Plasticizer Interaction With the Heart

Author:

Jaimes Rafael12,McCullough Damon1,Siegel Bryan2,Swift Luther12,McInerney Daniel1,Hiebert James1,Perez-Alday Erick A.3,Trenor Beatriz4,Sheng Jiansong5,Saiz Javier1,Tereshchenko Larisa G3,Posnack Nikki Gillum126

Affiliation:

1. Sheikh Zayed Institute for Pediatric Surgical Innovation (R.J., D. McCullough, L.S., D. McInerney, J.H., N.G.P.), Children’s National Health System, Washington DC.

2. Children’s National Heart Institute (R.J., B.S., L.S., N.G.P.), Children’s National Health System, Washington DC.

3. Knight Cardiovascular Institute, Oregon Health and Science University, Portland (E.A.P.-A., L.G.T.).

4. Ci2B-Universitat Politècnica de València, Spain (B.T., F.J.S.R.).

5. CiPA Lab, LLC, Rockville, MD (J.S.).

6. Departments of Pediatrics and Pharmacology and Physiology, School of Medicine and Health Sciences: George Washington University, Washington DC (N.G.P.).

Abstract

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 µmol/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.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Physiology (medical),Cardiology and Cardiovascular Medicine

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