Cardiac Myosin and Thin Filament as Targets for Lead and Cadmium Divalent Cations

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Oksana P. Gerzen^1,a*, Iulia K. Potoskueva¹, Alena E. Tzybina¹, Tatiana A. Myachina¹, Larisa V. Nikitina¹

¹Institute of Immunology and Physiology, Ural Branch of the Russian Academy of Sciences, 620078 Ekaterinburg, Russia

^* To whom correspondence should be addressed.

Received: May 18, 2024; Revised: June 10, 2024; Accepted: June 11, 2024

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Lead and cadmium are heavy metals widely distributed in the environment and contribute significantly to cardiovascular morbidity and mortality. Using Leadmium Green dye, we have shown that lead and cadmium enter cardiomyocytes, distributing throughout the cell. Using an in vitro motility assay, we have shown that sliding velocity of actin and native thin filaments over myosin decreases with increasing concentrations of Pb²⁺ and Cd²⁺. Significantly lower concentrations of Pb²⁺ and Cd²⁺ (0.6 mM) were required to stop sliding of thin filaments over myosin compared to the stopping actin sliding over the same myosin (1.1-1.6 mM). Lower concentration of Cd²⁺ (1.1 mM) needed to stop actin sliding over myosin compared to the Pb²⁺+Cd²⁺ combination (1.3 mM) and lead alone (1.6 mM). There were no differences found in the effects of lead and cadmium cations on relative force developed by myosin heads or number of actin filaments bound to myosin. Sliding velocity of actin over myosin in the left atrium, right and left ventricles changed equally when exposed to the same dose of the same metal. Thus, we have demonstrated for the first time that Pb²⁺ and Cd²⁺ can directly affect myosin and thin filament function, with Cd²⁺ exerting a more toxic influence on myosin function compared to Pb²⁺.

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KEY WORDS: myosin, thin filament, lead, cadmium, cardiac muscle

DOI: 10.1134/S0006297924070095

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