Growth hormone increases beta-cell proliferation in transplanted human and fetal rat islets

JOP. 2009 May 18;10(3):242-8.

Abstract

Objective: The aim of the study was to increase the number of human islet beta-cells after transplantation with injections of human growth hormone (hGH).

Interventions: Human islets and fetal rat islets were transplanted under the left kidney capsule and under the right kidney capsule, respectively in nude normoglycemic mice which were then given a daily injection of 200 microg hGH for 1-4 weeks.

Main outcome measure: Beta-cell proliferation was determined using thymidine incorporation and the beta-cell area was assessed using light microscopy.

Results: Mice given hGH increased their body weight one week after transplantation and had a more efficient removal of glucose after 3 and 4 weeks. Treatment with hGH resulted in increased beta-cell proliferation in human and fetal rat beta-cells, and the beta-cell area tended to increase. However, serum insulin concentrations and pancreas insulin content remained unchanged.

Conclusions: hGH increased the proliferation of transplanted human beta-cells as well as improving the glucose tolerance of the transplanted mice.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Animals
  • Blood Glucose / metabolism
  • Cell Division / physiology
  • Cell Survival / drug effects
  • Female
  • Fetal Tissue Transplantation
  • Graft Survival / drug effects*
  • Human Growth Hormone / blood
  • Human Growth Hormone / pharmacology*
  • Humans
  • Insulin / blood
  • Insulin-Secreting Cells* / cytology
  • Insulin-Secreting Cells* / drug effects
  • Insulin-Secreting Cells* / transplantation
  • Islets of Langerhans Transplantation*
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Mice, Nude
  • Middle Aged
  • Organ Culture Techniques
  • Pregnancy
  • Rats
  • Rats, Sprague-Dawley
  • Transplantation, Heterologous
  • Young Adult

Substances

  • Blood Glucose
  • Insulin
  • Human Growth Hormone