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Inhibitory Effect of 2‐0‐Octadecylascorbic Acid in Agglutination Assay with Concanavalin A; Short‐term Examination of Rat Urinary Bladder Carcinogenesis

A derivative of ascorbic acid, 2‐O‐octadecylascorbic acid (CV‐3611), is a strong scavenger of active oxygen species. We examined the effect of CV‐3611 on a short‐term test of bladder Carcinogenesis, using Concanavalin A (Con A) ‐dependent agglutination of isolated bladder epithelial cells. Rats were...

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Detalles Bibliográficos
Autores principales: Suzuki, Mika, Wakabayashi, Keiji, Sone, Hideko, Kushida, Hiromi, Sugiyama, Kiyoshi, Kakizoe, Tadao, Nagao, Minako, Sugimura, Takashi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 1991
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5918435/
https://www.ncbi.nlm.nih.gov/pubmed/1904418
http://dx.doi.org/10.1111/j.1349-7006.1991.tb01860.x
Descripción
Sumario:A derivative of ascorbic acid, 2‐O‐octadecylascorbic acid (CV‐3611), is a strong scavenger of active oxygen species. We examined the effect of CV‐3611 on a short‐term test of bladder Carcinogenesis, using Concanavalin A (Con A) ‐dependent agglutination of isolated bladder epithelial cells. Rats were given 0.01%N ‐butyl‐N(4‐hydroxybutyl)nitrosamine (BHBN) for 1 week, and then 5% sodium saccharin or 2% DL‐tryptophan or 0.01% BHBN alone or with 0.002, 0.006 or 0.02% CV‐3611 for 3 weeks. Treatment with CV‐3611 reduced the effects of the bladder tumor promoters sodium saccharin and DL‐tryptophan by 48–86 and 65–87%, respectively. CV‐3611 also reduced the number of aggregates of bladder epithelial cells from rats treated with BHBN for 4 weeks. These results suggest that CV‐3611 has a suppressive effect on rat bladder Carcinogenesis.