Oyama Yuji, Iigaya Kamon, Minoura Yoshino, Okabe Toshitaka, Izumizaki Masahiko, Onimaru Hiroshi
Department of Physiology, Showa University School of Medicine, 1-5-8 Hatanodai, Shinagawa-ku, Tokyo, 142-8555, Japan.
Division of Cardiology and Cardiac Catheterization Laboratories, Showa University Northern Yokohama Hospital, 35-1 Chigasaki-Chuo, Tsuzuki, Yokohama, Kanagawa, 224-8503, Japan.
J Physiol Sci. 2017 Sep;67(5):629-635. doi: 10.1007/s12576-017-0549-5. Epub 2017 Jun 10.
Newborn rat brainstem-spinal cord preparations are useful for in vitro analysis of various brainstem functions including respiratory activity. When studying the central control of sympathetic nerve activity (SNA), it is important to record peripheral outputs of the SNA. We developed an in vitro preparation in which neuronal connections between the cardiovascular center in the medulla and SNA peripheral outputs are preserved. Zero- to 1-day-old rats were deeply anesthetized with isoflurane, and the brainstem and spinal cord were isolated with a partial right thoracic cage to record sympathetic nerve discharge from the right thoracic sympathetic nerve trunk (T9-T11). SNA in this preparation was strongly modulated by inspiratory activity. Single-shot electrical stimulation of the ipsilateral rostral ventrolateral medulla (RVLM) induced a transient increase of SNA. Bath application of angiotensin II induced an increase of SNA, and local ipsilateral microinjection of angiotensin II to the RVLM induced a transient increase of SNA. This preparation allows analysis of the central control of the SNA in vitro.
新生大鼠脑干-脊髓标本对于体外分析包括呼吸活动在内的各种脑干功能很有用。在研究交感神经活动(SNA)的中枢控制时,记录SNA的外周输出很重要。我们开发了一种体外标本,其中延髓心血管中枢与SNA外周输出之间的神经元连接得以保留。将0至1日龄的大鼠用异氟醚深度麻醉,分离出脑干和脊髓,并带有部分右胸笼,以记录右侧胸交感神经干(T9-T11)的交感神经放电。该标本中的SNA受到吸气活动的强烈调节。单次电刺激同侧头端延髓腹外侧区(RVLM)可引起SNA短暂增加。浴槽中加入血管紧张素II可引起SNA增加,向RVLM局部同侧微量注射血管紧张素II可引起SNA短暂增加。这种标本允许在体外分析SNA的中枢控制。