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膳食脂肪水平影响组织铁水平,但不影响大鼠的铁调节基因 HAMP。

Dietary fat level affects tissue iron levels but not the iron regulatory gene HAMP in rats.

机构信息

Department of Physiology, National University of Sciences and Technology, Rawalpindi, Pakistan.

出版信息

Nutr Res. 2013 Feb;33(2):126-35. doi: 10.1016/j.nutres.2012.11.012. Epub 2012 Dec 20.

Abstract

Because dietary fats affect the regulation and use of body iron, we hypothesized that iron regulatory and transport genes may be affected by dietary fat. A model of early-stage I to II, nonalcoholic fatty liver was used in which rats were fed standard (35% energy from fat) or high-fat (71% energy from fat) liquid diets with normal iron content (STD/HF groups). In addition, intraperitoneal injections of iron dextran were given to iron-loaded (STD+/HF+ groups) and iron-deficient diets to STD-/HF- groups. Plasma osmolality, hemoglobin level, and mean corpuscular hemoglobin concentration were increased in all STD diet groups compared with all HF diet groups. Plasma iron and transferrin saturation were affected by an interaction between dietary fat and iron. They were high in the STD group (normal iron) compared with their respective HF group. Similarly, this group also showed a 4-fold increase in the messenger RNA expression of the hepatic hemochromatosis gene. Spleen iron was high in the iron-loaded STD+ group compared with all other groups. Hepatic iron and messenger RNA expression of peroxisome proliferator-activated receptor-γ, CCAAT/enhancer binding protein α, interleukin-6, and iron transport genes (transferrin receptor 2, divalent metal transporter 1 iron-responsive element, and divalent metal transporter 1 non-iron-responsive element) were increased, whereas tumor necrosis factor α was decreased in the HF diet groups. The expression of iron regulatory gene HAMP was not increased in the HF diet groups. Iron regulatory and transport genes involved in cellular and systemic iron homeostasis may be affected by the macronutrient composition of the diet.

摘要

由于膳食脂肪会影响机体铁的调节和利用,我们假设铁的调节和转运基因可能会受到膳食脂肪的影响。我们采用了一种早期 I 期至 II 期、非酒精性脂肪肝的模型,在该模型中,大鼠喂食标准(35%能量来自脂肪)或高脂肪(71%能量来自脂肪)液体饮食,铁含量正常(STD/HF 组)。此外,还对铁超载(STD+/HF+组)和缺铁饮食的 STD-/HF-组进行了铁右旋糖苷的腹腔注射。与所有 HF 饮食组相比,所有 STD 饮食组的血浆渗透压、血红蛋白水平和平均红细胞血红蛋白浓度均升高。血浆铁和转铁蛋白饱和度受到膳食脂肪和铁之间相互作用的影响。与各自的 HF 组相比,在 STD 组(正常铁)中,它们的值较高。同样,该组的肝脏血色病基因的信使 RNA 表达也增加了 4 倍。与所有其他组相比,铁超载的 STD+组的脾脏铁含量较高。与 HF 饮食组相比,肝铁和过氧化物酶体增殖物激活受体-γ、CCAAT/增强子结合蛋白-α、白细胞介素-6 和铁转运基因(转铁蛋白受体 2、二价金属转运蛋白 1 铁反应元件和二价金属转运蛋白 1 非铁反应元件)的信使 RNA 表达增加,而肿瘤坏死因子-α减少。HF 饮食组的铁调节基因 HAMP 的表达没有增加。涉及细胞和全身铁稳态的铁调节和转运基因可能会受到饮食宏量营养素组成的影响。

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