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扁柏酚诱导斑马鱼幼体发育和心血管毒性及潜在机制。

Hinokitiol induces developmental and cardiovascular toxicity in zebrafish larvae and potential mechanisms.

作者信息

Ge Chenkai, Wang Ziang, Hu Weitao, Shen Qinyuan, Li Weirong, Zha Wenwen, Xiao Zhonghao, Tang Jingrong, Huang Ling, Li Huimin, Cao Zigang, Chen Jianjun

机构信息

School of Ophthalmology and Optometry, Wenzhou Medical University, Wenzhou 325003, Zhejiang, China; Jiangxi Engineering Laboratory of Zebrafish Modeling and Drug Screening for Human Diseases, Jiangxi Key Laboratory of Developmental Biology of Organs and Epigenetics, College of Life Sciences, Clinical Research Center of Affiliated Hospital of Jinggangshan University, Jinggangshan University, Ji'an 343009, China.

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

出版信息

Toxicol Appl Pharmacol. 2025 Sep;502:117461. doi: 10.1016/j.taap.2025.117461. Epub 2025 Jul 8.

Abstract

Hinokitiol is a natural compound collected from the trunk of cypress, belonging to the tropolone family of compounds. It has anti-inflammatory, anti-tumour and antibacterial activities, making it a natural product with a wide range of applications. It is used as an additive in hair growth agents, toothpaste, make-up and furniture wood. However, the toxicity of hinokitiol remains poorly understood. Therefore, the cardiovascular and developmental toxicity of hinokitiol in organisms was investigated in zebrafish larvae. In the study, zebrafish embryos were exposed to hinokitiol for 3 days to study the developmental and cardiovascular toxicity of hinokitiol. Concentrations for the hinokitiol toxicity test were set at 0, 0.4, 0.8, 1.2, 1.6, 2.0 and 2.2 mg/L. The experimental concentrations of 0, 0.8, 1.2 and 1.6 mg/L were subsequently determined based on phenotype. The results showed that exposure to hinokitiol resulted in increased mortality, changes in hatching rates and abnormalities in the apparent morphology of zebrafish embryos/larvae (shortened body length, reduced eye area, pericardial edema, and abnormal heart rate). In addition, hinokitiol impaired the cardiovascular system of zebrafish larvae, as evidenced by the absence of morphological features of the atria and ventricles, linearization of the heart, and reduction in the area and abundance of blood vessels. In addition, hinokitiol affects mitochondrial function by affecting iron ion levels and generates oxidative stress leading to apoptosis and which then generates cardiovascular toxicity. Our findings suggest that hinokitiol causes mitochondrial dysfunction and oxidative stress through iron chelation, which in turn triggers apoptosis, ultimately leading to cardiovascular and developmental toxicity in zebrafish larvae. The study provides new insights into the safety of hinokitiol and natural products.

摘要

扁柏酚是一种从柏树树干中提取的天然化合物,属于托酚酮类化合物。它具有抗炎、抗肿瘤和抗菌活性,是一种具有广泛应用的天然产物。它被用作生发剂、牙膏、化妆品和家具木材中的添加剂。然而,扁柏酚的毒性仍知之甚少。因此,在斑马鱼幼体中研究了扁柏酚对生物体的心血管和发育毒性。在该研究中,将斑马鱼胚胎暴露于扁柏酚中3天,以研究扁柏酚的发育和心血管毒性。扁柏酚毒性试验的浓度设定为0、0.4、0.8、1.2、1.6、2.0和2.2mg/L。随后根据表型确定0、0.8、1.2和1.6mg/L的实验浓度。结果表明,暴露于扁柏酚会导致斑马鱼胚胎/幼体死亡率增加、孵化率变化以及明显形态异常(体长缩短、眼面积减小、心包水肿和心率异常)。此外,扁柏酚损害了斑马鱼幼体的心血管系统,表现为心房和心室无形态特征、心脏线性化以及血管面积和数量减少。此外,扁柏酚通过影响铁离子水平影响线粒体功能,并产生氧化应激导致细胞凋亡,进而产生心血管毒性。我们的研究结果表明,扁柏酚通过铁螯合导致线粒体功能障碍和氧化应激,进而引发细胞凋亡,最终导致斑马鱼幼体的心血管和发育毒性。该研究为扁柏酚和天然产物的安全性提供了新的见解。

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