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电压依赖性钙电流的突触前调制:加州海兔行为敏感化的机制

Presynaptic modulation of voltage-dependent Ca2+ current: mechanism for behavioral sensitization in Aplysia californica.

作者信息

Klein M, Kandel E R

出版信息

Proc Natl Acad Sci U S A. 1978 Jul;75(7):3512-6. doi: 10.1073/pnas.75.7.3512.

Abstract

Behavioral sensitization of the gill-withdrawal reflex of Aplysia is the result of a prolonged increase in transmitter release from the presynaptic terminals of sensory neurons. Earlier work suggested that this presynaptic facilitation might be mediated by a serotonin-sensitive adenylate cyclase in the sensory neuron terminals. Here we present evidence that presynaptic facilitation results from a cyclic AMP-dependent increase in the calcium current that underlies action potentials in the sensory neurons. The action potentials of sensory neuron cell bodies have, in addition to a sodium current, a calcium current that is enhanced by blocking the opposing potassium current with tetraethylammonium. Under these conditions, the action potentials show a slowly repolarizing plateau that follows the Nernst potential for a calcium electrode and serves as a sensitive assay for changes in calcium current. Stimulation of the pathway that mediates sensitization, incubation with serotonin or phosphodiesterase inhibitors, or intracellular injection of cyclic AMP produces an increase in the calcium plateau in the presence of tetraethylammonium. In addition, both before and after sensitizing stimulation, the duration of the plateau potential parallels transmitter release as measured by the amplitude of monosynaptic excitatory postsynaptic potentials evoked in the motor neurons by intracellular stimulation of single sensory neurons. These results are consistent with the idea that presynaptic facilitation is caused by a cyclic AMP-mediated increase in a voltage-sensitive calcium current in sensory neuron presynaptic terminals. This synaptic action is novel in that it can produce little or no change in the resting potential, is of long duration, and exerts its influence directly on a conductance triggered by the action potential, rather than on non-voltage-sensitive conductances, as is typical of conventional synaptic actions.

摘要

海兔鳃收缩反射的行为敏感化是感觉神经元突触前终末递质释放长期增加的结果。早期研究表明,这种突触前易化可能由感觉神经元终末中对5-羟色胺敏感的腺苷酸环化酶介导。在此,我们提供证据表明,突触前易化是由感觉神经元动作电位所依赖的钙电流的环磷酸腺苷(cAMP)依赖性增加引起的。感觉神经元胞体的动作电位,除了钠电流外,还有一种钙电流,用四乙铵阻断相反的钾电流可增强该钙电流。在这些条件下,动作电位表现出一个缓慢复极化的平台期,该平台期遵循钙电极的能斯特电位,并作为钙电流变化的灵敏检测指标。刺激介导敏感化的通路、用5-羟色胺或磷酸二酯酶抑制剂孵育,或细胞内注射cAMP,在存在四乙铵的情况下会使钙平台期增加。此外,在敏感化刺激之前和之后,平台电位的持续时间与递质释放平行,递质释放通过对单个感觉神经元进行细胞内刺激在运动神经元中诱发的单突触兴奋性突触后电位的幅度来测量。这些结果与以下观点一致,即突触前易化是由感觉神经元突触前终末中cAMP介导的电压敏感性钙电流增加引起的。这种突触作用是新颖的,因为它在静息电位上几乎不产生变化或不产生变化,持续时间长,并且直接作用于由动作电位触发的电导,而不是像传统突触作用那样作用于非电压敏感性电导。

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