Serotonergic modulation of the BNST–CeA pathway reveals sex differences in fear learning

IF 20 1区 医学 Q1 NEUROSCIENCES
Rebecca Ravenelle, Jinah Lee, Carolina Fernandes-Henriques, Jia Liu, Allyson K. Friedman, Ekaterina Likhtik, Nesha S. Burghardt
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Abstract

Post-traumatic stress disorder (PTSD) is characterized by intense fear memory formation and is diagnosed more often in women than men. Here we show that increasing serotonin pharmacologically before auditory fear conditioning promoted memory recall in female and male mice, and that females were more sensitive to this effect. Optogenetic stimulation of raphe terminals in the anterior dorsal bed nucleus of the stria terminalis (adBNST) during fear conditioning increased c-Fos expression in the BNST and central nucleus of the amygdala (CeA) and enhanced fear memory recall through activation of 5-HT2C receptors in the adBNST in females only. Likewise, serotonin stimulation during fear learning enhanced adBNST–CeA high gamma (90–140 Hz) synchrony and adBNST-to-CeA communication in high gamma during fear memory recall in females only. These findings suggest that sex differences in the raphe–BNST–CeA pathway may contribute to the higher risk of PTSD in women.

Abstract Image

bst - cea通路的血清素调节揭示了恐惧学习的性别差异
创伤后应激障碍(PTSD)的特点是形成强烈的恐惧记忆,女性比男性更常被诊断出来。在这里,我们发现在听觉恐惧条件反射之前,在药理学上增加5 -羟色胺可以促进雌性和雄性小鼠的记忆回忆,并且雌性对这种效果更敏感。在恐惧条件反射过程中,光遗传刺激尾纹前背床核中缝终端增加了尾纹前背床核和杏仁核中央核中c-Fos的表达,并通过激活尾纹前背床核中5-HT2C受体增强了女性恐惧记忆的回忆。同样,在恐惧学习过程中,5 -羟色胺刺激仅在女性中增强了恐惧记忆回忆过程中adBNST-CeA高伽马(90-140 Hz)同步和adBNST-CeA高伽马通信。这些发现表明,rape - bst - cea通路的性别差异可能导致女性患PTSD的风险更高。
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来源期刊
Nature neuroscience
Nature neuroscience 医学-神经科学
CiteScore
38.60
自引率
1.20%
发文量
212
审稿时长
1 months
期刊介绍: Nature Neuroscience, a multidisciplinary journal, publishes papers of the utmost quality and significance across all realms of neuroscience. The editors welcome contributions spanning molecular, cellular, systems, and cognitive neuroscience, along with psychophysics, computational modeling, and nervous system disorders. While no area is off-limits, studies offering fundamental insights into nervous system function receive priority. The journal offers high visibility to both readers and authors, fostering interdisciplinary communication and accessibility to a broad audience. It maintains high standards of copy editing and production, rigorous peer review, rapid publication, and operates independently from academic societies and other vested interests. In addition to primary research, Nature Neuroscience features news and views, reviews, editorials, commentaries, perspectives, book reviews, and correspondence, aiming to serve as the voice of the global neuroscience community.
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