Unger Erica L, Beard John L, Jones Byron C
Department of Nutritional Sciences, The Pennsylvania State University, University Park, PA 16802, USA.
Nutr Neurosci. 2007 Feb-Apr;10(1-2):89-95. doi: 10.1080/10284150701350653.
Many genes are likely involved in the control of iron metabolism in brain and in peripheral tissues, and genetically-defined murine strains present the opportunity to investigate genetic variations in iron metabolism. Weanling C57BL/6 (B6) and DBA/2 (D2) mice were divided into two treatment groups receiving distilled water with or without 5000 ppm ferric chloride ad libitum as their sole fluid source for 100 days. Iron overload increased liver, spleen and plasma iron levels in male and female B6 and female D2 mice. In D2 males, liver iron was increased relative to control, but spleen and plasma iron remained unaffected. Brain iron content was not different between control and iron-treated mice in ventral midbrain, caudate, pons or hippocampus, but D2 iron overloaded mice displayed lower iron levels in nucleus accumbens and prefrontal cortex. We conclude that genetic background influences the accumulation of excess iron in the periphery and iron regulation in the central nervous system.
许多基因可能参与大脑和外周组织中铁代谢的调控,而基因定义的小鼠品系为研究铁代谢的遗传变异提供了契机。将断乳的C57BL/6(B6)和DBA/2(D2)小鼠分为两个治疗组,分别给予含或不含5000 ppm氯化铁的蒸馏水作为唯一液体来源,持续100天。铁过载使雄性和雌性B6小鼠以及雌性D2小鼠的肝脏、脾脏和血浆铁水平升高。在D2雄性小鼠中,肝脏铁含量相对于对照组增加,但脾脏和血浆铁含量未受影响。在腹侧中脑、尾状核、脑桥或海马体中,对照小鼠和铁处理小鼠的脑铁含量没有差异,但D2铁过载小鼠伏隔核和前额叶皮质中的铁水平较低。我们得出结论,遗传背景会影响外周过量铁的积累以及中枢神经系统中的铁调节。