Therapeutic Concentrations of Mitoxantrone Elicit Energetic Imbalance in H9c2 Cells as an Earlier Event

• Tipo: Artigo em Revista Científica Internacional
• Data: 2013

Autores

Luciana Grazziotin Rossato (Autor) Outra; Vera Marisa Costa (Autor) Outra; Vania Vilas Boas (Autor) Outra; Maria de Lourdes Bastos (Autor) FFUP; Anabela Rolo (Autor) Outra; Carlos Palmeira (Autor) Outra; Fernando Remiao (Autor) FFUP

Revista

Título: Cardiovascular Toxicology

Vol. 13

Páginas: 413-425

ISSN: 1530-7905

Editora: Springer Nature

Indexação

ISI Web of Knowledge - 17 Citações

Scopus - 25 Citações

Classificação Científica

FOS: Ciências médicas e da saúde > Medicina clínica

Outras Informações

ID Authenticus: P-008-JWV

DOI: 10.1007/s12012-013-9224-0

Abstract (EN): Mitoxantrone (MTX) is a chemotherapeutic agent that emerged as an alternative to anthracycline therapy. However, MTX also causes late cardiotoxicity, being oxidative stress and mitochondrial-impaired function proposed as possible mechanisms. This work aimed to investigate the relevance of these mechanisms to the MTX toxicity in H9c2 cells, using therapeutic concentrations. The observed cytotoxicity of MTX was time and concentration dependent in both lactate dehydrogenase leakage assay and MTT reduction assay. Two therapeutic concentrations (100 nM and 1 mu M) and three time points were selected (24, 48, and 96 h) for further studies. Both MTX concentrations caused a significant increase in caspase-3 activity, which was not prevented by inhibiting MTX CYP450-metabolism. Significant decreases were observed in the total and reduced glutathione levels only in MTX 100 nM at 96 h; however, neither alterations in oxidized glutathione nor increases in the malondialdehyde levels were observed at any time or concentrations tested. On the other hand, changes in the intracellular ATP levels, mitochondrial membrane potential, and intracellular calcium levels were observed in both concentrations and all time tested. Noteworthy, decreased levels of ATP-synthase expression and activity and increases in the reactive species generation were observed at 96 h in both working concentrations. However, the radical scavenger N-acetylcysteine or the mitochondrial function enhancer L-carnitine did not prevent MTX cytotoxicity. Thus, this work evidenced the early MTX-induced energetic crisis as a possible key factor in the cell injury.

Idioma: Inglês

Tipo (Avaliação Docente): Científica

Nº de páginas: 13