首页> 外文期刊>Brain research >Modulation of extracellular monoamine transmitter concentrations in the hippocampus after weak and strong tetanization of the perforant path in freely moving rats.
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Modulation of extracellular monoamine transmitter concentrations in the hippocampus after weak and strong tetanization of the perforant path in freely moving rats.

机译:自由移动大鼠的穿刺路径弱弱和强壮性后,海马中细胞外单胺递质浓度的调节。

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摘要

Hippocampal long-term potentiation (LTP) is considered as a cellular model of memory formation. Specific, electrical weak tetanization of distinct afferents such as the medial perforant path results in a short-lasting, protein synthesis-independent early-LTP (up to 4 h) within the dentate gyrus. A stronger tetanization leads to late-LTP (>4 h), which is protein synthesis-dependent and requires heterosynaptic activation during its induction, the latter of which can be provided by afferents from cortical brain regions or subcortical nuclei during memory formation in the behaving animal. In particular, noradrenaline (NA) is required for late-LTP in the dentate gyrus and dopamine for late-LTP in the apical CA1-dendrites. However, little is known about the concentrations and temporal dynamics of such neuromodulators like NA, serotonin (5-HT) and dopamine (DA) during LTP. We now implemented the microdialysis method to study this topic after stimulating the dentate gyrus in more detail. A weak tetanus of the perforant path, which normally leads to early-LTP, transiently but significantly decreased the concentration of NA (3 h) and increased the concentration of 5-HT (about 2 h) and DA (about 1 h) in the hippocampus. A strong tetanus, normally resulting in late-LTP, increased concentrations of NA and DA significantly and long-lasting (for about 5 h), whereas 5-HT concentration was increased with a delay (after about 30 min) and only for a short time (30 min). Thus different stimulation protocols resulted in different release patterns of neuromodulators, that may support discriminative processing of incoming information in the hippocampus.
机译:海马长期增强(LTP)被认为是记忆形成的细胞模型。特异的,不同传入传入途径(例如内侧穿孔路径)的弱电镀膜作用导致齿状回内的持续时间短,不依赖蛋白质合成的早期LTP(长达4小时)。较强的金属化作用会导致后期LTP(> 4 h),后者依赖于蛋白质合成,并且在诱导过程中需要异突触激活,后者的行为可以由表现为记忆形成过程中皮质大脑区域或皮质下核的传入者提供动物。尤其是,齿状回中的晚期LTP需要去甲肾上腺素(NA),而顶端CA1-树突中的晚期LTP需要多巴胺。然而,人们对LTP期间诸如NA,5-羟色胺(5-HT)和多巴胺(DA)等神经调节剂的浓度和时间动态了解甚少。在更详细地刺激齿状回之后,我们现在采用微透析方法来研究该主题。穿孔路径的破伤风较弱,通常会导致早期LTP,短暂但明显降低了NA的浓度(3小时),并增加了5-HT(约2小时)和DA(约1小时)的浓度。海马。强烈的破伤风通常会导致LTP延迟,NA和DA的浓度显着增加并且持续很长时间(约5小时),而5-HT的浓度则有所延迟(约30分钟后)并且仅短暂出现时间(30分钟)。因此,不同的刺激方案导致神经调节剂的释放模式不同,这可能支持对海马中传入信息的判别处理。

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