Research Article | | Peer-Reviewed

Acute Lead Exposure Weakens Myocardial Contractile Function and the Therapeutic Effect of Alpha Lipoic Acid

Received: 21 November 2025     Accepted: 21 November 2025     Published: 22 November 2025
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Abstract

This study comprehensively utilized toad hearts and myocardial cell models to explore the effects of acute lead exposure on myocardial contractile function and the therapeutic effect of alpha lipoic acid (ALA). The results showed that lead acetate (PbAc) dose dependently inhibited the contractile function of toad hearts. Acute treatment with 50, 150, and 450 mM PbAc reduced the amplitude of heart contraction to 92.8%, 78.0%, and 69.7% of the control before medication (P<0.01), respectively, and reduced heart rate to 92.4%, 92.5%, and 54.9% of the control before medication (P<0.05). After treatment with a middle concentration of PbAc (150 mM) for 24 hours, the cell viability of H9c2 decreased to 71.9% of the control group (P<0.05). Compared with the lead exposure group, ALA at a concentration of 10 μM significantly improved cardiac contractile function, increasing the amplitude of cardiac contractions and heart rate to 109.4% and 134.2% of the control, respectively (P<0.05). Correspondingly, ALA at a concentration of 20 μM increased the cell viability of H9c2 to 112.6% of the control group (P<0.05). This study indicates that PbAc can significantly inhibit myocardial contractility and reduce cell viability, while ALA can antagonize lead induced myocardial injury and has significant cardioprotective potential.

Published in American Journal of Bioscience and Bioengineering (Volume 13, Issue 6)
DOI 10.11648/j.bio.20251306.11
Page(s) 106-110
Creative Commons

This is an Open Access article, distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution and reproduction in any medium or format, provided the original work is properly cited.

Copyright

Copyright © The Author(s), 2025. Published by Science Publishing Group

Keywords

Lead Exposure, Myocardial Cells, Cardiac Contractility, Heart Rate, Alpha Lipoic Acid

References
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Cite This Article
  • APA Style

    Zhou, Z., Tang, Z., Dai, Z., Xu, S., Ge, Y., et al. (2025). Acute Lead Exposure Weakens Myocardial Contractile Function and the Therapeutic Effect of Alpha Lipoic Acid. American Journal of Bioscience and Bioengineering, 13(6), 106-110. https://doi.org/10.11648/j.bio.20251306.11

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    ACS Style

    Zhou, Z.; Tang, Z.; Dai, Z.; Xu, S.; Ge, Y., et al. Acute Lead Exposure Weakens Myocardial Contractile Function and the Therapeutic Effect of Alpha Lipoic Acid. Am. J. BioSci. Bioeng. 2025, 13(6), 106-110. doi: 10.11648/j.bio.20251306.11

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    AMA Style

    Zhou Z, Tang Z, Dai Z, Xu S, Ge Y, et al. Acute Lead Exposure Weakens Myocardial Contractile Function and the Therapeutic Effect of Alpha Lipoic Acid. Am J BioSci Bioeng. 2025;13(6):106-110. doi: 10.11648/j.bio.20251306.11

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  • @article{10.11648/j.bio.20251306.11,
      author = {Zhengyi Zhou and Zhuo Tang and Zihao Dai and Shuhe Xu and Yujie Ge and Yuemin Ding and Xiong Zhang},
      title = {Acute Lead Exposure Weakens Myocardial Contractile Function and the Therapeutic Effect of Alpha Lipoic Acid
    },
      journal = {American Journal of Bioscience and Bioengineering},
      volume = {13},
      number = {6},
      pages = {106-110},
      doi = {10.11648/j.bio.20251306.11},
      url = {https://doi.org/10.11648/j.bio.20251306.11},
      eprint = {https://article.sciencepublishinggroup.com/pdf/10.11648.j.bio.20251306.11},
      abstract = {This study comprehensively utilized toad hearts and myocardial cell models to explore the effects of acute lead exposure on myocardial contractile function and the therapeutic effect of alpha lipoic acid (ALA). The results showed that lead acetate (PbAc) dose dependently inhibited the contractile function of toad hearts. Acute treatment with 50, 150, and 450 mM PbAc reduced the amplitude of heart contraction to 92.8%, 78.0%, and 69.7% of the control before medication (PPPPP<0.05). This study indicates that PbAc can significantly inhibit myocardial contractility and reduce cell viability, while ALA can antagonize lead induced myocardial injury and has significant cardioprotective potential.
    },
     year = {2025}
    }
    

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    T1  - Acute Lead Exposure Weakens Myocardial Contractile Function and the Therapeutic Effect of Alpha Lipoic Acid
    
    AU  - Zhengyi Zhou
    AU  - Zhuo Tang
    AU  - Zihao Dai
    AU  - Shuhe Xu
    AU  - Yujie Ge
    AU  - Yuemin Ding
    AU  - Xiong Zhang
    Y1  - 2025/11/22
    PY  - 2025
    N1  - https://doi.org/10.11648/j.bio.20251306.11
    DO  - 10.11648/j.bio.20251306.11
    T2  - American Journal of Bioscience and Bioengineering
    JF  - American Journal of Bioscience and Bioengineering
    JO  - American Journal of Bioscience and Bioengineering
    SP  - 106
    EP  - 110
    PB  - Science Publishing Group
    SN  - 2328-5893
    UR  - https://doi.org/10.11648/j.bio.20251306.11
    AB  - This study comprehensively utilized toad hearts and myocardial cell models to explore the effects of acute lead exposure on myocardial contractile function and the therapeutic effect of alpha lipoic acid (ALA). The results showed that lead acetate (PbAc) dose dependently inhibited the contractile function of toad hearts. Acute treatment with 50, 150, and 450 mM PbAc reduced the amplitude of heart contraction to 92.8%, 78.0%, and 69.7% of the control before medication (PPPPP<0.05). This study indicates that PbAc can significantly inhibit myocardial contractility and reduce cell viability, while ALA can antagonize lead induced myocardial injury and has significant cardioprotective potential.
    
    VL  - 13
    IS  - 6
    ER  - 

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Author Information
  • International Department, Hangzhou Wickham International School, Hangzhou, China

  • International Department, Hangzhou Wickham International School, Hangzhou, China

  • International Department, Hangzhou Xizi Experimental School, Hangzhou, China

  • International Department, Hangzhou Xizi Experimental School, Hangzhou, China

  • Department of Clinical Medicine, School of Medicine, Hangzhou City University, Hangzhou, China

  • Department of Clinical Medicine, School of Medicine, Hangzhou City University, Hangzhou, China; Institute of Translational Medicine, Zhejiang University City College, Hangzhou, China; Key Laboratory of Novel Targets and Drug Study for Neural Repair of Zhejiang Province, Zhejiang University City College, Hangzhou, China

  • Department of Basic Medical Science, Zhejiang University School of Medicine, Hangzhou, China

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