Aroniadou V A, Teyler T J
Neurobiology Department, Northeastern Ohio College of Medicine, Rootstown 44272.
Brain Res. 1992 Jul 3;584(1-2):169-73. doi: 10.1016/0006-8993(92)90891-c.
The aim of this study was to examine: (1) whether long-term potentiation (LTP) can be induced in slices from adult rat visual cortex under conditions where inhibition is not antagonized, and (2) the role of N-methyl-D-aspartate (NMDA) receptors in its induction. The field potential elicited in layer III in response to stimulation of the subcortical white matter consisted of a component with peak latency 5-8 ms (N1) and, in most slices, a second component with peak latency 13-19 ms (N2). N1 was generated via both kainate/alpha-amino-3-hydroxy-5-methyl-4-isoxazole propionic acid (AMPA) and NMDA receptor activation as revealed by bath application of 6,7-dinitroquinoxaline-2,3-dione (DNQX) and D,L-2-amino-5-phosphonovalerate (APV). N2 was insensitive to APV in most of the slices and was probably polysynaptic since it did not follow stimulation at 0.5 Hz. Tetanic stimulation of the white matter in normal medium induced LTP of N1; in some slices N2 also potentiated. Tetanic stimulation in the presence of APV also induced LTP of N1 and sometimes N2. LTP of N1 induced in APV was of a larger magnitude, and was expressed more quickly than LTP induced in normal medium. It appears that the known reduction of NMDA receptor activity in adult neocortex is accompanied by the development of other mechanisms that maintain synaptic plasticity; these mechanisms seem to operate more efficiently in absence of NMDA receptor activation.
(1)在不拮抗抑制作用的条件下,能否在成年大鼠视觉皮层切片中诱导长时程增强(LTP),以及(2)N-甲基-D-天冬氨酸(NMDA)受体在其诱导过程中的作用。对皮层下白质进行刺激时,III层引出的场电位由一个峰潜伏期为5-8毫秒的成分(N1)组成,并且在大多数切片中,还有一个峰潜伏期为13-19毫秒的第二个成分(N2)。如通过浴加6,7-二硝基喹喔啉-2,3-二酮(DNQX)和D,L-2-氨基-5-磷酸戊酸(APV)所揭示的,N1是通过海人藻酸/α-氨基-3-羟基-5-甲基-4-异恶唑丙酸(AMPA)和NMDA受体激活产生的。在大多数切片中,N2对APV不敏感,并且可能是多突触的,因为它在0.5赫兹刺激下不跟随刺激。在正常培养基中对白质进行强直刺激可诱导N1的LTP;在一些切片中,N2也增强。在存在APV的情况下进行强直刺激也可诱导N1的LTP,有时也可诱导N2的LTP。在APV中诱导的N1的LTP幅度更大,并且比在正常培养基中诱导的LTP表达更快。看来成年新皮层中已知的NMDA受体活性降低伴随着维持突触可塑性的其他机制的发展;这些机制在没有NMDA受体激活的情况下似乎运作得更有效。