Dexmedetomidine inhibits fear memory consolidation via the astrocyte-specific Srebf1-Phgdh pathway in the prelimbic prefrontal cortex

Post-traumatic stress disorder (PTSD) develops following exposure to a traumatic event. However, effective prevention and treatments remain elusive. In this study, we report that sub-anesthetic doses of dexmedetomidine can alleviate fear in mice by inhibiting the consolidation of fear memory. Transcriptomic analysis identifies sterol regulatory element-binding protein 1 (Srebf1) as a key mediator of dexmedetomidine's effects. The potential mechanism of this involves dexmedetomidine reducing the nuclear translocation of Srebf1 specifically in prelimbic prefrontal cortex astrocytes, thereby decreasing the active transcriptional form of Srebf1. This results in the downregulation of its target gene, phosphoglycerate dehydrogenase (Phgdh). Phgdh, as the main synthetase of the N-methyl-D-aspartate receptor co-agonist D-serine, plays a crucial role in regulating synaptic stability and ultimately inhibiting the consolidation of fear memory. This work identifies the mechanism by which dexmedetomidine inhibits fear memory consolidation, providing a rationale for its preventive application and uncovering novel targets for PTSD intervention.

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Publication Details

Journal
Cell Reports
Published
2026-03-17
DOI
https://doi.org/10.1016/j.celrep.2026.117125
Primary Topic
Memory and Neural Mechanisms
Type
article
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0.00
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article

Dexmedetomidine inhibits fear memory consolidation via the astrocyte-specific Srebf1-Phgdh pathway in the prelimbic prefrontal cortex

Mian Peng, Wei Wei, Han Zhang, Wei Wu et al.
Cell Reports
Memory and Neural Mechanisms
article

Dexmedetomidine inhibits fear memory consolidation via the astrocyte-specific Srebf1-Phgdh pathway in the prelimbic prefrontal cortex

Mian Peng, Wei Wei, Han Zhang, Wei Wu, Ke Li, Xin Liu, Xiang Li, Siyuan Wang
article en

Abstract

Post-traumatic stress disorder (PTSD) develops following exposure to a traumatic event. However, effective prevention and treatments remain elusive. In this study, we report that sub-anesthetic doses of dexmedetomidine can alleviate fear in mice by inhibiting the consolidation of fear memory. Transcriptomic analysis identifies sterol regulatory element-binding protein 1 (Srebf1) as a key mediator of dexmedetomidine's effects. The potential mechanism of this involves dexmedetomidine reducing the nuclear translocation of Srebf1 specifically in prelimbic prefrontal cortex astrocytes, thereby decreasing the active transcriptional form of Srebf1. This results in the downregulation of its target gene, phosphoglycerate dehydrogenase (Phgdh). Phgdh, as the main synthetase of the N-methyl-D-aspartate receptor co-agonist D-serine, plays a crucial role in regulating synaptic stability and ultimately inhibiting the consolidation of fear memory. This work identifies the mechanism by which dexmedetomidine inhibits fear memory consolidation, providing a rationale for its preventive application and uncovering novel targets for PTSD intervention.

Cell ReportsVol. 45(4)
Wuhan University (CN), Zhongnan Hospital of Wuhan University (CN)
Reduced inequalities
Openalex Percentile: Top 24%
Memory and Neural Mechanisms
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