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硫酸伊沙康唑通过上调氧化应激诱导斑马鱼幼鱼心脏发育缺陷。

Isavuconazonium sulfate induces heart development defects in zebrafish larvae by upregulation of oxidative stress.

机构信息

Affiliated Hospital of Jinggangshan University, Jiangxi Engineering Laboratory of Zebrafish Modeling and Drug Screening for Human Diseases, Jiangxi Key Laboratory of Developmental Biology of Organs and Epigenetics, Key Laboratory of Jiangxi Province for Biological Invasion and Biosecurity, Clinical Research Center of Affiliated Hospital of Jinggangshan University, College of Life Sciences, Jinggangshan University, 343009, Ji'an, China.

Affiliated Hospital of Jinggangshan University, Clinical Research Center of Affiliated Hospital of Jinggangshan University, 343000, Ji'an, Jiangxi Province, China.

出版信息

Chem Biol Interact. 2024 Dec 1;404:111267. doi: 10.1016/j.cbi.2024.111267. Epub 2024 Oct 11.

Abstract

Environmental pollution remains a pressing global concern, with a substantial number of annual fatalities attributed to pollution-induced diseases. One emerging facet of environmental pollution is drug contamination, whereby pharmaceutical compounds can readily infiltrate water sources during manufacturing or utilization, subsequently being detected in various aquatic ecosystems. Some drugs have been detected in many watersheds at concentrations that can cause toxicity to aquatic organisms. Isavuconazonium sulfate (ISAV-SF), a prevalent antifungal medication, is no exception, warranting an exploration of its potential toxicity. However, limited research has been conducted in this domain. In this investigation, zebrafish were employed as a model organism to scrutinize the cardiotoxicity of ISAV-SF. Exposure of zebrafish embryos to concentrations of 0.5, 0.75, and 1 mg/L of ISAV-SF resulted in noteworthy cardiac developmental aberrations. These anomalies encompassed enlarged pericardial area, diminished heart rate, alterations in SV-BA distance, and the detachment of cardiomyocytes from the endocardium. Exposure to ISAV-SF caused disruption of the expression of genes related to cardiac development (gata4, klf2a, nkx2.5, vmhc, tbx2b), especially in the high concentration group. Moreover, the Notch signaling pathway was inhibited and oxidative stress levels were upregulated in all exposed groups. Remarkably, the administration of the antioxidant astaxanthin effectively mitigated oxidative stress levels, thus ameliorating heart developmental impairments. These results suggest that ISAV-SF may contribute to cardiac developmental defects by upregulating oxidative stress. This study serves as a pivotal reference for the utilization of ISAV-SF within the market, emphasizing the necessity to curtail its introduction into aquatic environments during production and consumption and to evaluate its repercussions on aquatic organisms.

摘要

环境污染仍然是一个紧迫的全球问题,大量的年死亡人数归因于污染引起的疾病。环境污染的一个新出现的方面是药物污染,药物化合物在制造或使用过程中很容易渗透到水源中,随后在各种水生生态系统中被检测到。一些药物在许多流域的浓度被检测到,足以对水生生物造成毒性。伊曲康唑硫酸盐(ISAV-SF)是一种常见的抗真菌药物,也不例外,需要探索其潜在的毒性。然而,在这一领域的研究有限。在这项研究中,斑马鱼被用作模型生物来研究 ISAV-SF 的心脏毒性。将斑马鱼胚胎暴露于 0.5、0.75 和 1 mg/L 的 ISAV-SF 浓度下,导致明显的心脏发育异常。这些异常包括心包面积增大、心率降低、SV-BA 距离改变以及心肌细胞从心内膜分离。ISAV-SF 暴露导致与心脏发育相关的基因(gata4、klf2a、nkx2.5、vmhc、tbx2b)表达紊乱,特别是在高浓度组。此外,Notch 信号通路被抑制,所有暴露组的氧化应激水平升高。值得注意的是,抗氧化剂虾青素的给药有效地降低了氧化应激水平,从而改善了心脏发育损伤。这些结果表明,ISAV-SF 可能通过上调氧化应激导致心脏发育缺陷。这项研究为 ISAV-SF 在市场中的应用提供了重要参考,强调了在生产和消费过程中减少其引入到水生环境中的必要性,并评估其对水生生物的影响。

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