Glucagon Deficiency Reduces Hepatic Glucose Production and Improves Glucose Tolerance In Adult Mice
Author(s) -
Aidan S. Hancock,
Aiping Du,
Jingxuan Liu,
Mayumi F. Miller,
Catherine Lee May
Publication year - 2010
Publication title -
endocrine reviews
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 6.357
H-Index - 272
eISSN - 1945-7189
pISSN - 0163-769X
DOI - 10.1210/edrv.31.4.9983
Subject(s) - glucagon , medicine , endocrinology , glucose homeostasis , glucagon receptor , glycogenolysis , gluconeogenesis , postprandial , hyperglucagonemia , alpha cell , biology , pancreas , homeostasis , diabetes mellitus , insulin , beta cell , metabolism , insulin resistance , islet
The major role of glucagon is to promote hepatic gluconeogenesis and glycogenolysis to raise blood glucose levels during hypoglycemic conditions. Several animal models have been established to examine the in vivo function of glucagon in the liver through attenuation of glucagon via glucagon receptor knockout animals and pharmacological interventions. To investigate the consequences of glucagon loss to hepatic glucose production and glucose homeostasis, we derived mice with a pancreas specific ablation of the α-cell transcription factor, Arx, resulting in a complete loss of the glucagon-producing pancreatic α-cell. Using this model, we found that glucagon is not required for the general health of mice but is essential for total hepatic glucose production. Our data clarifies the importance of glucagon during the regulation of fasting and postprandial glucose homeostasis.
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