May Renee M, Tabatadze Nino, Czech Mary M, Woolley Catherine S
Department of Neurobiology, Northwestern University, 2205 Tech Drive, Evanston, IL, 60208, USA.
Brain Struct Funct. 2014 Nov;219(6):1947-54. doi: 10.1007/s00429-013-0614-7. Epub 2013 Jul 27.
Previous work has shown that the steroid hormone estradiol facilitates the release of anticonvulsant neuropeptides from inhibitory neurons in the hippocampus to suppress seizures. Because neuropeptides are packaged in large dense core vesicles, estradiol may facilitate neuropeptide release through regulation of dense core vesicles. In the current study, we used serial section electron microscopy in the hippocampal CA1 region of adult female rats to test three hypotheses about estradiol regulation of dense core vesicles: (1) Estradiol increases the number of dense core vesicles in axonal boutons, (2) Estradiol increases the size of dense core vesicles in axonal boutons, (3) Estradiol shifts the location of dense core vesicles toward the periphery of axonal boutons, potentially lowering the threshold for neuropeptide release during seizures. We found that estradiol increases the number and size of dense core vesicles in inhibitory axonal boutons, consistent with increased neuropeptide content, but does not shift the location of dense core vesicles closer to the bouton periphery. These effects were specific to large dense core vesicles (>80 nm) in inhibitory boutons. Estradiol had no effects on small dense core vesicles or dense core vesicles in excitatory boutons. Our results indicate that estradiol suppresses seizures at least in part by increasing the potentially releasable pool of neuropeptides in the hippocampus, and that estradiol facilitation of neuropeptide release involves a mechanism other than mobilization of dense core vesicles toward sites of release.
先前的研究表明,类固醇激素雌二醇可促进海马体中抑制性神经元释放抗惊厥神经肽,从而抑制癫痫发作。由于神经肽被包裹在大型致密核心囊泡中,雌二醇可能通过调节致密核心囊泡来促进神经肽的释放。在本研究中,我们使用成年雌性大鼠海马CA1区的连续切片电子显微镜,来检验关于雌二醇对致密核心囊泡调节的三个假设:(1)雌二醇增加轴突终扣中致密核心囊泡的数量;(2)雌二醇增加轴突终扣中致密核心囊泡的大小;(3)雌二醇使致密核心囊泡的位置向轴突终扣的周边移动,这可能会降低癫痫发作期间神经肽释放的阈值。我们发现,雌二醇增加了抑制性轴突终扣中致密核心囊泡的数量和大小,这与神经肽含量增加一致,但并没有使致密核心囊泡的位置更靠近终扣周边。这些效应仅限于抑制性终扣中的大型致密核心囊泡(>80纳米)。雌二醇对小型致密核心囊泡或兴奋性终扣中的致密核心囊泡没有影响。我们的结果表明,雌二醇至少部分地通过增加海马体中潜在可释放的神经肽池来抑制癫痫发作,并且雌二醇促进神经肽释放涉及的机制并非是将致密核心囊泡向释放位点移动。