Structure-related cytotoxicity and anti-hepatofibric effect of asiatic acid derivatives in rat hepatic stellate cell-line, HSC-T6

• Published in: Archives of pharmacal research 2004, 27(5), , pp.512-517
• Main Authors: Dong, Mi-Sook, Jung, Seung-Hyun, Kim, Hyun-jung, Kim, Jeong-Ran, Zhao, Long-Xuan, Lee, Eung-Seok, Lee, Eun-Joo, Yi, Jung Bum, Lee, Namkyu, Cho, Yong-Baik, Kwak, Wie Jong, Park, Young In
• Format: Article
• Language: English
• Subjects: Animals; Cell Line; Cell Line, Transformed; Cell Survival - drug effects; Cell Survival - physiology; Dose-Response Relationship, Drug; Hepatocytes - drug effects; Hepatocytes - physiology; Pentacyclic Triterpenes; Rats; Structure-Activity Relationship; Triterpenes - chemistry; Triterpenes - toxicity; 약학
• ISSN: 0253-6269; 1976-3786
• DOI: 10.1007/bf02980124

The structural relationship of 16 asiatic acid (AA) derivatives, including AA and asiaticoside (AS) to cytotoxicity and anti-hepatofibrotic activity in HSC-T6 cells, were investigated. Cytotoxicities of AA derivatives varied from 5.5 microM to over 2000 microM of IC50 depending on AA functional group modifications. Substituting the hydroxyl group at the C(2) to N[triple bond]C and substituting bulky groups for dihydroxyl groups at (3), (23) of the A-ring increased the cytotoxicity, but keto group at C(11) and benzoyl ester at C(2) were greatly reduced it. Modification of the carboxylic acid group at C28 also reduced the cytotoxicity. The collagen synthesis determined by hydroxyproline content in the cells was inhibited from a maximum of 48% (Zlx-i-85 and 87) to 15% (AS) by AA derivatives. The anti-hepatofibrotic effect of these compounds might be due to the reduced expression of prolyl 4-hydroxylase alpha and beta subunits and TIMP2. However, the inhibition of collagen by asiaticoside derivatives did not show any structural-activity relationship.