Neural correlates of glucocorticoids effects on autobiographical memory retrieval in healthy women
Neural correlates of glucocorticoids effects on autobiographical memory retrieval in healthy women
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DOI:
10.1016/j.bbr.2018.06.024
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发表时间:
2019-02-01
影响因子:
2.7
通讯作者:
Wingenfeld, Katja
中科院分区:
文献类型:
--
作者:
Fleischer, Juliane;Metz, Sophie;Wingenfeld, Katja
It is well known that elevated cortisol after stress or after exogenous administration impairs episodic memory retrieval including autobiographical memory (AM) retrieval. This impairment might be mediated by deactivation of a neural network associated with memory retrieval including the prefrontal cortex (PFC) and limbic structures. However, the neural underpinnings of these cortisol effects on AM retrieval have not been investigated yet.In this study, thirty-three healthy women received either placebo or 10 mg hydrocortisone in a double blind cross-over design before completing an AM test during fMRI. In this test, participants are asked to recall specific events from their own past in response to a cue word.In a first step, we analyzed the neural underpinnings of AM retrieval in the placebo condition. We found an activation pattern consistent with core regions involved in autobiographical memory recall, including the ventromedial PFC, anterior medial (am)PFC, inferior frontal gyms, the posterior cingulate cortex, the tempoparietal junction, the middle temporal gyms and the hippocampus. Further, we analyzed brain activation during AM retrieval after hydrocortisone compared to placebo. Region of interest (ROI) analyses revealed a hydrocortisone-induced deactivation during AM retrieval in the right amPFC. Results of the ROI analyses were nonsignificant in the left and right hippocampus, the left and right vmPFC and the left amPFCIn sum, during AM retrieval hydrocortisone had the most pronounced effects on the amPFC. This might be explained by the strong involvement of this brain region in self-referential behavior, which is essential for recalling autobiographic information.