Vyshedskiy A, Delaney K R, Lin J W
Department of Biology, Boston University, Boston, Massachusetts 02215, USA.
J Neurosci. 1998 Jul 15;18(14):5160-9. doi: 10.1523/JNEUROSCI.18-14-05160.1998.
A presynaptic voltage control method has been used to investigate the modulatory effects of serotonin (5-HT) and okadaic acid (OA) on the inhibitory junction of the crayfish opener muscle. Instead of using action potentials, we used 20 msec pulses depolarized to 0 mV to activate transmitter release. This approach allowed us to monitor two separate physiological parameters related to the release process. The first parameter, transmitter release kinetics, is characterized as the delay when inhibitory postsynaptic conductance reaches its half-maximum (IPSG50). The second parameter, the total area of IPSG (IPSGarea), estimates total transmitter output. We have reported previously that the F2 component of synaptic facilitation is associated with a decrease in IPSG50 but without a change in IPSGarea. These results raised the possibility that IPSG50 and IPSGarea could be mediated by separate mechanisms that were modulated independently. To explore this possibility, we investigated the effects of 5-HT (100-200 nM) and OA (2.5 microM) on the two parameters. 5-HT and OA enhanced IPSG neither by changing the sensitivity of postsynaptic receptors, as tested by iontophoretically ejected GABA, nor by elevating resting and action potential-activated presynaptic free calcium, as monitored by fura-2 imaging. 5-HT and OA decreased IPSG50 by 3.0 +/- 1.4 and 3.6 +/- 1.1 msec, respectively, and increased IPSGarea by 50 +/- 21 and 37 +/- 6%, respectively. The ability of F2 facilitation to accelerate release kinetics was reduced in the presence of the modulators, suggesting that the mechanism underlying the accelerated release kinetics was shared by the two modes of synaptic enhancement. This report demonstrates that the acceleration in release kinetics and the increase in total release are two separate mechanisms for enhancing transmitter output and that these two mechanisms can be activated without changes in presynaptic calcium dynamics.
一种突触前电压控制方法已被用于研究血清素(5-羟色胺,5-HT)和冈田酸(OA)对小龙虾开肌抑制性突触连接的调节作用。我们没有使用动作电位,而是使用去极化至0 mV的20毫秒脉冲来激活递质释放。这种方法使我们能够监测与释放过程相关的两个独立的生理参数。第一个参数,递质释放动力学,其特征是抑制性突触后电导达到其最大值一半时的延迟(IPSG50)。第二个参数,IPSG的总面积(IPSGarea),估计总的递质输出量。我们之前报道过,突触易化的F2成分与IPSG50的降低有关,但IPSGarea没有变化。这些结果提出了一种可能性,即IPSG50和IPSGarea可能由独立调节的不同机制介导。为了探究这种可能性,我们研究了5-HT(100 - 200 nM)和OA(2.5 microM)对这两个参数的影响。5-HT和OA既没有通过改变突触后受体的敏感性(通过离子电泳喷射γ-氨基丁酸进行测试)来增强IPSG,也没有通过提高静息和动作电位激活的突触前游离钙(通过fura-2成像监测)来增强IPSG。5-HT和OA分别使IPSG50降低了3.0±1.4毫秒和3.6±1.1毫秒,使IPSGarea分别增加了50±21%和37±6%。在存在调节剂的情况下,F2易化加速释放动力学的能力降低,这表明加速释放动力学的机制在两种突触增强模式中是相同的。本报告表明,释放动力学的加速和总释放量的增加是增强递质输出的两种不同机制,并且这两种机制可以在突触前钙动力学无变化的情况下被激活。