학술논문

Glucose metabolism in the Belgrade rat, a model of iron-loading anemia.
Document Type
Article
Source
American Journal of Physiology: Gastrointestinal & Liver Physiology. Jun2013 Part 2, Vol. 304 Issue 6, pG1095-G1102. 8p.
Subject
*GLUCOSE metabolism
*ANEMIA
*EPIDEMIOLOGY
*DISEASE prevalence
*PEOPLE with diabetes
*IRON in the body
*HEMOCHROMATOSIS
*LABORATORY rats
Language
ISSN
0193-1857
Abstract
The irondiabetes hypothesis proposes an association between iron overload and glucose metabolism that is supported by a number of epidemiological studies. The prevalence of type 2 diabetes in patients with hereditary hemochromatosis and iron-loading thalassemia supports this hypothesis. The Belgrade rat carries a mutation in the iron transporter divalent metal transporter 1 (DMT1) resulting in ironloading anemia. In this study, we characterized the glycometabolic status of the Belgrade rat. Belgrade rats displayed normal glycemic control. Insulin signaling and secretion were not impaired, and pancreatic tissue did not incur damage despite high levels of nonheme iron. These findings suggest that loss of DMT1 protects against oxidative damage to the pancreas and helps to maintain insulin sensitivity despite iron overload. Belgrade rats had lower body weight but increased food consumption compared with heterozygous littermates. The unexpected energy balance was associated with increased urinary glucose output. Increased urinary excretion of electrolytes, including iron, was also observed. Histopathological evidence suggests that altered renal function is secondary to changes in kidney morphology, including glomerulosclerosis. Thus, loss of DMT1 appears to protect the pancreas from injury but damages the integrity of kidney structure and function. [ABSTRACT FROM AUTHOR]