In this study, we further examined the effects of diallyl disulfide (DADS), one of the major components of oil-soluble garlic extracts (GE) and of raw water GE on SH-SY5Y and NSC34 neuronal cell lines. Both treatments with DADS and GE were able to induce growth arrest and apoptosis, and we observed an increased flux of reactive oxygen and nitrogen species as early signs of cytotoxicity. We demonstrated that the content of neuronal nitric oxide synthase (nNOS) increased as early as 1 h of treatment demonstrating to be a very early sensor of DADS and GE cytotoxicity. Treatments with L-nitropropyl-arginine, an inhibitor of nNOS, increased the rate of apoptosis whereas the overexpression of nNOS significantly reduced cell death by inhibiting DNA damage, protein oxidation, and the activation of the JNK/c-Jun apoptotic signaling cascade. Overall these results demonstrate that garlic derivatives may modulate nNOS and suggest an important contribution of nitric oxide in counteracting their reactive oxygen species-mediated cytotoxicity.

Aquilano, K., Filomeni, G., Baldelli, S., Piccirillo, S., De Martino, A., Rotilio, G., et al. (2007). Neuronal nitric oxide synthase protects neuroblastoma cells from oxidative stress mediated by garlic derivatives. JOURNAL OF NEUROCHEMISTRY, 101(5), 1327-1337 [10.1111/j.1471-4159.2006.04431.x].

Neuronal nitric oxide synthase protects neuroblastoma cells from oxidative stress mediated by garlic derivatives

AQUILANO, KATIA;FILOMENI, GIUSEPPE;ROTILIO, GIUSEPPE;CIRIOLO, MARIA ROSA
2007-01-01

Abstract

In this study, we further examined the effects of diallyl disulfide (DADS), one of the major components of oil-soluble garlic extracts (GE) and of raw water GE on SH-SY5Y and NSC34 neuronal cell lines. Both treatments with DADS and GE were able to induce growth arrest and apoptosis, and we observed an increased flux of reactive oxygen and nitrogen species as early signs of cytotoxicity. We demonstrated that the content of neuronal nitric oxide synthase (nNOS) increased as early as 1 h of treatment demonstrating to be a very early sensor of DADS and GE cytotoxicity. Treatments with L-nitropropyl-arginine, an inhibitor of nNOS, increased the rate of apoptosis whereas the overexpression of nNOS significantly reduced cell death by inhibiting DNA damage, protein oxidation, and the activation of the JNK/c-Jun apoptotic signaling cascade. Overall these results demonstrate that garlic derivatives may modulate nNOS and suggest an important contribution of nitric oxide in counteracting their reactive oxygen species-mediated cytotoxicity.
2007
Pubblicato
Rilevanza internazionale
Articolo
Sì, ma tipo non specificato
Settore MED/49 - SCIENZE TECNICHE DIETETICHE APPLICATE
English
Con Impact Factor ISI
arginine derivative; diallyl disulfide; DNA; garlic extract; neuronal nitric oxide synthase; nitric oxide; nitrogen; protein; reactive oxygen metabolite; stress activated protein kinase; water; animal cell; apoptosis; article; cell death; cell growth; cell line; cytotoxicity; DNA damage; drug effect; enzyme activation; human; human cell; modulation; mouse; muscle fibril; neuroblastoma cell; nonhuman; oxidation; oxidative stress; priority journal; protein expression; rat; sensor; statistical significance; Allyl Compounds; Animals; Antineoplastic Agents; Apoptosis; Cell Cycle; Cell Survival; Disulfides; Dose-Response Relationship, Drug; Drug Interactions; Enzyme Inhibitors; Garlic; Gene Expression Regulation, Neoplastic; Humans; Mice; Neuroblastoma; Nitric Oxide Synthase Type I; Oxidative Stress; Plant Extracts; Transfection; Allium sativum
Aquilano, K., Filomeni, G., Baldelli, S., Piccirillo, S., De Martino, A., Rotilio, G., et al. (2007). Neuronal nitric oxide synthase protects neuroblastoma cells from oxidative stress mediated by garlic derivatives. JOURNAL OF NEUROCHEMISTRY, 101(5), 1327-1337 [10.1111/j.1471-4159.2006.04431.x].
Aquilano, K; Filomeni, G; Baldelli, S; Piccirillo, S; De Martino, A; Rotilio, G; Ciriolo, Mr
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2108/35256
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