首页> 外文期刊>American Journal of Physiology >Hemochromatosis and pregnancy: iron stores in the Hfe-/- mouse are not reduced by multiple pregnancies.
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Hemochromatosis and pregnancy: iron stores in the Hfe-/- mouse are not reduced by multiple pregnancies.

机译:血色素沉着症和妊娠:多次怀孕不会减少Hfe-/-小鼠中的铁存储。

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摘要

Hereditary hemochromatosis (HH), a widespread hereditary iron metabolism disorder, is characterized by an excessive absorption of dietary iron, resulting in increased body iron stores. Some studies indicate a sex difference in disease expression, with women showing a slower disease progression and a less severe clinical profile. This is usually attributed to iron loss during menstruation and pregnancy. However, this link has not been clearly demonstrated. The Hfe-/- mouse model recapitulates key aspects of HH, including an iron overload phenotype similar to that observed in human patients. In this study, we use it to test the impact of multiple pregnancies in the iron stores. One-year-old nulliparous and pluriparous (averaging 29 weaned pups per female) C57BL/6 (B6) and Hfe-/- mice were euthanized, and blood and tissues were collected. Several serological and erythroid parameters were evaluated, as well as tissue nonheme iron content and serum ferritin. Hepcidin 1, hepcidin 2, and bone morphogenetic protein 6 (BMP6) expressions in the liver were determined by real-time PCR. No significant differences were observed for many serological and erythroid parameters although differences occurred in transferrin saturation and mean corpuscular volume in Hfe-/- mice and total iron-binding capacity in B6 mice. Hepatic iron concentration was similar for nulliparous and pluriparous mice of both genotypes, but total iron per organ (liver, spleen, heart, and pancreas) was higher overall in pluriparous females than nulliparous. Hepcidin 1 and 2 and BMP6 expressions were significantly decreased in pluriparous females, when compared with nulliparous, in both genotypes. In conclusion, multiple pregnancies do not reduce body iron stores in Hfe-/- mice.
机译:遗传性血色素沉着病(HH)是一种广泛的遗传性铁代谢紊乱,其特征是饮食中铁的过度吸收,导致体内铁储备增加。一些研究表明在疾病表达上存在性别差异,女性表现出较慢的疾病进展和较不严重的临床表现。这通常归因于月经和怀孕期间铁的流失。但是,此链接尚未明确说明。 Hfe //-小鼠模型概括了HH的关键方面,包括与人类患者相似的铁超负荷表型。在这项研究中,我们用它来测试多次怀孕对铁存储的影响。对一岁的未产卵和多胎(平均每只雌性29只断奶幼崽)的C57BL / 6(B6)和Hfe-/-小鼠实施安乐死,并收集血液和组织。评估了一些血清学和红系参数,以及组织中非血红素铁含量和血清铁蛋白。通过实时PCR检测肝中的铁调素1,铁调素2和骨形态发生蛋白6(BMP6)的表达。尽管在Hfe-/-小鼠的运铁蛋白饱和度和平均红细胞体积以及B6小鼠的总铁结合能力方面存在差异,但在许多血清学和红系参数上均未观察到显着差异。两种基因型的未出生和多胎小鼠的肝铁浓度均相似,但在多产雌性中,每个器官(肝脏,脾脏,心脏和胰腺)的总铁含量总体上高于未产肝。在两种基因型中,与不育相比,多产雌性中铁调素1和2以及BMP6的表达均显着降低。总之,多次怀孕不会减少Hfe-/-小鼠体内的铁储备。

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