Metabolism of glucagon by dipeptidyl peptidase IV (CD26)

Regul Pept. 2001 Jan 12;96(3):133-41. doi: 10.1016/s0167-0115(00)00170-1.


Glucagon is a 29-amino acid polypeptide released from pancreatic islet alpha-cells that acts to maintain euglycemia by stimulating hepatic glycogenolysis and gluconeogenesis. Despite its importance, there remains controversy about the mechanisms responsible for glucagon clearance in the body. In the current study, enzymatic metabolism of glucagon was assessed using sensitive mass spectrometric techniques to identify the molecular products. Incubation of glucagon with purified porcine dipeptidyl peptidase IV (DP IV) yielded sequential production of glucagon(3-29) and glucagon(5-29). In human serum, degradation to glucagon(3-29) was rapidly followed by N-terminal cyclization of glucagon, preventing further DP IV-mediated hydrolysis. Bioassay of glucagon, following incubation with purified DP IV or normal rat serum demonstrated a significant loss of hyperglycemic activity, while a similar incubation in DP IV-deficient rat serum did not show any loss of glucagon bioactivity. Degradation, monitored by mass spectrometry and bioassay, was blocked by the specific DP IV inhibitor, isoleucyl thiazolidine. These results identify DP IV as a primary enzyme involved in the degradation and inactivation of glucagon. These findings have important implications for the determination of glucagon levels in human plasma.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Blood Proteins / isolation & purification
  • Blood Proteins / metabolism
  • Blood Proteins / pharmacology
  • Dipeptidyl Peptidase 4 / blood
  • Dipeptidyl Peptidase 4 / isolation & purification
  • Dipeptidyl Peptidase 4 / metabolism*
  • Dipeptidyl Peptidase 4 / pharmacology
  • Glucagon / chemistry
  • Glucagon / metabolism*
  • Glucagon / pharmacology
  • Humans
  • Isoleucine / analogs & derivatives
  • Isoleucine / pharmacology
  • Kinetics
  • Male
  • Peptide Fragments / chemistry
  • Peptide Fragments / metabolism
  • Peptide Fragments / pharmacology
  • Rats
  • Rats, Wistar
  • Serine Proteinase Inhibitors / pharmacology
  • Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization
  • Swine
  • Thiazoles / pharmacology


  • Blood Proteins
  • Peptide Fragments
  • Serine Proteinase Inhibitors
  • Thiazoles
  • isoleucyl-thiazolidide
  • Isoleucine
  • Glucagon
  • Dipeptidyl Peptidase 4