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Chin J Nat Med ; 17(9): 663-671, 2019 Sep.
Article in English | MEDLINE | ID: mdl-31526501

ABSTRACT

Bioassay-guided fractionation of an ethanolic extract of Ochrosia borbonica led to the isolation of two known pyridocarbazole alkaloids, ellipticine (1) and 9-methoxyellipticine (2), and six known monoterpenoid indole alkaloids (3-8). Lipid-lowering assay in 3T3-L1 cell model revealed that 1 and 2 could significantly inhibit the lipid droplet formation (EC50 = 0.41 and 0.92 µmol·L-1, respectively) and lower triglyceride levels by 50%-60% at the concentration of 1 µmol·L-1, being more potent than the positive drug luteolin (EC50 = 2.63 µmol·L-1). A mechanistic study indicated that 1 and 2 could intercalate into supercoiled DNA, which consequently inhibited the mitotic clonal expansion of 3T3-L1 cells at the early differentiation phase, leading to the retardance of following adipogenesis and lipogenesis. These findings suggest that 1 and 2 may serve as promising leads for further development of anti-obesity drugs.


Subject(s)
Adipogenesis/drug effects , Carbazoles/pharmacology , Cell Proliferation/drug effects , DNA, Superhelical/chemistry , Hypolipidemic Agents/pharmacology , Ochrosia/chemistry , 3T3-L1 Cells , Adipocytes/drug effects , Adipocytes/metabolism , Adipocytes/pathology , Animals , Carbazoles/chemistry , Carbazoles/metabolism , DNA Damage , Ellipticines/chemistry , Ellipticines/metabolism , Ellipticines/pharmacology , Hypolipidemic Agents/chemistry , Hypolipidemic Agents/metabolism , Lipid Metabolism/drug effects , Mice , Molecular Structure , Plant Extracts/chemistry , Topoisomerase Inhibitors/chemistry , Topoisomerase Inhibitors/metabolism , Topoisomerase Inhibitors/pharmacology
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