Neurobiology Laboratory, National Institute of Environmental Health Sciences, National Institutes of Health, Department of Health and Human Services, 111 TW Alexander Dr., P.O. Box 12233, Mail Drop F2-08, Research Triangle Park, NC, 27709, USA.
J Mol Neurosci. 2024 Aug 30;74(3):82. doi: 10.1007/s12031-024-02260-0.
Hippocamposeptal (HS) neurons send GABAergic projections from the hippocampus to the medial septum/diagonal band of Broca (MS/DBB) as part of a reciprocal loop that is critical for memory. HS neurons are proposed to be particularly sensitive to the deleterious effects of pathological exposure to amyloid-β (Aβ), as would occur during Alzheimer's disease (AD). However, it is not known how HS GABA release in the MS/DBB is altered during the progression of AD. To target HS neurons in a mouse model of AD, we crossed SST-Cre mice to 5XFAD mice and performed stereotaxic injections of Cre-dependent AAV containing mCherry/channelrhodopsin-2 (ChR2) into the hippocampus of offspring at 4, 6, 9, and 12 months. We used optogenetics to selectively stimulate HS terminals while performing whole-cell patch-clamp recordings from MS/DBB neurons in slices. There was a transient reduction in HS-inhibitory postsynaptic current (IPSC) amplitude in female 5XFAD mice at 6 months, but no difference in males at any age, and no difference in paired-pulse ratio in either sex at any age. When bath applying the GABAR agonist, baclofen, we found a larger decrease in HS-IPSC amplitude in 5XFAD females at 9 months and 5XFAD males at 12 months. In 12-month-old 5XFAD females, response to baclofen was significantly reduced. These data suggest that there is a transient increase in responsiveness to GABAR activation in 5XFAD mice that occurs earlier in females than in males. These sex-specific changes to HS function are likely to impact the relay of information between the hippocampus and MS/DBB.
海马伞隔(HS)神经元从海马体投射 GABA 能性纤维到内侧隔核/布罗卡斜角带(MS/DBB),形成一个对记忆至关重要的反馈回路。HS 神经元被认为对淀粉样蛋白-β(Aβ)病理性暴露的有害影响特别敏感,如在阿尔茨海默病(AD)中发生的那样。然而,在 AD 进展过程中,MS/DBB 中的 HS GABA 释放如何改变尚不清楚。为了在 AD 小鼠模型中靶向 HS 神经元,我们将 SST-Cre 小鼠与 5XFAD 小鼠杂交,并在后代 4、6、9 和 12 个月时对其海马体进行立体定向注射 Cre 依赖性携带 mCherry/通道视紫红质-2(ChR2)的 AAV。我们使用光遗传学选择性地刺激 HS 末梢,同时在切片中对 MS/DBB 神经元进行全细胞膜片钳记录。在 6 个月龄的雌性 5XFAD 小鼠中,HS 抑制性突触后电流(IPSC)幅度出现短暂降低,但在任何年龄的雄性中均无差异,并且在任何年龄的任何性别中,配对脉冲比均无差异。当用 GABAR 激动剂巴氯芬进行灌流时,我们发现 9 个月龄的雌性 5XFAD 和 12 个月龄的雄性 5XFAD 中 HS-IPSC 幅度的降低更大。在 12 个月龄的雌性 5XFAD 中,对巴氯芬的反应明显减弱。这些数据表明,在 5XFAD 小鼠中存在对 GABAR 激活的反应性短暂增加,这种增加在雌性中比在雄性中更早出现。HS 功能的这些性别特异性变化可能会影响海马体和 MS/DBB 之间的信息传递。