Plasticizer Interaction With the Heart Chemicals Used in Plastic Medical Devices Can Interfere With Cardiac Electrophysiology

被引:34
|
作者
Jaimes, Rafael, III [1 ,2 ]
McCullough, Damon [1 ]
Siegel, Bryan [2 ]
Swift, Luther [1 ,2 ]
McInerney, Daniel [1 ]
Hiebert, James [1 ]
Perez-Alday, Erick A. [6 ]
Trenor, Beatriz [5 ]
Sheng, Jiansong [4 ]
Saiz, Javier
Tereshchenko, Larisa G. [2 ,6 ]
Posnack, Nikki Gillum [1 ,3 ]
机构
[1] Childrens Natl Hlth Syst, Sheikh Zayed Inst Pediat Surg Innovat, Washington, DC USA
[2] Childrens Natl Hlth Syst, Childrens Natl Heart Inst, Washington, DC USA
[3] George Washington Univ, Sch Med & Hlth Sci, Dept Pediat & Pharmacol & Physiol, Washington, DC 20052 USA
[4] CiPA Lab LLC, Rockville, MD USA
[5] Ci2B Univ Politecn Valencia, Valencia, Spain
[6] Oregon Hlth & Sci Univ, Knight Cardiovasc Inst, Portland, OR 97201 USA
来源
基金
美国国家卫生研究院;
关键词
action potentials; electrophysiology; heart; plasticizer; plastics; DI-2-ETHYLHEXYL PHTHALATE DEHP; BEAT RATE VARIABILITY; DI(2-ETHYLHEXYL) PHTHALATE; DI-(2-ETHYLHEXYL) PHTHALATE; NEWBORN-INFANTS; BISPHENOL-A; MONO-(2-ETHYLHEXYL) PHTHALATE; MONO(2-ETHYLHEXYL) PHTHALATE; ENDOCRINE DISRUPTORS; FREQUENCY CONTENT;
D O I
10.1161/CIRCEP.119.007294
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Phthalates are used as plasticizers in the manufacturing of flexible, plastic medical products. Patients can be subjected to high phthalate exposure through contact with plastic medical devices. We aimed to investigate the cardiac safety and biocompatibility of mono-2-ethylhexyl phthalate (MEHP), a phthalate with documented exposure in intensive care patients. Methods: Optical mapping of transmembrane voltage and pacing studies were performed on isolated, Langendorff-perfused rat hearts to assess cardiac electrophysiology after MEHP exposure compared with controls. MEHP dose was chosen based on reported blood concentrations after an exchange transfusion procedure. Results: Thirty-minute exposure to MEHP increased the atrioventricular node (147 versus 107 ms) and ventricular (117 versus 77.5 ms) effective refractory periods, compared with controls. Optical mapping revealed prolonged action potential duration at slower pacing cycle lengths, akin to reverse use dependence. The plateau phase of the action potential duration restitution curve steepened and became monophasic in MEHP-exposed hearts (0.18 versus 0.06 slope). Action potential duration lengthening occurred during late-phase repolarization resulting in triangulation (70.3 versus 56.6 ms). MEHP exposure also slowed epicardial conduction velocity (35 versus 60 cm/s), which may be partly explained by inhibition of Na(v)1.5 (874 and 231 mu mol/L half-maximal inhibitory concentration, fast and late sodium current). Conclusions: This study highlights the impact of acute MEHP exposure, using a clinically relevant dose, on cardiac electrophysiology in the intact heart. Heightened clinical exposure to plasticized medical products may have cardiac safety implications-given that action potential triangulation and electrical restitution modifications are a risk factor for early after depolarizations and cardiac arrhythmias.
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收藏
页数:13
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