Department of Endocrinology, The Second Affiliated Hospital of Guangzhou Medical University, Guangzhou, Guangdong, China (mainland).
Department of Endocrinology, Peking University First Hospital, Beijing, China (mainland).
Med Sci Monit. 2018 May 19;24:3293-3300. doi: 10.12659/MSM.907227.
BACKGROUND The aim of this study was to compare the effects of liraglutide, a long-acting glucagon-like peptide-1 (GLP-1) receptor agonist, and insulin glargine, a long-acting insulin analog, on glycemic control and pancreatic β-cell function in db/db mice. MATERIAL AND METHODS Eight-week-old male db/db mice (n=40) were divided into five groups: the vehicle-treated group (VG) (n=8); the insulin glargine-treated group (GG) (dose, 450 mg/kg) (n=8), the low-dose liraglutide-treated group (LLG) (dose, 75 μg/kg) (n=8), the mid-dose liraglutide-treated group (MLG) (150 μg/kg) (n=8), and the high-dose liraglutide-treated group (HLG) (300 μg/kg) (n=8), treated with subcutaneous injection once daily, from 8-14 weeks-of-age. Body weight, pancreatic weight, levels of blood glucose, triacylglycerol, C-peptide, and the intraperitoneal glucose tolerance test (IPGTT) were used. Expression levels of the INS1 gene were measured using reverse transcription polymerase chain reaction (RT-PCR), and pancreatic and duodenal homeobox 1 (Pdx1), paired box 4 (Pax4), and paired box 6 (Pax6) mRNA expression were measured. RESULTS Both insulin glargine and liraglutide improved glycemic control of db/db mice when compared with vehicle. The following were significantly increased in the HLG compared with the GG: the receiver operating characteristic (ROC) area under the curve (AUC) for the IPGTT; C-peptide levels; the pancreas to body weight coefficient; expression levels of the INS1 gene and pancreatic transcription factors Pdx1, Pax4 and Pax6. Liraglutide treatment was without hypoglycemic effects. CONCLUSIONS Liraglutide acted in a dose-dependent manner on glycemic control of db/db mice, and was more effective than insulin glargine, when administered at a high dose.
本研究旨在比较利拉鲁肽(一种长效胰高血糖素样肽-1(GLP-1)受体激动剂)和胰岛素甘精,一种长效胰岛素类似物,对 db/db 小鼠血糖控制和胰岛β细胞功能的影响。
8 周龄雄性 db/db 小鼠(n=40)分为五组:对照组(VG)(n=8);胰岛素甘精治疗组(GG)(剂量,450mg/kg)(n=8),低剂量利拉鲁肽治疗组(LLG)(剂量,75μg/kg)(n=8),中剂量利拉鲁肽治疗组(MLG)(150μg/kg)(n=8),高剂量利拉鲁肽治疗组(HLG)(300μg/kg)(n=8),每天皮下注射一次,从 8-14 周龄。测量体重、胰腺重量、血糖、三酰甘油、C 肽和腹腔葡萄糖耐量试验(IPGTT)。采用逆转录聚合酶链反应(RT-PCR)测量 INS1 基因的表达水平,并测量胰腺和十二指肠同源盒 1(Pdx1)、配对盒 4(Pax4)和配对盒 6(Pax6)mRNA 的表达。
与对照组相比,胰岛素甘精和利拉鲁肽均改善了 db/db 小鼠的血糖控制。与 GG 相比,HLG 以下指标明显升高:IPGTT 的受试者工作特征(ROC)曲线下面积(AUC);C 肽水平;胰腺与体重比;INS1 基因和胰腺转录因子 Pdx1、Pax4 和 Pax6 的表达水平。利拉鲁肽治疗无低血糖作用。
利拉鲁肽对 db/db 小鼠的血糖控制呈剂量依赖性,高剂量时的效果优于胰岛素甘精。