Tebano M T, Luzi M, Palazzesi S, Pomponi M, Loizzo A
Istituto Superiore di Sanità, Roma, Italia.
Neuropsychobiology. 1999;40(1):47-56. doi: 10.1159/000026596.
The effects of single intraperitoneal injection of two cholinesterase inhibitors, physostigmine (PHY; 0.01, 0.025, 0.05, 0. 1, 0.2 mg/kg) and heptylphysostigmine (HEP; 0.5, 2, 6 mg/kg) on electroencephalographic (EEG) activity and flash visual evoked potentials (f-VEP) in the occipital cortex were compared in DBA/2 mice. EEG spectral analysis of awake periods showed that PHY at all doses and HEP at 2 mg/kg induced an increase of power in the 4.25- to 7-Hz frequency band. Furthermore, PHY at the higher doses and HEP at all doses induced a decrease of power in the 7.25- to 12-Hz frequency band, while the lower doses of PHY (0.01, 0.025 mg/kg) produced an increase of this band. EEG effects elicited by the two drugs were similar, when doses displaying analogous biochemical effects (acetylcholinesterase inhibition) were used (i.e. 0.01 and 0. 025 mg/kg of PHY versus 0.5 and 2 mg/kg of HEP). PHY and HEP induced similar changes in f-VEPs. Amplitudes of early and late components (P1N1, N1P2, P4N4 and particularly N1P3) were enhanced, while amplitudes of middle components were depressed after all doses. The peak latency measures were generally delayed, even though, after the lower doses, a trend to a latency reduction was evident in late components. This finding might indicate a possible effect on stimulus speed diffusion by 'low therapeutic' doses, analogous to the ones used in men. Our data show that both drugs are effective in modifying EEG and f-VEP parameters connected with brain cholinergic function, although in a very narrow dose range.
在DBA/2小鼠中,比较了单次腹腔注射两种胆碱酯酶抑制剂毒扁豆碱(PHY;0.01、0.025、0.05、0.1、0.2mg/kg)和庚基毒扁豆碱(HEP;0.5、2、6mg/kg)对脑电图(EEG)活动及枕叶皮质闪光视觉诱发电位(f-VEP)的影响。清醒期的EEG频谱分析显示,所有剂量的PHY以及2mg/kg的HEP均可使4.25至7Hz频段的功率增加。此外,较高剂量的PHY和所有剂量的HEP可使7.25至12Hz频段的功率降低,而较低剂量的PHY(0.01、0.025mg/kg)则使该频段功率增加。当使用显示类似生化效应(乙酰胆碱酯酶抑制)的剂量时(即0.01和0.025mg/kg的PHY与0.5和2mg/kg的HEP),两种药物引起的EEG效应相似。PHY和HEP对f-VEP产生类似变化。所有剂量给药后,早期和晚期成分(P1N1、N1P2、P4N4,尤其是N1P3)的振幅增强,而中间成分的振幅降低。峰值潜伏期测量通常延迟,不过,较低剂量给药后,晚期成分有潜伏期缩短的趋势。这一发现可能表明“低治疗”剂量对刺激速度扩散有潜在影响,类似于用于人体的剂量。我们的数据表明,两种药物均能有效改变与脑胆碱能功能相关的EEG和f-VEP参数,尽管作用剂量范围很窄。