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作 者:陈生晓[1] 任昊[2] 刘郑荣[2] 刘宏发[2] 林晓明[1]
机构地区:[1]解放军第187医院肾内科,海口571159 [2]南方医科大学南方医院肾内科
出 处:《解放军医学杂志》2008年第1期72-74,共3页Medical Journal of Chinese People's Liberation Army
基 金:国家自然科学基金资助课题(30370665)
摘 要:目的探讨腹透液对大鼠腹膜间皮细胞水通道蛋白1(AQP1)表达的影响。方法将体外培养的大鼠腹膜间皮细胞分成4组,分别用含10%胎牛血清的1640培养液(阴性对照组)和3种不同腹透液(分别含4.25%葡萄糖、4.25%甘露醇、1.5%葡萄糖)刺激3h,采用间接免疫荧光标记法、流式细胞仪检测上述不同腹透液刺激后AQP1的表达。结果4.25%葡萄糖腹透液组和4.25%甘露醇腹透液组腹膜间皮细胞AQP1表达显著大于阴性对照组和1.5%葡萄糖腹透液组(P<0.01);4.25%葡萄糖腹透液组腹膜间皮细胞AQP1表达显著大于4.25%甘露醇腹透液组(P<0.01);1.5%葡萄糖腹透液组腹膜间皮细胞AQP1表达与阴性对照组相比无显著性差异(P>0.05)。结论高糖腹透液可以促进腹膜间皮细胞表面AQP1的表达,糖本身或糖降解产物可能是促进其表达的独立因素。Objective To discuss the effects of peritoneal dialysate (PDS) on the expression of aquaporin-1 in rat peritoneal mesothelial cells (RPMCs). Methods The in vitro cultured RPMCs were divided randomly into 4 groups, and stimulated respectively with 1640 culture medium containing 10% fetal calf serum (negative control), and three kinds of PDS (containing respectively 4. 25% glucose, 4. 25% rnannitol or 1. 5% glucose) for 3 hours. Indirect immunofluorescence assay (IFA) and flow cytometry (FCM)were employed to de tect the expression of aquaporin-1 in RPMCs stimulated by different kind of PDS as above. Results Compared with negative control and the group with PDS containing 1.5% glucose, the expression of aquaporin-1 on the mesothelial cells of the group with PDS containing 4. 25% glucose and that containing 4. 25% mannitol was significantly up-regulated ( P〈0. 01). Higher expression of aquaporin-1 was found in the group with PDS containing 4. 25 % glucose compared with that in the group with PDS containing 4. 250% rnannitol (P〈0. 01). No significant differences on the expressions of aquaporin-1 were found between the negative control and the group with PDS containing 1.5% glucose ( P〉0. 05). Conclusion PDS with higher osmotic pressure (OP) can enhance the expression of aquaporin-1 in RPMCs. For PDS with same OP (PDS containing 4. 25% glucose or PDS containing 4. 25% mannitol), those containing glucose can enhance the expres sion of aquaporin-1 more effectively than that PDS containing rnannitol. This result indicates that glucose or its degradation products may be the independent factors in enhancing the expression of aquaporin-1 of RPMCs.
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