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阿奇霉素通过干扰VEGF/Notch信号通路诱导斑马鱼产生神经毒性。

Azithromycin induces neurotoxicity in zebrafish by interfering with the VEGF/Notch signaling pathway.

作者信息

Chen Chen, Song Jie, Pu Qian, Liu Xingcheng, Yan Jin, Wang Xuedong, Wang Huili, Qian Qiuhui

机构信息

National and Local Joint Engineering Laboratory of Municipal Sewage Resource Utilization Technology, School of Environmental Science and Engineering, Suzhou University of Science and Technology, Suzhou 215009, China.

National and Local Joint Engineering Laboratory of Municipal Sewage Resource Utilization Technology, School of Environmental Science and Engineering, Suzhou University of Science and Technology, Suzhou 215009, China.

出版信息

Sci Total Environ. 2023 Dec 10;903:166505. doi: 10.1016/j.scitotenv.2023.166505. Epub 2023 Aug 23.

Abstract

Azithromycin (AZM) is a widely used antibiotic in both human and veterinary medicine, and its use has significantly increased during the COVID-19 pandemic. However, potential adverse effects of AZM on aquatic organisms have not been well studied. In this study, we explored the neurotoxicity of AZM in zebrafish and delved into its underlying mechanisms. Our results showed that AZM exposure resulted in a spectrum of detrimental effects in zebrafish, encompassing abnormal behaviors, damaged neuronal development, aberrant lateral line nervous system development, vascular malformations and perturbed expression of genes related to neural development. Moreover, we observed a concentration-dependent exacerbation of these neurotoxic manifestations with increasing AZM concentrations. Notably, AZM induced excessive cell apoptosis and oxidative stress damage. In addition, alterations in the expression levels of the genes involved in the VEGF/Notch signaling pathway were evident in AZM-exposed zebrafish. Consequently, we hypothesize that AZM may induce neurotoxicity by influencing the VEGF/Notch signaling pathway. To validate this hypothesis, we introduced a VEGF signaling inhibitor, axitinib, and a Notch signaling agonist, valproic acid, alongside AZM exposure. Remarkably, the administration of these rescue compounds significantly mitigated the neurotoxic effects induced by AZM. This dual verification provides compelling evidence that AZM indeed induces neurotoxicity during the early developmental stages of zebrafish, primarily through its interference with the VEGF/Notch pathway. Innovatively, our study reveals the molecular mechanism of AZM-induced neurotoxicity from the perspective of the close connection between blood vessels and nervous system. These findings provide new insights into the potential mechanisms underlying the neurotoxic effect of antibiotics and highlight the need for further investigation into the ecotoxicological effects of antibiotics on aquatic organisms and the potential risks to human health.

摘要

阿奇霉素(AZM)是一种在人类和兽医学中广泛使用的抗生素,在新冠疫情期间其使用量显著增加。然而,AZM对水生生物的潜在不良影响尚未得到充分研究。在本研究中,我们探究了AZM对斑马鱼的神经毒性,并深入研究了其潜在机制。我们的结果表明,暴露于AZM会对斑马鱼产生一系列有害影响,包括行为异常、神经元发育受损、侧线神经系统发育异常、血管畸形以及与神经发育相关基因的表达紊乱。此外,我们观察到随着AZM浓度的增加,这些神经毒性表现呈浓度依赖性加剧。值得注意的是,AZM诱导了过度的细胞凋亡和氧化应激损伤。此外,在暴露于AZM的斑马鱼中,参与VEGF/Notch信号通路的基因表达水平发生了明显变化。因此,我们推测AZM可能通过影响VEGF/Notch信号通路诱导神经毒性。为了验证这一假设,我们在暴露于AZM的同时引入了VEGF信号抑制剂阿西替尼和Notch信号激动剂丙戊酸。值得注意的是,给予这些拯救化合物显著减轻了AZM诱导的神经毒性作用。这种双重验证提供了有力证据,表明AZM在斑马鱼早期发育阶段确实会诱导神经毒性,主要是通过干扰VEGF/Notch通路。我们的研究创新性地从血管与神经系统紧密联系的角度揭示了AZM诱导神经毒性的分子机制。这些发现为抗生素神经毒性作用的潜在机制提供了新的见解,并强调了进一步研究抗生素对水生生物的生态毒理学影响以及对人类健康潜在风险的必要性。

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