Guy J, Bosler O, Dusticier G, Pelletier G, Calas A
Laboratoire de Physiologie des Interactions Cellulaires, UA 339 CNRS, Université de Bordeaux I, Talence, France.
Cell Tissue Res. 1987 Dec;250(3):657-62. doi: 10.1007/BF00218960.
The morphological substrate of putative serotonin (5-HT)/neuropeptide Y (NPY) interactions in the suprachiasmatic nucleus (SCN) was investigated by combined radioautography and immunocytochemistry after intraventricular administration of (3H)5-HT in the rat. In the ventral portion of the SCN, the distribution of (3H)5-HT uptake sites overlapped closely the NPY-immunoreactive terminals. Previous investigations have shown that the dense 5-HT and NPY innervations of the SCN originate in different structures, i.e., the midbrain raphe nuclei and the ventral lateral geniculate nucleus, respectively. Accordingly, in the present study, destruction of 5-HT afferents by 5,7-dihydroxytryptamine was not found to induce any modification in NPY staining and, in ultrastructural immuno-radioautographic preparations, two distinct pools of axonal varicosities could be identified. Both 5-HT and NPY terminals established morphologically defined synaptic junctions, sometimes on the same neuronal target. Some cases of direct axo-axonic appositions between the two types of terminals were also encountered. These data constitute additional criteria for characterizing the cytological basis of the multiple transmitter interactions presumably involved in the function of the SCN as a central regulator of circadian biological rhythms.
在大鼠脑室内注射(3H)5-羟色胺后,通过联合放射自显影和免疫细胞化学方法,研究了视交叉上核(SCN)中假定的5-羟色胺(5-HT)/神经肽Y(NPY)相互作用的形态学基础。在SCN的腹侧部分,(3H)5-HT摄取位点的分布与NPY免疫反应性终末紧密重叠。先前的研究表明,SCN中密集的5-HT和NPY神经支配分别起源于不同的结构,即中脑缝核和腹外侧膝状核。因此,在本研究中,未发现用5,7-二羟基色胺破坏5-HT传入纤维会引起NPY染色的任何改变,并且在超微结构免疫放射自显影片中,可以识别出两个不同的轴突膨体池。5-HT和NPY终末都形成了形态学上确定的突触连接,有时在同一神经元靶点上。还遇到了两种终末之间直接轴-轴并置的一些情况。这些数据为表征可能参与SCN作为昼夜生物节律中央调节器功能的多种递质相互作用的细胞学基础提供了额外的标准。