Comparative effects of parent and heated cinnamaldehyde on the function of human iPSC-derived cardiac myocytes. (December 2019)

• Record Type: Journal Article
• Authors: Nystoriak, Matthew A.; Kilfoil, Peter J.; Lorkiewicz, Pawel K.; Ramesh, Bhargav; Kuehl, Philip J.; McDonald, Jacob; Bhatnagar, Aruni; Conklin, Daniel J.
• Is Part Of: Toxicology in vitro. Volume 61(2019)
• Publication Date: 2019-12
• Subjects: Electronic cigarettes -- Electronic nicotine delivery systems (ENDS) -- Cellular impedance -- Cardiac action potential -- Arrhythmia -- Cytotoxicity; Toxicity testing -- In vitro -- Periodicals; Toxicology -- Periodicals; 615.9
• DOI: 10.1016/j.tiv.2019.104648
• Languages: English
• ISSNs: 0887-2333

Abstract

Abstract: Many e-cigarette products contain cinnamaldehyde as a primary constituent of cinnamon flavorings. When used as a food additive, cinnamaldehyde is generally regarded as safe for ingestion. However, little is known about the effects of cinnamaldehyde or its degradation products, generated after heating and inhalation, which may lead to elevated circulatory exposure to the heart. Hence, in this study, we tested the in vitro cardiac toxicity of cinnamaldehyde and its thermal degradation products generated by heating at low (200 ± 50 °C) and high temperatures (700 ± 50 °C) on the contractility, rhythmicity and electrical signaling properties of human induced pluripotent stem cell-derived cardiac myocytes (hiPSC-CMs). Cellular impedance measurements on spontaneously beating hiPSC-CMs revealed that cinnamaldehyde significantly alters contraction-dependent signal amplitude, beating rate, and cell morphology. These effects were attenuated after cinnamaldehyde was subjected to heating at low or high temperatures. Current clamp analysis of hiPSC-CM action potentials (APs) showed only modest effects of acute application of 1–100 μM cinnamaldehyde on resting membrane potential, while prolonged (~20 min) application of 100 μM cinnamaldehyde resulted in progressive depolarization and loss of rhythmic AP spiking activity. Collectively, these results suggest that micromolar levels of cinnamaldehyde could alter cardiac excitability, in part by impairing the processes that regulate membrane potential and depolarization. Our results further suggest that heating cinnamaldehyde by itself does not directly lead to the formation of products with greater cardiotoxicity in vitro. Highlights: Cinnamaldehyde impairs contractile activity of human induced pluripotent stem cell-derived cardiac myocytes (hiPSC-CMs). Exposure of hiPSC-CMs to cinnamaldehyde leads to depolarization of resting membrane potential. Heating cinnamaldehyde attenuates effects on hiPSC-CM function.