Barber W D, Yuan C S, Burks T F, Feldman J L, Greer J J
Department of Anatomy, College of Medicine, University of Arizona, Tucson 85724, USA.
J Auton Nerv Syst. 1995 Mar 2;51(3):181-9. doi: 10.1016/0165-1838(94)00129-8.
An in vitro neonatal rat preparation, consisting of the isolated caudal brainstem and stomach joined by the intact vagi, was developed using Sprague-Dawley rats. The animals were 0 to 4 days of age. This preparation provided an opportunity to investigate the extracellular and intracellular responses of neurons in the nucleus tractus solitarius (NTS) of the brainstem to electrical stimulation of subdiaphragmatic vagal fibers. The dorsal and ventral vagal branches were electrically stimulated at the point of the common subdiaphragmatic vagal trunk. The isolated preparation was superfused in a recording chamber at 28 degrees C with a modified Krebs solution, equilibrated with 95% O2 and 5% CO2. Suction microelectrodes, for electrical stimulation, were positioned on the common vagal trunk just below the diaphragm to evaluate extracellular and intracellular evoked responses in NTS. A total of 204 subdiaphragmatic vagally-evoked (SDVe) brainstem unitary responses in the NTS were recorded. The mean latency of the extracellular SDVe brainstem responses was 89 +/- 12.9 ms (mean +/- SD). The peripheral gastric effects of CCK-8 on SDVe unitary responses in NTS neurons were evaluated. The peptide caused a significant increase in the excitability of these NTS neurons which was blocked by the CCKA receptor antagonist L-364,718. Neurons in the NTS and the dorsal motor nucleus of the vagus which showed excitatory responses to vagal stimulation were filled with Lucifer Yellow to evaluate their morphology.
使用斯普拉格-道利大鼠建立了一种体外新生大鼠制备模型,该模型由孤立的尾端脑干和通过完整迷走神经相连的胃组成。动物年龄为0至4天。该制备模型为研究脑干孤束核(NTS)中神经元对膈下迷走神经纤维电刺激的细胞外和细胞内反应提供了机会。在膈下迷走神经总干处对迷走神经的背支和腹支进行电刺激。将分离的制备模型置于记录室中,在28℃下用改良的克雷布斯溶液进行灌流,该溶液用95% O₂和5% CO₂平衡。用于电刺激的吸引导电极置于膈下迷走神经总干刚好在膈肌下方的位置,以评估NTS中的细胞外和细胞内诱发反应。共记录了NTS中204个膈下迷走神经诱发(SDVe)的脑干单位反应。细胞外SDVe脑干反应的平均潜伏期为89±12.9毫秒(平均值±标准差)。评估了CCK-8对NTS神经元中SDVe单位反应的外周胃效应。该肽导致这些NTS神经元的兴奋性显著增加,这被CCKA受体拮抗剂L-364,718阻断。对迷走神经刺激表现出兴奋反应的NTS和迷走神经背运动核中的神经元用荧光黄填充以评估其形态。