Regional distribution of metallothionein and zinc in the mouse gut - Comparison with metallothionien-null mice

被引:30
|
作者
Tran, CD
Butler, RN
Philcox, JC
Rofe, AM
Howarth, GS
Coyle, P [1 ]
机构
[1] Inst Med & Vet Sci, Div Clin Biochem, Adelaide, SA 5000, Australia
[2] Womens & Childrens Hosp, Gastroenterol Unit, N Adelaide, SA 5006, Australia
[3] Univ Adelaide, Dept Physiol, Adelaide, SA 5005, Australia
[4] Child Hlth Res Inst, N Adelaide, SA 5006, Australia
[5] Cooperat Res Ctr Tissue Growth & Repair, Adelaide, SA 5000, Australia
关键词
metallothionein; zinc; gut; liver; diet; metallothionein-null mouse; glucagon;
D O I
10.1007/BF02778942
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
Gut Zn homeostatic responses to low, replete, and excess dietary Zn (10, 150, and 400 mg Zn/kg, respectively) were compared in mice with (MT+/+) and without (MT-/-) metallothionein (MT) expression. MT concentrations decreased progressively from stomach (12.9 nmol Cd bound/g) to colon (4.6 nmol Cd bound/g). Small intestinal MT was increased in mice fed the 400-mg Zn/kg diet (+130%, duodenum; +56%, jejunum; +29%, terminal ileum), but not in the stomach, cecum and colon. Zn concentrations were much higher in the distal gut at increasing Zn intakes in MT+/+ mice but to a lesser extent in MT-/- mice. On the 10-mg Zn/kg diet, MT-/- mice had 45% more Zn in the jejunum/ileum than MT+/+ mice. In fasted (20 h) mice, Zn concentrations in all gut regions were similar to those of MT+/+ mice fed the 10-mg Zn/kg diet, irrespective of prior Zn intake or genotype. Liver MT quadrupled in mice fasted after the 10-mg Zn/kg diet but only doubled after the 400-mg Zn/kg diet, a trend also present in gut MT. Glucagon administration stimulated gut as well as liver MT, implicating it as a major component of the MT response to fasting. MT-/- mice had five times more variation than MT+/+ mice in plasma Zn over all dietary groups. Together, these findings demonstrate that without MT, there is little modification of regional gut Zn concentrations in response to extremes of dietary Zn and poorer regulation of Zn homeostasis.
引用
收藏
页码:239 / 251
页数:13
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