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[铬作为一种必需元素]

[Chromium as an essential element].

作者信息

Racek J

机构信息

Ustav klinické biochemie a laboratorní diagnostiky LF UK a FN, Plzen.

出版信息

Cas Lek Cesk. 2003;142(6):335-9.

PMID:12924032
Abstract

Chromium was known for many years to be an element causing allergic reactions and having neurotoxic and carcinogenic effects. These effects can be observed especially in the case of hexavalent chromium. Only a little more than four decades ago trivalent chromium has been known as an essential element with relation to glycide and lipid metabolism. And only during several last years this chromium function has been revealed on a molecular level. After absorption in the gastrointestinal tract, chromium is most likely transported to cells bound to the plasma protein transferrin. Insulin initiates chromium transport into the cells where it is bound to the oligopeptide apochromodulin. This oligopeptide combined with four chromium(III) atoms forms chromodulin, which is important for amplifying the insulin signalling effect. After binding to insulin-activated receptor, chromodulin increases tyrosine kinase activity by one order. This enzyme forms a part of intracellular portion of insulin receptor. Chromium supplementation in people with chromium deficiency can improve glucose tolerance and some lipid metabolism parameters. The supplementation is indicated in persons with impaired glucose tolerance both in preclinical and manifested stadium of type 2 diabetes mellitus where increased lost of chromium in urine was documented. In these patients, chromium deficiency can participate in insulin resistance and hyperlipidaemia. Chromium is usually applied in the form of organic compounds: yeast extract or chromium(III) picolinate. Cr(III) picolinate can be reduced to compounds of Cr(II) in the cells which can then produce free hydroxyl radical in the so called Fenton reaction.

摘要

多年来,铬一直被认为是一种会引起过敏反应、具有神经毒性和致癌作用的元素。这些影响在六价铬的情况下尤其明显。仅仅在四十多年前,三价铬才被确认为与糖类和脂质代谢相关的必需元素。而且直到最近几年,这种铬的功能才在分子水平上被揭示出来。在胃肠道吸收后,铬很可能与血浆蛋白转铁蛋白结合运输到细胞中。胰岛素启动铬进入细胞的运输过程,在细胞内铬与寡肽脱辅基铬调节蛋白结合。这种寡肽与四个铬(III)原子结合形成铬调节蛋白,它对于放大胰岛素信号效应很重要。与胰岛素激活的受体结合后,铬调节蛋白使酪氨酸激酶活性提高一个数量级。这种酶是胰岛素受体细胞内部分的一部分。对铬缺乏的人补充铬可以改善葡萄糖耐量和一些脂质代谢参数。在2型糖尿病的临床前期和显性阶段,当尿中铬流失增加被记录时,葡萄糖耐量受损的人适合补充铬。在这些患者中,铬缺乏可能参与胰岛素抵抗和高脂血症。铬通常以有机化合物的形式应用:酵母提取物或吡啶甲酸铬(III)。吡啶甲酸铬(III)在细胞内可被还原为Cr(II)化合物,然后在所谓的芬顿反应中产生游离羟基自由基。

相似文献

1
[Chromium as an essential element].[铬作为一种必需元素]
Cas Lek Cesk. 2003;142(6):335-9.
2
Recent advances in the nutritional biochemistry of trivalent chromium.三价铬营养生物化学的最新进展。
Proc Nutr Soc. 2004 Feb;63(1):41-7. doi: 10.1079/PNS2003315.
3
Recent developments in the biochemistry of chromium(III).铬(III)生物化学的最新进展。
Biol Trace Elem Res. 2004 Summer;99(1-3):1-16. doi: 10.1385/BTER:99:1-3:001.
4
Comparing metabolic effects of six different commercial trivalent chromium compounds.比较六种不同商业三价铬化合物的代谢效应。
J Inorg Biochem. 2008 Nov;102(11):1986-90. doi: 10.1016/j.jinorgbio.2008.07.012. Epub 2008 Jul 31.
5
Chromium in metabolic and cardiovascular disease.铬与代谢和心血管疾病
Horm Metab Res. 2007 Oct;39(10):743-51. doi: 10.1055/s-2007-985847.
6
Chromium as an essential nutrient for humans.铬作为人类必需的营养素。
Regul Toxicol Pharmacol. 1997 Aug;26(1 Pt 2):S35-41. doi: 10.1006/rtph.1997.1136.
7
Chromium in the prevention and control of diabetes.铬在糖尿病防治中的作用
Diabetes Metab. 2000 Feb;26(1):22-7.
8
A comparison of the insulin-sensitive transport of chromium in healthy and model diabetic rats.健康大鼠与糖尿病模型大鼠中铬的胰岛素敏感性转运比较。
J Inorg Biochem. 2004 Mar;98(3):522-33. doi: 10.1016/j.jinorgbio.2004.01.003.
9
The trail of chromium(III) in vivo from the blood to the urine: the roles of transferrin and chromodulin.体内铬(III)从血液到尿液的踪迹:转铁蛋白和铬调节蛋白的作用。
J Biol Inorg Chem. 2001 Jun;6(5-6):608-17. doi: 10.1007/s007750100238.
10
The biochemistry of chromium.铬的生物化学
J Nutr. 2000 Apr;130(4):715-8. doi: 10.1093/jn/130.4.715.

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