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Heat stress stimulates hepcidin mRNA expression and C/EBPα protein expression in aged rodent liver
Journal article   Open access   Peer reviewed

Heat stress stimulates hepcidin mRNA expression and C/EBPα protein expression in aged rodent liver

Steven A Bloomer, Kevin C Kregel and Kyle E Brown
Archives of gerontology and geriatrics, Vol.58(1), pp.145-152
01/2014
DOI: 10.1016/j.archger.2013.07.012
PMCID: PMC3808518
PMID: 23993269
url
http://doi.org/10.1016/j.archger.2013.07.012View
Open Access

Abstract

Elevations in hepatic iron content occur with aging and physiological stressors, which may promote oxidative injury to the liver. Since dysregulation of the iron regulatory hormone, hepcidin, can cause iron accumulation, our goal was to characterize the regulation of hepcidin in young (6 mo) and old (24 mo) Fischer 344 rats exposed to environmental heat stress. Liver and blood samples were taken in the control condition and after heating. Hepcidin expression did not differ between young and old rats in the control condition, despite higher levels of hepatic iron and IL-6 mRNA in the latter. Following heat stress, pSTAT3 increased in both groups, but C/EBPα and hepcidin mRNA increased only in old rats. Despite this, serum iron decreased in both age groups 2h after heat stress, suggesting hepcidin-independent hypoferremia in the young rats. The differential regulation of hepcidin between young and old rats after hyperthermia may be due to the enhanced expression of C/EBPα protein in old rats. These data support the concept of “inflammaging” and suggest that repeated exposures to stressors may contribute to the development of anemia in older individuals.
Iron Inflammation IL-6 Hypoferremia STAT3

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