氯胺酮给药在青春期损害突触整合和抑制性突触传递在成人齿状回。

IF 6.1 2区 医学 Q1 NEUROSCIENCES
Odra Santander , Sebastián B. Arredondo , Francisca García-Rojas , Sebastián F. Estay , Juan E. Belforte , Andrés E. Chávez , Lorena Varela-Nallar , Marco Fuenzalida
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引用次数: 0

摘要

青春期服用氯胺酮会影响认知能力;然而,其对海马突触功能和神经元整合的长期影响尚不清楚。海马是大脑中对认知至关重要的区域。通过功能和分子分析,我们发现青春期长期服用氯胺酮会对突触整合产生长期影响,以特定的输入方式扩大时间窗口,影响内层分子层,但不影响成年小鼠海马背齿状回的内侧穿孔路径输入。氯胺酮还通过降低抑制输入的效力来改变兴奋/抑制平衡,这可能是由于小蛋白阳性中间神经元数量和功能的减少。这些发现表明,在青春期,氯胺酮对由小蛋白阳性神经元介导的抑制性突触功能产生强烈影响,最终影响成人背齿状回的突触整合,这有助于理解青少年大脑更容易受到伤害的神经生物学和功能基础。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Ketamine administration during adolescence impairs synaptic integration and inhibitory synaptic transmission in the adult dentate gyrus
Ketamine administration during adolescence affects cognitive performance; however, its long-term impact on synaptic function and neuronal integration in the hippocampus a brain region critical for cognition remains unclear. Using functional and molecular analyses, we found that chronic ketamine administration during adolescence exerts long-term effects on synaptic integration, expanding the temporal window in an input-specific manner affecting the inner molecular layer but not the medial perforant path inputs in the adult mouse dorsal hippocampal dentate gyrus. Ketamine also alters the excitatory/inhibitory balance by reducing the efficacy of inhibitory inputs likely due to a reduction in parvalbumin-positive interneurons number and function. These findings indicate that during adolescence, ketamine exerts a strong effect on inhibitory synaptic function mediated by parvalbumin-positive neurons that ultimately impact synaptic integration in the dorsal adult dentate gyrus, which could help to understand the neurobiological and functional bases that confer greater vulnerability to the adolescent brain.
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来源期刊
Progress in Neurobiology
Progress in Neurobiology 医学-神经科学
CiteScore
12.80
自引率
1.50%
发文量
107
审稿时长
33 days
期刊介绍: Progress in Neurobiology is an international journal that publishes groundbreaking original research, comprehensive review articles and opinion pieces written by leading researchers. The journal welcomes contributions from the broad field of neuroscience that apply neurophysiological, biochemical, pharmacological, molecular biological, anatomical, computational and behavioral analyses to problems of molecular, cellular, developmental, systems, and clinical neuroscience.
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