| First Author | Wu K | Year | 2001 |
| Journal | World J Gastroenterol | Volume | 7 |
| Issue | 1 | Pages | 60-5 |
| PubMed ID | 11819734 | Mgi Jnum | J:74407 |
| Mgi Id | MGI:2158208 | Doi | 10.3748/wjg.v7.i1.60 |
| Citation | Wu K, et al. (2001) Inhibitory effects of RRR-alpha-tocopheryl succinate on benzo(a)pyrene (B(a)P)-induced forestomach carcinogenesis in female mice. World J Gastroenterol 7(1):60-5 |
| abstractText | AIM:To study the inhibitory effects of VES (RRR-alpha-tocopheryl Succinate, VES),a derivative of natural Vitamin E, on benzo(a)pyrene(B(a)P)-induced forestomach tumor in female mice.METHODS:The model of B(a)P-induced forestomach tumor was established according to the methods of Wattenberg with slight modify-cations.One hundred and eighty female mice (6 weeks old) were divided into six groups equally; negative control (Succinic acid), vehicle control (Succinate+B(a)P),positive control(B(a)P), high VES(2.5g/kg.b.w+B(a)P), low VES(1.25g/kg.b.w+B(a)P)ig as well as VES by ip (20mg/kg.b.w+B(a)P). Except the negative control group, the mice were administrated with B(a)P ig. and corresponding treatments for 4 weeks to study the anti-carcinogenetic effect of VES during the initiation period. The experiment lasted 29 weeks, in which the inhibitory effects of VES both on tumor incidence and tumor size were tested.RESULTS:The models of B(a)P-induced forestomach tumor in female mice were established successfully. Some were cauliflower-like, others looked like papilla, even a few were formed into the ulcer cavities.VES at 1.25g/kg.b.w, 2.5g/kg.b.w. by ig and 20mg/kg.b.w. via ip could decrease the number of tumors per mouse (1.7 plus minus 0.41, 1.6 plus minus 0.34 and 1.1 plus minus 0.43), being lower than that of B(a)P group (5.4 plus minus 0.32, P<0.05). The tumor incidence was inhibited by 18.2%, 23.1% and 50.0%. VES at 1.25g/kg.b.w., 2.5g/kg.b.w. by ig and 20mg/kg.b.w. via ip reduced the total volume of tumors per mouse (54.8 plus minus 8.84, 28.4 plus minus 8.32 and 23.9 plus minus 16.05), being significantly lower than that of B(a)P group (150.2 plus minus 20.93, P < 0.01). The inhibitory rates were 63.5%, 81.1% and 84.1%, respectively.CONCLUSION:VES has inhibitory effects on B(a)P-induced forestomach carcinogenesis in female mice, especially by ip and it may be a potential anti-cancer agent in vivo. |
