Scharoun S L, Barone F C, Wayner M J, Jones S M
Brain Res Bull. 1984 Oct;13(4):573-83. doi: 10.1016/0361-9230(84)90040-6.
Horseradish peroxidase (HRP, Sigma Type VI) crystals were encased in a parafilm envelope and applied to the transected central ends of the left and right cervical vagus nerves and the anterior and posterior esophageal vagus nerves of adult male hooded rats. Injections of 30% HRP were made into the muscle wall of the fundus and antrum regions of the stomach. After 48 hr survival time, animals were perfused intracardially with a phosphate buffer plus sucrose wash followed by glutaraldehyde and paraformaldehyde fixative. The brain stem, spinal cord and corresponding dorsal root ganglia, superior cervical sympathetic ganglion, and the nodose ganglion were removed and cut into 50 micron sections. All tissue was processed with tetramethylbenzidine (TMB) for the blue reaction according to Mesulum and counterstained with neutral red. Sequential sections were examined under a microscope. Labeled neurons and nerve terminals were identified using bright and dark field condensers and polarized light. In tissue from animals that had HRP applied to the cervical vagus nerves, retrogradely labeled neurons were identified ipsilaterally in the medulla located in the dorsal motor nucleus of the vagus (DMN) and the nucleus ambiguus (NA). Labeled cells extended from the DMN into the spinal cord in ventral-medial and laminae X regions C1 and C2 of cervical segments. Many neurons were labeled in the nodose ganglion. Anterogradely labeled terminals were observed throughout and adjacent to the solitary nucleus (NTS) dorsal to the DMN and intermixed among labeled neurons located in the DMN. In tissue from animals that had HRP applied to the esophageal vagus nerves, similar labeling was observed. However, fewer neurons were identified in the NA, the nodose ganglion, and only in laminae X of the cervical spinal cord segments C1 and C2. Also, very little terminal labeling was observed in and adjacent to the NTS. Labeled neurons in tissue from animals that had HRP injected into the stomach wall were observed bilaterally in the DMN, nodose ganglion, and only in laminae X at the C1 and C2 levels of the spinal cord. Labeled neurons also were observed in the dorsal root ganglia of the thoracic cord. These data indicate that cervical cord and NA neurons are important in the supradiaphragmatic motor innervation by the vagus. Also, many afferents to the NTS originate above the diaphragm. In addition, some afferents from the stomach enter the central nervous system via the thoracic spinal cord.
辣根过氧化物酶(HRP,Sigma VI型)晶体被包裹在石蜡膜封套中,并应用于成年雄性带帽大鼠左右颈迷走神经以及食管迷走神经前后支的横断中央端。将30%的HRP注射到胃底和胃窦区域的肌壁中。在存活48小时后,经心脏用磷酸盐缓冲液加蔗糖冲洗,然后用戊二醛和多聚甲醛固定液灌注动物。取出脑干、脊髓以及相应的背根神经节、颈上交感神经节和结状神经节,并切成50微米厚的切片。所有组织按照Mesulum的方法用四甲基联苯胺(TMB)进行蓝色反应处理,并用中性红复染。连续切片在显微镜下检查。使用明场和暗场聚光镜以及偏振光来识别标记的神经元和神经末梢。在将HRP应用于颈迷走神经的动物组织中,在同侧延髓的迷走神经背运动核(DMN)和疑核(NA)中发现了逆行标记的神经元。标记的细胞从DMN延伸到脊髓颈段的腹内侧和X层C1和C2区域。在结状神经节中有许多神经元被标记。在DMN背侧的孤束核(NTS)及其周围观察到顺行标记的终末,并且与位于DMN中的标记神经元混合在一起。在将HRP应用于食管迷走神经的动物组织中,观察到类似的标记。然而,在NA、结状神经节中识别出的神经元较少,并且仅在颈脊髓节段C1和C2的X层中发现。此外,在NTS及其附近观察到的终末标记很少。在将HRP注射到胃壁的动物组织中,在DMN、结状神经节中双侧观察到标记的神经元,并且仅在脊髓C1和C2水平的X层中发现。在胸段脊髓的背根神经节中也观察到标记的神经元。这些数据表明,颈脊髓和NA神经元在迷走神经膈上运动神经支配中很重要。此外,许多传入NTS的神经纤维起源于膈肌上方。另外,一些来自胃的传入神经通过胸段脊髓进入中枢神经系统。