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光鸡蛋试验中外源性原卟啉IX和δ-氨基乙酰丙酸的光毒性

Phototoxicity of exogenous protoporphyrin IX and delta-aminolevulinic acid in the photo hen's egg test.

作者信息

Neumann Norbert J, Hanneken Sandra, Ruzicka Thomas, Lehmann Percy

机构信息

Department of Dermatology, Heinrich-Heine-University Duesseldorf, Moorenstrasse 5, D-40225 Duesseldorf, Germany.

出版信息

Photodermatol Photoimmunol Photomed. 2004 Oct;20(5):224-9. doi: 10.1111/j.1600-0781.2004.00112.x.

Abstract

BACKGROUND

Oxygen, appropriate light sources, and special photosensitizers are necessary to induce photochemical damage in tumor cells via photodynamic therapy (PDT) delta-aminolevulinic acid (ALA) is increasingly used in PDT, because topical or systemic administration of ALA induces accumulation of endogenous porphyrins preferentially in neoplastic tissues. Subsequent radiation with light of approximately 630 nm leads to selective damage of tumor cells. PDT should optimally leave peritumoral tissues unaffected, but only few data are reported on the effects and the time course of ALA-induced porphyrins in tumor-free tissues.

METHODS

Therefore, we studied the phototoxic effects of protoporphyrin IX (PP) and ALA-induced porphyrins in a recently established phototoxic model based on tumor-free tissue, the photo hen's egg test (PHET).

RESULTS

Employing this test procedure, PP provoked strong phototoxic reactions when irradiated with Ultraviolet A immediately and up to 30 h after substance application. In contrast, ALA induced a significant phototoxic effect only if irradiated 24 h after application.

CONCLUSION

Thus, we observed a delayed phototoxic effect of ALA in tumor-free tissue of the yolk sac (YS) blood vessel system. This delayed phototoxic response 24 h after ALA application is probably caused by endogenously synthesized porphyrins. In contrast, epithelial tumors show a maximum porphyrin accumulation 4-8 h after ALA application whereas in healthy human skin porphyrin synthesis is less intensive but prolonged with maximum levels 24-48 h after ALA application. Thus, ALA induced virtually the same delayed phototoxic effect in the tumor-free YS blood vessel tissue as in healthy human skin. These results show that the PHET is a useful model for the predictive preclinical risk assessment of exogenous or endogenous photosensitizers.

摘要

背景

通过光动力疗法(PDT)诱导肿瘤细胞发生光化学损伤需要氧气、合适的光源和特殊的光敏剂。δ-氨基乙酰丙酸(ALA)在PDT中应用越来越广泛,因为局部或全身给予ALA可使内源性卟啉优先在肿瘤组织中蓄积。随后用约630nm的光照射可导致肿瘤细胞的选择性损伤。PDT应尽量不影响瘤周组织,但关于ALA诱导的卟啉在无瘤组织中的作用及时间进程的报道较少。

方法

因此,我们在一个基于无瘤组织建立的光毒性模型——光鸡蛋试验(PHET)中研究了原卟啉IX(PP)和ALA诱导的卟啉的光毒性作用。

结果

采用该试验程序,在应用物质后立即及30小时内用紫外线A照射时,PP引发强烈的光毒性反应。相比之下,ALA仅在应用后24小时照射时才诱导出显著的光毒性作用。

结论

因此,我们观察到ALA在卵黄囊(YS)血管系统的无瘤组织中具有延迟的光毒性作用。ALA应用后24小时出现的这种延迟光毒性反应可能是由内源性合成的卟啉引起的。相比之下,上皮性肿瘤在ALA应用后4 - 8小时卟啉蓄积达到最大值,而在健康人皮肤中,卟啉合成强度较低但持续时间较长,在ALA应用后24 - 48小时达到最高水平。因此,ALA在无瘤的YS血管组织中诱导的延迟光毒性作用与在健康人皮肤中几乎相同。这些结果表明,PHET是用于预测外源性或内源性光敏剂临床前风险评估的有用模型。

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