Pancreatic peptides in young and elderly zucker type 2 diabetic fatty rats

Frank Christopher Howarth, Mey Khalfan Ahmed Ali Al Kitbi, Rasheed Shaul Hameed, Ernest Adeghate

Research output: Contribution to journalArticlepeer-review

10 Citations (Scopus)

Abstract

Context The global prevalence of diabetes mellitus, and in particular type 2 diabetes mellitus is increasing at an alarming rate. Risk factors for development of diabetes include obesity and advancing age. Objectives The distribution of insulin, glucagon, somatostatin and pancreatic polypeptide in the pancreatic islets has been investigated in young and elderly type 2 Zucker diabetic fatty (ZDF) rats and age-matched Zucker lean (ZL) controls. Methods Experiments were performed in male animals aged either 9-13 weeks or 30-34 weeks. Immunohistochemistry was used to label insulin, glucagon, somatostatin and pancreatic polypeptide in islet cells. Results The percentage of insulin-positive cells was unaltered in young but decreased in elderly ZDF (35.5±2.5%) rats compared to ZL controls (57.9±1.8%). The percentage of glucagon-positive cells was increased in young ZDF (58.7±3.4%) compared to ZL controls (23.4±2.1%). However, in elderly rats the percentage of glucagon-positive cells declined in ZDF rats and was no longer different from ZL controls. The percentage of somatostatin-positive cells was unaltered in young and elderly ZDF rats compared to ZL controls. The percentage of pancreatic polypeptide-positive cells was unaltered in young but increased in elderly ZDF (22.0±2.5%) rats compared to ZL controls (13.8±1.8%). Conclusions The distribution of pancreatic hormones is altered to varying extents in the ZDF rat and during the normal aging process.

Original languageEnglish
Pages (from-to)567-573
Number of pages7
JournalJournal of the Pancreas
Volume12
Issue number6
Publication statusPublished - Nov 2011

Keywords

  • Diabetes mellitus
  • Glucagon
  • Insulin
  • Pancreas
  • Pancreatic polypeptide
  • Rats
  • Somatostatin
  • Type 2
  • Zucker

ASJC Scopus subject areas

  • Endocrinology, Diabetes and Metabolism
  • Hepatology
  • Endocrinology

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