Pancreatic peptides, neuropeptides and neurotransmitters in diabetes mellitus: A review

Ernest Adeghate, Abdulsamad Ponery

Research output: Contribution to journalReview articlepeer-review

7 Citations (Scopus)


Diabetes mellitus is due to defective secretion and/or function of insulin. It is a common chronic disease affecting up to 6% of the world population. This prevalence increases to about 24% in the island of Nauru and some Middle Eastern countries. Diabetes mellitus is associated with profound changes in the endocrine pancreas. These changes include a significant decrease in the number of beta cells, the cell type that produces and secretes insulin. A decrease in the number of insulin producing cells is more evident in type I diabetes. The decrease in the number of insulin-secreting cells is associated with a concomitant increase in the number of glucagon, somatostatin and pancreatic-polypeptide producing cells. The increase in glucagon producing cells results in hyperglucagonaemia, which further exacerbates the hyperglycaemia induced by lack of insulin. In addition to the changes in the number and plasma levels of pancreatic hormones, the number of calcitonin-gene-related peptide- and galanin-positive cells in the islet of Langerhans decreases after the onset of diabetes. Pancreatic amino butyric acid is also decreased in diabetes. These abnormal changes in the pattern of distribution of peptides, neuropeptides and neurotransmitters may contribute to the pathogenesis of diabetes mellitus.

Original languageEnglish
Pages (from-to)1-6
Number of pages6
JournalInternational Journal of Diabetes and Metabolism
Issue number1-2
Publication statusPublished - 2003


  • Diabetes mellitus
  • Hormones
  • Neuropeptides
  • Neurotransmitters
  • Peptides

ASJC Scopus subject areas

  • Endocrinology, Diabetes and Metabolism


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