Daniel E E, Cowan W, Daniel V P
Can J Physiol Pharmacol. 1983 Nov;61(11):1247-73. doi: 10.1139/y83-183.
The ultrastructure of normal and neurotoxin-treated human detrusor muscle was studied to define the bases for myogenic and neurogenic control and to determine the extent and selectivity of effects of the toxins. No gap junctions were observed in the 30 strips studied but there were other cell-to-cell junctions which may allow cell-to-cell coupling. Nerve varicosities in the muscle bundles were present in high frequency (9 to 15 profiles per 100 muscle cell profiles); they sometimes formed close contacts with muscle and most were bare or partly bare of glial covering. They were often present as single axons or in bundles of only a few nerves. No myelinated nerves or nerve cell bodies were seen in or near muscle bundles. This muscle seemed to be designed primarily for neural control of contractile function with single nerves innervating discrete muscle regions. Most of the nerve varicosities contained a large majority of small agranular vesicles along with some large granular vesicles, but about 20% contained a few small granular vesicles as well. The proportion of the small granular vesicles was not increased but the percentage of varicosities containing them increased slightly after treatment with 5- or 6-hydroxydopamine. Scorpion venom seriously damaged 80% of nerve varicosities, sparing no particular class, but spared axons from structural damage. Beta-bungarotoxin had similar effects. 4-Aminopyridine did not induce gap junction formation but had neurotoxic effects. These data suggest that scorpion venom is a useful tool to eliminate selectively physiological functions dependent on synaptic vesicles, that all nerve types contain scorpion venom binding Na channels and that the persistent atropine- and tetrodotoxin-insensitive responses of this muscle involve mechanisms independent of synaptic vesicles observable by electron microscopy. The common occurrence of multilamellar membranous structures in bladder muscle cells was reported and their origin suggested.
研究了正常和经神经毒素处理的人逼尿肌的超微结构,以确定肌源性和神经源性控制的基础,并确定毒素作用的程度和选择性。在所研究的30条肌条中未观察到缝隙连接,但存在其他细胞间连接,这可能允许细胞间偶联。肌束中的神经膨体高频出现(每100个肌细胞轮廓中有9至15个轮廓);它们有时与肌肉形成紧密接触,大多数裸露或部分裸露神经胶质覆盖。它们常以单根轴突或仅几根神经的束状形式存在。在肌束内或其附近未见到有髓神经或神经细胞体。这种肌肉似乎主要是为收缩功能的神经控制而设计,单根神经支配离散的肌肉区域。大多数神经膨体含有绝大多数小的无颗粒小泡以及一些大的有颗粒小泡,但约20%也含有一些小的有颗粒小泡。在用5-或6-羟基多巴胺处理后,小的有颗粒小泡的比例没有增加,但含有它们的膨体百分比略有增加。蝎毒严重损伤了80%的神经膨体,无特定类型幸免,但轴突未受结构损伤。β-银环蛇毒素有类似作用。4-氨基吡啶未诱导缝隙连接形成,但有神经毒性作用。这些数据表明,蝎毒是一种有用的工具,可选择性消除依赖突触小泡的生理功能,所有神经类型均含有蝎毒结合钠通道,且该肌肉对阿托品和河豚毒素持续不敏感的反应涉及电子显微镜下可观察到的与突触小泡无关的机制。报道了膀胱肌细胞中多层膜结构的常见情况并提出了其来源。