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向海马锥体细胞注射蛋白激酶C可引发长时程增强的特征。

Protein kinase C injection into hippocampal pyramidal cells elicits features of long term potentiation.

作者信息

Hu G Y, Hvalby O, Walaas S I, Albert K A, Skjeflo P, Andersen P, Greengard P

出版信息

Nature. 1987;328(6129):426-9. doi: 10.1038/328426a0.

Abstract

Long-term potentiation (LTP) in the hippocampus is an interesting example of synaptic plasticity because of its induction by physiological discharge rates and its long duration. Of the possible biochemical mechanisms that regulate prolonged changes in cell function, protein phosphorylation is a particularly attractive candidate. We have therefore examined the effect of intracellular injection of calcium/diacylglycerol-dependent protein kinase (protein kinase C (PKC] in CA1 pyramidal neurones in hippocampal slices. Injection of the active enzyme elicited long-lasting enhancement of synaptic transmission, similar to LTP, whereas inactivated kinase failed to do so. The observed changes included an increased amplitude of the excitatory post-synaptic potential (e.p.s.p.) and an increased probability of firing and a reduced latency of the associated actin potential.

摘要

海马体中的长时程增强(LTP)是突触可塑性的一个有趣例子,因为它可由生理放电率诱导产生且持续时间长。在调节细胞功能长期变化的可能生化机制中,蛋白质磷酸化是一个特别有吸引力的候选机制。因此,我们研究了在海马切片的CA1锥体神经元中细胞内注射钙/二酰甘油依赖性蛋白激酶(蛋白激酶C,PKC)的效果。注射活性酶可引起突触传递的持久增强,类似于长时程增强,而失活的激酶则不能。观察到的变化包括兴奋性突触后电位(e.p.s.p.)幅度增加、放电概率增加以及相关动作电位潜伏期缩短。

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