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首页> 外文期刊>Neurobiology of disease >Dopamine loss alters the hippocampus-nucleus accumbens synaptic transmission in the Tg2576 mouse model of Alzheimer's disease
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Dopamine loss alters the hippocampus-nucleus accumbens synaptic transmission in the Tg2576 mouse model of Alzheimer's disease

机译:多巴胺损失改变了阿尔茨海默病的TG2576小鼠模型中的海马 - 核突触突触传播

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摘要

The functional loop involving the ventral tegmental area (VTA), dorsal hippocampus and nucleus accumbens (NAc) plays a pivotal role in the formation of spatial memory and persistent memory traces. In particular, the dopaminergic innervation from the VTA to the hippocampus is critical for hippocampal-related memory function and alterations in the midbrain dopaminergic system are frequently reported in Alzheimer's disease (AD), contributing to age-related decline in memory and non-cognitive functions. However, much less is known about the hippocampus-NAc connectivity in AD. Here, we evaluated the functioning of the hippocampus-to-NAc core connectivity in the Tg2576 mouse model of AD that shows a selective and progressive degeneration of VTA dopaminergic neurons. We show that reduced dopaminergic innervation in the Tg2576 hippocampus results in reduced synaptic plasticity and excitability of dorsal subiculum pyramidal neurons. Importantly, the glutamatergic transmission from the hippocampus to the NAc core is also impaired. Chemogenetic depolarisation of Tg2576 subicular pyramidal neurons with an excitatory Designer Receptor Exclusively Activated by Designer Drugs, or systemic administration of the DA precursor levodopa, can both rescue the deficits in Tg2576 mice. Our data suggest that the dopaminergic signalling in the hippocampus is essential for the proper functioning of the hippocampus-NAc excitatory synaptic transmission.
机译:涉及腹侧区域(VTA),背部海马和核心(NAC)的功能环在空间存储器和持久存储器迹线的形成中起着枢转作用。特别地,从VTA到海马的多巴胺能原理对于海马相关的记忆功能至关重要,并且在阿尔茨海默病(AD)中经常报道中脑多巴胺能系统的改变,有助于记忆和非认知功能的年龄相关下降。然而,关于广告中的海马-NAC连接是众所周知的更少。在这里,我们评估了在AD的TG2576小鼠模型中的海马到NAC核心连接的运作,显示了VTA多巴胺能神经元的选择性和进行性变性。我们表明,TG2576海马的多巴胺能物质降低导致背部粒度锥体神经元的突触可塑性和兴奋性降低。重要的是,来自海马到NAC芯的谷氨酸谷氨酸酯传播也受到损害。 TG2576亚奇金字塔神经元的化学型去氧与设计师药物的兴奋性设计者受体,或DA前体左旋多巴的全身施用,可以在TG2576小鼠中拯救缺陷。我们的数据表明海马中的多巴胺能信号传导对于海马-NAC兴奋性突触传递的正常运作至关重要。

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