Abstract
AIM: To study the anti-fibrotic mechanism of amygdalin, a component of Semen Persicae, on fat-storing cells (FSC).
METHODS: Livers of normal adult rats were perfused with Pronas E and collagenase in situ. FSC were isolated by centrifugation with 11% Metrizamide. The subcultured FSC were incubated with 10-4-10-8 mol/L amygdalin for 72 h, and then FSC proliferation and collagen production were assayed, respectively.
RESULTS: Low doses of amygdalin reduced incorporation of L-[3H]-thymidine into FSC and L-[5-3H]-proline into secreted collagenase-sensitive proteins and cell layer-associated collagenase-sensitive proteins. the strongest effects were seen for the 10-8 mol/L dose of amygdalin, which inhibited the proliferation of FSC by 25.0%, and decreased collagen production in medium and cell layer by 24.2% and 26.8%, respectively.
CONCLUSION: An anti-fibrotic mechanism of amygdalin is to inhibit the proliferation and collagen production of active FSC.
Keywords: Amygdalin, Pharmacology, Liver, Drug effects, Cirrhosis, Drug therapy, Collagen, Biosynthesis
Footnotes
Original title: China National Journal of New Gastroenterology (1995-1997) renamed World Journal of Gastroenterology (1998-)
S- Editor: Filipodia L- Editor: Jennifer E- Editor: Liu WX
