Niel J P, Gonella J, Roman C
J Physiol (Paris). 1980 Nov;76(6):591-9.
The localization of the parasympathetic preganglionic and sympathetic postganglionic neuronal cell bodies innervating the lower oesophageal sphincter (l.o.s.) has been investigated in cats, using the technique of horseradish peroxidase (HRP) retrograde axonal transport. HRP was injected into the sphincteric muscle layers (under aseptic conditions). The animals were sacrificed 72 hours later and fixed by perfusion via the aorta. The medulla oblongata and the sympathetic chains from the stellate to T12 ganglia were removed and processed for HRP identification. 1. Labelled cell bodies were identified in the medulla, the stellate and other thoracic ganglia and in the caeliac ganglia. 2. In the medulla, the labelled neurones were located mainly in the vagal dorsal motor nucleus and, to a lesser extent, in the nucleus ambiguus. A few cell bodies were observed between both nuclei. The medullary labelled cell bodies are presumably those of the preganglionic vagal neurones innervating the l.o.s. 3. In the stellate ganglia, the labelled neurones were exclusively located in the ventromedial area. It is likely that they correspond to the postganglionic adrenergic neurones of the sympathetic pathway controlling the lower oesophageal sphincter, the axons of which leave the ganglia through cardiac branches and pass in the thoracic vagus nerve to reach the sphincter (see GONELLA et al., 1979). 4. Labelled neurones were no longer observed in the medulla and in the stellate ganglia when HRP was injected in the l.o.s. after a thoracic bilateral vagotomy. 5. Labelled neurones were also observed in other thoracic ganglia from T3 to T11, most of them lying in T9 and T10. They are probably the postganglionic neurones of a second sympathetic pathway controlling the lower oesophageal sphincter, via the splanchnic nerve (see GONELLA et al., 1979). 6. A homogenous distribution of labelled neurones has been observed in the caeliac ganglia. Its functional significance is discussed.
运用辣根过氧化物酶(HRP)逆行轴突运输技术,对支配猫食管下括约肌(l.o.s.)的副交感神经节前神经元和交感神经节后神经元细胞体的定位进行了研究。在无菌条件下,将HRP注入括约肌肌层。72小时后处死动物,并通过主动脉灌注进行固定。取出延髓以及从星状神经节到T12神经节的交感神经链,进行HRP鉴定处理。1. 在延髓、星状神经节和其他胸段神经节以及腹腔神经节中发现了标记的细胞体。2. 在延髓中,标记的神经元主要位于迷走神经背运动核,在疑核中的数量较少。在两个核之间观察到一些细胞体。延髓中标记的细胞体可能是支配食管下括约肌的迷走神经节前神经元的细胞体。3. 在星状神经节中,标记的神经元仅位于腹内侧区域。它们可能对应于控制食管下括约肌的交感神经通路的节后肾上腺素能神经元,其轴突通过心脏分支离开神经节,经胸段迷走神经到达括约肌(见GONELLA等人,1979年)。4. 双侧胸段迷走神经切断后,在食管下括约肌注射HRP时,延髓和星状神经节中不再观察到标记的神经元。5. 在T3至T11的其他胸段神经节中也观察到标记的神经元,其中大多数位于T9和T10。它们可能是通过内脏神经控制食管下括约肌的第二条交感神经通路的节后神经元(见GONELLA等人,1979年)。6. 在腹腔神经节中观察到标记神经元的均匀分布。对其功能意义进行了讨论。