Jensen K, Jensen M S, Lambert J D
Department of Physiology, Institute of Anatomy, University of Aarhus, DK-8000 Aarhus C, Denmark.
J Neurophysiol. 1999 Mar;81(3):1225-30. doi: 10.1152/jn.1999.81.3.1225.
Using dual whole cell patch-clamp recordings of monosynaptic GABAergic inhibitory postsynaptic currents (IPSCs) in cultured rat hippocampal neurons, we have previously demonstrated posttetanic potentiation (PTP) of IPSCs. Tetanic stimulation of the GABAergic neuron leads to accumulation of Ca2+ in the presynaptic terminals. This enhances the probability of GABA-vesicle release for up to 1 min, which underlies PTP. In the present study, we have examined the effect of altering the probability of release on PTP of IPSCs. Baclofen (10 microM), which depresses presynaptic Ca2+ entry through N- and P/Q-type voltage-dependent Ca2+ channels (VDCCs), caused a threefold greater enhancement of PTP than did reducing [Ca2+]o to 1.2 mM, which causes a nonspecific reduction in Ca2+ entry. This finding prompted us to investigate whether presynaptic L-type VDCCs contribute to the Ca2+ accumulation in the boutons during spike activity. The L-type VDCC antagonist, nifedipine (10 microM), had no effect on single IPSCs evoked at 0.2 Hz but reduced the PTP evoked by a train of 40 Hz for 2 s by 60%. Another L-type VDCC antagonist, isradipine (5 microM), similarly inhibited PTP by 65%. Both L-type VDCC blockers also depressed IPSCs during the stimulation (i.e., they increased tetanic depression). The L-type VDCC "agonist" (-)BayK 8644 (4 microM) had no effect on PTP evoked by a train of 40 Hz for 2 s, which probably saturated the PTP process, but enhanced PTP evoked by a train of 1 s by 91%. In conclusion, the results indicate that L-type VDCCs do not participate in low-frequency synchronous transmitter release, but contribute to presynaptic Ca2+ accumulation during high-frequency activity. This helps maintain vesicle release during tetanic stimulation and also enhances the probability of transmitter release during the posttetanic period, which is manifest as PTP. Involvement of L-type channels in these processes represents a novel presynaptic regulatory mechanism at fast CNS synapses.
利用对培养的大鼠海马神经元单突触GABA能抑制性突触后电流(IPSCs)进行双全细胞膜片钳记录,我们之前已经证明了IPSCs的强直后增强(PTP)。对GABA能神经元的强直刺激导致突触前终末中Ca2+的积累。这会使GABA囊泡释放的概率增加,持续长达1分钟,这是PTP的基础。在本研究中,我们研究了改变释放概率对IPSCs的PTP的影响。巴氯芬(10微摩尔)通过N型和P/Q型电压依赖性Ca2+通道(VDCCs)抑制突触前Ca2+内流,与将[Ca2+]o降低到1.2毫摩尔相比,其对PTP的增强作用大三倍,将[Ca2+]o降低到1.2毫摩尔会导致Ca2+内流的非特异性减少。这一发现促使我们研究突触前L型VDCCs在动作电位活动期间是否有助于突触小体中Ca2+的积累。L型VDCC拮抗剂硝苯地平(10微摩尔)对以0.2赫兹诱发的单个IPSCs没有影响,但将40赫兹持续2秒的一串刺激诱发的PTP降低了60%。另一种L型VDCC拮抗剂伊拉地平(5微摩尔)同样抑制PTP达65%。两种L型VDCC阻滞剂在刺激期间也抑制IPSCs(即,它们增加了强直抑制)。L型VDCC“激动剂”(-)BayK 8644(4微摩尔)对40赫兹持续2秒的一串刺激诱发的PTP没有影响,这可能使PTP过程饱和,但使1秒的一串刺激诱发的PTP增强了91%。总之,结果表明L型VDCCs不参与低频同步递质释放,但在高频活动期间有助于突触前Ca2+的积累。这有助于在强直刺激期间维持囊泡释放,也增加了强直后时期递质释放的概率,这表现为PTP。L型通道参与这些过程代表了中枢神经系统快速突触处一种新的突触前调节机制。