【摘要】 目的研究槟榔碱对Hacat细胞上皮模型通透性的影响及Ca²⁺对其的调节作用。方法建立Hacat细胞上皮体外模型;设置对照组（A组）、槟榔碱处理组（B组）及Ca²⁺+槟榔碱处理组（C组）,以荧光黄表观通透系数(P_app)评价槟榔碱及Ca²⁺对细胞模型通透性的影响。结果在B组,各小组荧光黄P_app均大于相应A组（P<0.05）,且荧光黄P_app随槟榔碱浓度及干预时间增加而增大（P<0.05）。在C组,各小组荧光黄P_app分别比相同浓度和时间点的B组低（P<0.05）,各小组荧光黄P_app均大于A组（P<0.05）,且荧光黄P_app随槟榔碱浓度及干预时间增加而增大（P<0.05）。结论槟榔碱导致上皮屏障通透性增大,可能是口腔黏膜下纤维性变（oral submucous fibrosis,OSF）发病作用机制之一。Ca²⁺预处理使槟榔碱增加上皮通透性的作用减弱。更多还原

【Abstract】 Objective To study the effect of arecoline on the permeability of Hacat cell epithelia model in vitro and the adjustment of Ca²⁺on it.Methods Establish the Hacat cell epithelia monolayer model in vitro by culturing Hacat cell.The models were divided into control group（group A）,arecoline treatment group（group B）and"calcium+arecoline"treatment group（group C）.The values of Lucifer Yellow P_appwere used to estimate the permeability changes of models after treatment with arecoline and calcium.Results In group B,the Lucifer Yellow P_appof each subgroup was higher than that of group A（P<0.05）and the Lucifer Yellow P_appincreased as the arecoline concentration and treatment time were increased（P<0.05）.In group C,after pretreatment with calcium,the Lucifer Yellow P_appof each subgroup were lower than that of group B at corresponding concentration and time points（P<0.05）;while the P_appof each subgroup was higher than that of group A（P<0.05）.Besides,the Lucifer Yellow P_appincreased as the arecoline concentration and treating time were increased（P<0.05）.ConclusionThe increase of permeability of oral epithelia model by arecoline may play an important role in the pathogenesis and development of oral submucous fibrosis.The pretreatment with calcium,to some extent,can weaken the effect of arecoline on the permeability of Hacat cell monolayer model.更多还原