Abstract
Scutellaria barbata has long been used as a Chinese medicine for the treatment of liver diseases such
as hepatitis and hepatocellular carcinoma. In the present study, a bioassay-guided
method was used to isolate the most active components from Scutellaria barbata. The anti-proliferative effects on human hepatoma HepG2 and Hep3B cells of each fraction
at every stage of the purification were monitored. An active component, which is 97
% pure by high performance liquid chromatographic analysis, was isolated. Based on
nuclear magnetic resonance (NMR) and mass spectrophotometric (MS) analysis, this active
component was identified to be pheophorbide a (C35H36N4O5). Mechanistic studies showed that pheophorbide a induced apoptosis in Hep3B cells,
a viral-induced hepatoma cell line. However, it was found to be non-toxic in normal
human liver cells WRL-68. DNA fragmentation, sub-G1 cell cycle arrest, as well as suppression of the anti-apoptotic protein Bcl-2, release
of cytochrome c to the cytosol, and activation of pro-caspase 3 and pro-caspase 9
were observed when Hep3B cells were treated with 40 μg/mL (i. e., 67.5 μM) pheophorbide
a for 48 hours. In conclusion, this is the first report describing the isolation of
pheophorbide a from Scutellaria barbata using a bioassay-guided isolation method. The anti-proliferative activity and possible
mechanisms of action of pheophorbide a on hepatoma Hep3B cells are also discussed.
Key words
Scutellaria barbata
- pheophorbide a - apoptosis - HepG2 - Hep3B
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Dr. K. P. Fung
Department of Biochemistry
Faculty of Medicine
Room 603
Mong Man Wai Building
The Chinese University of Hong Kong
Shatin
Hong Kong
People’s Republic of China
Phone: +852-2609-6873
Fax: +852-2603-7732
Email: kpfung@cuhk.edu.hk