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Eudesmols Induce Apoptosis through Release of Cytochrome c in HL-60 Cells  

Hoang, Duc Manh (Korea Research Institute of Bioscience and Biotechnology (KRIBB))
Trung, Trinh Nam (College of Pharmacy, Chungnam National University)
He, Long (Korea Research Institute of Bioscience and Biotechnology (KRIBB))
Ha, Do Thi (College of Pharmacy, Chungnam National University)
Lee, Myoung-Sook (Research Institute of Obesity Science, Sungshin Women's University)
Kim, Bo-Yeon (Korea Research Institute of Bioscience and Biotechnology (KRIBB))
Luong, Hoang Van (Vietnam Military Medical University)
Ahn, Jong-Seog (Korea Research Institute of Bioscience and Biotechnology (KRIBB))
Bae, Ki-Hwan (College of Pharmacy, Chungnam National University)
Publication Information
Natural Product Sciences / v.16, no.2, 2010 , pp. 88-92 More about this Journal
Abstract
We verified that the apoptosis activities were examined by DNA fragmentation, flow cytometric analysis with annexin V staining, activation of caspase-3, and cytochrome c release. In the result, $\alpha$- and $\beta$-eudesmol induced DNA fragmentation in HL-60 cells at a concentration of $80\;{\mu}M$, respectively. Additionally, pro-apoptotic cells sorted by flow cytometry analysis were detected in HL-60 cells to 31.77 and 29.67% with $\acute{a}$- and $\beta$-eudesmol of $80\;{\mu}M$. Thus, both $\alpha$- and $\beta$-eudesmol exerted caspase-3 activation and cytochrome c release at $80\;{\mu}M$ in HL-60 cells. These results are firstly reported that the sesquiterpenes, $\alpha$- and $\beta$-eudesmol are apoptosis inducers through mitochondria-dependent caspase cascade in HL-60 cells.
Keywords
Magnolia obovata; sesquiterpene; eudesmols; apoptosis inducer; phytochemical;
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1 Vera, N., Misico, R., Sierra, M.G., Asakawa, Y., and Bardon, A., Eudesmanes from Pluchea sagittalis. Their antifeedant activity on Spodoptera frugiperda. Phytochemistry. 69, 1689-94 (2008).   DOI   ScienceOn
2 Hamasaki, Y., Kobayashi, I., Zaitu, M., Tsuji, K., Kita, M., Hayasaki, R., Muro, E., Yamamoto S., Matsuo, M., Ichimaru, T., and Miyazaki, S., Magnolol inhibits leukotriene synthesis in rat basophilic leukemia- 2H3 cells. Planta Med., 65, 222-226 (1999).   DOI   ScienceOn
3 Ikeda, K. and Nagase, H., Magnolol has the ability to induce apoptosis in tumor cells. Biol. Pharm. Bull., 25, 1546-1549 (2002).   DOI   ScienceOn
4 Kimura, M., Kimura, I., Kondoh, T., and Tsuneki, H., Noncontractile acetylcholine receptor-operated $ Ca^{++} $mobilization: suppression of activation by open channel blockers and acceleration of desensitization by closed channel blockers in mouse diaphragm muscle. J. Pharmacol. Exp. Ther., 256, 18-23 (1991).
5 Raharivelomanana, P., Bianchini, J.P., Ramanoelina, A.R.P., Rasoarahona, J.R.E., Faure, R., and Cambon, A., Eudesmane sesquiterpenes from Laggera alata. Phytochemistry. 47, 1085-1088 (1998).   DOI
6 Sun, Z., Chen, B., Zhang, S., and Hu C., Four new eudesmanes from Caragana intermedia and their biological activities. J Nat Prod. 67, 1975-1979 (2004).   DOI   ScienceOn
7 Teng, C.M., Yu, S.M., Chen, C.C., Huang, Y.L., and Huang ,T.F., EDRFrelease and $ Ca^{+(+)}$-channel blockade by magnolol, an antiplatelet agent isolated from Chinese herb Magnolia officinalis, in rat thoracic aorta. Life Sci., 47, 1153-1161 (1990).   DOI   ScienceOn
8 El-Gammal, M.H. and Wolff, P., A further contribution to the sesquiterpenoid constituents of Cymbopogon proximus. Planta Med., 53, 293-294 (1987).   DOI   ScienceOn
9 Al-Dabbas, M.M., Suganuma, T., Kitahara, K., Hou, D.X., and Fujii, M., Cytotoxic, antioxidant and antibacterial activities of Varthemia iphionoides Boiss. extracts. J Ethnopharmacol. 108, 287-293 (2006).   DOI   ScienceOn
10 Denyer, C.V., Jackson, P., Loakers, D.M., Ellis, M.R., and Young, D. A.B., Isolation of antirhinoviral sesquiterpenes from ginger (Zingiber officinale). J. Nat. Prod. 57, 658-662 (1994).   DOI   ScienceOn
11 Bae, E.A., Han, M.J., Kim, N.J., and Kim, D.H., Anti-Helicobacter pylori activity of herbal medicines. Biol. Pharm. Bull. 21, 990-992 (1998).   DOI   ScienceOn