کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
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4410438 | 1307544 | 2012 | 6 صفحه PDF | دانلود رایگان |

Although a number of manufactured nanoparticles are applied for the medical and clinical purposes, the understanding of interaction between nanomaterials and biological systems are still insufficient. Using nematode Caenorhabditis elegans model organism, we here investigated the in vivo toxicity or safety of hydroxylated fullerene nanoparticles known to detoxify anti-cancer drug-induced oxidative damages in mammals. The survival ratio of C. elegans rapidly decreased by the uptake of nanoparticles from their L4 larval stage with resulting in shortened lifespan (20 d). Both reproduction rate and body size of C. elegans were also reduced after exposure to 100 μg mL−1 of fullerol. We found ectopic cell corpses caused by apoptotic cell death in the adult worms grown with fullerol nanoparticles. By the mutation of core pro-apoptotic regulator genes, ced-3 and ced-4, these nanoparticle-induced cell death were significantly suppressed, and the viability of animals consequently increased despite of nanoparticle uptake. The apoptosis-mediated toxicity of nanoparticles particularly led to the disorder of digestion system in the animals containing a large number of undigested foods in their intestine. These results demonstrated that the water-soluble fullerol nanoparticles widely used in medicinal applications have a potential for inducing apoptotic cell death in multicellular organisms despite of their antioxidative detoxifying property.
► Hydroxylated fullerene nanoparticles shortened lifespan of Caenorhabditis elegans with an acute lethality in the adulthood.
► Hydroxylated fullerene nanoparticles reduced both reproduction rate and body growth of C. elegans.
► Hydroxylated fullerene nanoparticles induced apoptosis in the adult C. elegans.
► Suppression of apoptosis by genetic mutation rescued the toxicity caused by hydroxylated fullerene nanoparticles.
► Apoptosis-mediated toxicity in C. elegans was not dependent on oxidative stress.
Journal: Chemosphere - Volume 87, Issue 1, March 2012, Pages 49–54