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应激前而非应激后单次给予氟西汀治疗可预防大鼠应激诱导的海马长时程抑制和空间记忆提取障碍。

Single fluoxetine treatment before but not after stress prevents stress-induced hippocampal long-term depression and spatial memory retrieval impairment in rats.

作者信息

Han Huili, Dai Chunfang, Dong Zhifang

机构信息

1] Ministry of Education Key Laboratory of Child Development and Disorders, Children's Hospital of Chongqing Medical University, Chongqing 400014, PR China [2] Chongqing Key Laboratory of Translational Medical Research in Cognitive Development and Learning and Memory Disorders, Children's Hospital of Chongqing Medical University, Chongqing 400014, PR China.

出版信息

Sci Rep. 2015 Jul 28;5:12667. doi: 10.1038/srep12667.

DOI:10.1038/srep12667
PMID:26218751
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4517509/
Abstract

A growing body of evidence has shown that chronic treatment with fluoxetine, a widely prescribed medication for treatment of depression, can affect synaptic plasticity in the adult central nervous system. However, it is not well understood whether acute fluoxetine influences synaptic plasticity, especially on hippocampal CA1 long-term depression (LTD), and if so, whether it subsequently impacts hippocampal-dependent spatial memory. Here, we reported that LTD facilitated by elevated-platform stress in hippocampal slices was completely prevented by fluoxetine administration (10 mg/kg, i.p.) 30 min before stress. The LTD was not, however, significantly inhibited by fluoxetine administration immediately after stress. Similarly, fluoxetine incubation (10 μM) during electrophysiological recordings also displayed no influence on the stress-facilitated LTD. In addition, behavioral results showed that a single fluoxetine treatment 30 min before but not after acute stress fully reversed the impairment of spatial memory retrieval in the Morris water maze paradigm. Taken together, these results suggest that acute fluoxetine treatment only before, but not after stress, can prevent hippocampal CA1 LTD and spatial memory retrieval impairment caused by behavioral stress in adult animals.

摘要

越来越多的证据表明,长期使用氟西汀(一种广泛用于治疗抑郁症的药物)会影响成年中枢神经系统的突触可塑性。然而,急性使用氟西汀是否会影响突触可塑性,尤其是对海马CA1区的长时程抑制(LTD),以及如果有影响,随后是否会影响海马依赖的空间记忆,目前尚不清楚。在此,我们报告,在应激前30分钟腹腔注射氟西汀(10mg/kg)可完全阻止海马切片中由高架平台应激促进的LTD。然而,在应激后立即注射氟西汀并不能显著抑制LTD。同样,在电生理记录期间用氟西汀孵育(10μM)对应激促进的LTD也没有影响。此外,行为学结果表明,在急性应激前30分钟而非应激后单次给予氟西汀可完全逆转Morris水迷宫实验中空间记忆提取的损伤。综上所述,这些结果表明,仅在应激前而非应激后进行急性氟西汀治疗,可以预防成年动物行为应激引起的海马CA区LTD和空间记忆提取损伤。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a30/4517509/95283ad5c0b6/srep12667-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a30/4517509/00ae9d3a4419/srep12667-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a30/4517509/3c56cd7427e4/srep12667-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a30/4517509/a8ac7039bafb/srep12667-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a30/4517509/95283ad5c0b6/srep12667-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a30/4517509/00ae9d3a4419/srep12667-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a30/4517509/3c56cd7427e4/srep12667-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a30/4517509/a8ac7039bafb/srep12667-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a30/4517509/95283ad5c0b6/srep12667-f4.jpg

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