Aicher S A, Kurucz O S, Reis D J, Milner T A
Department of Neurology and Neuroscience, Cornell University Medical College, New York, NY 10021, USA.
Brain Res. 1995 Sep 25;693(1-2):51-63. doi: 10.1016/0006-8993(95)00660-i.
The caudal ventrolateral medulla (CVL) contains neurons that are vasodepressor and are a critical component of the baroreceptor reflex pathway. While electrophysiological studies suggest that CVL neurons are intercalated in the baroreceptor pathway between the nucleus tractus solitarius (NTS) and the rostral ventrolateral medulla (RVL), there is no direct evidence for this projection. Therefore, we identified CVL neurons that project to RVL by retrogradely labelling them with wheat germ agglutinin-apo-horseradish peroxidase conjugated to colloidal gold (WAHG) injected into the RVL. Retrogradely labelled neurons were seen in previously identified vasodepressor areas of the rostral CVL that are critical for the baroreceptor reflex. Double labelling for WAHG and tyrosine hydroxylase (TH) immunocytochemistry indicated that CVL neurons that project to the RVL (CVL --> RVL neurons) are distinct from the noradrenergic neurons of the A1 cell group. To establish the presence of a direct projection from the NTS to CVL --> RVL neurons, the retrograde tracer WAHG was pressure injected into the RVL and the anterograde tracer biocytin was iontophoresed into the NTS of anesthetized rats. After 4-6 h, anesthetized rats were perfused transcardially with 3.75% acrolein in 2% paraformaldehyde and sections through the CVL were processed for both markers. By light microscopy, numerous biocytin-labelled varicose processes overlapped neurons containing WAHG in the CVL. By electron microscopy, biocytin was found in myelinated and unmyelinated axons and in axon terminals (0.9 + 0.02 microns) that contained primarily small clear vesicles. These terminals formed predominantly asymmetric synapses on large (1.5-6.0 microns in diameter) dendrites within the CVL. Some of the post-synaptic perikarya and large dendrites contained WAHG associated with lysosomes and multivesicular bodies, indicating that they belong to neurons which project to the RVL. We conclude that CVL --> RVL neurons are (a) distinct from A1 noradrenergic cells; (b) receive direct synaptic contacts from NTS efferent terminals; (c) are potently and monosynaptically excited (asymmetric synapses) by NTS efferent terminals. These data support the hypothesis that CVL neurons are intercalated between the NTS and the RVL in the baroreceptor reflex pathway.
延髓尾端腹外侧区(CVL)含有具有血管减压作用的神经元,是压力感受器反射通路的关键组成部分。虽然电生理研究表明CVL神经元插在孤束核(NTS)和延髓头端腹外侧区(RVL)之间的压力感受器通路中,但尚无该投射的直接证据。因此,我们通过向RVL注射与胶体金偶联的麦胚凝集素 - 脱辅基辣根过氧化物酶(WAHG)逆行标记,来识别投射至RVL的CVL神经元。在先前确定的对压力感受器反射至关重要的头端CVL血管减压区域中可见逆行标记的神经元。对WAHG和酪氨酸羟化酶(TH)免疫细胞化学进行双重标记表明,投射至RVL的CVL神经元(CVL→RVL神经元)与A1细胞群的去甲肾上腺素能神经元不同。为了确定从NTS到CVL→RVL神经元是否存在直接投射,将逆行示踪剂WAHG压力注射到RVL中,并将顺行示踪剂生物胞素离子电泳到麻醉大鼠的NTS中。4 - 6小时后,用含3.75%丙烯醛的2%多聚甲醛经心灌注麻醉大鼠,对通过CVL的切片进行两种标记物的处理。通过光学显微镜观察,在CVL中,大量生物胞素标记的曲张突起与含有WAHG的神经元重叠。通过电子显微镜观察,在有髓和无髓轴突以及主要含有小而清亮囊泡的轴突终末(0.9 + 0.02微米)中发现了生物胞素。这些终末主要在CVL内的大(直径1.5 - 6.0微米)树突上形成不对称突触。一些突触后胞体和大树突含有与溶酶体和多囊泡体相关的WAHG,表明它们属于投射至RVL的神经元。我们得出结论,CVL→RVL神经元:(a)与A1去甲肾上腺素能细胞不同;(b)接受来自NTS传出终末的直接突触联系;(c)被NTS传出终末强烈且单突触兴奋(不对称突触)。这些数据支持了CVL神经元在压力感受器反射通路中插在NTS和RVL之间的假说。