小鼠与女性研究提示卵巢周期和雌二醇调节皮层网络状态与听觉夹带
The ovarian cycle and estradiol modulate cortical network state and auditory entrainment in mice and women
一项尚未完成同行评审的预印本研究在小鼠和人类中报告,内源性或外源性雌二醇水平较高与更陡的非周期功率谱斜率相关,并伴随40Hz刺激后听觉夹带减弱。研究在男女被试中记录EEG、在雌雄小鼠中记录皮层内局部场电位,女性被试在低雌二醇与高雌二醇两个卵巢周期阶段接受测试。
该预印本以小鼠与人类跨物种对照,将卵巢周期与雌二醇水平同皮层非周期功率谱斜率及40Hz听觉夹带联系起来,为激素—脑耦合研究提供初步证据,但仅依据摘要,样本量与统计细节未报告。
The human brain is remarkably dynamic, continuously adapting to internal and external signals across rapid and protracted timescales. While both male and female brains are influenced by sex hormones to drive adaptive behavioural and physiological changes, the ovarian cycle in female mammals represents a conserved naturalistic model to understand how hormones such as estradiol (E2) alter cellular and network states to shape brain function. To understand whether and how the ovarian cycle influences sensory cortical processing, we investigated cortical network activity at rest and upon auditory stimulation across the ovarian cycle in mice and human subjects. We recorded EEG activity in men and women and intracortical local field potentials in male and female mice. Female participants were tested during two phases of their ovarian cycle characterized by low E2 levels (early follicular phase in women; late estrus in mice) and high E2 levels (late follicular phase in women; proestrus in mice). Across species, high endogenous or exogenous estradiol was associated with a steeper aperiodic power spectral slope, indicating decreased excitatory/inhibitory drive and attenuated auditory entrainment following a 40Hz stimulation. At the single-cell level, high E2 selectively increased the baseline and sustained 40-Hz firing of putative fast-spiking interneurons while reducing their temporal coherence during both spontaneous and stimulus-evoked activity, suggesting that E2 enhances inhibitory tone, while disrupting the temporal coordination of inhibitory networks. Altogether, these findings demonstrate that estradiol dynamically modulates cortical network states and auditory responsiveness. This underscores the necessity of investigating hormone-brain coupling as an evolutionarily conserved model essential for yielding translational insights into sex-specific neurobiology.
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来源:bioRxiv · Neuroscience · biorxiv.org