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膳食葡萄籽原花青素抑制 UVB 暴露皮肤和 SKH-1 无毛小鼠皮肤肿瘤中 COX-2 的表达和其他炎症介质。

Dietary grape seed proanthocyanidins inhibit UVB-induced cyclooxygenase-2 expression and other inflammatory mediators in UVB-exposed skin and skin tumors of SKH-1 hairless mice.

机构信息

Department of Dermatology, University of Alabama, 1670 University Boulevard, Volker Hall 557, Birmingham, Alabama 35294, USA.

出版信息

Pharm Res. 2010 Jun;27(6):1092-102. doi: 10.1007/s11095-010-0050-9. Epub 2010 Feb 9.

Abstract

PURPOSE

The purpose of this study was to determine the chemopreventive mechanism of dietary grape seed proanthocyanidins (GSPs) against ultraviolet (UV) radiation-induced skin tumor development in mice.

METHODS

Six-to-seven-week-old SKH-1 hairless mice were subjected to photocarcinogenesis protocol, and exposed to UVB radiation (180 mJ/cm(2)) three times/week for 24 weeks. Mice were fed a standard AIN76A control diet with or without supplementation with grape seed proanthocyanidins (GSPs; 0.2% or 0.5%, w/w). At the termination of the experiment, mice were sacrificed, and skin and skin tumor samples were harvested and subjected to the analysis of biomarkers related to inflammation using immunostaining, western blot analysis, ELISA and real-time PCR.

RESULTS

Dietary GSPs inhibited UVB-induced infiltration of proinflammatory leukocytes and the levels of myeloperoxidase, cyclooxygenase-2 (COX-2), prostaglandin (PG) E(2), cyclin D1 and proliferating cell nuclear antigen (PCNA) in the skin and skin tumors compared to non-GSPs-treated UVB irradiated mouse skin and skin tumors. GSPs also significantly inhibited the levels of proinflammatory cytokines, tumor necrosis factor-alpha (P < 0.01), IL-1beta (P < 0.001) and IL-6 (P < 0.001), in UVB-exposed skin and skin tumors.

CONCLUSION

The results from this study clearly suggest that dietary GSPs inhibit photocarcinogenesis in mice through the inhibition of UVB-induced inflammation and mediators of inflammation in mouse skin.

摘要

目的

本研究旨在确定膳食葡萄籽原花青素(GSP)对紫外线(UV)辐射诱导的小鼠皮肤肿瘤发生的化学预防机制。

方法

6-7 周龄 SKH-1 无毛小鼠接受光致癌发生方案,并接受 UVB 辐射(180mJ/cm²),每周 3 次,共 24 周。小鼠喂食标准 AIN76A 对照饮食,或添加 0.2%或 0.5%(w/w)的葡萄籽原花青素(GSP)。实验结束时,处死小鼠,采集皮肤和皮肤肿瘤样本,并使用免疫染色、Western blot 分析、ELISA 和实时 PCR 分析与炎症相关的生物标志物。

结果

与未用 GSP 处理的 UVB 照射小鼠皮肤和皮肤肿瘤相比,膳食 GSP 抑制了 UVB 诱导的促炎白细胞浸润以及皮肤和皮肤肿瘤中髓过氧化物酶、环氧化酶-2(COX-2)、前列腺素(PG)E2、细胞周期蛋白 D1 和增殖细胞核抗原(PCNA)的水平。GSP 还显著抑制了促炎细胞因子肿瘤坏死因子-α(P<0.01)、IL-1β(P<0.001)和 IL-6(P<0.001)在 UVB 暴露皮肤和皮肤肿瘤中的水平。

结论

本研究结果清楚地表明,膳食 GSP 通过抑制 UVB 诱导的炎症和小鼠皮肤中的炎症介质,抑制了小鼠的光致癌作用。

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