Fiorentino Teresa Vanessa, Owston Michael, Abrahamian Gregory, La Rosa Stefano, Marando Alessandro, Perego Carla, Di Cairano Eliana S, Finzi Giovanna, Capella Carlo, Sessa Fausto, Casiraghi Francesca, Paez Ana, Adivi Ashwin, Davalli Alberto, Fiorina Paolo, Guardado Mendoza Rodolfo, Comuzzie Anthony G, Sharp Mark, DeFronzo Ralph A, Halff Glenn, Dick Edward J, Folli Franco
Division of Diabetes, Department of Medicine, University of Texas Health Science Center at San Antonio, San Antonio, Texas; Department of Medical and Surgical Sciences, University Magna Graecia of Catanzaro, Catanzaro, Italy.
Southwest National Primate Research Center, Texas Biomedical Research Institute, San Antonio, Texas.
Am J Pathol. 2015 Jan;185(1):139-50. doi: 10.1016/j.ajpath.2014.09.009. Epub 2014 Nov 6.
In this study, we aimed to evaluate the effects of exenatide (EXE) treatment on exocrine pancreas of nonhuman primates. To this end, 52 baboons (Papio hamadryas) underwent partial pancreatectomy, followed by continuous infusion of EXE or saline (SAL) for 14 weeks. Histological analysis, immunohistochemistry, Computer Assisted Stereology Toolbox morphometry, and immunofluorescence staining were performed at baseline and after treatment. The EXE treatment did not induce pancreatitis, parenchymal or periductal inflammatory cell accumulation, ductal hyperplasia, or dysplastic lesions/pancreatic intraepithelial neoplasia. At study end, Ki-67-positive (proliferating) acinar cell number did not change, compared with baseline, in either group. Ki-67-positive ductal cells increased after EXE treatment (P = 0.04). However, the change in Ki-67-positive ductal cell number did not differ significantly between the EXE and SAL groups (P = 0.13). M-30-positive (apoptotic) acinar and ductal cell number did not change after SAL or EXE treatment. No changes in ductal density and volume were observed after EXE or SAL. Interestingly, by triple-immunofluorescence staining, we detected c-kit (a marker of cell transdifferentiation) positive ductal cells co-expressing insulin in ducts only in the EXE group at study end, suggesting that EXE may promote the differentiation of ductal cells toward a β-cell phenotype. In conclusion, 14 weeks of EXE treatment did not exert any negative effect on exocrine pancreas, by inducing either pancreatic inflammation or hyperplasia/dysplasia in nonhuman primates.
在本研究中,我们旨在评估艾塞那肽(EXE)治疗对非人灵长类动物外分泌胰腺的影响。为此,52只狒狒(阿拉伯狒狒)接受了部分胰腺切除术,随后连续输注EXE或生理盐水(SAL)14周。在基线和治疗后进行了组织学分析、免疫组织化学、计算机辅助立体学工具箱形态测量和免疫荧光染色。EXE治疗未诱发胰腺炎、实质或导管周围炎性细胞积聚、导管增生或发育异常病变/胰腺上皮内瘤变。在研究结束时,与基线相比,两组中Ki-67阳性(增殖)腺泡细胞数量均未改变。EXE治疗后Ki-67阳性导管细胞增加(P = 0.04)。然而,EXE组和SAL组之间Ki-67阳性导管细胞数量的变化无显著差异(P = 0.13)。SAL或EXE治疗后,M-30阳性(凋亡)腺泡和导管细胞数量未改变。EXE或SAL治疗后,未观察到导管密度和体积的变化。有趣的是,通过三重免疫荧光染色,我们仅在研究结束时的EXE组中检测到导管中共同表达胰岛素的c-kit(细胞转分化标志物)阳性导管细胞,这表明EXE可能促进导管细胞向β细胞表型分化。总之,14周的EXE治疗在非人灵长类动物中未通过诱发胰腺炎症或增生/发育异常对外分泌胰腺产生任何负面影响。