Farmer J, Zhao X, van Praag H, Wodtke K, Gage F H, Christie B R
Department of Psychology, Division of Neuroscience and The Brain Research Centre, University of British Columbia, 2136 West Mall, Vancouver, BC, Canada V6T 1Z4.
Neuroscience. 2004;124(1):71-9. doi: 10.1016/j.neuroscience.2003.09.029.
We have previously shown that voluntary exercise produces enhanced neurogenesis and long-term potentiation (LTP) in the dentate gyrus (DG) of mice in vitro. In the present experiments we show that rats given access to a running wheel (Runners) exhibit significantly more short-term potentiation and LTP with theta-patterned conditioning stimulation in vivo than do age-matched litter mates (Controls). This increase in LTP appears to reflect an alteration in the induction threshold for synaptic plasticity that accompanies voluntary exercise. Weak theta-patterned stimulation, which did not produce LTP in control subjects, produced a robust and long-lasting LTP in Runners. LTP induction in both groups was dependent upon the activation of N-methyl-D-aspartate (NMDA) receptors, and could be blocked by the competitive antagonist [+/-]-3-[2-carboxypiperazin-4-yl] propanephosphonic acid. Consistent with these findings, we found that mRNA levels for NR2B subtype of NMDA receptor were increased specifically in the DG of Runners. In addition to changes in NR2B mRNA levels, quantitative polymerase chain reaction analysis revealed that brain-derived neurotrophic factor (BDNF) and glutamate receptor 5 mRNA levels were also significantly elevated in the DG of Runners, but not in other areas of the hippocampus. Thus, alterations in the expression of BDNF, and specific glutamate receptor subtypes, may underlie the ability of exercise to enhance neurogenesis and reduce the threshold for LTP in the DG.
我们之前已经表明,自愿运动在体外可使小鼠齿状回(DG)中的神经发生增强以及长时程增强(LTP)增强。在本实验中,我们发现有机会使用跑步轮的大鼠(跑步组)与年龄匹配的同窝小鼠(对照组)相比,在体内进行θ波模式条件刺激时表现出明显更多的短时程增强和LTP。这种LTP的增加似乎反映了伴随自愿运动的突触可塑性诱导阈值的改变。在对照组中不能产生LTP的弱θ波模式刺激,在跑步组中却能产生强烈且持久的LTP。两组中的LTP诱导均依赖于N-甲基-D-天冬氨酸(NMDA)受体的激活,并且可被竞争性拮抗剂[+/-]-3-[2-羧基哌嗪-4-基]丙烷磺酸阻断。与这些发现一致,我们发现NMDA受体NR2B亚型的mRNA水平在跑步组的DG中特异性增加。除了NR2B mRNA水平的变化外,定量聚合酶链反应分析显示,脑源性神经营养因子(BDNF)和谷氨酸受体5的mRNA水平在跑步组的DG中也显著升高,但在海马体的其他区域则没有。因此,BDNF以及特定谷氨酸受体亚型表达的改变,可能是运动增强神经发生和降低DG中LTP阈值能力的基础。