Bickford M E, Günlük A E, Guido W, Sherman S M
Department of Neurobiology, State University of New York, Stony Brook 11794-5230.
J Comp Neurol. 1993 Aug 15;334(3):410-30. doi: 10.1002/cne.903340307.
We investigated the source of axons and terminals in the cat's lateral geniculate nucleus that stain positively for NADPH-diaphorase. The functional significance of such staining is that NADPH-diaphorase is identical to the enzyme nitric oxide synthetase, and thus it is thought to reveal cells and axons that use nitric oxide as a neuromodulator. Within the lateral geniculate and adjacent perigeniculate nuclei, a dense network of axons and terminals is labeled for NADPH-diaphorase. The pattern of NADPH-diaphorase staining here is remarkably similar to that of choline acetyltransferase (ChAT) staining, suggesting that the source of these axons and terminals might be the parabrachial region of the brainstem because this provides the major cholinergic input to the lateral geniculate nucleus. In other areas of the brain to which parabrachial axons project, there is also a similar staining pattern for NADPH-diaphorase and ChAT. Furthermore, the patterns of cell staining within the parabrachial region for NADPH-diaphorase and ChAT are virtually identical. However, the relationship between ChAT and NADPH-diaphorase staining for the parabrachial region is not a general property of cholinergic neurons. Other cholinergic cells and axons, such as the trochlear nerve, the oculomotor nerve and nucleus, and the parabigeminal nucleus, which all label densely for ChAT, stain poorly or not at all for NADPH-diaphorase. It is significant that the parabigeminal nucleus, which provides a cholinergic input to the lateral geniculate nucleus, has no cells that label for NADPH-diaphorase. We used double labeling methods to identify further the source of NADPH-diaphorase staining in the lateral geniculate nucleus. We found that parabrachial cells co-localize NADPH-diaphorase and ChAT. Noradrenergic and serotoninergic cells in the brainstem also innervate the lateral geniculate nucleus, but we found that none of these co-localize NADPH-diaphorase. Finally, by combining NADPH-diaphorase histochemistry with retrograde labeling of cells that project to the lateral geniculate nucleus, we found that the cholinergic cells of the parabrachial region are essentially the sole source of NADPH-diaphorase in the lateral geniculate nucleus. We thus conclude that cells from the parabrachial region that innervate the lateral geniculate nucleus use both acetylcholine and nitric oxide for neurotransmission, and that this is virtually the only afferent input to this region that uses nitric oxide.
我们研究了猫外侧膝状核中对还原型辅酶Ⅱ-黄递酶(NADPH-d)呈阳性染色的轴突和终末的来源。这种染色的功能意义在于,NADPH-d与一氧化氮合酶是同一种酶,因此人们认为它能揭示那些以一氧化氮作为神经调质的细胞和轴突。在外侧膝状核及相邻的膝周核内,有一个密集的轴突和终末网络被标记为NADPH-d。此处NADPH-d的染色模式与胆碱乙酰转移酶(ChAT)的染色模式极为相似,这表明这些轴突和终末的来源可能是脑干的臂旁区域,因为该区域为外侧膝状核提供了主要的胆碱能输入。在臂旁轴突投射到的脑的其他区域,也存在类似的NADPH-d和ChAT染色模式。此外,臂旁区域内NADPH-d和ChAT的细胞染色模式几乎完全相同。然而,臂旁区域ChAT与NADPH-d染色之间的关系并非胆碱能神经元的普遍特性。其他胆碱能细胞和轴突,如滑车神经、动眼神经及其核以及脑桥旁核,它们都对ChAT有密集标记,但对NADPH-d染色不佳或根本不染色。重要的是,为外侧膝状核提供胆碱能输入的脑桥旁核没有对NADPH-d进行标记的细胞。我们使用双重标记方法进一步确定外侧膝状核中NADPH-d染色的来源。我们发现臂旁细胞同时表达NADPH-d和ChAT。脑干中的去甲肾上腺素能和5-羟色胺能细胞也支配外侧膝状核,但我们发现它们都不与NADPH-d共定位。最后,通过将NADPH-d组织化学与投射到外侧膝状核的细胞的逆行标记相结合,我们发现臂旁区域的胆碱能细胞基本上是外侧膝状核中NADPH-d的唯一来源。因此,我们得出结论,支配外侧膝状核的臂旁区域的细胞在神经传递中同时使用乙酰胆碱和一氧化氮,并且这几乎是该区域使用一氧化氮的唯一传入输入。