Tanaka Junichi, Mashiko Norifumi, Kawakami Ayako, Hatakenaka Satoko, Fujisawa Shigeko, Nomura Masahiko
Department of Curriculum, Teaching and Memory, Naruto University of Education, Naruto, Tokushima 772-8502, Japan.
Neurosci Lett. 2002 Oct 25;332(1):41-4. doi: 10.1016/s0304-3940(02)00913-8.
Electrical stimulation of the A1 noradrenergic region of the ventrolateral medulla produced synatic excitation (n = 19, 9%), inhibition (n = 5, 2%) or no effect (n = 184, 89%) in the activity of a total of 208 neurons in the subfornical organ (SFO) in male rats under urethane anesthesia. Almost all (n = 18) of the excitatory responses (n = 19) were blocked by microiontophoretically-applied phentolamine, an alpha-adrenergic antagonist, but not by timolol, a beta-adrenergic antagonist. The inhibitory response of all the neurons (n = 5) tested was prevented by iontophoretically applied timolol, but not by phentolamine. Approximately a half (n = 9) of SFO neurons that demonstrated the excitatory response to A1 region stimulation exhibited an increase in neuronal activity in response to hemorrhage (10 ml/kg b.w.t.), while remaining neurons (n = 10) were unresponsive. Hemorrhage did not cause any change in the activity of all the neurons (n = 5) that demonstrated the inhibitory response to A1 region stimulation. These results suggest that the medullary inputs to approximately 10% of SFO neurons tested are mediated by alpha-adrenergic excitatory and beta-adrenergic inhibitory pathways, and imply that a part of the excitatory pathways may transmit the peripheral baroreceptor information.
在乌拉坦麻醉的雄性大鼠中,电刺激延髓腹外侧的A1去甲肾上腺素能区域,终板器官(SFO)中总共208个神经元的活动产生突触兴奋(n = 19,9%)、抑制(n = 5,2%)或无影响(n = 184,89%)。几乎所有(n = 18)的兴奋反应(n = 19)都被微离子透入法施加的α-肾上腺素能拮抗剂酚妥拉明阻断,但未被β-肾上腺素能拮抗剂噻吗洛尔阻断。所有被测试神经元(n = 5)的抑制反应都被离子透入法施加的噻吗洛尔阻止,但未被酚妥拉明阻止。对A1区域刺激表现出兴奋反应的SFO神经元中约一半(n = 9)在出血(10 ml/kg体重)后神经元活动增加,而其余神经元(n = 10)无反应。出血对所有对A1区域刺激表现出抑制反应的神经元(n = 5)的活动没有任何影响。这些结果表明,延髓对约10%被测试的SFO神经元的输入由α-肾上腺素能兴奋和β-肾上腺素能抑制途径介导,这意味着部分兴奋途径可能传递外周压力感受器信息。