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非相干近红外辐射可保护正常人皮肤成纤维细胞免受太阳紫外线毒性的影响。

Non-coherent near infrared radiation protects normal human dermal fibroblasts from solar ultraviolet toxicity.

作者信息

Menezes S, Coulomb B, Lebreton C, Dubertret L

机构信息

Institut de Recherche sur la Peau, INSERM U312, Hôpital Saint Louis, Paris, France.

出版信息

J Invest Dermatol. 1998 Oct;111(4):629-33. doi: 10.1046/j.1523-1747.1998.00338.x.

Abstract

The sun is the most important and universal source of non-ionizing radiation shed on human populations. Life evolved on Earth bathed by this radiation. Solar UV damages cells, leading to deleterious conditions such as photoaging and carcinogenesis in human skin. During the process of evolution, the cells selected dark- and light-dependent repair mechanisms as a defence against these hazardous effects. This study describes the induction by non-coherent infrared radiation (700-2000 nm), in the absence of rising temperature, of a strong cellular defense against solar UV cytotoxicity as well as induction of cell mitosis. Blocking mitoses with arabinoside-cytosine or protein synthesis with cycloheximide did not abolish the protection, leading to the conclusion that this protection is independent of cell division and of protein neosynthesis. The protection provided by infrared radiation against solar UV radiation is shown to be a long-lasting (at least 24 h) and cumulatif phenomenon. Infrared radiation does not protect the lipids in cellular membranes against UVA induced peroxidation. The protection is not mediated by heat shock proteins. Living organisms on the Earth's surface are bathed by infrared radiation every day, before being submitted to solar UV. Thus, we propose that this as yet undescribed natural process of cell protection against solar UV, acquired and preserved through evolutional selection, plays an important role in life maintenance. Understanding and controlling this mechanism could provide important keys to the prevention of solar UV damage of human skin.

摘要

太阳是照射到人类群体的最重要且最普遍的非电离辐射源。地球上的生命在这种辐射的沐浴下进化。太阳紫外线会损伤细胞,导致诸如人类皮肤光老化和致癌等有害状况。在进化过程中,细胞选择了依赖黑暗和依赖光照的修复机制来抵御这些有害影响。本研究描述了在温度未升高的情况下,非相干红外辐射(700 - 2000纳米)可诱导细胞对太阳紫外线细胞毒性产生强大的防御作用以及诱导细胞有丝分裂。用阿糖胞苷阻断有丝分裂或用环己酰亚胺抑制蛋白质合成并不能消除这种保护作用,从而得出结论:这种保护作用与细胞分裂和蛋白质新合成无关。红外辐射对太阳紫外线辐射提供的保护作用被证明是一种持久的(至少24小时)累积现象。红外辐射不能保护细胞膜中的脂质免受紫外线A诱导的过氧化作用。这种保护作用不是由热休克蛋白介导的。地球表面的生物在受到太阳紫外线照射之前,每天都沐浴在红外辐射中。因此,我们提出这种尚未被描述的细胞对太阳紫外线的自然保护过程,是通过进化选择获得并保留下来的,在维持生命方面起着重要作用。理解和控制这一机制可能为预防人类皮肤的太阳紫外线损伤提供重要线索。

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