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首页> 外文期刊>The Journal of Comparative Neurology >Ultrastructural evidence for direct projections from the pontine micturition center to glycine-immunoreactive neurons in the sacral dorsal gray commissure in the cat.
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Ultrastructural evidence for direct projections from the pontine micturition center to glycine-immunoreactive neurons in the sacral dorsal gray commissure in the cat.

机译:从脑桥排尿中心直接投射到猫the背灰色连合中甘氨酸免疫反应神经元的超微结构证据。

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摘要

During micturition, according to the concept of Blok, Holstege, and colleagues ([1997] Neurosci. Lett. 233:109-112), the pontine micturition center (PMC) elicits bladder contraction by way of direct excitation of the parasympathetic bladder motoneurons. At the same time, the PMC elicits relaxation of the external urethral sphincter (EUS) by excitation of gamma-aminobutyric acid (GABA)-ergic interneurons in the sacral dorsal gray commissure (DGC), which, in turn, inhibit EUS motoneurons. The question is whether the inhibitory neurotransmitter glycine is also involved in this system. The present study investigated, first, whether there are glycine immunoreactive interneurons in the sacral DGC and, second, whether they receive direct PMC afferents. Finally, it was determined whether glycine and GABA are colocalized in DGC interneurons. In two adult male cats, the PMC was identified by electrical stimulation. Subsequently, the identified region was injected with the anterograde tracer WGA-HRP. Sections of sacral cord segments were processed for light and electron microscopic detection of anterograde labeling, as well as for glycine and GABA, using postembedding immunogold labeling with antibodies. In total 128 labeled PMC terminals were found in the DGC, which contained many round vesicles and asymmetric synapses. About 31.3% (40 of 128) made contact with glycine-immunoreactive dendrites. Eleven of them were selected for serial sectioning, which showed that 54.6% (6 of 11) of the glycine-immunoreactive dendrites were also immunoreactive for GABA. The results demonstrate that the PMC projects directly to dendrites of interneurons in the sacral DGC, which are immunoreactive for both glycine and GABA. These interneurons are thought to inhibit the EUS motoneurons during micturition.
机译:在排尿期间,根据Blok,Holstege及其同事的概念([1997] Neurosci。Lett。233:109-112),桥脑排尿中心(PMC)通过副交感神经系统膀胱运动神经元的直接激发来引起膀胱收缩。同时,PMC通过激发the背灰色连合部(DGC)中的γ-氨基丁酸(GABA)增能中神经元而引起尿道外括约肌(EUS)的松弛,进而抑制EUS运动神经元。问题是抑制性神经递质甘氨酸是否也参与该系统。本研究首先调查the骨DGC中是否存在甘氨酸免疫反应性中间神经元,其次调查它们是否接受直接PMC传入。最后,确定甘氨酸和GABA是否在DGC间神经元中共定位。在两只成年雄性猫中,通过电刺激鉴定出PMC。随后,向识别出的区域注射顺行示踪剂WGA-HRP。使用植入后的免疫金标抗体处理for神经节的切片,以进行光学和电子显微镜检测顺行性标记以及甘氨酸和GABA。在DGC中总共发现了128个标记的PMC末端,其中包含许多圆形囊泡和不对称突触。约31.3%(128个中的40)与甘氨酸免疫反应性树突接触。选择了其中的11个进行连续切片,结果表明54.6%(11个中的6个)的甘氨酸免疫反应性树突对GABA也具有免疫反应性。结果表明,PMC直接投射到s DGC中的中间神经元树突上,这些树突对甘氨酸和GABA都具有免疫活性。这些中间神经元被认为在排尿期间抑制EUS运动神经元。

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