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胰岛素抵抗细胞模型的胰岛素降解酶表达 被引量:6
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作者 李晨钟 张素华 +2 位作者 舒昌达 任伟 何军 《中华内分泌代谢杂志》 CAS CSCD 北大核心 2000年第5期302-305,共4页
目的 了解胰岛素降解酶 (IDE)基因、酶蛋白表达水平与胰岛素敏感性的关系 ,并初步探讨胰岛素降解抑制剂氯喹改善胰岛素敏感性的分子机制。方法 以原代大鼠肝细胞胰岛素抵抗(IR)模型为研究对象 ,分别采用免疫印迹技术和逆转录 聚合酶... 目的 了解胰岛素降解酶 (IDE)基因、酶蛋白表达水平与胰岛素敏感性的关系 ,并初步探讨胰岛素降解抑制剂氯喹改善胰岛素敏感性的分子机制。方法 以原代大鼠肝细胞胰岛素抵抗(IR)模型为研究对象 ,分别采用免疫印迹技术和逆转录 聚合酶链反应 (RT PCR)技术检测IR细胞模型的IDE酶蛋白表达 (EIP)及基因表达水平 (EIG) ,同时检测IDE活性和反映细胞胰岛素敏感性的14 C 2 脱氧葡萄糖掺入率及14 C 醋酸盐掺入率 ,并观察氯喹对IR细胞模型上述指标的影响。结果IR细胞模型的EIG及EIP水平显著高于对照细胞 ,并与其IDE活性呈显著正相关 ,与两种掺入率呈显著负相关。同时氯喹可明显抑制IR细胞模型以及对照细胞的EIG及EIP水平 ,而且抑制的程度与氯喹作用时间的长短密切相关。结论 大鼠肝细胞的EIG和EIP与其胰岛素敏感性之间呈负相关关系 ;高浓度胰岛素可刺激大鼠肝细胞的IDE基因mRNA及酶蛋白的表达 ,而氯喹则对其起明显的抑制作用 ;胰岛素和氯喹对大鼠肝细胞EIG的影响可能是通过影响IDE基因转录来实现。 展开更多
关键词 氯喹 胰岛素溶解 基因表达 胰岛素抵抗 细胞模型
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Effect of Chitosan-Cysteine Conjugate on Enzymatic Degradation and Hypoglycemic effect of Insulin
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作者 祁荣 平其能 +1 位作者 徐瑞阳 石勇平 《Journal of Chinese Pharmaceutical Sciences》 CAS 2004年第2期124-129,共6页
Aim To evaluate the inhibitory effect of chitosan-cysteine conjugate onenzymatic degradation and hypogly-cemic enhancement effect of insulin. Methods Chitosan-cysteineconjugate was synthesized. The protective effect o... Aim To evaluate the inhibitory effect of chitosan-cysteine conjugate onenzymatic degradation and hypogly-cemic enhancement effect of insulin. Methods Chitosan-cysteineconjugate was synthesized. The protective effect of the conjugate against degradation of insulin byα-chymotrypsin and trypsin was evaluated in vitro. Insulin enteric- microspheres were prepared byusing O_1 /Q_2 emulsion solvent evaporation method. The hypoglycemic enhancement effect of theconjugate was studied by oral administration of insulin solution or enteric-microspheres to rats.Results The thiol group content of the synthesized conjugate was about 200 μmol·g^(-1) polymer,which showed a strong protective effect on insulin from enzymatic degradation in vitro. Almost allthe insulin incubated in a-chymotrypsin solution or trypsin solution without chitosan-cysteineconjugate was degraded entirely within 1 h and 5 h respectively, whereas above 75% of insulinremained in the same content of the enzymatic solution containing 4 mg·mL^(-1) conjugate. The drugloading of insulin enteric-microspheres was about 7% . In vivo experiment, chitosan-cysteineconjugate (85 μg·kg^(-1)) prolonged the hypoglycemic time of insulin solution orenteric-microspheres when administered simultaneously with the absorption enhancer SNAC. ConclusionChitosan-cysteine conjugate has a marked inhibitory effect on the enzymatic degradation of insulinin vitro, and it displays a significant hypoglycemic enhancement effect on insulin oral formulationin vivo. 展开更多
关键词 chitosan-cysteine conjugate INSULIN enzymatic degradation enteric-microspheres hypoglycemic enhancement
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