J4 ›› 2012, Vol. 38 ›› Issue (3): 443-446.

• 基础研究 • 上一篇    下一篇

新型肝X受体激动剂ATI-829对糖尿病小鼠的治疗作用

彭璐1|赵兴山1|谢景田2|彭大成2|兰玲3   

  1. (1.北京积水潭医院心血管内科|北京 100035;2.芝加哥大学医学院Ben |May研究中心|美国 芝加哥 |60637;3.北京积水潭医院内分泌科|北京 |100035)
  • 收稿日期:2012-01-11 出版日期:2012-05-28 发布日期:2012-05-28
  • 通讯作者: 兰 玲 E-mail:(Tel: 010-58516688,E-mail: lupeng11@163.com)
  • 作者简介:彭 璐 (1974-)|女|北京市人|主治医师|医学硕士|主要从事代谢疾病的基础及临床研究。
  • 基金资助:

    国家自然科学基金资助课题(30901725)

Effect of |novel liver X receptor agonist ATI-829 in |treatment of diabetic mice

PENG |Lu1,ZHAO Xing-shan1,XIE Jing-tian2,PENG Da-cheng2,LAN Ling3   

  1. (1.Department of |Cardiology,Beijing Jishuitan Hospital,Beijing 100035,China|2.Ben May Research Center,School of Medical Science,Chicago University,Chicago 60637,USA|3.Department of |Endocrinology,Beijing Jishuitan Hospital,Beijing 100035,China)
  • Received:2012-01-11 Online:2012-05-28 Published:2012-05-28

摘要:

目的: 观察新型肝X受体激动剂ATI-829对2型糖尿病KKAy小鼠的血糖、体质量和摄食量及NOD小鼠1型糖尿病发生率的影响,为ATI-829的临床应用提供依据。方法:  将15只12周龄雄性KKAy 2型糖尿病小鼠分为溶媒对照组、吡格列酮治疗组和ATI-829治疗组。每周进行1次血糖、体质量和摄食量的监测,共给药2周。40只6周龄的雌性1型糖尿病NOD小鼠分为溶媒对照组、传统肝X受体激动剂T1317治疗组和ATI-829治疗组,共给药8周,从小鼠20周龄起,每2周监测1次血糖水平,持续监测至34周龄。结果:在KKAy2型糖尿病小鼠实验中,治疗1周后,各组小鼠血糖水平、体质量和摄食量变化与治疗前比较差异均无统计学意义(P<0.05)。治疗2周后吡格列酮治疗组血糖浓度由(30.11±3.94) mmol.L-1降至(14.00±2.78) mmol.L-1,小鼠体质量由(36.96±1.17) g升高到(41.14±0.99) g,与溶媒对照组比较差异均有统计学意义(P<0.05)。ATI-829治疗组血糖浓度由(33.28±1.89) mmol.L-1降至(15.89±1.06) mmol.L-1,与溶媒对照组比较差异有统计学意义(P<0.05),小鼠体质量由(37.82± 0.96) g降至(37.11±0.26) g,但与溶媒对照组比较差异无统计学意义(P> 0.05)。吡格列酮和ATI-829均不影响小鼠摄食量。在1型糖尿病NOD小鼠实验中,溶媒对照组最终小鼠糖尿病发病率为50%,T1317治疗组发病率达90%,而ATI-829 治疗组无小鼠发病,T1317组和ATI-829治疗组发病率与溶媒对照组比较差异均有统计学意义(P<0.05)。结论: 新型肝X受体激动剂ATI-829能有效降低2型糖尿病小鼠血糖浓度,且不诱导其体质量增加,同时亦可降低小鼠1型糖尿病的发生率。

关键词: 肝X受体;激动剂;糖尿病

Abstract:

To observe the influence  of  novel liver X receptor (LXR) agonist ATI-829 on the blood glucose level,body weight and dietary consumption of type 2 diabetes mellitus KKAy mice and  the incidence of type 1 diabetic NOD mice, and to provide evidence for clinical application.Methods Fifteen 12-week male type 2 diabetes mellitus KKAy mice were randomly divided into vehicle control group,pioglitazone treatment group,and ATI-829 treatment group.The mice were treated for 2 weeks, and the  blood glucose levels,body weights,and the dietary consumptions of mice were measured every week.Forty 6-week female type 1 diabetes mellitus NOD mice were divided into vehicle control group,classic LXR agonist T1317 treatment group,and ATI-829 treatment group.The mice were treated for 8 weeks, and the cumulative incidence was  measured every two weeks from 20 to 34 week.Results In type 2 diabetes mellitus mice,after 1 week treatment,the glucose level,body wieght and the dietry consumption of mice in various groups didn’t change significantly compared with those before treatment.After 2 weeks treatment, the blood glucose level of mice in pioglitazone treatment group was decreased from (30.11±3.94) mmol.L-1 to (14.00±2.78) mmol.L-1,and the body weight was  increased from (36.96±1.17) g to (41.14±0.99) g,there were significant differences compared with vehicle control group(P<0.05).The blood glucose level of mice  in ATI-829 treatment group was decreased from(33.28±1.89) mmol.L-1 to (15.89±1.06) mmol.L-1,there was significant difference compared with vehicle control group(P<0.05);and the body weight was  decreased from (37.82±0.96) g to (37.11±0.26) g,there was no significant difference compared with vehicle control group(P>0.05).The dietary consumption didn’t change significantly in various groups before and after treatment.In type 1 diabetic NOD mice,ATI-829 was able to totally prevent the disease occurrence and the disease incidence in T1317 treatment group rose to 90%,which was 50%  in vehicle control group,there were  significant differences between T1317 group,ATI-829 treatment  group and    vehicle control group(P<0.05).Conclusion The novel   liver X receptor  agonist ATI-829 can decrease the blood glucose levels of type 2 diabetes mellitus mice and avoid body weight gain.Meanwhile,ATI-829 can also decrease the incidence of type 1 diabetes mellitus in mice.

中图分类号: 

  • R587.1