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猕猴(食蟹猴)肾脏神经支配的起源

Origins of the renal innervation in the primate, Macaca fascicularis.

作者信息

Marfurt C F, Echtenkamp S F, Jones M A

机构信息

Department of Anatomy, Indiana University School of Medicine, Gary 46408.

出版信息

J Auton Nerv Syst. 1989 Jul;27(2):113-26. doi: 10.1016/0165-1838(89)90093-3.

DOI:10.1016/0165-1838(89)90093-3
PMID:2476474
Abstract

The origins of the renal efferent and afferent nerves in 5 cynomolgus monkeys (Macaca fascicularis) were studied by using the retrograde transport of horseradish peroxidase (HRP) and horseradish peroxidase-wheat germ agglutinin (HRP-WGA). The cut ends of the right renal nerves were soaked for 30-45 min in solutions consisting of 15% HRP and 1% HRP-WGA. Three or four days later the animals were killed and the tissues examined for the presence of retrogradely labeled neurons, HRP-filled cells were observed, with rare exceptions, only in ganglia ipsilateral to the side of tracer application. Renal efferent neurons (4648-14565 cells per animal) were found in relatively equal numbers in prevertebral and paravertebral (sympathetic chain) ganglia. Labeled prevertebral cells were distributed among the renal (52%), aorticorenal (32%) and superior mesenteric (16%) ganglia, whereas labeled paravertebral neurons were mainly located in chain ganglia T11-L3, with 94% of these located in L1-3. Labeled renal sensory neurons (31-543 per animal) constituted less than 5% of all labeled cells and were found in ipsilateral dorsal root ganglia T10-L3, with (80%) in T12 and L1. The labeled sensory neurons ranged from 18-64 microns in diameter (X = 32.4 microns). With the exception of a single cell in one animal, no labeled neurons were observed in the nodose ganglia. Many parallels were observed between the organization of the renal plexuses of macaques and humans, suggesting the utility of the non-human primate as an experimental model for functional studies of renal innervation in humans.

摘要

利用辣根过氧化物酶(HRP)和辣根过氧化物酶-小麦胚凝集素(HRP-WGA)的逆行运输法,对5只食蟹猴(猕猴)的肾传出神经和传入神经的起源进行了研究。将右侧肾神经的断端浸泡在含有15% HRP和1% HRP-WGA的溶液中30 - 45分钟。三四天后处死动物,检查组织中是否存在逆行标记的神经元。除极少数情况外,仅在应用示踪剂一侧的同侧神经节中观察到HRP填充的细胞。在椎前和椎旁(交感神经链)神经节中发现的肾传出神经元数量相对相等(每只动物4648 - 14565个细胞)。标记的椎前细胞分布在肾神经节(52%)、主动脉肾神经节(32%)和肠系膜上神经节(16%)之间,而标记的椎旁神经元主要位于T11 - L3节段的神经链神经节中,其中94%位于L1 - 3。标记的肾感觉神经元(每只动物31 - 543个)占所有标记细胞的比例不到5%,位于同侧T10 - L3背根神经节中,其中80%位于T12和L1。标记的感觉神经元直径在18 - 64微米之间(平均值 = 32.4微米)。除一只动物中的单个细胞外,在结状神经节中未观察到标记的神经元。在猕猴和人类的肾丛组织之间观察到许多相似之处,这表明非人类灵长类动物作为人类肾神经支配功能研究的实验模型具有实用性。

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