Cox Aaron R, Lam Carol J, Rankin Matthew M, Rios Jacqueline S, Chavez Julia, Bonnyman Claire W, King Kourtney B, Wells Roger A, Anthony Deepti, Tu Justin X, Kim Jenny J, Li Changhong, Kushner Jake A
McNair Medical Institute, Pediatric Diabetes and Endocrinology, Baylor College of Medicine, Texas Children's Hospital, Houston, Texas 77030.
Division of Endocrinology and Diabetes, Children's Hospital of Philadelphia, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania 19104.
Endocrinology. 2017 Jun 1;158(6):1701-1714. doi: 10.1210/en.2017-00027.
The impact of incretins upon pancreatic β-cell expansion remains extremely controversial. Multiple studies indicate that incretin-based therapies can increase β-cell proliferation, and incretins have been hypothesized to expand β-cell mass. However, disagreement exists on whether incretins increase β-cell mass. Moreover, some reports indicate that incretins may cause metaplastic changes in pancreatic histology. To resolve these questions, we treated a large cohort of mice with incretin-based therapies and carried out a rigorous analysis of β-cell turnover and pancreatic histology using high-throughput imaging. Young mice received exenatide via osmotic pump, des-fluoro-sitagliptin, or glipizide compounded in diet for 2 weeks (short-term) on a low-fat diet (LFD) or 4.5 months (long-term) on a LFD or high-fat diet (HFD). Pancreata were quantified for β-cell turnover and mass. Slides were examined for gross anatomical and microscopic changes to exocrine pancreas. Short-term des-fluoro-sitagliptin increased serum insulin and induced modest β-cell proliferation but no change in β-cell mass. Long-term incretin therapy in HFD-fed mice resulted in reduced weight gain, improved glucose homeostasis, and abrogated β-cell mass expansion. No evidence for rapidly dividing progenitor cells was found in islets or pancreatic parenchyma, indicating that incretins do not induce islet neogenesis or pancreatic metaplasia. Contrasting prior reports, we found no evidence of β-cell mass expansion after acute or chronic incretin therapy. Chronic incretin administration was not associated with histological abnormalities in pancreatic parenchyma; mice did not develop tumors, pancreatitis, or ductal hyperplasia. We conclude that incretin therapies do not generate β-cells or alter pancreatic histology in young mice.
肠促胰岛素对胰腺β细胞增殖的影响仍极具争议。多项研究表明,基于肠促胰岛素的疗法可增加β细胞增殖,并且有人推测肠促胰岛素可扩大β细胞量。然而,对于肠促胰岛素是否能增加β细胞量存在分歧。此外,一些报告表明,肠促胰岛素可能会导致胰腺组织学发生化生改变。为了解决这些问题,我们用基于肠促胰岛素的疗法治疗了一大群小鼠,并使用高通量成像技术对β细胞更新和胰腺组织学进行了严格分析。幼鼠通过渗透泵接受艾塞那肽、去氟西他列汀或饮食中混合的格列吡嗪,在低脂饮食(LFD)下为期2周(短期),或在LFD或高脂饮食(HFD)下为期4.5个月(长期)。对胰腺进行β细胞更新和量的定量分析。检查切片以观察外分泌胰腺的大体解剖和微观变化。短期给予去氟西他列汀可增加血清胰岛素并诱导适度的β细胞增殖,但β细胞量无变化。在高脂饮食喂养的小鼠中进行长期肠促胰岛素治疗可导致体重增加减少、血糖稳态改善以及β细胞量扩张消失。在胰岛或胰腺实质中未发现快速分裂的祖细胞的证据,这表明肠促胰岛素不会诱导胰岛新生或胰腺化生。与先前的报告相反,我们发现在急性或慢性肠促胰岛素治疗后没有β细胞量扩张的证据。长期给予肠促胰岛素与胰腺实质的组织学异常无关;小鼠未发生肿瘤、胰腺炎或导管增生。我们得出结论,肠促胰岛素疗法不会在幼鼠中产生β细胞或改变胰腺组织学。