Department of Anatomy and Neurobiology, University of Tennessee, 855 Monroe Ave., Memphis, TN 38163, USA.
Brain Res. 2010 Oct 28;1358:123-39. doi: 10.1016/j.brainres.2010.08.065. Epub 2010 Aug 27.
Using intrachoroidal injection of the transneuronal retrograde tracer pseudorabies virus (PRV) in rats, we previously localized preganglionic neurons in the superior salivatory nucleus (SSN) that regulate choroidal blood flow (ChBF) via projections to the pterygopalatine ganglion (PPG). In the present study, we used higher-order transneuronal retrograde labeling following intrachoroidal PRV injection to identify central neuronal cell groups involved in parasympathetic regulation of ChBF via input to the SSN. These prominently included the hypothalamic paraventricular nucleus (PVN) and the nucleus of the solitary tract (NTS), both of which are responsive to systemic BP and are involved in systemic sympathetic vasoconstriction. Conventional pathway tracing methods were then used to determine if the PVN and/or NTS project directly to the choroidal subdivision of the SSN. Following retrograde tracer injection into SSN (biotinylated dextran amine 3K or Fluorogold), labeled perikarya were found in PVN and NTS. Injection of the anterograde tracer, biotinylated dextran amine 10K (BDA10K), into PVN or NTS resulted in densely packed BDA10K+terminals in prechoroidal SSN (as defined by its enrichment in nitric oxide synthase-containing perikarya). Double-label studies showed these inputs ended directly on prechoroidal nitric oxide synthase-containing neurons of SSN. Our study thus establishes that PVN and NTS project directly to the part of SSN involved in parasympathetic vasodilatory control of the choroid via the PPG. These results suggest that control of ChBF may be linked to systemic blood pressure and central control of the systemic vasculature.
我们先前使用大鼠脉络丛内注射顺行性跨神经元追踪病毒(PRV)的方法,定位了通过投射到翼腭神经节(PPG)来调节脉络膜血流(ChBF)的节前神经元,这些神经元位于上涎核(SSN)中。在本研究中,我们使用脉络丛内 PRV 注射后的高级跨神经元逆行标记来鉴定涉及通过输入 SSN 来调节 ChBF 的副交感神经的中枢神经元细胞群。这些神经元主要包括下丘脑室旁核(PVN)和孤束核(NTS),它们均对全身血压有反应,并参与全身交感神经血管收缩。然后使用传统的通路追踪方法来确定 PVN 和/或 NTS 是否直接投射到 SSN 的脉络膜亚区。在将逆行示踪剂(生物素化葡聚糖胺 3K 或荧光金)注射到 SSN 后,在 PVN 和 NTS 中发现了标记的神经元胞体。将顺行示踪剂,生物素化葡聚糖胺 10K(BDA10K)注射到 PVN 或 NTS 中,导致在 SSN 的前脉络膜中出现密集的 BDA10K+终末(如富含含一氧化氮合酶的神经元胞体所定义的)。双标记研究表明,这些输入直接终止于 SSN 的前脉络膜含一氧化氮合酶的神经元上。因此,我们的研究确立了 PVN 和 NTS 通过 PPG 直接投射到参与副交感神经血管舒张性调节脉络膜的 SSN 部分。这些结果表明,ChBF 的控制可能与全身血压和全身血管的中枢控制有关。
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