Kauer J A, Fisher T E, Kaczmarek L K
Department of Pharmacology, Yale University School of Medicine, New Haven, Connecticut 06510.
J Neurosci. 1987 Nov;7(11):3623-32. doi: 10.1523/JNEUROSCI.07-11-03623.1987.
Brief electrical or hormonal stimulation of the bag cell neurons of Aplysia triggers a long-lasting discharge during which alpha bag cell peptide (alpha-BCP) and other neuropeptides are released from the cells. We have carried out experiments, using both intact abdominal ganglia and isolated neurons, demonstrating that alpha-BCP acts directly on the bag cell neurons to influence cAMP levels and voltage-dependent potassium currents. Exposure of the bag cell neurons within intact ganglia to alpha-BCP, at concentrations greater than 1 nM, inhibited an ongoing discharge. alpha-BCP also significantly reduced both basal and forskolin-stimulated levels of cAMP in bag cell clusters. The inhibition of the discharge by alpha-BCP could be prevented and reversed by pharmacological elevation of intracellular cAMP levels. Immunohistochemical staining of neurons maintained in cell culture showed that all isolated bag cell neurons exhibit immunoreactivity with antisera against alpha-BCP. Application of the adenylate cyclase activator forskolin to such isolated cells, in the presence of a phosphodiesterase inhibitor, attenuates the amplitude of the delayed voltage-dependent outward currents measured in voltage-clamp experiments. Pretreatment of the cells with alpha-BCP significantly reduced the ability of forskolin to attenuate these currents, demonstrating that alpha-BCP acts directly at autoreceptors on bag cell neurons. Experiments with the isolated cells showed that a second autoreceptor-mediated effect of alpha-BCP was the enhancement of an inwardly rectifying potassium current that was activated at potentials more negative than -40 mV. The reversal potential and conductance of the current induced by alpha-BCP were dependent on the external K+ concentration. This response to alpha-BCP could be blocked by rubidium, cesium, and barium ions. Our data demonstrate that alpha-BCP can exert inhibitory biochemical and electrophysiological actions on the bag cell neurons that release it and suggest that autoreceptors for alpha-BCP play an important role in the termination of a discharge in the bag cell neurons.
对海兔的包细胞神经元进行短暂的电刺激或激素刺激,会引发持续较长时间的放电,在此期间,α包细胞肽(α-BCP)和其他神经肽会从细胞中释放出来。我们使用完整的腹神经节和分离的神经元进行了实验,证明α-BCP直接作用于包细胞神经元,以影响环磷酸腺苷(cAMP)水平和电压依赖性钾电流。将完整神经节内的包细胞神经元暴露于浓度大于1 nM的α-BCP下,会抑制正在进行的放电。α-BCP还显著降低了包细胞簇中基础cAMP水平和福斯可林刺激的cAMP水平。通过药理学方法提高细胞内cAMP水平,可以预防和逆转α-BCP对放电的抑制作用。对细胞培养中维持的神经元进行免疫组织化学染色显示,所有分离的包细胞神经元都与抗α-BCP抗血清表现出免疫反应性。在磷酸二酯酶抑制剂存在的情况下,将腺苷酸环化酶激活剂福斯可林应用于此类分离的细胞,会减弱在电压钳实验中测量的延迟电压依赖性外向电流的幅度。用α-BCP预处理细胞可显著降低福斯可林减弱这些电流的能力,表明α-BCP直接作用于包细胞神经元上的自身受体。对分离细胞的实验表明,α-BCP的另一种自身受体介导效应是增强内向整流钾电流,该电流在电位比-40 mV更负时被激活。α-BCP诱导的电流的反转电位和电导取决于外部钾离子浓度。铷、铯和钡离子可阻断对α-BCP的这种反应。我们的数据表明,α-BCP可对释放它的包细胞神经元发挥抑制性生化和电生理作用,并表明α-BCP的自身受体在包细胞神经元放电的终止中起重要作用。