[No authors listed]
Methamphetamine (MA) is a highly abused amphetamineâlike psychostimulant. At present, the mechanisms underlying MAâinduced cardiotoxicity are poorly understood. The cardiotoxic effects have yet not been clearly elucidated with respect to the apoptotic pathway. Insulinâlike growth factor binding proteinâ5 (IGFBP5) is important for cell growth control and the induction of apoptosis. The aim of the present study was to analyze whether IGFBP5 is involved in MAâinduced apoptosis as a novel target. MAâinduced apoptosis was observed in neonatal rat ventricular myocytes (NRVMs) in a concentrationâdependent manner using a terminal deoxyribonucleotide transferaseâmediated dUTP nick endâlabeling assay. Using reverse transcription polymerase chain reaction and western blotting, MA was demonstrated to induce concentrationâdependent increases in the expression of IGFBP5. Silencing IGFBP5 with small interfering RNA significantly reduced apoptosis and suppressed the expression of caspaseâ3 in NRVMs following treatment with MA. To the best of our knowledge, the present study provided the first evidence suggesting that IGFBP5 is a potential therapeutic target in MAâinduced apoptosis in vitro, providing a foundation for future in vivo studies.
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