posttraumatic stress disorder (PTSD), a disorders characterized by dysregulations in fear learning mechanisms, as well as exaggerated arousal and salience processing. Against this background, the present study examined the effects of sleep deprivation (SD) on the acquisition of fear and the subsequent neural consolidation. To this end, the present study assessed fear acquisition and associated changes in fMRI-based amygdala-functional connectivity following 24 h of SD. Relative to non-sleep deprived controls, SD subjects demonstrated increased fear ratings and skin conductance responses (SCR) during fear acquisition. During fear consolidation SD inhibited increased amygdala-ventromendial prefrontal cortex (vmPFC) connectivity and concomitantly increased changes in amygdala-insula connectivity. Importantly, whereas in controls fear indices during acquisition were negatively associated with amygdala-vmPFC connectivity during consolidation, fear indices were positively associated with amygdala-insula coupling following SD. Together the findings suggest that SD may interfere with vmPFC control of the amygdala and increase bottom-up arousal signaling in the amygdala-insula pathway during fear consolidation, which might mediate the negative impact of sleep disturbances on PSTD symptomatology.
引用
收藏
页码:145 / 155
页数:11
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