Polyhexamethylene Guanidine Phosphate Enhanced Procoagulant Activity through Oxidative-Stress-Mediated Phosphatidylserine Exposure in Platelets

被引:1
|
作者
Choi, Ju Hee [1 ]
Kim, Keunyoung [1 ]
机构
[1] Kangwon Natl Univ, Coll Pharm, Chunchon 24341, South Korea
基金
新加坡国家研究基金会;
关键词
polyhexamethylene guanidine phosphate (PHMG-p); platelets; phosphatidylserine (PS) exposure; procoagulant activation; humidifier disinfectant; cardiovascular disease; HUMIDIFIER DISINFECTANT; LUNG INJURY; HYDROCHLORIDE; MITOCHONDRIA; CALCIUM; RAT; MICROPARTICLES; CYTOTOXICITY; MECHANISMS; GENERATION;
D O I
10.3390/toxics12010050
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Polyhexamethylene guanidine phosphate (PHMG-p) is a common biocidal disinfectant that is widely used in industry and household products. However, PHMG-p was misused as a humidifier disinfectant (HD) in South Korea, which had fatal health effects. Various health problems including cardiovascular diseases were observed in HD-exposed groups. However, the potential underlying mechanism of HD-associated cardiovascular diseases is poorly understood. Here, we examined the procoagulant activity of platelets caused by PHMG-p and clarified the underlying mechanism. PHMG-p enhanced phosphatidylserine (PS) exposure through alteration of phospholipid transporters, scramblase, and flippase. Intracellular calcium elevation, intracellular ATP depletion, and caspase-3 activation appeared to underlie phospholipid transporter dysregulation caused by PHMG-p, which was mediated by oxidative stress and mitochondrial dysfunction. Notably, antioxidant enzyme catalase and calcium chelator EGTA reversed PHMG-p-induced PS exposure and thrombin generation, confirming the contributive role of oxidative stress and intracellular calcium in the procoagulant effects of PHMG-p. These series of events led to procoagulant activation of platelets, which was revealed as enhanced thrombin generation. Collectively, PHMG-p triggered procoagulant activation of platelets, which may promote prothrombotic risks and cardiovascular diseases. These findings improve our understanding of HD-associated cardiovascular diseases.
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页数:12
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