Islet auto-transplantation into an omental or splenic site results in a normal beta cell but abnormal alpha cell response to mild non-insulin-induced hypoglycemia

Am J Transplant. 2005 Oct;5(10):2368-77. doi: 10.1111/j.1600-6143.2005.01041.x.

Abstract

The present studies were designed to determine if totally pancreatectomized dogs that underwent islet auto-transplantation retained a functional pancreatic counterregulatory response to mild non-insulin-induced hypoglycemia. Six dogs underwent total pancreatectomy followed by islet auto-transplantation to spleen or omentum. The animals recovered and fasting plasma glucose and insulin levels were normal. Each study consisted of a 40-min control and 2-h test period. At the onset of the test period, a glycogen phosphorylase inhibitor was administered to create mild hypoglycemia. Plasma glucose in the transplanted dogs fell from 120 +/- 4 to 80 +/- 3 mg/dL, similar to the minimum in control dogs without islet auto-transplantation (108 +/- 2 to 84 +/- 5 mg/dL). The fall in plasma insulin was similar in both groups. Glucagon, however, rose in response to hypoglycemia in the control dogs (Delta24 +/- 7 pg/mL; p < 0.05), but failed to rise significantly in the transplanted dogs (Delta9 +/- 6 pg/mL). In fact, only 1 of 7 control dogs failed to increase plasma glucagon by at least 25%, whereas 4 of 6 transplanted dogs failed to do so. In conclusion, in conscious dogs with successfully auto-transplanted islets, the beta cell response to mild non-insulin-induced hypoglycemia was normal, whereas the alpha cell response was not.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Area Under Curve
  • Arginine / chemistry
  • Blood Glucose / metabolism
  • Cell Survival
  • Cell Transplantation
  • Dogs
  • Female
  • Glucagon / metabolism
  • Glucagon-Secreting Cells / metabolism*
  • Glucagon-Secreting Cells / physiology*
  • Glycogen Phosphorylase / antagonists & inhibitors
  • Graft Survival
  • Hypoglycemia / pathology*
  • Insulin / blood
  • Insulin / metabolism*
  • Insulin / pharmacology
  • Insulin-Secreting Cells / cytology*
  • Islets of Langerhans / cytology*
  • Islets of Langerhans Transplantation / methods*
  • Male
  • Pancreas / pathology
  • Pancreas / physiology
  • Spleen / cytology*
  • Spleen / pathology
  • Time Factors
  • Transplantation, Autologous / methods*

Substances

  • Blood Glucose
  • Insulin
  • Glucagon
  • Arginine
  • Glycogen Phosphorylase