Antiapoptotic effects of dietary antioxidants towards N-nitrosopiperidine and N-nitrosodibutylamine-induced apoptosis in HL-60 and HepG2 cells

✍ Scribed by Almudena García; Paloma Morales; Nuria Arranz; Ma Eugenia Delgado; Joseph Rafter; Ana I. Haza

• Publisher: John Wiley and Sons
• Year: 2009
• Tongue: English
• Weight: 738 KB
• Volume: 29
• Category: Article
• ISSN: 0260-437X
• DOI: 10.1002/jat.1426

✦ Synopsis

Abstract

The aim of this work was to determine the effect of vitamin C, diallyl disulfide (DADS) and dipropyl disulfide (DPDS) towards N‐nitrosopiperidine (NPIP) and N‐nitrosodibutylamine (NDBA)‐induced apoptosis in human leukemia (HL‐60) and hepatoma (HepG2) cell lines using the terminal deoxynucleotidyl transferase‐mediated dUTP nick end labeling assay. None of the vitamin C (5–50 µm), DADS and DPDS (1–5 µm) concentrations selected induced a significant percentage of apoptosis. In simultaneous treatments, vitamin C, DADS and DPDS reduced the apoptosis induced by NPIP and NDBA in HL‐60 and HepG2 cells (around 70% of reduction). We also investigated its scavenging activities towards reactive oxygen species (ROS) produced by NPIP and NDBA using 2',7'‐dichlorodihydrofluorescein diacetate in both cell lines. ROS production induced by both N‐nitrosamine was reduced to control levels by vitamin C (5–50 µm) in a dose‐dependent manner. However, DADS (5 µm) increased ROS levels induced by NPIP and NDBA in HL‐60 (40 and 20% increase, respectively) and HepG2 cells (18% increase), whereas DPDS was more efficient scavenger of ROS at the lowest concentration (1 µm) in both HL‐60 (52 and 25% reduction, respectively) and HepG2 cells (24% reduction). The data demonstrated that the scavenging ability of vitamin C and DPDS could contribute to inhibition of the NPIP‐ and NDBA‐induced apoptosis. However, more than one mechanism, such as inhibition of phase I and/or induction of phase II enzymes, could be implicated in the protective effect of dietary antioxidants towards NPIP‐ and NDBA‐induced apoptosis in HL‐60 and HepG2 cells. Copyright © 2009 John Wiley & Sons, Ltd.