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缺铁性认知障碍的分子机制:脑源性神经营养因子和胰岛素样生长因子在中枢神经系统中的表达及功能改变

Molecular mechanisms of cognitive impairment in iron deficiency: alterations in brain-derived neurotrophic factor and insulin-like growth factor expression and function in the central nervous system.

作者信息

Estrada José A, Contreras Irazú, Pliego-Rivero F Bernardo, Otero Gloria A

出版信息

Nutr Neurosci. 2014 Sep;17(5):193-206. doi: 10.1179/1476830513Y.0000000084. Epub 2013 Nov 26.

DOI:10.1179/1476830513Y.0000000084
PMID:24074845
Abstract

OBJECTIVE

The present review examines the relationship between iron deficiency and central nervous system (CNS) development and cognitive impairment, focusing on the cellular and molecular mechanisms related to the expression and function of growth factors, particularly the insulin-like growth factors I and II (IGF-I/II) and brain-derived neurotrophic factor (BDNF), in the CNS.

METHODS

Nutritional deficiencies are important determinants in human cognitive impairment. Among these, iron deficiency has the highest prevalence worldwide. Although this ailment is known to induce psychomotor deficits during development, the precise molecular and cellular mechanisms underlying these alterations have not been properly elucidated. This review summarizes the available information on the effect of iron deficiency on the expression and function of growth factors in the CNS, with an emphasis on IGF-I/II and BDNF.

RESULTS AND DISCUSSION

Recent studies have shown that specific growth factors, such as IGF-I/II and BDNF, have an essential role in cognition, particularly in processes involving learning and memory, by the activation of intracellular-signaling pathways involved in cell proliferation, differentiation, and survival. It is known that nutritional deficiencies promote reductions in systemic and CNS concentrations of growth factors, and that altered expression of these molecules and their receptors in the CNS leads to psychomotor and developmental deficits. Iron deficiency may induce these deficits by decreasing the expression and function of IGF-I/II and BDNF in specific areas of the brain.

摘要

目的

本综述探讨缺铁与中枢神经系统(CNS)发育及认知障碍之间的关系,重点关注与生长因子表达和功能相关的细胞和分子机制,特别是中枢神经系统中的胰岛素样生长因子I和II(IGF-I/II)以及脑源性神经营养因子(BDNF)。

方法

营养缺乏是人类认知障碍的重要决定因素。其中,缺铁在全球范围内的患病率最高。尽管已知这种疾病在发育过程中会诱发精神运动缺陷,但这些改变背后的确切分子和细胞机制尚未得到充分阐明。本综述总结了关于缺铁对中枢神经系统中生长因子表达和功能影响的现有信息,重点是IGF-I/II和BDNF。

结果与讨论

最近的研究表明,特定的生长因子,如IGF-I/II和BDNF,通过激活参与细胞增殖、分化和存活的细胞内信号通路,在认知中发挥重要作用,特别是在涉及学习和记忆的过程中。已知营养缺乏会导致全身和中枢神经系统中生长因子浓度降低,并且这些分子及其受体在中枢神经系统中的表达改变会导致精神运动和发育缺陷。缺铁可能通过降低大脑特定区域中IGF-I/II和BDNF的表达和功能来诱发这些缺陷。

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