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首页> 外文期刊>Acta Cirurgica Brasileira >Preparation of Zoledronate liposome and its impact on apoptosis of Kupffer cells in rat liver 1
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Preparation of Zoledronate liposome and its impact on apoptosis of Kupffer cells in rat liver 1

机译:唑来膦酸盐脂质体的制备及其对大鼠肝库普弗细胞凋亡的影响1

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Purpose: To establish a method for the preparation of zoledronate liposome and to observe its effect on inducing the apoptosis of rat liver Kupffer cells. Methods: Zoledronate was encapsulated in liposomes, and then the entrapment rate was detected on a spectrophotometer. The prepared Zoledronate liposome (0.01 mg/mL) was injected into the tail vein of SD rats. Three days later, the number of Kupffer cells (CD68 positive) in rat liver tissue was detected by immunohistochemistry. Flow cytometry was used to detect the apoptosis rate of the isolated liver Kupffer cell cultured in vitro. Results: The entrapment rate of Zoledronate was 43.4±7.8%. Immunohistochemistry revealed that the number of Kupffer cells was 19.3±2.1 in PBS group and 5.5±1.7 in Zoledronate liposome group, with a significant difference (P0.05). The apoptosis rate of Kupffer cells was 4.1±0.8% in PBS group, while it was 9±2.2% and 23.3±5.9% in Zoledronate liposomes groups with different concentrations of Zoledronate liposome (P0.05). Conclusions: Zoledronate liposomes can effectively induce the apoptosis of Kupffer cells in vivo and in vitro, and the apoptosis rate is related to the concentration of Zoledronate liposome. To establish a rat liver Kupffer cell apoptosis model can provide a new means for further study on Kupffer cell function.
机译:目的:建立唑来膦酸脂质体的制备方法,观察其诱导大鼠肝库普弗细胞凋亡的作用。方法:将唑来膦酸盐包裹在脂质体中,然后用分光光度计检测其包封率。将制备的唑来膦酸盐脂质体(0​​.01 mg / mL)注射到SD大鼠的尾静脉中。三天后,通过免疫组织化学检测大鼠肝组织中的枯否细胞(CD68阳性)的数目。流式细胞仪用于检测离体培养的分离的肝Kupffer细胞的凋亡率。结果:唑来膦酸盐的包封率为43.4±7.8%。免疫组织化学分析显示,PBS组库普弗细胞数为19.3±2.1,唑来膦酸盐脂质体组库普弗细胞数为5.5±1.7,差异有统计学意义(P <0.05)。在不同浓度的唑来膦酸盐脂质体中,PBS组的库普弗细胞凋亡率为4.1±0.8%,在唑来膦酸盐脂质体组中分别为9±2.2%和23.3±5.9%(P <0.05)。结论:唑来膦酸盐脂质体可有效地诱导体内外Kupffer细胞凋亡,其凋亡率与唑来膦酸盐脂质体浓度有关。建立大鼠肝库普弗细胞凋亡模型可以为进一步研究库普弗细胞功能提供新的手段。

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