Relative inhibitory activity of bile acids against 12-O-tetradecanoylphorbol-13-acetate-induced inflammation, and chenodeoxycholic acid inhibition of tumour promotion in mouse skin two-stage carcinogenesis. The Journal of pharmacy and pharmacology [J Pharm Pharmacol] Journal article | | Title | Relative inhibitory activity of bile acids against 12-O-tetradecanoylphorbol-13-acetate-induced inflammation, and chenodeoxycholic acid inhibition of tumour promotion in mouse skin two-stage carcinogenesis. | | Author(s) | Yasukawa K, Iida T, Fujimoto Y | | Institution | College of Pharmacy, Nihon University, Funabashi-shi, Chiba, Japan. self-med@pha.nihon-u.ac.jp | | Source | J Pharm Pharmacol 2009 Aug; 61(8):1051-6. | | MeSH | 9,10-Dimethyl-1,2-benzanthracene
Animals
Anti-Inflammatory Agents
Anticarcinogenic Agents
Bile Acids and Salts
Carcinogens
Chenodeoxycholic Acid
Disease Models, Animal
Edema
Female
Indomethacin
Inflammation
Inhibitory Concentration 50
Mice
Mice, Inbred ICR
Neoplasms, Experimental
Skin Neoplasms
Structure-Activity Relationship
Tetradecanoylphorbol Acetate
| | Abstract | OBJECTIVES: Bile acids are present in Bezoar Bovis and Fel Ursi, traditionally used as antipyretics and antispasmodics. However the anti-inflammatory activity of individual bile acids and related compounds has not yet been investigated. In this paper, we report the structure-activity relationships influencing the anti-inflammatory activity of a variety of structurally different bile acid derivatives and also the inhibitory activity of chenodeoxycholic acid against tumour promotion.
METHODS: Fifty derivatives of bile acids were examined for their inhibitory activity against the induction of oedema in mouse ear by application of 12-O-tetradecanoylphorbol-13-acetate (TPA). Also, the effect of chenodeoxycholic acid was studied in mouse skin in which tumours had been induced by topical application of 7,12-dimethylbenz[a]anthracene (DMBA) and promoted by TPA. KEY
FINDINGS: Many bile acid derivatives had an inhibitory effect against TPA-induced ear oedema at a similar grade to that of indometacin. Chenodeoxycholic acid, methyl 3alpha,7alpha,15alpha-trihydroxy-5beta-cholan-24-oate and methyl 3alpha,7alpha,15beta-trihydroxy-5beta-cholan-24-oate showed the most potent activity with an ID50 value of 71-110 nmol/ear, a level corresponding to that of hydrocortisone (69 nmol/ear). Furthermore, chenodeoxycholic acid markedly suppressed tumour-promoting activity by TPA following initiation by DMBA in mouse skin.
CONCLUSIONS: This is the first report on the anti-inflammatory activity of bile acids on TPA-induced inflammatory ear oedema in mice. Chenodeoxycholic acid, methyl 3alpha,7alpha,15alpha-trihydroxy-5beta-cholan-24-oate and methyl 3alpha,7alpha,15beta-trihydroxy-5beta-cholan-24-oate showed the most potent activity, at a level corresponding to that of hydrocortisone. Furthermore, chenodeoxycholic acid markedly inhibited tumour promotion in a two-stage carcinogenesis model in mouse skin. | | Language | eng | | Pub Type(s) | Comparative Study
Journal Article
Research Support, Non-U.S. Gov't
| | PubMed ID | 19703349 |
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