Institute of Human Nutrition and Dietetics, Department of Bromatology and Food Toxicology, Poznań University of Life Sciences, ul. Wojska Polskiego 31, 60-624, Poznań, Poland.
Department of Clinical Psychology, Poznań University of Medical Sciences, ul. Bukowska 70, 60-812, Poznań, Poland.
Biol Trace Elem Res. 2018 Aug;184(2):398-408. doi: 10.1007/s12011-017-1203-z. Epub 2017 Nov 21.
Inadequate iron supply has significant consequences to health. There are some relations between the metabolism of different trace elements, such as iron, zinc, copper and chromium. However, the direction of these interactions can be antagonistic or synergistic, and it depends on many factors. The aim of the study was to evaluate the combined effects of supplementary of chromium(III) propionate complex (Cr3) with iron excess on the Cr and Fe status in healthy female rats. The 36 healthy female Wistar rats were divided into six experimental groups (six animals in each) with different Fe levels-adequate (45 mg kg-100% RDA) and high (excessive-180 mg kg-400% RDA). At the same time, they were supplemented with Cr(III) at doses of 1, 50 and 500 mg kg of diet: C1-control (Fe 45 mg kg, Cr 1 mg kg); C50 (Fe 45 mg kg, Cr 50 mg kg); C500 (Fe 45 mg kg, Cr 500 mg kg); H1 (Fe 180 mg kg, Cr 1 mg kg); H50 (Fe 180 mg kg, Cr 50 mg kg); H500 (Fe 180 mg kg, Cr 500 mg kg). The serum iron level and total iron binding capacity (TIBC) were measured with colorimetric methods. The serum ferritin level was measured by means of electrochemiluminescence immunoassay. The serum transferrin level was measured with the ELISA method. Haematological measurements were made with an automated blood analyser. The Cr and Fe tissular levels were measured with the AAS method. The exposure to a high level of Fe(III) alone or in combination with Cr caused Fe accumulation in tissues, especially in the liver and kidneys, but there were no significant changes in the TIBC, transferrin, ferritin concentration in the serum and most haematological parameters. Moreover, the serum, hepatic and renal Cr concentrations decreased. The doses of supplementary Cr(III) given separately or in combination with high level of Fe(III) disturbed the Cr content in the liver and kidneys of healthy female rats. However, they did not change most of the parameters of Fe metabolism, except the Fe kidney concentration. Supplementary Cr3 decreased the renal Fe level in groups with adequate Fe content in the diet. However, the renal Fe levels increased along with a higher Cr level in the diet in groups with high Fe content. The findings proved a relationship between Fe(III) and Cr(III) metabolism in healthy female rats. However, the direction of change varied and depended on relative amounts of these elements in the diet.
铁元素供给不足对健康有重大影响。不同微量元素(如铁、锌、铜和铬)的代谢之间存在一定联系。然而,这些相互作用的方向可能是拮抗的或协同的,这取决于许多因素。本研究的目的是评估补充三价铬丙酸复合物(Cr3)与铁过量对健康雌性大鼠体内铬和铁状况的联合影响。36 只健康雌性 Wistar 大鼠被分为六组实验(每组 6 只),具有不同的铁水平——适量(45mg/kg-100%RDA)和过量(180mg/kg-400%RDA)。同时,它们被补充不同剂量的 Cr(III):1、50 和 500mg/kg 饮食:C1-对照(铁 45mg/kg,Cr 1mg/kg);C50(铁 45mg/kg,Cr 50mg/kg);C500(铁 45mg/kg,Cr 500mg/kg);H1(铁 180mg/kg,Cr 1mg/kg);H50(铁 180mg/kg,Cr 50mg/kg);H500(铁 180mg/kg,Cr 500mg/kg)。用比色法测量血清铁水平和总铁结合能力(TIBC)。用电化学发光免疫分析法测量血清铁蛋白水平。用 ELISA 法测量血清转铁蛋白水平。用自动血液分析仪进行血液学测量。用原子吸收光谱法(AAS)测量 Cr 和 Fe 组织水平。单独或联合暴露于高浓度 Fe(III)会导致组织中铁的积累,特别是在肝脏和肾脏中,但 TIBC、转铁蛋白、血清铁蛋白浓度以及大多数血液学参数均无显著变化。此外,血清、肝脏和肾脏中的 Cr 浓度降低。单独或联合高浓度 Fe(III)给予补充 Cr(III)会干扰健康雌性大鼠肝脏和肾脏中的 Cr 含量。然而,除了肾脏铁浓度外,它们并没有改变铁代谢的大多数参数。补充 Cr3 降低了饮食中铁含量适中组的肾脏铁水平。然而,在饮食中 Cr 水平较高的情况下,肾脏铁水平会增加。研究结果证明了健康雌性大鼠 Fe(III)和 Cr(III)代谢之间存在关系。然而,变化的方向有所不同,取决于饮食中这些元素的相对含量。