Extract of caterpillar medicinal mushroom, cordyceps militaris (Ascomycetes), mycelia attenuates doxorubicin-induced cardiotoxicity and upregulates mitochondrial electron transport chain activity in rats

Ravindran K. Veena, Haridas Ramya, Thekkuttuparambil A. Ajith, Kainoor K. Janardhanan, Solomon P. Wasser

Research output: Contribution to journalArticlepeer-review

Abstract

The anthracycline antibiotic doxorubicin (DOX) is extensively used in cancer chemotherapy. Cumulative dose-dependent cardiotoxicity may develop even several years after DOX treatment. This study aimed to evaluate the protective effect of aqueous ethanol extract of Cordyceps militaris mycelia (CM) against DOX-induced cardiotoxicity in rats. DOX was administered intraperitoneally at a cumulative dose of 18 mg/kg of body weight (BW). The protective effect was evaluated using CM at doses of 150 and 300 mg/kg BW administered orally. DL-alpha-lipoic acid (100 mg/ kg BW) was used as the reference control. Both serum creatine kinase and lactate dehydrogenase activities were elevated significantly (P < 0.01) in the group treated with DOX alone compared to the control or CM + DOX-treated groups. DOX administration significantly decreased (P < 0.01) adenosine triphosphate levels and activity of complexes I, III, and IV and Krebs cycle dehydrogenases. CM treatment (300 mg/kg BW) upregulated decreased mitochondrial enzyme activity consequent to DOX administration. Histopathological observations revealed the amelioration of cardiac myocyte necrosis and hypertrophy, which supported the protective effect of CM.

Original languageEnglish
Pages (from-to)17-26
Number of pages10
JournalInternational Journal of Medicinal Mushrooms
Volume23
Issue number1
DOIs
StatePublished - 2021

Bibliographical note

Publisher Copyright:
© 2021 by Begell House, Inc.

Keywords

  • ATP
  • Cordyceps militaris
  • DL-alpha-lipoic acid
  • Doxorubicin
  • Electron transport chain
  • Heart failure
  • Krebs cycle dehydrogenases
  • Medicinal mushrooms

ASJC Scopus subject areas

  • Applied Microbiology and Biotechnology
  • Pharmacology
  • Drug Discovery

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