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西他氯铵对角膜上皮细胞的体外毒性

In Vitro Toxicity of Cetalkonium Chloride on Corneal Epithelial Cells.

作者信息

Park Joo-Hee, Park Choul Yong

机构信息

Department of Ophthalmology, Dongguk University Ilsan Hospital, Goyang 10326, Republic of Korea.

Department of Ophthalmology, Samsung Medical Center, Sungkyunkwan University School of Medicine, Suwon 06351, Republic of Korea.

出版信息

Pharmaceutics. 2025 Apr 16;17(4):522. doi: 10.3390/pharmaceutics17040522.

Abstract

: To investigate the toxicity of cetalkonium chloride (CKC) on primary cultured human corneal epithelial cells (HCECs). : HCECs were subjected to various concentrations (0.03125 × 10 to 2.0 × 10% ()) of CKC for durations ranging from 24 to 72 h. Cell viability was evaluated using the CCK-8 kit along with live and dead cell staining. Intracellular reactive oxygen species (ROS) levels were measured 20 min following CKC exposure. Observations of changes in cell morphology, cytoplasmic actin filaments, and mitochondrial distribution were conducted using immunocytochemistry and MitoTracker assays. Protein expression levels related to cell survival pathways, including mTOR, ERK, Akt, Bcl-xL, and BAX, were examined via Western blot analysis. : CKC exhibited dose-dependent toxicity in HCECs. Exposure to CKC concentrations below 0.125 × 10% resulted in no significant decrease in HCEC viability for up to 72 h. Conversely, exposure to CKC at concentrations of 1.0 × 10% or higher led to significantly decreased HCEC viability. Following exposure to higher concentrations of CKC, elevated levels of intracellular ROS and LDH release were observed. This toxicity was further characterized by decreased levels of phosphorylated mTOR, phosphorylated Akt, phosphorylated ERK, and Bcl-xL, as well as an increase in BAX expression. As the CKC concentration increased, HCECs decreased in size, and mitochondria displayed a loss of characteristic punctate staining. : Our findings indicated that exposure to CKC caused significant toxicity in HCECs, which varied with concentration and duration of exposure. This toxicity was associated with an increase in ROS, mitochondrial alterations, and a decline in activity of the cell survival pathways.

摘要

: 研究西他氯铵(CKC)对原代培养的人角膜上皮细胞(HCECs)的毒性。: 将HCECs暴露于不同浓度(0.03125×10至2.0×10%())的CKC中,持续时间为24至72小时。使用CCK-8试剂盒以及活细胞和死细胞染色评估细胞活力。在CKC暴露20分钟后测量细胞内活性氧(ROS)水平。使用免疫细胞化学和MitoTracker分析观察细胞形态、细胞质肌动蛋白丝和线粒体分布的变化。通过蛋白质印迹分析检测与细胞存活途径相关的蛋白质表达水平,包括mTOR、ERK、Akt、Bcl-xL和BAX。: CKC在HCECs中表现出剂量依赖性毒性。暴露于低于0.125×10%浓度的CKC中,长达72小时HCEC活力无显著下降。相反,暴露于1.0×10%或更高浓度的CKC会导致HCEC活力显著下降。暴露于较高浓度的CKC后,观察到细胞内ROS水平升高和乳酸脱氢酶(LDH)释放增加。这种毒性的进一步特征是磷酸化mTOR、磷酸化Akt、磷酸化ERK和Bcl-xL水平降低,以及BAX表达增加。随着CKC浓度的增加,HCECs体积减小,线粒体呈现出特征性点状染色的丧失。: 我们的研究结果表明,暴露于CKC会对HCECs造成显著毒性,其毒性随暴露浓度和持续时间而变化。这种毒性与ROS增加、线粒体改变以及细胞存活途径活性下降有关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/81ed/12030407/049a285d316a/pharmaceutics-17-00522-g001.jpg

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