利拉鲁肽对2型糖尿病肥胖患者胰岛细胞功能及NLRP3炎症小体、IL-1β、IL-18的影响
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Impact of liraglutide onislet cells function and NLRP3 inflammasome, IL-1β, IL-18 in obese and overweight type 2 diabetic patients
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    目的 探讨利拉鲁肽对2型糖尿病肥胖患者核苷酸结合寡聚化结构域(NOD)样受体家族3(NLRP3)炎症小体、白细胞介素1β(IL1β)、白细胞介素18(IL18)及稳态模型胰岛素抵抗指数(HOMAIR)、胰岛β细胞功能指数(HOMAβ)的影响。方法 选取2型糖尿病肥胖患者44例,按随机数字表法分为观察组和对照组各22例,对照组给予口服二甲双胍降糖方案,观察组在对照组基础上给予利拉鲁肽降糖方案。分析两组治疗前和治疗后空腹胰高血糖素、C肽、空腹血糖、HbA1c、总胆固醇水平、NLRP3 mRNA、IL1β、IL18及HOMAIR、HOMAβ的变化。结果 治疗前两组各指标均没有显著性差异。治疗后观察组患者BMI、空腹血糖、餐后2小时血糖及HbA1c均显著降低,且显著低于对照组;30min、60minC肽及AUCC肽显著增大,30min、60min、120min胰高血糖素及AUC胰高血糖素显著下降;两组NLRP3 mRNA、IL1β、IL18均显著性降低,且观察组显著低于对照组;两组患者HOMAIR均显著性降低,且观察组HOMAIR显著低于对照组,而HOMAβ均显著性升高,且观察组HOMAβ显著高于对照组。 结论 利拉鲁肽可以抑制NLRP3激活减小IL1β、IL18炎症因子的释放,改善胰岛β细胞功能。

    Abstract:

    Objective To evaluate effects of liraglutide on NLRP3 inflammasome, IL1β,IL18, homeostasis model insulin resistance index (HOMAIR) and homeostasis model assessmentβ in obese type 2 diabetic patients (T2DM). Methods A total of 44 T2DM patients were divided into observation group (n=22) and control group (n=22) by random digital table. Control group was given melbine. Observation group was additionally given Liraglutide on the basis of control group. Before and after treatment, glucagon,Cpeptide, blood glucose, HbA1c, total cholesterol, NLRP3 mRNA, IL1β, IL18, HOMAIR and HOMAβ were analyzed. Results There was no significant difference in every measurements between two groups. After treatment, the levels of glucagon,Cpeptide, blood glucose and HbA1c were significantly decreased in observation group and lower than those in the control group. Cpetide level at 30, 60minutes after standard meals and its area under the curve (AUC) significantly increased. Glucagon concentration at 30, 60 and 120minutes after standard meals and its AUC were significantly lower than that before liraglutide therapy. NLRP3 mRNA, IL1β and IL1 were significantly decreased in both groups. HOMAIR in the observation group was significantly lower than that in the control group, while HOMAIR was significantly lower than that in the control group. HOMAβ was significantly higher, and HOMAβ in the observation group was significantly higher than that in the control group. Conclusion Liraglutide could reduce the level of NLRP3 and downstream proinflammatory cytokine, and improve the function of islet beta cells.

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  • 在线发布日期: 2020-10-22
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