Glycaemic regulation and insulin secretion are abnormal in cystic fibrosis pigs despite sparing of islet cell mass

Aliye Uc, Alicia K. Olivier, Michelle A. Griffin, David K. Meyerholz, Jianrong Yao, Maisam Abu-El-Haija, Katherine M. Buchanan, Oriana G. Vanegas Calderón, Marwa Abu-El-Haija, Alejandro A. Pezzulo, Leah R. Reznikov, Mark J. Hoegger, Michael V. Rector, Lynda S. Ostedgaard, Peter J. Taft, Nick D. Gansemer, Paula S. Ludwig, Emma E. Hornick, David A. Stoltz, Katie L. OdeMichael J. Welsh, John F. Engelhardt, Andrew W. Norris

Research output: Contribution to journalArticlepeer-review

52 Scopus citations

Abstract

Diabetes is a common and significant co-morbidity in cystic fibrosis (CF). The pathogenesis of cystic fibrosis related diabetes (CFRD) is incompletely understood. Because exocrine pancreatic disease is similar between humans and pigs with CF, the CF pig model has the potential to contribute significantly to the understanding of CFRD pathogenesis. We determined the structure of the endocrine pancreas in fetal, newborn and older CF and non-CF pigs and assessed endocrine pancreas function by intravenous glucose tolerance test (IV-GTT). In fetal pigs, pancreatic insulin and glucagon density was similar between CF and non-CF. In newborn and older pigs, the insulin and glucagon density was unchanged between CF and non-CF per total pancreatic area, but increased per remnant lobular tissue in CF reflecting exocrine pancreatic loss. Although fasting glucose levels were not different between CF and non-CF newborns, CF newborns demonstrated impaired glucose tolerance and increased glucose area under the curve during IV-GTT. Second phase insulin secretion responsiveness was impaired in CF newborn pigs and significantly lower than that observed in non-CF newborns. Older CF pigs had elevated random blood glucose levels compared with non-CF. In summary, glycaemic abnormalities and insulin secretion defects were present in newborn CF pigs and spontaneous hyperglycaemia developed over time. Functional changes in CF pig pancreas were not associated with a decline in islet cell mass. Our results suggest that functional islet abnormalities, independent of structural islet loss, contribute to the early pathogenesis of CFRD.

Original languageEnglish
Pages (from-to)131-142
Number of pages12
JournalClinical Science
Volume128
Issue number2
DOIs
StatePublished - 2015

Keywords

  • Cystic fibrosis-related diabetes
  • Exocrine pancreas
  • Glucagon
  • Glucose tolerance test
  • Pancreas
  • Pig

Fingerprint

Dive into the research topics of 'Glycaemic regulation and insulin secretion are abnormal in cystic fibrosis pigs despite sparing of islet cell mass'. Together they form a unique fingerprint.

Cite this