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Transcriptional Responses in Adult Zebrafish (Danio rerio) Exposed to Propranolol and Metoprolol

机译:成年斑马鱼(Danio rerio)中的转录反应暴露于普萘洛尔和美托洛尔

摘要

beta-adrenergic receptor blockers (beta-blockers) are widely detected in the aquatic environment; however, the effects of these pharmaceuticals on aquatic organisms remain uncertain. In this study, adult zebrafish were exposed to two different beta-blockers, propranolol and metoprolol, for 96 h. After exposure, the transcriptional responses of genes encoding the beta-adrenergic receptor (i.e., adrb1, adrb2a, adrb2b, adrb3a and adrb3b), genes involved in detoxification and the stress response (i.e., hsp70, tap, mt1 and mt2), and genes related to the antioxidant system (i.e., cu/zn-sod, mn-sod, cat and gpx) were examined in the brain, liver and gonad. Our results show that both propranolol and metoprolol exposure changes the mRNA level of beta-adrenergic receptors, indicating clear pharmacological target engagement of the beta-blockers. The transcription of genes related to antioxidant responses and detoxification process were induced, suggesting that beta-blocker exposure can activate the detoxification process and result in oxidative stress in fish. Moreover, the transcriptional responses displayed substantial tissue- and gender-specific effects. Considering the environmental concentrations of propranolol and metoprolol, these results suggest that these pharmaceuticals are unlikely to pose a risk to fish. However, the impacts in prolonged exposure, along with other possible side effects due to beta-adrenergic receptor blockade, should be further assessed.
机译:β-肾上腺素受体阻滞剂(β-受体阻滞剂)在水生环境中被广泛发现;然而,这些药物对水生生物的影响仍不确定。在这项研究中,成年斑马鱼暴露于两种不同的β受体阻滞剂普萘洛尔和美托洛尔96小时。暴露后,编码β-肾上腺素受体的基因(即adrb1,adrb2a,adrb2b,adrb3a和adrb3b),涉及排毒和应激反应的基因(即hsp70,tap,mt1和mt2)和基因的转录反应在大脑,肝脏和性腺中检查了与抗氧化剂系统(即cu / zn-sod,mn-sod,cat和gpx)相关的物质。我们的结果表明,普萘洛尔和美托洛尔的暴露都会改变β-肾上腺素受体的mRNA水平,这表明β-受体阻滞剂具有明确的药理靶点。诱导了与抗氧化剂反应和排毒过程相关的基因的转录,这表明暴露于β-受体阻滞剂可以激活排毒过程并导致鱼的氧化应激。此外,转录反应显示出实质性的组织和性别特异性作用。考虑到普萘洛尔和美托洛尔的环境浓度,这些结果表明这些药物不太可能对鱼类构成威胁。但是,应进一步评估延长暴露时间的影响以及由于β-肾上腺素受体阻滞而引起的其他可能的副作用。

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