Austin K B, Beiswanger C, Bronzino J D, Austin-Lafrance R J, Galler J R, Morgane P J
Worcester Foundation for Experimental Biology, Shrewsbury, MA 01545.
Brain Res Bull. 1992 Feb;28(2):245-55. doi: 10.1016/0361-9230(92)90186-2.
We have examined the effects of prenatal protein malnutrition on interneuronally mediated inhibition and facilitation in the dentate gyrus of the rat using the paired-pulse technique. Field potentials were recorded in the dentate gyrus in response to paired stimuli delivered to the perforant path. The paired-pulse index (PPI) was used as a measure of the net short-term facilitation or interneuronally mediated inhibition effective at the time of the paired-pulse test and was computed by dividing the amplitude of the second population spike (p2) by the amplitude of the first population spike (p1). PPIs were classified according to p1 in order to compare PPIs between behavioral states and dietary treatments since population spike amplitudes in the dentate gyrus vary in relation to behavioral state. Testing was performed during 4 behavioral states: slow-wave sleep (SWS), paradoxical sleep (REM), immobile waking (IW) and exploratory locomotion (AW) using interpulse intervals (IPI) from 20 to 400 ms. The magnitude and duration of interneuronally mediated inhibition was significantly increased in prenatal protein malnourished animals when compared with controls. Paired-pulse tests performed using an IPI of 20 ms under the high p1 (p1 greater than median) condition showed significantly smaller PPIs in prenatal protein malnourished rats regardless of behavioral state. For IPIs greater than 20 ms PPIs were consistently smaller in prenatal protein malnourished rats during SWS and IW. These data indicate that both the magnitude and duration of interneuronally mediated inhibition are increased in prenatally malnourished rats. No consistent diet-related differences were found during AW and REM using IPIs greater than 20 ms because interneuronally mediated inhibition was relatively suppressed during these behavioral states for both dietary groups. There was no consistent behavioral state modulation of paired-pulse facilitation (IPI = 40 to 80 ms) or late inhibition (IPI = 400 ms) in either diet group. In addition, a new relation between PPI and IPI was found under the low p1 (p1 greater than median) condition. During AW the PPIs observed using IPIs of 40 and 50 ms were smaller than those observed using IPIs of 30 and 60 ms. This depression interrupts what is generally considered the "facilitatory" phase of paired-pulse response and may indicate an interaction between perforant path stimulation and hippocampal theta rhythm which is masked when p1 amplitude is high.(ABSTRACT TRUNCATED AT 400 WORDS)
我们使用双脉冲技术研究了产前蛋白质营养不良对大鼠齿状回中间神经元介导的抑制和易化作用的影响。记录齿状回中的场电位,以响应施加到穿通路径的双脉冲刺激。双脉冲指数(PPI)用作衡量双脉冲测试时有效净短期易化或中间神经元介导抑制的指标,通过将第二个群体峰电位(p2)的幅度除以第一个群体峰电位(p1)的幅度来计算。根据p1对PPI进行分类,以便比较行为状态和饮食处理之间的PPI,因为齿状回中的群体峰电位幅度会因行为状态而变化。在4种行为状态下进行测试:慢波睡眠(SWS)、异相睡眠(REM)、静止清醒(IW)和探索性运动(AW),使用的脉冲间隔(IPI)为20至400毫秒。与对照组相比,产前蛋白质营养不良的动物中,中间神经元介导的抑制的幅度和持续时间显著增加。在高p1(p1大于中位数)条件下,使用20毫秒的IPI进行的双脉冲测试显示,无论行为状态如何,产前蛋白质营养不良的大鼠的PPI均显著较小。对于大于20毫秒的IPI,在SWS和IW期间,产前蛋白质营养不良的大鼠的PPI始终较小。这些数据表明,产前营养不良的大鼠中,中间神经元介导的抑制的幅度和持续时间均增加。在使用大于20毫秒的IPI的AW和REM期间,未发现与饮食相关的一致差异,因为在这两种行为状态下,两个饮食组的中间神经元介导的抑制均相对受到抑制。在任何一个饮食组中,双脉冲易化(IPI = 40至80毫秒)或晚期抑制(IPI = 400毫秒)均未出现一致的行为状态调节。此外,在低p1(p1大于中位数)条件下发现了PPI与IPI之间的新关系。在AW期间,使用40和50毫秒的IPI观察到的PPI小于使用30和60毫秒的IPI观察到的PPI。这种抑制中断了通常被认为是双脉冲反应“易化”阶段的过程,可能表明穿通路径刺激与海马θ节律之间的相互作用,当p1幅度较高时这种相互作用被掩盖。(摘要截断于400字)