Liraglutide Compromises Pancreatic β Cell Function in a Humanized Mouse Model

被引:64
作者
Abdulreda, Midhat H. [1 ]
Rodriguez-Diaz, Rayner [2 ]
Caicedo, Alejandro [2 ]
Berggren, Per-Olof [1 ,3 ]
机构
[1] Univ Miami, Miller Sch Med, Diabet Res Inst, 1450 NW 10th Ave, Miami, FL 33136 USA
[2] Univ Miami, Miller Sch Med, Dept Med, Div Endocrinol Diabet & Metab, 1580 NW 10th Ave, Miami, FL 33136 USA
[3] Karolinska Univ Hosp L1, Karolinska Inst, Rolf Luft Res Ctr Diabet & Endocrinol, SE-17176 Stockholm, Sweden
基金
瑞典研究理事会;
关键词
INCRETIN-BASED THERAPIES; GLUCAGON-LIKE PEPTIDE-1; ONCE-DAILY LIRAGLUTIDE; WEIGHT-LOSS; ENDOCRINE PANCREAS; GLYCEMIC CONTROL; HIGH-RESOLUTION; OPEN-LABEL; BIOLOGY; SAFETY;
D O I
10.1016/j.cmet.2016.01.009
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Incretin mimetics are frequently used in the treatment of type 2 diabetes because they potentiate beta cell response to glucose. Clinical evidence showing short-term benefits of such therapeutics (e.g., liraglutide) is abundant; however, there have been several recent reports of unexpected complications in association with incretin mimetic therapy. Importantly, clinical evidence on the potential effects of such agents on the beta cell and islet function during long-term, multiyear use remains lacking. We now show that prolonged daily liraglutide treatment of >200 days in humanized mice, transplanted with human pancreatic islets in the anterior chamber of the eye, is associated with compromised release of human insulin and deranged overall glucose homeostasis. These findings raise concern about the chronic potentiation of beta cell function through incretin mimetic therapy in diabetes.
引用
收藏
页码:541 / 546
页数:6
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