Yin Jiufeng, Wang Hui, Zhao Feng, Liang Dan, Yang Wenqing, Zhang Dan
Institute for Chinese Medicine Innovation, Shandong University of Traditional Chinese Medicine, Jinan 250300, China.
Laboratory Centre, Shandong University of Traditional Chinese Medicine, Jinan 250300, China.
Toxics. 2024 Nov 3;12(11):799. doi: 10.3390/toxics12110799.
Protocatechuic aldehyde (PCA) is a natural phenolic acid compound with pharmacological effects such as anti-oxidative stress, antibacterial, anti-apoptotic, anti-inflammatory, anti-platelet aggregation, and anti-tumor. Despite the favorable therapeutic effects of PCA, it is imperative to recognize that adverse drug reactions can arise even with satisfactory quality assurance measures and during standard clinical application and dosing. Additionally, the acute toxicity and cardiotoxic sequelae of PCA are frequently under reported in the available documentation. To investigate the acute toxicity and cardiotoxic effects of PCA, the present study comprehensively assessed the acute toxicity and cardiotoxic effects of PCA by administering different concentrations of PCA and by monitoring the phenotypic changes in zebrafish, using AB wild-type zebrafish as the experimental model organism. Meanwhile, the target genes of PCA that may cause cardiotoxicity were predicted and validated using a network pharmacology approach. Our findings indicated that PCA exhibited severe acute toxicity and cardiotoxic effects in zebrafish at 70 μg/mL and 80 μg/mL. Furthermore, PIK3CA, PARP1, and GSK3β may be involved in the mechanism of action of the cardiotoxicity-inducing effects of this compound. The present investigation has afforded a deeper insight into the acute toxicity and cardiotoxic impacts of PCA on zebrafish and has established a significant theoretical foundation for the evaluation of toxicity in pharmaceuticals incorporating PCA.
原儿茶醛(PCA)是一种天然酚酸化合物,具有抗氧化应激、抗菌、抗凋亡、抗炎、抗血小板聚集和抗肿瘤等药理作用。尽管PCA具有良好的治疗效果,但必须认识到,即使采取了令人满意的质量保证措施,在标准临床应用和给药过程中仍可能出现药物不良反应。此外,PCA的急性毒性和心脏毒性后遗症在现有文献中经常报道不足。为了研究PCA的急性毒性和心脏毒性作用,本研究以AB野生型斑马鱼为实验模型生物,通过给予不同浓度的PCA并监测斑马鱼的表型变化,全面评估了PCA的急性毒性和心脏毒性作用。同时,采用网络药理学方法预测并验证了可能导致心脏毒性的PCA靶基因。我们的研究结果表明,PCA在70μg/mL和80μg/mL时对斑马鱼表现出严重的急性毒性和心脏毒性作用。此外,PIK3CA、PARP1和GSK3β可能参与了该化合物诱导心脏毒性作用的机制。本研究为深入了解PCA对斑马鱼的急性毒性和心脏毒性影响提供了更深刻的认识,并为评估含PCA药物的毒性奠定了重要的理论基础。