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

生物 腺苷 斑马鱼 腺苷受体 戊四氮 达尼奥 腺苷A1受体 抗惊厥药 兴奋剂 内分泌学 内科学 药理学 基因表达 受体 癫痫 基因 神经科学 生物化学 医学
作者
Giovanna Trevisan Couto,Higor Arruda Caetano,Guilherme Pietro da Silva,Liliana Rockenbach,Jéssica Scheid da Silva,Mônica Ryff Moreira Roca Vianna,Rosane Souza da Silva
出处
期刊:Zebrafish [Mary Ann Liebert, Inc.]
卷期号:20 (5): 210-220 被引量:1
标识
DOI:10.1089/zeb.2023.0002
摘要

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.
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