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高脂饮食C57BL/6小鼠PAI-1表达及罗格列酮干预效果研究
作者:刘莉  
单位:中国医科大学公共卫生学院营养与食品卫生学教研室
关键词:血浆纤溶酶原激活物抑制物-1 内脏脂肪 皮下脂肪 罗格列酮 
分类号:
出版年·卷·期(页码):2011·39·第六期(653-657)
摘要:

目的:研究正常体重和肥胖C57BL/6小鼠血清PAI-1及内脏和皮下脂肪组织PAI-1表达情况及罗格列酮的干预效果。方法:雄性C57BL/6小鼠按体重随机分为对照组、高脂组和高脂+RSG组(喂饲4周添加罗格列酮的高脂饲料),共12周。测定血脂、血清PAI-1及附睾、皮下脂肪组织PAI-1 mRNA表达。结果:高脂+RSG组小鼠体重显著高于高脂组和对照组。罗格列酮干预可降低总甘油三酯水平。高脂饲料喂养后小鼠血清PAI-1水平均显著高于对照组,而罗格列酮干预可降低血清PAI-1水平。三组小鼠附睾脂肪组织PAI-1 mRNA表达均显著高于皮下脂肪组织。罗格列酮干预可显著降低皮下脂肪组织PAI-1表达,而对附睾脂肪组织却无明显影响。结论:正常体重和肥胖小鼠的血清PAI-1水平及内脏和皮下脂肪组织PAI-1表达均存在差别,罗格列酮有助于改善血脂、降低血清PAI-1及皮下脂肪组织PAI-1 mRNA表达。

Objective: To study the level of serum plasminogen activator inhibitor 1(PAI-1) and expression of PAI-1 mRNA in visceral and subcutaneous adipose tissues of C57BL/6 mice which were normal weight or obesity and the effect of rosiglitazone (RSG) treatment. Methods: Male C57BL/6 mice were divided into control group fed with chow diet, high-fat group fed with high fat diet and high fat+RSG group fed with high fat diet for 8 weeks and supplemented with rosiglitazone for other 4 weeks, randomly. 12 weeks later, serum total triglyceride, total cholesterol and PAI-1 level were detected and the expression of PAI-1 mRNA in adipose tissues was also measured. Results: The body weight of mice in high-fat + RSG group was significantly higher than that in high-fat group and control. RSG treatment could decrease serum total triglyceride. High-fat diet could increase serum PAI-1 level, but RSG treatment could decreasePAI-1 level of mice with high feeding. The expression of PAI-1 mRNA of epididymal adipose tissues in all groups was all significantly higher than subcutaneous adipose tissues. RSG treatment could decrease the expression of PAI-1 mRNA in subcutaneous adipose tissues, but no effect in epididymal adipose tissues. Conclusion: The level of serum PAI-1 and the expression of PAI-1 mRNA were different between visceral and subcutaneous adipose tissues in both normal and obese mice. RSG treatment contributed to improve blood fat, decreased the level of serum PAI-1 and the expression of PAI-1 mRNA in subcutaneous adipose tissues.

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