首页> 外文期刊>Neuroscience: An International Journal under the Editorial Direction of IBRO >High intracellular calcium levels during and after electrical discharges in molluscan peptidergic neurons.
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High intracellular calcium levels during and after electrical discharges in molluscan peptidergic neurons.

机译:软体动物肽能神经元放电期间和放电后细胞内钙水平高。

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Intracellular calcium levels ([Ca2+]i) during and following electrical activity of the neuroendocrine caudodorsal cells of the pond snail (Lymnaea stagnalis) were measured in situ and is dissociated cells by combining electrical recordings and Fura-2 measurements. Caudodorsal cells are typical neuroendocrine cells that control egg laying via the release of a set of peptides during a stereotyped discharge of action potentials. Single action potentials or short trains of spikes in dissociated caudodorsal cells induced only small but consistent increases in [Ca2+]i. With longer or repeated spike trains, larger [Ca2+]i transients were measured, indicating accumulation of calcium. The calcium channel blocker Ni2+ suppressed the calcium elevation, suggesting that calcium influx occurred through voltage-activated calcium channels. Calcium levels in caudodorsal cells in situ were measured before, during and after the stereotyped firing pattern, a approximately 35-min discharge of regular spiking. Basal calciumlevels in caudodorsal cells in situ were about 125 nM. During the initial phase of the discharge, the intracellular calcium level increased to approximately 250 nM. Maximal calcium levels (300-600 nM) were only reached at the final phase of the discharge or several minutes after the cessation of firing. Calcium levels remained elevated for up to 1 h after the end of the discharge. During this time, caudodorsal cells were characterized by very low excitability. We suggest that the prolonged, elevated level of calcium following the discharge need not be directly dependent on action potentials. The long-lasting [Ca2+]i elevation may cause the release of neuropeptides to outlast the duration of electrical activity, thus uncoupling release from spiking. In addition, it may cause reduced excitability of neuroendocrine cells following a period of spiking, thereby inducing a refractory period.
机译:在池蜗牛(Lymnaea stagnalis)的神经内分泌尾odor神经细胞电活动期间和之后的细胞内钙水平([Ca2 +] i)进行了原位测量,并结合电记录和Fura-2测量将其分离。尾嗅细胞是典型的神经内分泌细胞,通过定型释放动作电位,通过释放一组肽来控制卵的产卵。在分离的尾嗅细胞中,单动作电位或短时间的尖峰序列仅引起[Ca2 +] i的微小但一致的增加。使用更长或重复的尖峰序列,可以测量到较大的[Ca2 +] i瞬变,表明钙的积累。钙通道阻滞剂Ni2 +抑制了钙的升高,表明钙流入通过电压激活的钙通道而发生。在定型射击模式之前,期间和之后,定期放电约35分钟,测量尾部原位钙含量。原位尾尾细胞中的基础钙水平约为125 nM。在放电的初始阶段,细胞内钙水平增加到约250 nM。最高钙水平(300-600 nM)仅在放电的最后阶段或停止烧制后的几分钟达到。放电结束后长达1小时,钙水平仍保持升高。在这段时间内,尾嗅细胞的兴奋性很低。我们建议放电后钙的长期升高水平不必直接取决于动作电位。持久的[Ca2 +] i升高可能导致神经肽的释放超过电活动的持续时间,从而使释放与峰脱钩。此外,它可能会导致一段时间的刺突后神经内分泌细胞的兴奋性降低,从而导致不应期。

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