Stepanichev M Yu, Kudryashova I V, Yakovlev A A, Onufriev M V, Khaspekov L G, Lyzhin A A, Lazareva N A, Gulyaeva N V
Department of Functional Biochemistry of the Nervous System, Institute of Higher Nervous Activity and Neurophysiology, Russian Academy of Sciences, Butlerov Street 5A, Moscow 117485, Russia.
Neuroscience. 2005;136(2):579-91. doi: 10.1016/j.neuroscience.2005.08.010. Epub 2005 Sep 28.
Recent studies suggest that caspase-3-mediated mechanisms are essential for neuronal plasticity. N-benzyloxycarbonyl-Asp(OMe)-Glu(OMe)-Val- Asp(OMe)-fluoromethyl ketone (z-DEVD-fmk), a caspase inhibitor with predominant specificity toward caspase-3, has been shown to block long-term potentiation in hippocampal slices. Intrahippocampal infusion of a caspase-3 inhibitor to rats has been shown to significantly impair spatial memory in the water maze. The present work was designed to study whether i.c.v. administration of a caspase-3 inhibitor z-DEVD-fmk impairs learning in other tasks related to specific forms of memory in rats. The rats received bilateral injections of z-DEVD-fmk or N-benzyloxycarbonyl-Phe-Ala-fluoromethyl ketone (z-FA-fmk) ("control" peptide) at a dose of 3 nmol. Administration of z-DEVD-fmk significantly decreased the number of avoidance reactions in some blocks of trials in the active avoidance (shuttle box) learning, while z-FA-fmk had no effect as compared with intact rats. However, only a slight effect of the caspase inhibitor across the session was found. z-DEVD-fmk impaired development of some essential components of the two-way active avoidance performance, such as escape reaction, conditioned fear reaction, and inter-trial crossings. Measurement of caspase-3 activity in rat brain regions involved in active avoidance learning revealed most expressed z-DEVD-fmk-related inhibition of the enzyme activity (about 30%) in the fronto-parietal cortex. A similar effect was close to significant in the hippocampus, but not in the other cerebral structures studied. In primary cultures of cerebellar neurons z-DEVD-fmk (2-50 microM) inhibited caspase-3 activity by 60-87%. We suggest that moderate inhibition of caspase-3 resulting from the central administration of z-DEVD-fmk to rats may impair active avoidance learning. Taking into account previous data on the involvement of neuronal caspase-3 in neuroplasticity phenomena we assume that the enzyme may be important for selected forms of learning.
最近的研究表明,半胱天冬酶-3介导的机制对神经元可塑性至关重要。N-苄氧羰基-天冬氨酸(甲氧基)-谷氨酸(甲氧基)-缬氨酸-天冬氨酸(甲氧基)-氟甲基酮(z-DEVD-fmk)是一种对半胱天冬酶-3具有主要特异性的半胱天冬酶抑制剂,已被证明可阻断海马切片中的长时程增强。向大鼠脑室内注射半胱天冬酶-3抑制剂已被证明会显著损害水迷宫中的空间记忆。本研究旨在探讨脑室内注射半胱天冬酶-3抑制剂z-DEVD-fmk是否会损害大鼠与特定记忆形式相关的其他任务中的学习能力。大鼠接受双侧注射剂量为3 nmol的z-DEVD-fmk或N-苄氧羰基-苯丙氨酸-丙氨酸-氟甲基酮(z-FA-fmk)(“对照”肽)。在主动回避(穿梭箱)学习的某些试验组中,注射z-DEVD-fmk显著减少了回避反应的次数,而与未处理大鼠相比,z-FA-fmk没有影响。然而,在整个实验过程中仅发现半胱天冬酶抑制剂有轻微作用。z-DEVD-fmk损害了双向主动回避行为的一些基本组成部分的发展,如逃避反应、条件恐惧反应和试验间期穿越。对参与主动回避学习的大鼠脑区的半胱天冬酶-3活性的测量显示,在额顶叶皮质中,z-DEVD-fmk相关的酶活性抑制最为明显(约30%)。在海马体中也有类似的接近显著的效果,但在其他研究的脑结构中没有。在小脑神经元的原代培养物中,z-DEVD-fmk(2-50 microM)可将半胱天冬酶-3活性抑制60-87%。我们认为,向大鼠脑室内注射z-DEVD-fmk导致的半胱天冬酶-3的适度抑制可能会损害主动回避学习。考虑到先前关于神经元半胱天冬酶-3参与神经可塑性现象的数据,我们推测该酶可能对特定形式的学习很重要。