[Cell kinetic effects of crude coal tar application plus long wave ultraviolet radiation on normal and hyperproliferative epidermis of guinea pig skin].

A Taniguchi
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Abstract

This study investigated the cell kinetic effects of combined treatment with crude coal tar and long wave ultraviolet (UVA) radiation on the normal and n-hexadecane-induced hyperproliferative epidermis of guinea pig skin. Flow cytometry was used to determine the proportion of cells in S phase (S fraction) and G2 + M phase (G2 + M fraction). Bromodeoxyuridine incorporation was used to determine the labeling index. Conventional histologic techniques were used to observe the mitotic index. In the normal epidermis after a single treatment with tar and UVA (1 J/cm2) or tar alone, the labeling index showed an initial decrease of 4 hr duration followed by moderate increase. The initial decrease was more pronounced in the tar-UVA-treated epidermis than in the tar-treated epidermis. The mitotic index was depressed during the first 12 hr. S- and G2 + M fraction showed no changes during the first 12 to 18 hour, and then increased in varying degrees. In the hyperproliferative epidermis after two applications of tar and UVA (1 and 4J/cm2) or tar alone, the labeling index was depressed during the first 12 hr, and mitotic index was below the control level until the 36 hr. The inhibitory effects on DNA synthesis and mitosis were more pronounced in the tar-UVA-treated epidermis than in the tar-treated epidermis. The S- and G2 + M fraction exceeded the control level in varying degrees during the whole experimental period. The results indicate that tar inhibits the epidermal DNA synthesis and mitosis by itself, and that the inhibitory effects of tar are intensified by the radiation of UVA.

[粗煤焦油加长波紫外线辐射对豚鼠正常表皮和增生性表皮细胞动力学的影响]。
本文研究了粗煤焦油和长波紫外线(UVA)辐射联合处理对豚鼠正常皮肤和正十六烷诱导的增生性表皮细胞动力学的影响。流式细胞术测定S期(S部分)和G2 + M期(G2 + M部分)细胞比例。采用溴脱氧尿苷掺入法测定标记指数。采用常规组织学技术观察有丝分裂指数。在正常表皮中,分别用焦油和UVA (1 J/cm2)或单独用焦油处理后,标记指数在4小时内开始下降,然后适度上升。与焦油处理的表皮相比,焦油- uva处理的表皮最初的减少更为明显。前12小时有丝分裂指数下降。S-和G2 + M组分在前12 ~ 18 h内没有变化,随后有不同程度的增加。在高增殖表皮中,分别施用焦油和UVA(1和4J/cm2)或单独施用焦油后,标记指数在前12小时下降,有丝分裂指数在36小时前低于对照水平。对DNA合成和有丝分裂的抑制作用在焦油- uva处理的表皮中比在焦油处理的表皮中更为明显。整个试验期间,S-和G2 + M组分均不同程度地超过对照水平。结果表明,焦油本身具有抑制表皮DNA合成和有丝分裂的作用,并在UVA照射下增强其抑制作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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