Evidence map›Paper›PMID 40551683›Full record

ArticleCardiovascular & hematological disorders drug targets2025

Cardioprotective Activity of Oroxylin-A in Doxorubicin-induced Myocardial Toxicity: Antioxidant and

Nagaraju Bandaru, Naga Venkata Indira Devi Jajula, Dodda TulaseNadhreddy, Alla Narayana Rao, Nuziveeti Lakshmi Durga Bhavani, Makarand Suresh Gambhire

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Article in Cardiovascular & hematological disorders drug targets, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

6 authors.

Nagaraju BandaruSchool of Pharmaceutical Sciences, Sandip University, Nashik, Maharashtra, India.
Naga Venkata Indira Devi JajulaDepartment of Pharmaceutical Analysis, Emmanuel College of Pharmacy, Visakhapatnam, Andhra Pradesh, 531162, India.
Dodda TulaseNadhreddySchool of Pharmaceutical Sciences, Sandip University, Nashik, Maharashtra, India.
Alla Narayana RaoCollege of Pharmacy, Koneru Lakshmaiah Education Foundation, Vaddesweram, Andhra Pradesh, India.
Nuziveeti Lakshmi Durga BhavaniShri Vishnu College of Pharmacy, Vishnupur, Bhimavaram, Andhra Pradesh, India.
Makarand Suresh GambhireSchool of Pharmaceutical Sciences, Sandip University, Nashik, Maharashtra, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionOroxylin A is primarily sourced from the roots of Scutellaria baicalensis, a medicinal plant commonly used in traditional Chinese medicine. It can also be found in other Scutellaria species. The plant's rich bioactive profile makes it a significant source of various flavonoids, including Oroxylin A.

aimsThe proposed aim of this study is to investigate

methodsThe total phenolic content was estimated using Folin-Ciocalteu test and in-vitro activity was performed using DPPH assay. Acute toxicity studies were performed according to OECD 423 guidelines. In vitro cardioprotective activity was performed on H9c2 cells and was estimated for the biomarkers.

resultsOroxylin-A showed good antioxidant activity. No abnormalities were found in animals upon its usage, indicating that Oroxylin-A was safe at 2000 mg/kg. 150ug/ml of Oroxylin-A significantly increased the cell viability up to 99% and also decreased the LDH and ROS generation indicating that Oroxylin-A showed significant cardioprotective activity on H9c2 cells. DISCUSSION: Oroxylin-A demonstrated potent antioxidant and cardioprotective effects by reducing ROS generation and LDH release while enhancing H9c2 cell viability against doxorubicininduced toxicity. Its safety at higher doses further supports its therapeutic potential. These findings highlight Oroxylin-A as a promising natural cardioprotective agent, warranting further in vivo and mechanistic studies to validate its clinical applicability.

conclusionThis research underscores the potential of Oroxylin A as a candidate for further investigation as a cardioprotective agent. Also, the present study contributes to the growing body of knowledge aimed at identifying natural compounds that may offer protective effects against myocardial damage, providing hope for future therapeutic interventions in the field of cardiovascular medicine.

Indexed as

AntioxidantsCardiotonic AgentsDoxorubicinFlavonoidsMyocytes, CardiacAnimalsCardiotoxicityCell LineRats5,7-dihydroxy-6-methoxy-2-phenylchromen-4-oneAntioxidantsCardiotonic AgentsDoxorubicinFlavonoidsantioxidantcardioprotective agentcell linesin-vitroOroxylin-AScutellaria baicalensis.

Identifiers

PMID40551683

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