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1,25-二羟基维生素D3对紫外线B诱导的角质形成细胞损伤的光保护作用及其作用机制。

The photoprotective effect of 1,25-dihydroxyvitamin D3 on ultraviolet light B-induced damage in keratinocyte and its mechanism of action.

作者信息

Lee J, Youn J I

机构信息

Department of Dermatology, Inha University Medical School/Hospital, Incheon, South Korea.

出版信息

J Dermatol Sci. 1998 Sep;18(1):11-8. doi: 10.1016/s0923-1811(98)00015-2.

DOI:10.1016/s0923-1811(98)00015-2
PMID:9747657
Abstract

We investigated the photoprotective effect of 1,25-dihydroxyvitamin D3 (1,25(OH)2D3) both in vivo and in vitro, revealing its relationship with glutathione, a well-known antioxidant. We also probed into the possible mechanism of photoprotection of 1,25(OH)2D3 through immunohistochemical study for metallothionein (MT). At the same time, endogenous antioxidant effect of 1,25(OH)2D3 was examined. Survival of cultured human keratinocytes was decreased when the cells were irradiated with ultraviolet light-B (UVB) at doses above 30 mJ/cm2. But in the presence of 1,25(OH)2D3 (12 nM), the decrease of survival of keratinocytes by UVB was diminished. The formation of sunburn cells by UVB irradiation in the skin of ICR mice was inhibited by topical application of 1,25(OH)2D3, regardless of prior glutathione depletion. Immunohistochemical staining revealed that 1,25(OH)2D3 induced the expression of MT, a potent radical scavenger, mainly in the basal layer of ICR mice skin. 1,25(OH)2D3 neither inhibited peroxidation of plasma lipids nor interacted with superoxide, nor removed hydrogen peroxide as an antioxidant. These findings suggest that 1,25(OH)2D3 has photoprotective effect not related with glutathione or its endogenous antioxidant property. Rather, it could be attributed to 1,25(OH)2D3-induced MT and its capacity to prevent radical-related damage in UVB irradiation.

摘要

我们在体内和体外研究了1,25 - 二羟基维生素D3(1,25(OH)2D3)的光保护作用,揭示了其与谷胱甘肽(一种著名的抗氧化剂)的关系。我们还通过对金属硫蛋白(MT)的免疫组织化学研究,探究了1,25(OH)2D3光保护的可能机制。同时,检测了1,25(OH)2D3的内源性抗氧化作用。当培养的人角质形成细胞受到剂量高于30 mJ/cm2的紫外线B(UVB)照射时,细胞存活率降低。但在存在1,25(OH)2D3(12 nM)的情况下,UVB导致的角质形成细胞存活率下降有所减轻。无论先前谷胱甘肽是否耗竭,通过局部应用1,25(OH)2D3均可抑制ICR小鼠皮肤中UVB照射引起的晒伤细胞形成。免疫组织化学染色显示,1,25(OH)2D3诱导主要在ICR小鼠皮肤基底层表达MT(一种有效的自由基清除剂)。1,25(OH)2D3既不抑制血浆脂质的过氧化,也不与超氧化物相互作用,也不作为抗氧化剂去除过氧化氢。这些发现表明,1,25(OH)2D3具有与谷胱甘肽或其内源抗氧化特性无关的光保护作用。相反,这可能归因于1,25(OH)2D3诱导的MT及其预防UVB照射中自由基相关损伤的能力。

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