Vitisin B
Vitisin B can stimulate osteoblastogenesis via estrogen receptor-mediated pathway, it can inhibits migration through inhibition of PDGF signaling and enhancement of cell adhesiveness in cultured vascular smooth muscle cells. (-)-Vitisin B can significantly inhibit cell proliferation through inducing cell apoptosis in human HL-60 promyelocytic leukemia cells, it induces apoptosis of leukemia cells might be mediated through activation of JNK and Fas death-signal transduction.
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24 months(2-8C).
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Toxicol Appl Pharmacol. 2011 Oct 15;256(2):198-208.
Vitisin B, a resveratrol tetramer, inhibits migration through inhibition of PDGF signaling and enhancement of cell adhesiveness in cultured vascular smooth muscle cells.[Pubmed:
21871475 ]
Vascular smooth muscle cells (VSMCs) play an important role in normal vessel formation and in the development and progression of cardiovascular diseases. Grape plants contain resveratrol monomer and oligomers and drinking of wine made from grape has been linked to "French Paradox". In this study we evaluated the effect of Vitisin B, a resveratrol tetramer, on VSMC behaviors.
METHODS AND RESULTS:
Vitisin B inhibited basal and PDGF-induced VSMC migration. Strikingly, it did not inhibit VSMC proliferation but inversely enhanced cell cycle progression and proliferation. Among the tested resveratrol oligomers, Vitisin B showed an excellent inhibitory activity and selectivity on PDGF signaling. The anti-migratory effect by Vitisin B was due to direct inhibition on PDGF signaling but was independent of interference with PDGF binding to VSMCs. Moreover, the enhanced VSMC adhesiveness to matrix contributed to the anti-migratory effect by Vitisin B. Fluorescence microscopy revealed an enhanced reorganization of actin cytoskeleton and redistribution of activated focal adhesion proteins from cytosol to the peripheral edge of the cell membrane. This was confirmed by the observation that enhanced adhesiveness was repressed by the Src inhibitor. Finally, among the effects elicited by Vitisin B, only the inhibitory effect toward basal migration was partially through estrogen receptor activation.
CONCLUSIONS:
We have demonstrated here that a resveratrol tetramer exhibited dual but opposite actions on VSMCs, one is to inhibit VSMC migration and the other is to promote VSMC proliferation. The anti-migratory effect was through a potent inhibition on PDGF signaling and novel enhancement on cell adhesion.
Integrative Medicine Research, 2015,May 4(1):76-7.
Vitisin B stimulates osteoblastogenesis via estrogen receptor-mediated pathway[Reference:
WebLink]
METHODS AND RESULTS:
Vitisin B stimulates osteoblastogenesis via estrogen receptor-mediated pathway
Drug Chem Toxicol. 2013 Jul;36(3):313-9.
Cytotoxicity of (-)-vitisin B in human leukemia cells.[Pubmed:
23030068 ]
Vitis thunbergii var. taiwaniana (VTT) is an indigenous Taiwanese wild grape and is used as a folk medicine in Taiwan. VTT is rich in polyphenols, especially quercetin and resveratrol derivatives, which were demonstrated to exhibit inhibitory activities against carcinogenesis and prevent some neurodegenerative diseases. (-)-Vitisin B is one of the resveratrol tetramers extracted from VTT. In this study, we investigated the mechanisms of (-)-Vitisin B on the induction of apoptosis in human HL-60 promyelocytic leukemia cells.
METHODS AND RESULTS:
First, (-)-Vitisin B significantly inhibited cell proliferation through inducing cell apoptosis. This effect appeared to occur in a time- and dose-dependent manner. Cell-cycle distribution was also examined, and we found that (-)-Vitisin B significantly induced a sub-G1 population in a dose-dependent manner. In addition, (-)-Vitisin B exhibited stronger inhibitory effects on cell proliferation than resveratrol. Second, (-)-Vitisin B dose dependently induced apoptosis-related protein expressions, such as the cleavage form of caspase-3, caspase-8, caspase-9, poly(ADP ribose) polymerase, and the proapoptotic Bax protein. Third, (-)-Vitisin B treatment also resulted in increases in c-Jun N-terminal kinase (JNK) phosphorylation and Fas ligand (FasL) expression. Moreover, the (-)-Vitisin B-induced FasL expression and caspase-3 activation could be reversed by a JNK inhibitor.
CONCLUSIONS:
These results suggest that (-)-Vitisin B-induced apoptosis of leukemia cells might be mediated through activation of JNK and Fas death-signal transduction.
