[1]潘道延,沈洁,朱筱,等.利格列汀对2型糖尿病大鼠代谢性内毒素血症的影响[J].国际内分泌代谢杂志,2015,(04):230-233.[doi:10.3760/cma.j.issn.1673-4157.2015.04.004]
 Pan Daoyan,Shen Jie,Zhu Xiao,et al.Effects of linagliptin on metabolic endotoxemia in type 2 diabetic rats[J].International Journal of Endocrinology and Metabolism,2015,(04):230-233.[doi:10.3760/cma.j.issn.1673-4157.2015.04.004]
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利格列汀对2型糖尿病大鼠代谢性内毒素血症的影响()
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《国际内分泌代谢杂志》[ISSN:1673-4157/CN:12-1383/R]

卷:
期数:
2015年04
页码:
230-233
栏目:
论著
出版日期:
2015-07-20

文章信息/Info

Title:
Effects of linagliptin on metabolic endotoxemia in type 2 diabetic rats
作者:
潘道延沈洁朱筱赵德福陈志韩亚娟李文婷陈远程
300202 天津市河西区妇产科医院产科
Author(s):
Pan DaoyanShen JieZhu XiaoZhao DefuChen ZhiHan YajuanLi WentingChen Yuancheng.
Department of Endocrinology and Metabolism,The Third Affiliated Hospital of Southern Medical University,Guangzhou 510630,China Corresponding author:Shen Jie,Email:shenjiedr@163.com
关键词:
利格列汀2型糖尿病代谢性内毒素血症炎症
Keywords:
LinagliptinType 2 diabetes mellitusMetabolic endotoxemiaInflammation
DOI:
10.3760/cma.j.issn.1673-4157.2015.04.004
摘要:
目的 探讨利格列汀对高脂饮食联合小剂量链脲佐菌素(STZ)诱导的2型糖尿病大鼠代谢性内毒素血症的影响。方法 30只健康雄性Sprague-Dawley大鼠按随机数字法选择10只作为正常对照组,以正常饲料喂养,其余20只以高脂饲料饲喂8周后,予一次性腹腔注射STZ(35 mg/kg)制备2型糖尿病模型。将造模成功大鼠共16只按随机数字法分为利格列汀干预组(3 mg·kg-1·d-1灌胃,n=8)和糖尿病对照组(等量生理盐水灌胃,n=8),干预4周后测定大鼠空腹血糖、空腹胰岛素(FINS)、甘油三酯、总胆固醇、门静脉血浆脂多糖、肿瘤坏死因子-α(TNF-α)、白细胞介素-6(IL-6)、二胺氧化酶(DAO)的水平,计算稳态模型评估-胰岛素敏感指数(HOMA-ISI)及稳态模型评估-胰岛素抵抗指数(HOMA-IR)。结果 与正常对照组相比,糖尿病对照组空腹血糖、FINS、HOMA-IR、甘油三酯、总胆固醇及体重等指标明显升高,ln(HOMA-ISI)明显降低,而利格列汀干预组上述指标除体重外较糖尿病对照组均有改善(F =39.18~136.74,P均<0.01)。糖尿病对照组门静脉血浆脂多糖、TNF-α、IL-6、血浆DAO水平明显高于正常对照组,而利格列汀干预组上述指标较糖尿病对照组有所下降(F =18.13~51.43,P均<0.05)。结论 利格列汀可以改善高脂饮食联合STZ诱导的2型糖尿病大鼠代谢性内毒素血症,并减轻全身系统性炎性反应。
Abstract:
Objective To investigate the effects of linagliptin on metabolic endotoxemia in rats with type 2 diabetes mellitus(T2DM) induced by high fat feeding and low dose streptozotocin(STZ). Methods Ten of the 30 healthy male Sprague-Dawley rats were selected as normal control group according to random number and received basic diet,whereas the other 20 rats were fed with high-fat diet for 8 weeks and then treated with STZ intraperitoneal injection (35 mg/kg) once to induce T2DM. Diabetes was successfully induced in 16 rats which were then randomly divided into linagliptin treatment group(3 mg·kg-1·d-1 gavage,n=8) and T2DM control group(equivalent normal saline,n=8) according to random number. Four weeks later,fasting blood glucose,fasting blood insulin(FINS),triglyceride,total cholesterol,portal blood plasma lipopolysaccharide(LPS),tumor necrosis factor-α(TNF-α),interleukin 6(IL-6) and diamine oxidase(DAO) were measured. Homeostasis model assessment-insulin sensitive index (HOMA-ISI) and homeostasis model assessment-insulin resistance index(HOMA-IR) were calculated. Results Compared with normal control group,the levels of fasting blood glucose,FINS,HOMA-IR,triglyceride,total cholesterol and body weight were all significantly increased in T2DM control group,whereas the ln(HOMA-ISI) was signifi-cantly reduced; compared with T2DM group,indexes mentioned above except body weight were all improved in linagliptin treatment group(F =39.18-136.74, all P <0.01);compared with normal control group,the levels of portal blood plasma LPS,TNF-α,IL-6 and plasma DAO increased in T2DM control group,but indexes mentioned above were all decreased in linagliptin treatment group(F =18.13-51.43, all P<0.05). Conclusion Linagliptin can improve the metabolic endotoxemia in rats with T2DM induced by high fat feeding and STZ,and attenuate systemic inflammation response.

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备注/Memo

备注/Memo:
基金项目:广东省科技计划项目(2011B010500027);广东省自然科学基金资助项目(S2013010016045)   通信作者:沈洁,Email: shenjiedr@163.com
更新日期/Last Update: 2015-07-20