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KMID : 0380420150390010003
Journal of Prventive Veterinary Medicine
2015 Volume.39 No. 1 p.3 ~ p.14
Comparison of the bioavailability of nano- and micro-sized copper oxide particles in copper-deficient mice
Seol Ja-Kyung

Jeong Jae-Hwang
Nam Sang-Yoon
Yun Young-Won
Kim Jong-Soo
Lee Beom-Jun
Abstract
Copper is an essential micronutrient whose deficiency is often seen to occur in humans. Although many biomedicalstudies have focused on the use of nanoparticles, the nutritional effects of nano-sized copper oxide particles are not wellknown. This aim of this study was to investigate the nutritional bioavailability of nano- and micro-sized copper oxide (CuO)particles in copper-deficient (CuD) mice. Copper deficiency was induced in mice by feeding a CuD diet (0.93 mg Cu/kg diet)for 7 weeks. After the induction of copper deficiency, nano- or micro-sized copper oxide particles were administered orallyat two different doses (0.8 and 4.0 mg CuO/kg body weight) to mice in the following groups: (1) normal control (NC), (2)CuD, (3) low dose micro-sized CuO, (4) high dose micro-sized CuO, (5) low dose nano-sized CuO, and (6) high dosenano-sized CuO. The hepatic copper concentration in the CuD group was significantly lower than that in the NC group. Compared to the NC group, the CuD group exhibited lower serum ceruloplasmin (CP) activity and CP level. Thecopper/zinc-superoxide dismutase activity in the CuD group was significantly lower than that in the NC group. Treatment withnano- or micro-sized copper oxide particles for 2 weeks restored the hepatic copper levels and serum CP activities to valuessimilar to those observed in the NC group. The CP levels and copper/zinc-superoxide dismutase activities in all the copperoxide treatment groups also recovered to normal values after 3 weeks of copper oxide treatment. These results show thatoral administration of either nano- or micro-sized copper oxide particles for 2?3 weeks restored the normal condition inpreviously CuD mice.
KEYWORD
copper deficiency, nanosized CuO particles, microsized CuO particles bioavailability, ceruloplasmin, copper/zinc-superoxide dismutase
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