Functioning and Gene Expression of Adenosine A1 Receptor During Zebrafish (Danio rerio) Development.

Zebrafish Pub Date : 2023-10-01 DOI:10.1089/zeb.2023.0002
Giovanna Trevisan Couto, Higor Arruda Caetano, Guilherme Pietro da Silva, Liliana Rockenbach, Jéssica Scheid da Silva, Monica Ryff Vianna, Rosane Souza Da Silva
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Abstract

The A1 adenosine receptor is the most widely expressed P1 receptor in vertebrates, performing inhibitory tone of the nervous system. Increased levels of adenosine are crucial to promote tissue protection in threatening situations, such as convulsion and hypoxia. Zebrafish is an established model organism for studies on health and disease. In this study, we evaluated the functionality of A1 adenosine receptor through development of zebrafish (6-7-day-, 3-, 8-, and 24-month-old), assessing: (I) the effects of the agonist N6-cyclopenthyladenosine (CPA) over locomotor parameters, (II) the anticonvulsant properties of CPA and adenosine per se in the pentylenetetrazol-induced seizure, and (III) the gene expression of adora1b through development. CPA promoted decreased distance traveled in the highest concentrations/doses tested (larvae: 75 to 500 μM; adults: 20 mg.kg-1), altered mean velocity (larvae: 50-500 μM; adults: 20 mg.kg-1) and time in the bottom zone of apparatus (adults: decrease in 20 mg.kg-1). Adenosine increased the latency of the larvae to reach stage II at 5 and 10 μM. CPA anticonvulsant effect against convulsive stage II was reached at 75 μM, although it decreased basal locomotor activity in larvae. For adults, CPA 10 mg.kg-1 was effective as anticonvulsant without locomotory effects. Adenosine had minor anticonvulsant effects in the concentration tested (larvae: 5 and 10 μM). The level of gene expression of adora1b was stable in brain from adult animals (8- and 24-month-old animals). These results suggest that zebrafish has similar responses to CPA as mammals. To avoid confounding factors, such as locomotor effects, during any brain function investigation using A1 adenosine receptor as a target, the concentration below 75 μM or below the dose of 20 mg.kg-1 of CPA is ideal for zebrafish at larval and adult stages, respectively.

斑马鱼(Danio rerio)发育过程中腺苷A1受体的功能和基因表达。
A1腺苷受体是脊椎动物中表达最广泛的P1受体,对神经系统起抑制作用。腺苷水平的提高对于在惊厥和缺氧等威胁情况下促进组织保护至关重要。斑马鱼是一种已建立的健康和疾病研究模式生物。在这项研究中,我们评估了A1腺苷受体在斑马鱼(6-7天、3个月、8个月和24个月大)发育过程中的功能,评估了:(I)激动剂N6-环戊腺苷(CPA)对运动参数的影响,(II)CPA和腺苷本身在戊四氮诱导的癫痫发作中的抗惊厥特性,以及(III)adora1b通过发育的基因表达。CPA在测试的最高浓度/剂量下促进旅行距离的减少(幼虫:75至500 μM;成年人:20 mg.kg-1),改变平均速度(幼虫:50-500 μM;成年人:20 mg.kg-1)和在器械底部区域的时间(成人:20岁时减少 mg.kg-1)。腺苷增加了幼虫在5和10时达到II期的潜伏期 μM。CPA对痉挛II期的抗惊厥作用在75岁时达到 μM,尽管它降低了幼虫的基础运动活性。对于成年人,CPA 10 mg.kg-1是一种有效的抗惊厥药物,对运动无明显影响。腺苷在测试浓度下具有轻微的抗惊厥作用(幼虫:5和10 μM)。在成年动物(8月龄和24月龄动物)的大脑中,adora1b的基因表达水平是稳定的。这些结果表明,斑马鱼对CPA的反应与哺乳动物相似。为了避免混淆因素,如运动效应,在使用A1腺苷受体作为靶点的任何脑功能研究中,浓度低于75 μM或低于20的剂量 mg.kg-1的CPA分别是斑马鱼幼虫期和成虫期的理想选择。
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