Vera P L, Nadelhaft I
Veteran's Administration Medical Center, R&D Service (151), Bay Pines, FL 33744, USA.
Brain Res. 2000 Nov 10;883(1):107-18. doi: 10.1016/s0006-8993(00)02732-3.
We labeled interneurons in the L1-L2 and L6-S1 spinal cord segments of the rat that are involved in bladder innervation using transneuronal retrograde transport of pseudorabies virus (PRV) in normal animals and in animals with selected nerve transections. Preganglionic neurons were identified using antisera against choline acetyltransferase (ChAT). In some experiments we labelled parasympathetic preganglionic neurons (PPNs) in the L6-S1 spinal cord by retrograde transport of Fluorogold from the major pelvic ganglion. We identified bladder afferent terminals using the transganglionic transport of the anterograde tracer cholera toxin subunit b. We present anatomical evidence for two spinal pathways involved in innervation of the bladder. First, in the intact rat, afferent information from the bladder connects, via interneurons in L6-S1, to the PPNs that provide the efferent innervation of the bladder. The afferent terminals were located mainly in close apposition to interneurons located dorsal to the retrogradely labeled PPNs. Second, using L6-S1 ganglionectomies or L6-S1 ventral root rhizotomies we limited viral transport to the sympathetic pathways innervating the bladder. This procedure also labelled interneurons (but not PPNs) with PRV in the L6-S1 spinal cord in a location very similar to those described in the intact rat. These interneurons also receive bladder afferent terminals but we propose that they project to sympathetic preganglionic neurons, most of which are in the L1-L2 spinal segments. Based on this anatomical evidence, we propose the existence of two spinal reflex pathways involved in micturition: a pathway limited to a reflex arc in the pelvic nerve (presumably excitatory to the detrusor muscle); and a pathway involving the pelvic nerve and sympathetic nerve fibers, some of which may travel in the hypogastric (presumably inhibitory to the detrusor muscle).
我们利用伪狂犬病病毒(PRV)在正常动物和进行了特定神经横断的动物中的跨神经元逆行运输,标记了大鼠L1-L2和L6-S1脊髓节段中参与膀胱神经支配的中间神经元。使用抗胆碱乙酰转移酶(ChAT)的抗血清鉴定节前神经元。在一些实验中,我们通过从主要盆神经节逆行运输荧光金来标记L6-S1脊髓中的副交感节前神经元(PPN)。我们利用顺行示踪剂霍乱毒素亚基b的跨神经节运输来鉴定膀胱传入终末。我们提供了解剖学证据,证明存在两条参与膀胱神经支配的脊髓通路。首先,在完整大鼠中,来自膀胱的传入信息通过L6-S1中的中间神经元,连接到为膀胱提供传出神经支配的PPN。传入终末主要位于与逆行标记的PPN背侧的中间神经元紧密相邻处。其次,通过L6-S1神经节切除术或L6-S1腹侧神经根切断术,我们将病毒运输限制在支配膀胱的交感神经通路。该操作还在L6-S1脊髓中用PRV标记了中间神经元(但不是PPN),其位置与完整大鼠中描述的非常相似。这些中间神经元也接收膀胱传入终末,但我们认为它们投射到交感节前神经元,其中大多数位于L1-L2脊髓节段。基于这一解剖学证据,我们提出存在两条参与排尿的脊髓反射通路:一条限于盆神经中的反射弧(可能对逼尿肌有兴奋作用);另一条涉及盆神经和交感神经纤维,其中一些可能走行于腹下神经(可能对逼尿肌有抑制作用)。