Distinct acute stressors produce different intensity of anxiety-like behavior and differential glutamate release in zebrafish brain.

IF 2.6 3区 医学 Q2 BEHAVIORAL SCIENCES
Frontiers in Behavioral Neuroscience Pub Date : 2024-10-23 eCollection Date: 2024-01-01 DOI:10.3389/fnbeh.2024.1464992
Milena Letícia Martins, Emerson Feio Pinheiro, Geovanna Ayami Saito, Caroline Araújo Costa De Lima, Luana Ketlen Reis Leão, Evander de Jesus Oliveira Batista, Adelaide da Conceição Fonseca Passos, Amauri Gouveia, Karen Renata Herculano Matos Oliveira, Anderson Manoel Herculano
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Abstract

Anxiety disorder is one of the most well-characterized behavioral disorders in individuals subjected to acute or chronic stress. However, few studies have demonstrated how different types of stressors can modulate the neurochemical alterations involved in the generation of anxiety. In this study, we hypothesize that subjects exposed to different aversive stimuli (mechanical, chemical, and spatial restriction) present varied intensities of anxiety-like responses associated with distinct patterns of gamma-aminobutyric acid (GABA) and glutamate release in the brain. Adult zebrafish, Danio rerio (n = 60), were randomly divided into four experimental groups; control, acute restraint stress (ARS), conspecific alarm substance (CAS), and chasing with net (CN). After the stress protocols, the animals were individually transferred to a novel tank diving test for behavioral analysis. Subsequently, their brains were collected and subjected to GABA and glutamate release assay for quantification by HPLC. Our behavioral results showed that all aversive stimuli were capable of inducing anxiety-like behavior. However, the impact of anxiogenic behavior was more prominent in the CN and CAS groups when compared to ARS. This phenomenon was evident in all analyzed behavioral parameters (time on top, freezing, mean speed, maximum speed, and erratic swimming). Our data also showed that all aversive stimuli significantly decreased GABA release compared to the control group. Only animals exposed to CN and CAS presented an increase in extracellular glutamate levels. Different acute stressors induced different levels of anxiety-like behavior in zebrafish as well as specific alterations in GABAergic and glutamatergic release in the brain. These results demonstrate the complexity of anxiety disorders, highlighting that both behavioral and neurochemical responses are highly context-dependent.

不同的急性应激源会在斑马鱼大脑中产生不同强度的焦虑样行为和不同的谷氨酸释放。
焦虑症是受急性或慢性压力影响的人中特征最明显的行为障碍之一。然而,很少有研究证明不同类型的应激源如何调节产生焦虑的神经化学变化。在本研究中,我们假设受试者暴露于不同的厌恶刺激(机械、化学和空间限制)时,会出现不同强度的焦虑样反应,这些反应与大脑中γ-氨基丁酸(GABA)和谷氨酸的不同释放模式有关。成年斑马鱼(n = 60)被随机分为四个实验组:对照组、急性束缚应激组(ARS)、同种警报物质组(CAS)和带网追逐组(CN)。应激方案结束后,动物被单独转移到一个新的水槽潜水试验中进行行为分析。随后,收集动物大脑并进行GABA和谷氨酸释放测定,通过高效液相色谱法进行定量。我们的行为结果表明,所有的厌恶刺激都能诱发类似焦虑的行为。然而,与ARS相比,CN组和CAS组的焦虑行为影响更为显著。这一现象在所有分析的行为参数(上浮时间、冻结、平均速度、最大速度和不规则游动)中都很明显。我们的数据还显示,与对照组相比,所有厌恶刺激都会显著减少 GABA 的释放。只有受到 CN 和 CAS 刺激的动物细胞外谷氨酸水平有所上升。不同的急性应激源会诱发斑马鱼不同程度的焦虑样行为,以及大脑中 GABA 能和谷氨酸能释放的特定改变。这些结果表明了焦虑症的复杂性,强调了行为和神经化学反应都是高度依赖于环境的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Frontiers in Behavioral Neuroscience
Frontiers in Behavioral Neuroscience BEHAVIORAL SCIENCES-NEUROSCIENCES
CiteScore
4.70
自引率
3.30%
发文量
506
审稿时长
6-12 weeks
期刊介绍: Frontiers in Behavioral Neuroscience is a leading journal in its field, publishing rigorously peer-reviewed research that advances our understanding of the neural mechanisms underlying behavior. Field Chief Editor Nuno Sousa at the Instituto de Pesquisa em Ciências da Vida e da Saúde (ICVS) is supported by an outstanding Editorial Board of international experts. This multidisciplinary open-access journal is at the forefront of disseminating and communicating scientific knowledge and impactful discoveries to researchers, academics, clinicians and the public worldwide. This journal publishes major insights into the neural mechanisms of animal and human behavior, and welcomes articles studying the interplay between behavior and its neurobiological basis at all levels: from molecular biology and genetics, to morphological, biochemical, neurochemical, electrophysiological, neuroendocrine, pharmacological, and neuroimaging studies.
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