WU Wen-hui, ZHANG Qi, LI Huan, DING Yong, LU Xiao-ting, WU Xiao-bing, SONG Jing, ZHANG Ling, NIU Qiao, ZHANG Qin-li. Effect of Nano Aluminum Oxide Particles on Non-Specific Immune Function in Mice[J]. Journal of Environmental and Occupational Medicine, 2016, 33(2): 184-188. DOI: 10.13213/j.cnki.jeom.2016.15229
Citation: WU Wen-hui, ZHANG Qi, LI Huan, DING Yong, LU Xiao-ting, WU Xiao-bing, SONG Jing, ZHANG Ling, NIU Qiao, ZHANG Qin-li. Effect of Nano Aluminum Oxide Particles on Non-Specific Immune Function in Mice[J]. Journal of Environmental and Occupational Medicine, 2016, 33(2): 184-188. DOI: 10.13213/j.cnki.jeom.2016.15229

Effect of Nano Aluminum Oxide Particles on Non-Specific Immune Function in Mice

  • Objective To explore the effect of nano aluminum oxide (A2O3) on neutrophil phagocytosis in mice exposed to different sizes of nano A2O3 particles, and to assess the impact on non-specific immune function in mice.
    Methods Threemonth-old healthy ICR male (n=20) and female (n=20) mice were randomly divided into five groups with four male mice and four female mice per group:blank control, solvent control (daily infusion of saline), 10 μm A2O3, 50 nm A2O3, and 13 nm A2O3 groups. Continuous exposure was conducted 3 times/d for 60 d by nasal drip and exposure dose was 50 mg/kg. Neutrophil phagocytosis was evaluated by oil immersion lens microscopy observation of 150 neutrophils on each Wright's stained blood smear which was prepared by mixing bacterial suspension and inner canthus blood sample of mice. Routine blood tests were also conducted.
    Results The phagocytic percentages of the three A2O3 exposed groups were significantly lower than those of the blank control group and the solvent control group (all Ps<0.05). Compared with the 10 μm A2O3 group, the 50 nm A2O3 group had no obvious change in phagocytic percentage (P=0.06), but the 13 nm A2O3 group showed significantly lowered phagocytic percentage (P=0.01). Compared with the 50 nm A2O3 group, the 13 nm A2O3 had no obvious change in phagocytic percentage (P=0.08). The phagocytic indices of the three A2O3 exposed groups were lower than those of the blank control group and the solvent control group (all Ps<0.05). Compared with the 10 μm A2O3 group, the 50 nm A2O3 group and the 13 nm A2O3 group were significantly decreased in phagocytic index (both Ps<0.05). Compared with the 50 nm A2O3 group, the 13nm A2O3 group reported no significant change (P=0.85). Total white blood cells, lymphocyte counts, and lymphocyte percentages were higher in the 13 nm A2O3 group than in the blank control group and the solvent control group, and the differences were statistically significant (all Ps<0.05). No significant differences were found in the number of neutrophils (P>0.05).
    Conclusion Nano A2O3 could decrease neutrophil phagocytosis and influence the non-specific immune function in mice, and the phagocytosis would decrease with smaller sizes, indicating a potential size effect. Nano A2O3 could also cause an increase in the number of lymphocytes in peripheral blood.
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