Ezure K, Tanaka I
Department of Neurobiology, Tokyo Metropolitan Institute for Neuroscience, Japan.
Neuroreport. 2000 Jun 5;11(8):1709-12. doi: 10.1097/00001756-200006050-00023.
Pulmonary slowly adapting receptors (SARs) and rapidly adapting receptors (RARs) are important components of various respiratory reflexes. In anesthetized, paralyzed and artificially ventilated rats, we found an inhibitory linkage from the former to the latter system at the level of their second-order relay neurons (P cells and RAR cells, respectively). Lung inflation which activates RARs as well as SARs suppressed RAR cell activity evoked by electrical stimulation of the vagus nerve. Intracellular recordings from RAR cells showed IPSPs locked to electrical stimulation of the ipsilateral and contralateral vagus nerves at an intensity just above the threshold for P cell activation. Activation of P cells with glutamate suppressed RAR cell firing. Since P cells project to the area of RAR cells, taken together, these results strongly suggest that P cells synaptically inhibit RAR cells.
肺慢适应感受器(SARs)和快适应感受器(RARs)是各种呼吸反射的重要组成部分。在麻醉、麻痹并进行人工通气的大鼠中,我们发现在其二级中继神经元(分别为P细胞和RAR细胞)水平上,从前一个系统到后一个系统存在抑制性联系。激活RARs以及SARs的肺充气抑制了迷走神经电刺激诱发的RAR细胞活动。对RAR细胞的细胞内记录显示,在略高于P细胞激活阈值的强度下,与同侧和对侧迷走神经电刺激锁定的抑制性突触后电位(IPSPs)。用谷氨酸激活P细胞可抑制RAR细胞放电。由于P细胞投射到RAR细胞区域,综上所述,这些结果强烈表明P细胞通过突触抑制RAR细胞。