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水蛭中枢神经系统中抑制性突触传递的调制。

Modulation of transmission at an inhibitory synapse in the central nervous system of the leech.

作者信息

Nicholls J, Wallace B G

出版信息

J Physiol. 1978 Aug;281:157-70. doi: 10.1113/jphysiol.1978.sp012414.

Abstract

The synaptic interactions among a group of cells in the leech C.N.S. that regulate the animal's heartbeat exhibit several remarkable features (Thompson & Stent, 1976 a, b, c). We have examined in detail the properties of the inhibitory synapse between two of these cells, the heart interneurone (HN cell) and the heart excitor motoneurone (HE cell). 1. Impulses in the presynaptic HN cell gave rise to monosynaptic i.p.s.p.s in the HE cell that were blocked by high concentrations of Mg and were reversed when the membrane potential of the post-synaptic motoneurone was hyperpolarized beyond--75 m V or when Cl was injected into the cell body. These i.p.s.p.s were chemically mediated, and involved an increase in chloride conductance. 2. In contrast to chemical synapses between sensory and motor cells in the leech C.N.S., little facilitation or depression of transmission occurred when the HN cell was stimulated at frequencies of 0.1--50 Hz. 3. Steady subthreshold depolarization of the presynaptic HN interneurone evoked a maintained hyperpolarization of the post-synaptic HE cell, indicating that currents injected into the HN cell body could spread to the terminals and cause continuous release of transmitter. 4. The size of the i.p.s.p. evoked in the HE motoneurone by an action potential in the HN interneurone varied with the resting membrane potential of the presynaptic cell. An impulse superimposed on a prolonged, subthreshold, depolarizing pulse produced a larger i.p.s.p.; conversely, prolonged hyperpolarization of the HN interneurone reduced the i.p.s.p. amplitude recorded in the HE cell. This effect was most obvious when the natural, rhythmical bursts of activity in the HN interneurone were interrupted by bathing the preparation in leech Ringer fluid containing elevated concentrations of Mg. Under these conditions a 10 mV depolarization of the HN cell increased the size of the i.p.s.p. in the HE cell approximately sixfold. Significant changes in i.p.s.p. amplitude occurred without any noticeable change in the amplitude and duration of the presynaptic action potential. With large presynaptic depolarizations, which produced the biggest i.p.s.p.s, there was some reduction in the amplitude and increase in the duration of the action potential. 5. Following a step depolarization of the presynaptic cell, the size of successive i.p.s.p.s increased with a time constant of about 1 sec. Upon repolarization the i.p.s.p.s decreased in amplitude to the original level. 6. stimulation of one HN cell also gives rise to an i.p.s.p. in its contralateral homologue (Thompson & Stent, 1976c). Trains of i.p.s.p.s produced in this way hyperpolarized at HN cell to such an extent that the size of the synaptic potential it evoked in an HE cell was reduced. 7. Thus, an HN interneurone inhibitis transmission between the contralateral HN and HE cells presynapitcally in addition to inhibiting directly the ipsilateral HE motoneurone.

摘要

水蛭中枢神经系统中调节动物心跳的一组细胞间的突触相互作用呈现出几个显著特征(汤普森和施特恩特,1976年a、b、c)。我们已经详细研究了这些细胞中的两个细胞,即心脏中间神经元(HN细胞)和心脏兴奋运动神经元(HE细胞)之间抑制性突触的特性。1. 突触前HN细胞的冲动在HE细胞中产生单突触抑制性突触后电位(i.p.s.p.s),高浓度的镁可阻断该电位,当突触后运动神经元的膜电位超极化超过 -75 mV 时,或者当向细胞体注入氯离子时,该电位会反转。这些抑制性突触后电位是化学介导的,涉及氯离子电导的增加。2. 与水蛭中枢神经系统中感觉细胞和运动细胞之间的化学突触不同,当以0.1 - 50 Hz的频率刺激HN细胞时,传递很少出现易化或抑制现象。3. 突触前HN中间神经元的稳定阈下去极化引起突触后HE细胞的持续超极化,这表明注入HN细胞体的电流可以扩散到终末并导致递质的持续释放。4. HN中间神经元的动作电位在HE运动神经元中诱发的抑制性突触后电位的大小随突触前细胞的静息膜电位而变化。叠加在延长的阈下去极化脉冲上的冲动产生更大的抑制性突触后电位;相反,HN中间神经元的延长超极化会降低在HE细胞中记录到的抑制性突触后电位的幅度。当用含有高浓度镁的水蛭林格液浸泡标本,打断HN中间神经元自然的节律性活动爆发时,这种效应最为明显。在这些条件下,HN细胞10 mV的去极化使HE细胞中抑制性突触后电位的大小增加约六倍。抑制性突触后电位幅度发生显著变化时,突触前动作电位的幅度和持续时间没有任何明显变化。在产生最大抑制性突触后电位的大的突触前去极化情况下,动作电位的幅度有所降低,持续时间有所增加。5. 突触前细胞进行阶跃去极化后,连续的抑制性突触后电位的大小以约1秒的时间常数增加。复极化时,抑制性突触后电位的幅度降至原始水平。6. 刺激一个HN细胞也会在其对侧同源细胞中产生抑制性突触后电位(汤普森和施特恩特,1976年c)。以这种方式产生的一连串抑制性突触后电位使HN细胞超极化到这样一种程度,以至于它在HE细胞中诱发的突触电位的大小减小。7. 因此,一个HN中间神经元除了直接抑制同侧HE运动神经元外,还在突触前抑制对侧HN和HE细胞之间的传递。

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