Fermented Prunus mume with Probiotics Inhibits 7,12-Dimethylbenz[a] anthracene and 12-O-Tetradecanoyl phorbol-13-acetate Induced Skin Carcinogenesis through Alleviation of Oxidative Stress

被引:16
作者
Lee, Jin-A [1 ]
Ko, Jae-Hyung [2 ]
Jung, Bock-Gie [1 ]
Kim, Tae-Hoon [1 ]
Hong, Ji-In [1 ]
Park, Young-Seok [3 ]
Lee, Bong-Joo [1 ]
机构
[1] Chonnam Natl Univ, Coll Vet Med, Dept Vet Infect Dis, Kwangju, South Korea
[2] Kyonggido Livestock & Vet Serv, Suwon, Kyonggi, South Korea
[3] Kongju Natl Univ, Dept Compan & Lab Anim Sci, Kong Ju 314701, Chungnam, South Korea
基金
新加坡国家研究基金会;
关键词
Prunus mume; maesil; skin cancer; oxidative stress; inhibitory potential; JAPANESE APRICOT; MOUSE SKIN; ATOPIC-DERMATITIS; CANCER; CELLS; MK615; DMBA; CHEMOPREVENTION; TUMORIGENESIS; ANTIOXIDANT;
D O I
10.7314/APJCP.2013.14.5.2973
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Maesil (Prunus mume Siebold & Zucc.), a member of the genus Rosaceae, has been reported to have antioxidative effects, as well as anticancer influence in many cancer lines. Thus, this present study was designed to investigate the inhibitory effect of fermented Maesil with probiotics against 7,12-dimethylbenz[a]anthracene (DMBA), 12-O-tetradecanoyl phorbol 13-acetate (TPA)-induced mouse skin carcinogenesis via its antioxidative potential. Mice were fed a diet containing fermented Maesil, containing either 1% (1% FM fed group) or 2% (2% FM fed group) along with probiotics following DMBA and TPA exposure. Continuous ingestion of the experimental feed markedly inhibited skin carcinogenesis, as evidenced by a marked decrease in papilloma numbers and epidermal hyperplasia as well as cellular proliferation and the percentage of proliferating-cell nuclear antigen positive cells. Also, the FM fed group showed an increase of total antioxidant capacity as well as an increased level of phase II detoxifying enzymes such as superoxide dismutase, concurrent with a decreased lipid peroxidation activity level. Taken together, these results suggest that fermented Maesil has the ability to suppress the development of DMBA-TPA induced skin carcinogenesis, via the reduction of lipid peroxidation, enhancing total antioxidant capacity and phase II detoxifying enzyme.
引用
收藏
页码:2973 / 2978
页数:6
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