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过敏性接触性皮炎引起的差异性色素沉着过度

Differential hypermelanosis induced by allergic contact dermatitis.

作者信息

Imokawa G, Kawai M

机构信息

Tochigi Research Laboratories, Kao Corporation, Japan.

出版信息

J Invest Dermatol. 1987 Dec;89(6):540-6. doi: 10.1111/1523-1747.ep12461181.

Abstract

In moderately colored guinea-pig skin, UVB, PUVA (psoralen plus UVA), and allergic contact dermatitis were shown to induce visibly well-defined hyperpigmentation that resembled the pigmentary changes observed in Mongoloid human skin. To clarify mechanisms of allergen-induced hyperpigmentation, we compared the effects of allergic contact dermatitis on pigmentation by using 6 different allergens: dinitrochlorobenzene (DNCB), 1-phenylazo-2-naphthol (PAN), benzyl salicylate (BS), jasmine oil (JO), hydroxycitronella (HC), and ylang ylang oil (YYO). The PAN-, JO-, HC-, and YYO-induced allergic reactions caused a definite visible hyperpigmentation that began to appear within 14 days, reaching maximum intensity about 40 days after the induction of the allergic reaction. These hyperpigmentations were accompanied by a significant increase in the population of dopa-positive melanocytes on day 24 following allergic reactions. In contrast, BS- and DNCB-induced allergic reactions did not give rise to visibly distinct hyperpigmentation in spite of the intensive allergic reactions following their challenge application. In a nonsensitized group, primary irritant reactions were induced by the application of 100% JO, but no distinctive hyperpigmentation was found 40 days after the last application. Quantitative analysis of the number of melanophages in the dermis showed that there was a marked increase in the number of melanophages in PAN, YYO, and HC allergy-induced hyperpigmented areas, with PAN showing a significant increase compared with those in non-treated areas of the same animals, whereas JO was associated with no such increase in hyperpigmented area, despite the stimulated pigmentation. In the case of the lack of induced hyperpigmentation, as seen in BS and DNCB allergy and JO irritation, there was also no substantial increase in the number of melanophages. Our findings indicate that allergic contact dermatitis is a unique melanogenic stimulant different from UV irradiation.

摘要

在中等肤色的豚鼠皮肤中,紫外线B(UVB)、补骨脂素加紫外线A(PUVA)以及过敏性接触性皮炎被证明可诱导出明显界限清晰的色素沉着过度,这类似于在蒙古人种人类皮肤中观察到的色素变化。为了阐明变应原诱导色素沉着过度的机制,我们使用6种不同的变应原比较了过敏性接触性皮炎对色素沉着的影响:二硝基氯苯(DNCB)、1-苯基偶氮-2-萘酚(PAN)、水杨酸苄酯(BS)、茉莉油(JO)、羟基香茅醛(HC)以及依兰油(YYO)。PAN、JO、HC和YYO诱导的过敏反应引起了明确可见的色素沉着过度,在14天内开始出现,在过敏反应诱导后约40天达到最大强度。这些色素沉着过度伴随着过敏反应后第24天多巴阳性黑素细胞数量的显著增加。相比之下,尽管BS和DNCB诱导的过敏反应在激发应用后会引发强烈的过敏反应,但并未引起明显不同的色素沉着过度。在未致敏组中,应用100%JO可诱导原发性刺激反应,但在最后一次应用后40天未发现明显的色素沉着过度。对真皮中噬黑素细胞数量的定量分析表明,PAN、YYO和HC过敏诱导的色素沉着过度区域中噬黑素细胞数量显著增加,与同一动物的未处理区域相比,PAN显示出显著增加,而JO尽管有色素沉着刺激,但色素沉着过度区域中未出现这种增加。在缺乏诱导性色素沉着过度的情况下,如在BS和DNCB过敏以及JO刺激中所见,噬黑素细胞数量也没有实质性增加。我们的研究结果表明,过敏性接触性皮炎是一种不同于紫外线照射的独特黑素生成刺激物。

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