时间干扰和酒精消耗对雌性大鼠奖赏相关脑区基因表达的影响。

IF 3.5 3区 医学 Q2 NEUROSCIENCES
Frontiers in Molecular Neuroscience Pub Date : 2024-11-18 eCollection Date: 2024-01-01 DOI:10.3389/fnmol.2024.1493862
Christiane Meyer, Konrad Schoettner, Shimon Amir
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引用次数: 0

摘要

在人类和动物模型中,暴露于异常明暗条件下引起的昼夜节律障碍与异常饮酒有关。饮酒行为的改变与大脑奖励相关区域的生物钟基因表达的改变有关,这可能归因于时间干扰或酒精的影响。然而,到目前为止,昼夜节律紊乱和酒精对大脑功能的综合影响还不太清楚。此外,尽管已知饮酒行为存在性别差异,但大多数研究仅针对男性受试者进行,因此对女性的影响尚不清楚。为了解决这一差距,在11小时/11小时光暗周期(LD22)或标准光照条件(LD24, 12小时/12小时光暗)下饲养的成年雌性大鼠被给予间歇性饮酒方案(IA20%),以评估对涉及酒精消耗和奖励的大脑区域基因表达的影响:前额叶皮层(PFC),伏隔核(NAc)和背纹状体(DS)。在相对于运动活动周期的两个时间点测量核心时钟基因(Bmal1、clock、Per2)、性激素受体(ERβ、PR)、谷氨酸受体(mGluR5、GluN2B)、钙激活通道(Kcnn2)和炎症细胞因子(TNF-α)的mRNA表达。LD22下的住房不影响酒精摄入量,但显著破坏了昼夜活动节律并减少了运动。Bmal1、ERβ和TNF-α表达的显著变化主要与畸变光条件有关,而Per2和PR表达的变化与酒精的影响有关。总的来说,这些结果表明,昼夜节律的破坏和/或间歇性酒精暴露对女性大脑中的基因表达有明显的影响,这可能对饮酒、成瘾以及最终的大脑健康的调节有影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effects of chronodisruption and alcohol consumption on gene expression in reward-related brain areas in female rats.

Circadian dysfunction caused by exposure to aberrant light-dark conditions is associated with abnormal alcohol consumption in humans and animal models. Changes in drinking behavior have been linked to alterations in clock gene expression in reward-related brain areas, which could be attributed to either the effect of chronodisruption or alcohol. To date, however, the combinatory effect of circadian disruption and alcohol on brain functions is less understood. Moreover, despite known sex differences in alcohol drinking behavior, most research has been carried out on male subjects only, and therefore implications for females remain unclear. To address this gap, adult female rats housed under an 11 h/11 h light-dark cycle (LD22) or standard light conditions (LD24, 12 h/12 h light-dark) were given access to an intermittent alcohol drinking protocol (IA20%) to assess the impact on gene expression in brain areas implicated in alcohol consumption and reward: the prefrontal cortex (PFC), nucleus accumbens (NAc), and dorsal striatum (DS). mRNA expression of core clock genes (Bmal1, Clock, Per2), sex hormone receptors (ERβ, PR), glutamate receptors (mGluR5, GluN2B), a calcium-activated channel (Kcnn2), and an inflammatory cytokine (TNF-α) were measured at two-time points relative to the locomotor activity cycle. Housing under LD22 did not affect alcohol intake but significantly disrupted circadian activity rhythms and reduced locomotion. Significant changes in the expression of Bmal1, ERβ, and TNF-α were primarily related to the aberrant light conditions, whereas changes in Per2 and PR expression were associated with the effect of alcohol. Collectively, these results indicate that disruption of circadian rhythms and/or intermittent alcohol exposure have distinct effects on gene expression in the female brain, which may have implications for the regulation of alcohol drinking, addiction, and, ultimately, brain health.

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来源期刊
CiteScore
5.70
自引率
2.10%
发文量
669
审稿时长
14 weeks
期刊介绍: Frontiers in Molecular Neuroscience is a first-tier electronic journal devoted to identifying key molecules, as well as their functions and interactions, that underlie the structure, design and function of the brain across all levels. The scope of our journal encompasses synaptic and cellular proteins, coding and non-coding RNA, and molecular mechanisms regulating cellular and dendritic RNA translation. In recent years, a plethora of new cellular and synaptic players have been identified from reduced systems, such as neuronal cultures, but the relevance of these molecules in terms of cellular and synaptic function and plasticity in the living brain and its circuits has not been validated. The effects of spine growth and density observed using gene products identified from in vitro work are frequently not reproduced in vivo. Our journal is particularly interested in studies on genetically engineered model organisms (C. elegans, Drosophila, mouse), in which alterations in key molecules underlying cellular and synaptic function and plasticity produce defined anatomical, physiological and behavioral changes. In the mouse, genetic alterations limited to particular neural circuits (olfactory bulb, motor cortex, cortical layers, hippocampal subfields, cerebellum), preferably regulated in time and on demand, are of special interest, as they sidestep potential compensatory developmental effects.
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