Herbo‐Mineral Medicine, Cardiogrit Gold, Exhibits Protective Effects in <i>Caenorhabditis elegans</i> Model of Doxorubicin‐Induced Cardiotoxicity

Doxorubicin, an effective antineoplastic agent, is often prescribed for the treatment of various carcinomas. However, the use of doxorubicin becomes limited due to its adverse effects like cardiotoxicity, dysmenorrhea, and leucopenia. Cardiogrit Gold (CG) is a herbo-mineral Ayurvedic medicine prescribed for the treatment of various cardiovascular ailments. The current study aimed to investigate the therapeutic potential of CG in imparting protection against doxorubicin-induced cardiotoxicity. Wild-type (N2) and genetically modified <i>Caenorhabditis elegans</i>(SJ4005 and DA597) were used as model organisms to assess the bioactivity of CG against doxorubicin-induced cardiotoxicity. Chemical characterization of CG was performed by HPLC-based analysis. Calcium, a key mineral component of CG, was measured in CG-treated <i>C. elegans</i> using inductively coupled plasma mass spectrometry (ICP-MS) analysis, as the marker of CG internalization in <i>C. elegans</i>. Toxicity induced by doxorubicin and its recovery upon CG treatment was determined by various toxicologically important endpoints. CG treatment rescued N2 <i>C. elegans</i> from doxorubicin-induced reduction in their growth, reproduction, locomotory behavior, pharyngeal pumping, feeding ability, and increased ROS generation. CG treatment modulated the expression of hsp-4 in SJ4005 <i>C. elegans</i> suggestive of decreased ER stress and normalized the pharyngeal grinder damage in DA597 <i>C. elegans,</i> indicating a robust induction of cardio-normalcy. Novel analytical methods were developed to detect and quantify doxorubicin in <i>C. elegans</i> on HPLC and UPLC/QToF-MS platforms. Interestingly, CG treatment decreased bioaccumulation of doxorubicin in <i>C. elegans,</i> robustly correlating with the observed cardioprotective effects. Taken together, CG has a strong cardioprotective profile against doxorubicin-induced damages and could be taken for further preclinical and clinical assessments.

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Publication Details

Journal
Journal of Toxicology
Published
2025-01-01
DOI
https://doi.org/10.1155/jt/4609428
Primary Topic
Nanoparticles: synthesis and applications
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article
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article

Herbo‐Mineral Medicine, Cardiogrit Gold, Exhibits Protective Effects in Caenorhabditis elegans Model of Doxorubicin‐Induced Cardiotoxicity

Rishabh Dev, Meenu Tomer, Anurag Varshney, Acharya Balkrishna et al.
Journal of Toxicology
Nanoparticles: synthesis and applications
article

Herbo‐Mineral Medicine, Cardiogrit Gold, Exhibits Protective Effects in Caenorhabditis elegans Model of Doxorubicin‐Induced Cardiotoxicity

Rishabh Dev, Meenu Tomer, Anurag Varshney, Acharya Balkrishna, Saurabh Bhatti, Sudeep Verma
article en

Abstract

Doxorubicin, an effective antineoplastic agent, is often prescribed for the treatment of various carcinomas. However, the use of doxorubicin becomes limited due to its adverse effects like cardiotoxicity, dysmenorrhea, and leucopenia. Cardiogrit Gold (CG) is a herbo-mineral Ayurvedic medicine prescribed for the treatment of various cardiovascular ailments. The current study aimed to investigate the therapeutic potential of CG in imparting protection against doxorubicin-induced cardiotoxicity. Wild-type (N2) and genetically modified <i>Caenorhabditis elegans</i>(SJ4005 and DA597) were used as model organisms to assess the bioactivity of CG against doxorubicin-induced cardiotoxicity. Chemical characterization of CG was performed by HPLC-based analysis. Calcium, a key mineral component of CG, was measured in CG-treated <i>C. elegans</i> using inductively coupled plasma mass spectrometry (ICP-MS) analysis, as the marker of CG internalization in <i>C. elegans</i>. Toxicity induced by doxorubicin and its recovery upon CG treatment was determined by various toxicologically important endpoints. CG treatment rescued N2 <i>C. elegans</i> from doxorubicin-induced reduction in their growth, reproduction, locomotory behavior, pharyngeal pumping, feeding ability, and increased ROS generation. CG treatment modulated the expression of hsp-4 in SJ4005 <i>C. elegans</i> suggestive of decreased ER stress and normalized the pharyngeal grinder damage in DA597 <i>C. elegans,</i> indicating a robust induction of cardio-normalcy. Novel analytical methods were developed to detect and quantify doxorubicin in <i>C. elegans</i> on HPLC and UPLC/QToF-MS platforms. Interestingly, CG treatment decreased bioaccumulation of doxorubicin in <i>C. elegans,</i> robustly correlating with the observed cardioprotective effects. Taken together, CG has a strong cardioprotective profile against doxorubicin-induced damages and could be taken for further preclinical and clinical assessments.

Journal of ToxicologyVol. 2025(1)
Jawaharlal Nehru University (IN), Patanjali Research Foundation (IN)
Openalex Percentile: Top 87%
Nanoparticles: synthesis and applications
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