Suppr超能文献

在齿状回中诱导长时程增强后,突触后膜组分中花生四烯酸浓度增加。

Increase in arachidonic acid concentration in a postsynaptic membrane fraction following the induction of long-term potentiation in the dentate gyrus.

作者信息

Clements M P, Bliss T V, Lynch M A

机构信息

Division of Neurophysiology and Neuropharmacology, National Institute for Medical Research, Mill Hill, London, U.K.

出版信息

Neuroscience. 1991;45(2):379-89. doi: 10.1016/0306-4522(91)90235-g.

Abstract

We have determined the concentration of free fatty acids in membranes of slices prepared from the dentate gyrus following the induction of long-term potentiation in the anaesthetized rat. Compared to unpotentiated tissue, there was a significant increase in the concentration of free arachidonic acid 2.5 min, 45 min and 3 h after induction of long-term potentiation. There was no corresponding increase in oleic, stearic or palmitic acids. To account for the increase in free arachidonate, the activities of phospholipase A2, phospholipase A1 and phospholipase C were determined at the same three time intervals in control and potentiated tissue. Two-and-a-half minutes after the induction of long-term potentiation, activity of phospholipase A2 was enhanced, while at 45 min, and at 3 h phospholipase C activity was increased. These results suggest that the liberation of free arachidonate is due initially to phospholipase A2 activity, but that at later stages of long-term potentiation, control switches to phospholipase C. Subcellular fractionation experiments revealed an increase in free arachidonate in the postsynaptic density fraction 45 min after induction of long-term potentiation, without significant changes in synaptosomal- or glial-enriched fractions. These results are consistent with the hypothesis that arachidonic acid, released from a postsynaptic site, acts as a trophic retrograde synaptic signal in long-term potentiation in the dentate gyrus.

摘要

我们测定了在麻醉大鼠中诱导长时程增强后,从齿状回制备的切片膜中游离脂肪酸的浓度。与未增强的组织相比,在诱导长时程增强后2.5分钟、45分钟和3小时,游离花生四烯酸的浓度显著增加。油酸、硬脂酸或棕榈酸没有相应增加。为了解释游离花生四烯酸的增加,在对照和增强组织的相同三个时间间隔测定了磷脂酶A2、磷脂酶A1和磷脂酶C的活性。诱导长时程增强后2.5分钟,磷脂酶A2的活性增强,而在45分钟和3小时,磷脂酶C的活性增加。这些结果表明,游离花生四烯酸的释放最初是由于磷脂酶A2的活性,但在长时程增强的后期阶段,控制转向磷脂酶C。亚细胞分级分离实验显示,诱导长时程增强后45分钟,突触后致密部分的游离花生四烯酸增加,而富含突触体或胶质细胞的部分没有显著变化。这些结果与以下假设一致:从突触后位点释放的花生四烯酸在齿状回的长时程增强中作为一种营养性逆行突触信号。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验