Department of Animal and Human Physiology, University of Gdańsk, Wita Stwosza 59, 80-308 Gdańsk, Poland.
Brain Res. 2013 May 13;1510:63-77. doi: 10.1016/j.brainres.2013.03.021. Epub 2013 Mar 26.
Hippocampal rhythmic slow activity (RSA, theta) is regulated by many brainstem structures, including the midbrain ventral tegmental area (VTA). This work aimed at assessing the role of the dopaminergic (DA) transmission of the VTA in this regulation. Male Wistar rats (n=35) in urethane anaesthesia received an intra-VTA microinjection of either flupenthixol (FLU; doses of 5.0, 2.5, 1.25 and 0.625 μg) or amphetamine (AMPH; 2.5 and 5.0 μg) following control solvent microinjection. Peak power (Pmax) and corresponding peak frequency (Fmax) for delta and theta bands were extracted from EEG recording. Flupenthixol at a dose of 1.25 μg evoked long-lasting theta, continuing for 32.0 min on average, with a mean latency of 7.1 min. Other doses of FLU caused an increase of Pmax theta and reduction of Pmax delta without generating visually recognizable, regular theta rhythm. 5 μg of AMPH evoked theta continuing for 24.4 min on average, with a mean latency of 9.7 min. The lower dose was much less effective, with its outcome resembling the one after the less active FLU doses. During pharmacologically induced theta rhythm, both after FLU and AMPH, brief episodes of asynchronous activity appeared periodically, and they were more frequent and longer in AMPH groups. AMPH may act locally on multiple sites, inhibiting DA cells in somatodendritic region but also increasing dopamine release in target structures, and this, depending on AMPH dose, can lead to induction of theta rhythm. Locally administered DA antagonist on the other hand, when used at a proper dose, can produce theta most likely by the mechanism of inhibiting autoreceptors.
海马节律性慢波活动(RSA,θ波)受许多脑干结构调节,包括中脑腹侧被盖区(VTA)。本研究旨在评估 VTA 中的多巴胺(DA)传递在这种调节中的作用。雄性 Wistar 大鼠(n=35)在氨基甲酸乙酯麻醉下,在对照溶剂微注射后,接受 VTA 内微注射氟哌噻吨(FLU;剂量为 5.0、2.5、1.25 和 0.625 μg)或安非他命(AMPH;2.5 和 5.0 μg)。从 EEG 记录中提取 delta 和 theta 频段的峰值功率(Pmax)和相应的峰值频率(Fmax)。氟哌噻吨 1.25 μg 剂量诱发持久的θ波,平均持续 32.0 分钟,平均潜伏期为 7.1 分钟。其他氟哌噻吨剂量引起 Pmax theta 增加和 Pmax delta 减少,但没有产生可识别的规则θ节律。5 μg 的 AMPH 诱发的θ波平均持续 24.4 分钟,平均潜伏期为 9.7 分钟。较低的剂量效果差得多,其结果类似于不太活跃的氟哌噻吨剂量后的结果。在药物诱导的θ节律期间,无论是在氟哌噻吨还是 AMPH 之后,都会周期性地出现短暂的异步活动期,在 AMPH 组中更为频繁和持续时间更长。AMPH 可能在多个部位局部作用,抑制躯体树突区的 DA 细胞,但也增加靶结构中的多巴胺释放,这取决于 AMPH 剂量,可导致 θ 节律的诱导。另一方面,局部给予适当剂量的 DA 拮抗剂可能通过抑制自身受体的机制产生θ波。