Changes in adenosine A1 receptor-mediated regulation of hippocampal area CA2 following chronic high-dose caffeine treatment during adolescence in rats

大鼠青春期长期大剂量咖啡因治疗后腺苷 A1 受体介导的海马区 CA2 调节的变化

• 批准号: BB/P008143/1
• 负责人: Douglas Caruana
• 金额: $ 52.26万
• 依托单位: Keele University
• 依托单位国家: 英国
• 项目类别: Research Grant
• 财政年份: 2017
• 资助国家: 英国
• 起止时间: 2017 至 无数据
• 项目状态: 已结题
• 来源: https://gtr.ukri.org/projects?ref=BB%2FP008143%2F1
• 关键词: Changes; adenosine; A1; receptor; mediated

Memory is a highly complex cognitive function that involves interactions between numerous brain structures, proteins and signalling molecules. Indeed, experience-dependent changes in the strength of synaptic connections between neurons are though to underlie information storage in the brain. Thus, understanding the highly elastic nature, or the 'plasticity', of synapses is critical to uncovering how the brain converts our individual experiences into lasting memories. To this end, modulatory neurotransmitter systems play a central role in shaping synaptic processes involved in the encoding and retention of information within neural circuits. A fundamental problem remains, though, in understanding how extrinsic factors recruit, mimic or even hijack these endogenous regulatory signals to affect the development of brain systems critical to cognitive and mnemonic function.The mammalian nervous system undergoes several critical periods during early postnatal development in which cognitive and sensory functions are sensitive to lasting disruption by an array of environmental factors. Indeed, there is growing evidence to suggest that the hippocampal purinergic system in rodents also undergoes a period of significant maturation related to the expression pattern of the adenosine A1 receptor (A1R). Adenosine acts as a neuromodulator in the brain, and signalling at adenosine receptors in the hippocampus has been shown to influence memory formation and behaviour by regulating synaptic plasticity. In rats, the expression pattern of the A1R is not static during early development. In particular, the surface expression of the A1R increases significantly during adolescence in a specific part of the hippocampus, known as area Cornu Ammonis 2 (or CA2). However, changes in synaptic function and neuronal physiology in area CA2 following manipulations to disrupt adenosinergic signalling during development have yet to be explored in animal models.Consistent with the high expression of A1Rs in CA2 is the observation that caffeine and other A1R blockers preferentially enhance excitatory synaptic transmission in area CA2 at concentrations that have little effect on responses in other parts of the hippocampus. This suggests that A1Rs in CA2 may play a central role in mediating the cognitive enhancing effects of caffeine. Caffeine is a naturally-occurring cognitive enhancer that is widely-consumed to improve attention and augment memory. Its primary mechanism of action is thought to be through blockade of A1Rs, however, little is known about hippocampal area CA2 where A1Rs are highly expressed and where the surface expression of the A1R changes dramatically during adolescent development. The popularity of highly-caffeinated so-called 'energy' drinks has increased dramatically in the past 15 years, and recent trends highlight how teenagers consume energy drinks regularly and in quantities that exceed recommended daily limits. It is currently unknown, though, whether habitual consumption of energy drinks during adolescence is associated with lasting changes in brain function. Given that A1Rs increase dramatically during adolescence, together with the specificity that caffeine has in modifying synaptic function in CA2, the aim of this proposal is to evaluate the long-term effects of chronic caffeine administration on CA2 physiology and CA2-dependent forms of cognition. To achieve this, human adolescent energy drink consumption patterns will be modelled experimentally in rats and caffeine-induced changes in synaptic function, neuronal morphology and protein expression in CA2 will be assessed at the end of the dosing regimen. Evidence in support of a developmental window during which adolescents may be susceptible to lasting neurological dysfunction resulting from habitual caffeine consumption may provide justification to amend policy and regulate the sale of highly caffeinated products to vulnerable populations.

记忆是一种高度复杂的认知功能，涉及许多大脑结构，蛋白质和信号分子之间的相互作用。事实上，神经元之间突触连接强度的经验依赖性变化被认为是大脑信息存储的基础。因此，了解突触的高度弹性或“可塑性”对于揭示大脑如何将我们的个人经历转化为持久记忆至关重要。为此，调节性神经递质系统在塑造参与神经回路内的信息编码和保留的突触过程中发挥核心作用。然而，一个根本性的问题仍然是，在理解外部因素如何招募，模仿甚至劫持这些内源性调节信号，影响大脑系统的发展至关重要的认知和记忆功能，哺乳动物的神经系统在出生后的早期发育过程中经历了几个关键时期，在这些时期，认知和感觉功能对一系列环境因素的持续干扰很敏感。事实上，有越来越多的证据表明，啮齿动物的海马嘌呤能系统也经历了一个时期的腺苷A1受体（A1 R）的表达模式相关的显着成熟。腺苷在大脑中充当神经调质，并且已经显示海马体中腺苷受体的信号传导通过调节突触可塑性来影响记忆形成和行为。在大鼠中，A1R的表达模式在早期发育过程中不是静态的。特别是，A1R的表面表达在青春期海马体的特定部分显著增加，称为角Ammonis 2（或CA2）。然而，突触功能和神经元生理学的变化，在CA2区以下的操作，以破坏adenosinergic信号在发展过程中还有待探讨在动物models.Consistent高表达的A1受体在CA2区的观察，咖啡因和其他A1受体阻滞剂优先增强兴奋性突触传递在CA2区的浓度，在海马体的其他部分的反应几乎没有影响。这表明CA2中的A1R可能在介导咖啡因的认知增强作用中发挥核心作用。咖啡因是一种天然的认知增强剂，被广泛用于提高注意力和增强记忆力。其主要作用机制被认为是通过阻断A1R，然而，对海马CA2区知之甚少，其中A1R高度表达，并且A1R的表面表达在青少年发育期间发生显著变化。在过去的15年里，高咖啡因的所谓“能量”饮料的流行程度急剧上升，最近的趋势突出了青少年如何定期饮用能量饮料，并且数量超过了建议的每日限制。然而，目前尚不清楚青春期习惯性饮用能量饮料是否与大脑功能的持久变化有关。考虑到A1Rs在青春期急剧增加，以及咖啡因在修改CA2突触功能方面的特异性，本提案的目的是评估长期咖啡因给药对CA2生理学和CA2依赖性认知形式的长期影响。为了实现这一目标，将在大鼠中对人类青少年能量饮料消费模式进行实验建模，并在给药方案结束时评估咖啡因诱导的突触功能、神经元形态和CA2中蛋白质表达的变化。证据支持发育窗口期，在此期间，青少年可能容易受到持久的神经功能障碍，导致习惯性的咖啡因消费可能提供合理的修改政策和规范高咖啡因产品的销售给弱势群体。