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Ecto-CD38-NADase inhibition modulates cardiac metabolism and protects mice against doxorubicin-induced cardiotoxicity.

Eduardo Nunes ChiniGuillermo AgorrodyLaura ColmanSonu KashyapJulianna D ZeidlerClaudia Christiano Silva ChiniGina M WarnerKatie L ThompsonPranjali DalviFelipe Cesar BeckedorffSanam EbtehajJoerg HerrmannWim van SchootenEduardo Nunes Chini
Published in: Cardiovascular research (2024)
NAD+-preserving strategies by inactivation of CD38 via a genetic or a pharmacological-based approach improve cardiac energetics and reduce cardiac inflammation and dysfunction otherwise seen in an acute DXR cardiotoxicity model.
Keyphrases
  • left ventricular
  • oxidative stress
  • drug induced
  • drug delivery
  • diabetic rats
  • heart failure
  • intensive care unit
  • high glucose
  • nk cells
  • skeletal muscle
  • copy number
  • cancer therapy