Sequential changes in Fe, Cu, and Zn in target organs during early coxsackievirus B3 infection in mice

被引:30
|
作者
Ilbäck, NG
Benyamin, G
Lindh, U
Friman, G
机构
[1] Univ Uppsala Hosp, Dept Med Sci, Infect Dis Sect, Uppsala, Sweden
[2] Ctr Met Biol Uppsala, Rudbeck Lab, Uppsala, Sweden
[3] Uppsala Univ, Rudbeck Lab, Sect Biomed Radiat Sci, Uppsala, Sweden
[4] Natl Food Adm Toxicol Lab, Div Toxicol, Uppsala, Sweden
关键词
copper; infection; iron; organ; virus; zinc;
D O I
10.1385/BTER:91:2:111
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
In Coxsackievirus B3 (CB3) infection, the heart and pancreas are major target organs and, as a general host response, an associated immune activation and acute phase reaction develops. Although iron (Fe), copper (Cu), and zinc (Zn) are involved in these responses, sequential trace element changes in different target organs of infection have not been studied to date. In the present study, Fe, Cu, and Zn were measured through inductively coupled plasma mass spectrometry (ICP-MS) in the plasma, liver, spleen, heart, and pancreas during the early phase (d I and 3) of CB3 infection in female Balb/c mice. The severity of the infection was assessed through clinical signs of disease and histopathology of the heart and pancreas, including staining of CD4 and CD8 cells in the pancreas. During infection, the concentrations of Fe, Cu, and Zn changed in the plasma, liver, and pancreas, but not in the spleen and heart. The changes in plasma Cu, Zn, and Fe seemed to be biphasic with a decrease at d 1 that turned into increased levels by d 3. Cu showed similar biphasic changes in the liver, spleen, and pancreas, whereas, for Zn and Fe, this pattern was only evident in the liver. In the pancreas, the reverse response occurred with pronounced decreases in Fe (23%, p < 0.05) and Zn (64%, p < 0.01) at d 3. Although the pathophysiological interpretation of these findings requires further research, the sequential determination of these elements may be of clinical value in enterovirus infections in deciding the stage of disease development.
引用
收藏
页码:111 / 123
页数:13
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