Trikha P, Sharma N, Athar M
Department of Medical Elementology and Toxicology, Hamdard University, Hamdard Nagar, New Delhi 110 062, India.
Carcinogenesis. 2001 Aug;22(8):1207-11. doi: 10.1093/carcin/22.8.1207.
Nitroglycerin (GTN), a nitric oxide (NO) generating vasodilator has been used in the present study to assess the role of NO during tumor promotion in murine skin. Administration of GTN to 12-O tetradecanoyl phorbol 13-acetate (TPA)-treated mice resulted in a dose-dependent inhibition in the level of glutathione and the activity of antioxidant enzymes by approximately 16-40% of acetone-treated control. We also observed that GTN application led to a significant reduction in the ornithine decarboxylase (ODC) activity and decreased the rate of [3H]thymidine incorporation into epidermal DNA when compared with the acetone-treated control (P < 0.001). Treatment of DMBA-initiated TPA-promoted mice with GTN increased the latency period, decreased the tumor incidence by 32% and there was a 2-fold decrease in tumor yield (tumor/mouse) as compared with the TPA (alone)-treated group by 20 weeks. From these data, it can be concluded that NO can abrogate the toxic and tumor promoting effects of TPA and GTN can be used as a chemopreventive agent to inhibit tumorigenesis in murine skin.
硝酸甘油(GTN)是一种可产生一氧化氮(NO)的血管舒张剂,在本研究中用于评估NO在小鼠皮肤肿瘤促进过程中的作用。给经12-O-十四烷酰佛波醇-13-乙酸酯(TPA)处理的小鼠施用GTN,导致谷胱甘肽水平和抗氧化酶活性呈剂量依赖性抑制,与丙酮处理的对照组相比,抑制率约为16%-40%。我们还观察到,与丙酮处理的对照组相比,施用GTN导致鸟氨酸脱羧酶(ODC)活性显著降低,且[3H]胸腺嘧啶核苷掺入表皮DNA的速率下降(P < 0.001)。用GTN处理经二甲基苯并蒽(DMBA)启动、TPA促进的小鼠,延长了潜伏期,肿瘤发生率降低了32%,与单独用TPA处理20周的组相比,肿瘤产量(每只小鼠的肿瘤数)降低了2倍。从这些数据可以得出结论,NO可以消除TPA的毒性和肿瘤促进作用,并且GTN可以用作化学预防剂来抑制小鼠皮肤肿瘤发生。