Brazhnik E S, Vinogradova O S
Brain Res. 1986 Aug 13;380(1):94-106. doi: 10.1016/0006-8993(86)91433-2.
The drugs, described as blocking the high-frequency (pentobarbital) or low-frequency (scopolamine, atropine) theta rhythm of the hippocampal electroencephalogram, were tested upon the rhythmically bursting septal cells. Three groups of chronic, unanaesthetized rabbits were used for the experiments: with intact septum; with septohippocampal disconnection; with complete basal undercutting of the septum, depriving it of ascending brainstem influences (MFB lesion). While the frequency and other parameters of theta bursts did not differ in the first two groups (5.2-5.5 Hz), in MFB-lesioned septum their frequency was significantly lower (3.5 Hz). Intravenous injection of pentobarbital suppressed theta bursts in some cells with unstable, periodic rhythmic activity and lowered the frequency of the bursts in continuously bursting cells. The parameters of bursts in intact and hippocampectomized septum under pentobarbital did not differ from those of undercut septum in undrugged state. Acetylcholine-blocking drugs suppressed theta modulation in some intermittently bursting cells, but only slightly decreased regularity of the bursts in some cells with continuous theta bursting even in sublethal doses; physostigmine has the opposite effect. Neither scopolamine and atropine, nor physostigmine influenced frequency of theta bursts in any way. Sensory or reticular stimulation could temporarily restore both the theta rhythm of hippocampal EEG and the rhythmic bursting of some septal cells under pentobarbital or anticholinergic drugs. On the basis of the experiments a unitary concept of theta rhythm origin is proposed. Pentobarbital influences ascending excitatory input to the septum, which results in a decrease of the burst frequency in the limited group of septal cells, regarded as endogenous bursting pacemakers, and in restriction of the population of high-threshold secondary rhythmic cells, synaptically involved in the rhythmic process. Anticholinergic drugs do not influence the pacemaker cells, but block intraseptal and septohippocampal cholinergic transmission. Both cholinergic and non-cholinergic neurons projecting to the hippocampus exist among septal cells synaptically involved in the rhythmic activity.
这些药物被描述为可阻断海马脑电图的高频(戊巴比妥)或低频(东莨菪碱、阿托品)θ节律,并在有节律性爆发的隔区细胞上进行了测试。实验使用了三组慢性未麻醉兔子:隔区完整;隔海马切断;完全切断隔区基底,使其失去来自脑干的上行影响(中脑被盖束损伤)。在前两组中,θ波爆发的频率和其他参数没有差异(5.2 - 5.5赫兹),而在中脑被盖束损伤的隔区,其频率显著降低(3.5赫兹)。静脉注射戊巴比妥可抑制一些具有不稳定、周期性节律活动的细胞中的θ波爆发,并降低持续爆发细胞中爆发的频率。在戊巴比妥作用下,完整和海马切除的隔区中爆发的参数与未用药状态下切断隔区的参数没有差异。乙酰胆碱阻断药物可抑制一些间歇性爆发细胞中的θ调制,但即使在亚致死剂量下,也只能略微降低一些持续θ波爆发细胞中爆发的规律性;毒扁豆碱则有相反的作用。东莨菪碱和阿托品以及毒扁豆碱均未以任何方式影响θ波爆发的频率。感觉或网状刺激可在戊巴比妥或抗胆碱能药物作用下暂时恢复海马脑电图的θ节律以及一些隔区细胞的节律性爆发。基于这些实验,提出了θ节律起源的统一概念。戊巴比妥影响隔区的上行兴奋性输入,这导致被视为内源性爆发起搏器的有限隔区细胞群中爆发频率降低,并限制了参与节律过程的高阈值次级节律细胞的数量。抗胆碱能药物不影响起搏器细胞,但阻断隔区内和隔海马胆碱能传递。投射到海马的胆碱能和非胆碱能神经元都存在于参与节律活动的隔区突触细胞中。