在高血糖斑马鱼中,钝化的皮质醇和改变的抗氧化防御作为全身应激的生物标志物。

IF 2.9 3区 医学 Q2 ENDOCRINOLOGY & METABOLISM
Roseleena Minz, Praveen Kumar Sharma
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引用次数: 0

摘要

背景/目的:新出现的证据表明,作为“糖尿病的标志”的高血糖不仅与外周代谢功能障碍有关,而且还与其对大脑健康的有害影响有关,经常导致与压力相关的病理,如抑郁和认知能力下降。斑马鱼具有良好的血管系统特征和行为分析,为研究蔗糖诱导的高血糖的影响提供了独特的模型。本研究旨在利用斑马鱼研究蔗糖诱导的高血糖对2型糖尿病应激机制的影响。方法:将雄性斑马鱼分为对照组和55.5mM蔗糖浸泡组。在两周的时间里,这些老鼠接受了行为分析——新水箱测试(NTT)和光/暗测试(LDT)。NTT通过测量在新水箱的不同垂直区域中花费的时间来评估焦虑相关行为,而光/暗测试则根据在照明隔间和黑暗隔间中花费的时间来评估焦虑反应。使用ZebraZoom软件对轨迹、体坐标和尾部运动学进行量化,以评估运动指标状态。测量皮质醇水平以评估下丘脑轴功能。测定抗氧化酶,包括超氧化物歧化酶(SOD)和过氧化氢酶(CAT),以评估氧化应激。结果:结果显示,暴露于蔗糖的斑马鱼表现出显著的高血糖(**p)。结论:斑马鱼系统有效地模拟了蔗糖诱导的高血糖的负面影响,为研究2型糖尿病的应激机制提供了有价值的见解。这些发现表明,高血糖改变内分泌应激反应和抗氧化系统,可能作为全身性应激的生物标志物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Blunted cortisol and altered antioxidant defense as biomarkers of systemic stress in hyperglycemic Zebrafish.

Background/aim: Emerging evidence links hyperglycemia, a "hallmark of diabetes mellitus" not only to peripheral metabolic dysfunction but also to its detrimental impact on brain health, often contributing to stress-related pathologies such as depression and cognitive decline. Zebrafish, with their well-characterized vascular system and behavioral assays, offer a unique model to study the impacts of sucrose-induced hyperglycemia. This study aims to investigates the effects of sucrose-induced hyperglycemia on stress mechanisms in type 2 diabetes using the zebrafish.

Methods: Male zebrafish were divided into two groups: control, and 55.5mM sucrose immersed. Over two weeks, these were subjected to behavioural assays- the novel tank test (NTT) and the light/dark test (LDT). The NTT assessed anxiety-related behaviour by measuring the time spent in different vertical zones of a novel tank, while the light/dark test evaluated anxiety responses based on the time spent in illuminated versus dark compartments. Trajectory body coordinates and tail kinematics were quantified using ZebraZoom software to asses locomotor metrics status. Cortisol levels were measured to assess HPA axis function. Antioxidant enzymes, including superoxide dismutase (SOD) and catalase (CAT), were quantified to evaluate oxidative stress.

Results: The results revealed that zebrafish exposed to sucrose exhibited significant hyperglycemia (**p < 0.01) and behavioural changes compared to those on control. Specifically, in the NTT, the hyperglycemic group demonstrated heightened anxiety-like behaviour, spending more time at the bottom zone of the tank. In the light/dark test, male zebrafish showed increased anxiety by spending more time in the dark compartment. Hyperglycemic zebrafish showed a significant blunting of the cortisol response, indicating impaired stress regulation. Additionally, SOD activity was increased, while CAT activity was decreased, suggesting an imbalance in antioxidative defense mechanisms.

Conclusion: The zebrafish system effectively models the negative impacts of sucrose-induced hyperglycemia, providing valuable insights into the stress mechanisms associated with type 2 diabetes. These findings demonstrate that hyperglycemia alters both endocrine stress response and antioxidant systems, potentially serving as biomarkers of systemic stress.

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来源期刊
Acta Diabetologica
Acta Diabetologica 医学-内分泌学与代谢
CiteScore
7.30
自引率
2.60%
发文量
180
审稿时长
2 months
期刊介绍: Acta Diabetologica is a journal that publishes reports of experimental and clinical research on diabetes mellitus and related metabolic diseases. Original contributions on biochemical, physiological, pathophysiological and clinical aspects of research on diabetes and metabolic diseases are welcome. Reports are published in the form of original articles, short communications and letters to the editor. Invited reviews and editorials are also published. A Methodology forum, which publishes contributions on methodological aspects of diabetes in vivo and in vitro, is also available. The Editor-in-chief will be pleased to consider articles describing new techniques (e.g., new transplantation methods, metabolic models), of innovative importance in the field of diabetes/metabolism. Finally, workshop reports are also welcome in Acta Diabetologica.
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