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作 者:何庆[1] 刘铭[2] 苏京[3] 王保平[3] 王晶[3] 陈克勤[3] 尹潍[1]
机构地区:[1]天津医科大学总医院内分泌科,300052 [2]天津医科大学总医院老年病研究室,300052 [3]丹麦诺和诺德中国研究发展中心
出 处:《天津医药》2006年第3期176-179,共4页Tianjin Medical Journal
基 金:天津市自然科学基金资助课题(项目编号:983702411;043607911)
摘 要:目的:观察高浓度葡萄糖体外对胰岛细胞凋亡及凋亡相关基因表达的影响,探讨葡萄糖毒性及其分子机制。方法:应用TUNEL法检测高浓度葡萄糖培养后大鼠胰岛细胞和小鼠βTc3细胞凋亡百分率;应用定量RT-PCR(QRT-PCR)检测培养后大鼠胰岛细胞和小鼠βTc3细胞bcl-2和baxmRNA的表达;应用定量RT-PCR检测低剂量链脲佐菌素糖尿病大鼠胰岛bcl-2和baxmRNA的表达。结果:高浓度葡萄糖使原代培养的大鼠胰岛细胞和βTc-3的凋亡细胞比例明显增加;胰岛细胞凋亡过程中,诱导凋亡基因bax的mRNA表达水平明显升高,抵抗凋亡基因bcl-2mRNA表达水平明显下降,致使bcl-2/bax比率明显降低;对低剂量链脲佐菌素糖尿病大鼠胰岛凋亡相关基因QRT-PCR检测也显示同样的结果。结论:高浓度葡萄糖可能通过诱导胰岛细胞凋亡增加而加重糖尿病,其中bcl-2/baxmRNA表达比率变化可能起重要作用。Objective: To study the effects of high concentration glucose on islet cell apoptosis and apoptosis related genes, and discuss the glucose toxicity and its molecular mechanism. Methods: Apoptosis percentages of primary rat islet cells and βTc3 cells cultured with high concentration glucose medium were measured by TUNEL method, mRNA expressions of bcl-2 and bax of cultured.rat islet cells and mouse βTc3 cells were detected by QRT-PCR. mRNA expressions of bcl-2 and bax of low dosage streptozotocin (STZ) diabetic rat islet cells were measured by QRT-PCR. Results: Apoptosis percentages of islet cells and βTc3 cells increased significantly in high concentration glucose cultured medium, mRNA expression of apoptosis-induced gene bax increased significantly and that of apoptosis-resistant gene bcl-2 decreased significantly in the islet cell apoptosis process, and bd-2Poax ratio decreased significantly. The same results were obtained in the study of apoptosis related gene of diabetic rat islet cells by QRT-PCR. Conclusion: High concentration glucose may aggravate low dosage (STZ) diabetes by increasing islet cell apoptosis, and the change of bcl-2/bax mRNA expression ratio may play an important role in this process.
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