Izumi H, Ito Y, Sato M, Karita K, Iwatsuki N
Department of Physiology, Tohoku University School of Dentistry, Sendai, Japan.
Am J Physiol. 1997 Jul;273(1 Pt 2):R168-74. doi: 10.1152/ajpregu.1997.273.1.R168.
The present experiments were designed to examine the effects of inhalation anesthetics (isoflurane, halothane, and sevoflurane) on the parasympathetic reflex vasodilation in the lower lip and palate elicited by electrical stimulation of the central cut end of the lingual nerve in vagosympathectomized cats. Isoflurane (1.5%), halothane (1.0%), and sevoflurane (2.5%), each at a concentration of 1.0 minimum alveolar concentration, markedly suppressed the evoked blood flow increases in the lower lip, whereas nitrous oxide (70% in 30% oxygen) and morphine (2 mg/kg iv) did not. Prior administration of picrotoxin, a gamma-aminobutyric acid (GABA) antagonist (2 mg/kg iv), reversed the inhibitory effect of isoflurane on the parasympathetic reflex response. Decerebration had no significant effect on the isoflurane-induced inhibition. These findings suggest that there is a GABA-mediated suppressive mechanism acting on this parasympathetic reflex response; the sites at which inhalation anesthetics exert such an inhibitory action could be in the midbrain, pons, or medulla, but not in the hypothalamus or higher structure.
本实验旨在研究吸入麻醉药(异氟烷、氟烷和七氟烷)对迷走神经交感神经切除猫舌神经中枢切断端电刺激引起的下唇和腭部副交感神经反射性血管舒张的影响。异氟烷(1.5%)、氟烷(1.0%)和七氟烷(2.5%),每种浓度为1.0最低肺泡浓度,均显著抑制下唇诱发的血流增加,而氧化亚氮(70%含30%氧气)和吗啡(2mg/kg静脉注射)则无此作用。预先静脉注射γ-氨基丁酸(GABA)拮抗剂苦味毒(2mg/kg)可逆转异氟烷对副交感神经反射反应的抑制作用。去大脑对异氟烷诱导的抑制无显著影响。这些发现表明,存在一种GABA介导的抑制机制作用于这种副交感神经反射反应;吸入麻醉药发挥这种抑制作用的部位可能在中脑、脑桥或延髓,而不在下丘脑或更高结构。