The physiological and pharmacological actions of noradrenaline (NA) on neurons of the medial septum and diagonal band of Broca (MSDB) were examined using extracellular, intracellular and whole-cell patch-clamp recordings in an in vitro rat brain slice preparation. 2. In current- and voltage-clamp recordings with KCl- or potassium gluconate-containing electrodes, bath-applied NA increased the number of tetrodoxin- and bicuculline-sensitive synaptic events in > 80% of cholinergic- and GABA-type neurons tested. The NA-induced synaptic activity originated from GABAergic neurons located within the MSDB itself, as a similar effect occurred in brain slices in which the MSDB had been surgically isolated from neighbouring structures. 3. In antidromic studies, NA dose-dependently increased firing in a subpopulation of septohippocampal neurons with fast conducting fibres (mean conduction velocity, 1.78 +/- 0.10 m s-1; presumably GABAergic). The NA excitation was mimicked by the alpha 1-agonist phenylephrine (PE) and blocked by the alpha 1-antagonists prazosin and WB-4101, suggesting the presence of alpha 1-receptors on septohippocampal GABAergic neurons. 4. Similarly, in whole-cell recordings in both cholinergic- and non-cholinergic-type MSDB neurons, prazosin blocked the effects of NA and PE mimicked the effects of NA by inducing IPSCs with a similar amplitude distribution. 5. Consistent with the above findings, GABA-type neurons that responded directly to NA and PE with a prazosin-sensitive inward current were found within the MSDB. 6. In conclusion, NA, via alpha 1-adrenoceptors, excites MSDB septohippocampal GABAergic neurons and influences both septal and septohippocampal circuitry.
摘要
采用细胞外、细胞内和全细胞膜片钳记录技术,在体外大鼠脑片制备中研究了去甲肾上腺素(NA)对内侧隔核和布罗卡斜角带(MSDB)神经元的生理和药理作用。2. 在使用含氯化钾或葡萄糖酸钾电极的电流钳和电压钳记录中,浴加NA使超过80%受试的胆碱能和GABA能神经元中对河豚毒素和荷包牡丹碱敏感的突触事件数量增加。NA诱导的突触活动源于MSDB本身内的GABA能神经元,因为在MSDB已从相邻结构手术分离的脑片中也出现了类似效应。3. 在逆向刺激研究中,NA剂量依赖性地增加了一群具有快速传导纤维(平均传导速度,1.78±0.10 m s-1;推测为GABA能)的隔海马神经元的放电。NA兴奋作用可被α1激动剂苯肾上腺素(PE)模拟,并被α1拮抗剂哌唑嗪和WB-4101阻断,提示隔海马GABA能神经元上存在α1受体。4. 同样,在胆碱能和非胆碱能型MSDB神经元的全细胞记录中,哌唑嗪阻断了NA的作用,而PE通过诱导具有相似幅度分布的抑制性突触后电流(IPSCs)模拟了NA的作用。5. 与上述发现一致,在MSDB内发现了直接对NA和PE产生哌唑嗪敏感内向电流反应的GABA能神经元。6. 总之,NA通过α1肾上腺素能受体兴奋MSDB隔海马GABA能神经元,并影响隔核和隔海马环路。