Effects of endocrine disrupting chemicals on myelin development and diseases

被引:16
|
作者
Naffaa, Vanessa [1 ]
Laprevote, Olivier [1 ,2 ]
Schang, Anne-Laure [3 ]
机构
[1] Univ Paris, UMR 8038 CiTCoM, CNRS, Fac Pharm Paris, 4 Ave Observ, F-75006 Paris, France
[2] Hop Europeen Georges Pompidou, AP HP, Serv Biochim, 20 Rue Leblanc, F-75015 Paris, France
[3] Univ Paris, UMR 1153 CRESS, Fac Pharm Paris, 4 Ave Observ, F-75006 Paris, France
关键词
Myelin; Oligodendrocyte; Schwann cell; Endocrine disrupting chemical; Hypomyelination; Demyelination;
D O I
10.1016/j.neuro.2020.12.009
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
In the central and peripheral nervous systems, myelin is essential for efficient conduction of action potentials. During development, oligodendrocytes and Schwann cells differentiate and ensure axon myelination, and disruption of these processes can contribute to neurodevelopmental disorders. In adults, demyelination can lead to important disabilities, and recovery capacities by remyelination often decrease with disease progression. Among environmental chemical pollutants, endocrine disrupting chemicals (EDCs) are of major concern for human health and are notably suspected to participate in neurodevelopmental and neurodegenerative diseases. In this review, we have combined the current knowledge on EDCs impacts on myelin including several persistent organic pollutants, bisphenol A, triclosan, heavy metals, pesticides, and nicotine. Besides, we presented several other endocrine modulators, including pharmaceuticals and the phytoestrogen genistein, some of which are candidates for treating demyelinating conditions but could also be deleterious as contaminants. The direct impacts of EDCs on myelinating cells were considered as well as their indirect consequences on myelin, particularly on immune mechanisms associated with demyelinating conditions. More studies are needed to describe the effects of these compounds and to further understand the underlying mechanisms in relation to the potential for endocrine disruption.
引用
收藏
页码:51 / 68
页数:18
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