Effect of Prunellae Spica on Oxidative Stress and Mitochondrial Dysfunction in the Hepatocyte |
Jang, Mihee
(Medical Research Center (MRC-GHF), College of Korean Medicine, Daegu Haany University)
Seo, Hye Lim (Medical Research Center (MRC-GHF), College of Korean Medicine, Daegu Haany University) Kim, Sang Chan (Medical Research Center (MRC-GHF), College of Korean Medicine, Daegu Haany University) Kim, Young Woo (Medical Research Center (MRC-GHF), College of Korean Medicine, Daegu Haany University) |
1 | Beckman, K.B., Ames, B.N. The free radical theory of aging matures. Physiol Rev. 78: 547-581, 1998. DOI |
2 | Wiseman, H. and Halliwell, B. Damage to DNA by reactive oxygen and nitrogen species: role in inflammatory disease and progression to cancer. Biochem. J. 313: 17-20, 1996. DOI |
3 | Kim, T.S., Kang, S.J., Park, W.C. Changes in antioxidants and antioxidants enzymes activities of soybean leaves subject to water stress. J. Korean Soc. Agric. Chem. Biol. pp 246-251, 1999. |
4 | Oh, J.M., Lee, J.Y., Lee, G.H., Kim, B.H., Kim, S.K. Evaluation oxidative stress and antioxidant enzyme expression in human hepatocarcinoma SK-Hep-1 cells treated with stearic acid. Yakhak Hoeji. 56(1):14-19, 2012. |
5 | Choi, S.H., Kim, Y.W., Kim, S.G. AMPK-mediated GSK3b inhibition by isoliquiritigenin contributes to protecting mitochondria against iron-catalyzed oxidative stress. Biochemical Pharmacology. 79: 1352-1362, 2009. DOI |
6 | Larson, R.A. The antioxidant of higher plants. Phytochemistry. 27: 969-978, 1988. DOI |
7 | Yang, J.M., Jun, Y.J., Nam, J.Y., Son, M.Y., Sung, J.S., Kim, D.I. The Cell protective Effects of Dioscoreae Rhizoma by Antioxidant Activities on HeLa Cells. J Orient Obstet Gynecol. 21(2):97-107, 2008. |
8 | Lee, C.H. Effect of reactive oxygen species against hepatic vascular resistance. Korean Society of Gastroenterology. 513(16):271-272, 2006. |
9 | Park, S.Y., Cho, J.H. Effect of Vitamin A on Hepatic Mitochondrial Activity. Kor. J. Vet. Publ. Hlth. 27(1):53-58, 2003. |
10 | Shimizu, T., Wolfe, L.S. Arachidonic acid cascade and intercellular signal transduction. J Neurochem. 55(1):1-15, 1990. DOI |
11 | Balboa, M.A., Balsinde, J. Oxidative stress and arachidonic acid mobilization. Biochim Biophys Acta. 1761: 385-391, 2006. DOI |
12 | Shin, S.M., Kim, S.G. Inhibition of arachidonic acid and iron-induced mitochondrial dysfunction and apoptosis by oltipraz and novel 1,2-dithiole-3-thione congeners. Mol Pharmacol. 75: 242-253, 2009. DOI |
13 | Gunter, T.E., Pfeiffer, D.R. Mechanisms by which mitochondria transport calcium. Am J Physiol. 258: 755-786, 1990. DOI |
14 | Haworth, R.A., Hunter, D.R. The Ca2+-induced membrane transition in mitochondria. II. Nature of the Ca2+ trigger site. Arch Biochem Biophys. 195: 460-467, 1979. DOI |
15 | Ryu, S.Y., Oak, M.H., Yoon, S.K., Cho, D.I., Yoo, G.S., Kim, T.S., Kim, K.M. Anti-allergic and anti-inflammatory tri-terpenes from the herb of Prunella vulgaris. Planta Med 66: 358-360, 2000. DOI |
16 | Hunter, D.R., Haworth, R.A. The Ca2+-induced membrane transition in mitochondria. I. The protective mechanisms. Arch Biochem Biophys. 195: 453-459, 1979. DOI |
17 | Lee, J.W., Shim, Y.H. Mitochondrial Permeability Transition Pore and Cardioprotection Against Ischemia-reperfusion Injury. J Korean Med Assoc. 52(10):1007-1019, 2009. DOI |
18 | Kim, J.S., Kang, S.S., Lee, K.S., Chang, S.Y., Won, D.H. Quantitative determination of ursolic acid from Prunellae herba. Kor J Pharmacogn. 31: 416-420, 2000. |
19 | Liu, F., Ng, T.B. Antioxidative and free radical scavenging activities of selected medicinal herbs. Life Sci 66: 725-735, 2000. DOI |
20 | You, J.K., Chung, M.J., Kim, D.J., Seo, D.J., Park, J.H., Kim, T.W., Choe, M. Antioxidant and tyrosinase inhibitory effects of Paeonia suffruticosa water extract. J Korean Soc Food Sci Nutr. 38(3):292-296, 2009. DOI |
21 | Kim, B.H., Oh, J.M., Yun, K.U., Kim, C.H., Kim, S.K. Effects of Glucagon and Insulin on Glutathione Homeostasis: Role of Cellular Signaling Pathways and Glutathione Transport System. J. Environ. Toxicol. 22(3):227-233, 2007. |
22 | Sandra, J. Phytochemical studies of Prunella vulgaris and Prunella grandiflora-Ⅰ. Saponin and triterpene compounds. Dissertations Pharm 15: 333-341, 1963. |
23 | Ronot, X., Benel, L., Adolphe, M. and Mounolou, J. C. Mitochondrial analysis in living cells: the use of rhodamine 123 and flow cytometry. Biology of the Cell. 57(1):1-7, 1986. DOI |
24 | Bernardi, P. Mitochondrial transport of cations: channels, exchangers, and permeability transition. Physiol Rev. 79: 1127-1155, 1999. DOI |
25 | Ljubica Vucicevic, et al. Compound C induces protective autophagy in cancer cells through AMPK inhibition-independent blockade of Akt/mTOR pathway. Autophagy. 7(1):40-50, 2011. DOI |
26 | Jo, Y.S. Asthma and oxidative stress. Korean journal of asthma, allergy and clinical immunology. 28(3):167, 2008. |
27 | Daiber, A., Di Lisa, F., Oelze, M., Kröller-Schön, S., Steven, S., Schulz, E., Münzel, T. Crosstalk of mitochondria with NADPH oxidase via reactive oxygen and nitrogen species signalling and its role for vascular function. Br J Pharmacol. 2015 Dec 9. doi: 10.1111/bph.13403. DOI |
28 | Kokoszka, J.E., Waymire, K.G., Levy, S.E., Sligh, J.E., Cai, J., Jones, D.P., MacGregor, G.R., Wallace, D.C. The ADP/ATP translocator is not essential for the mitochondrial permeability transition pore. Nature. 427: 461-465, 2004. DOI |
29 | Kim, J.S., Jin, Y.J., Lemasters, J.J. Reactive oxygen species, but not Ca2+ overloading, trigger pH- and mitochondrial permeability transition-dependent death of adult rat myocytes after ischemia-reperfusion. Am J Physiol, Heart Circ Physiol. 290: 2024-2034, 2006. DOI |
30 | Juhaszova, M., Wang, S., Zorov, N.H., Bradley, D.B., Gleichmann, M., Mattson, M.P. et al., The identity and regulation of the mitochondrial permeability transition pore: where the known meets the unknown. Ann NY Acad Sci. 1123: 197-212, 2008. DOI |
31 | Rasola, A., Bernardi, P. The mitochondrial permeability transition pore and its involvement in cell death and in disease pathogenesis. Apoptosis. 12: 815-833, 2007. DOI |
32 | Ouchi, N., Shibata, R., Walsh, K. AMP-activated protein kinase signaling stimulates VEGF expression and angiogenesis in skeletal muscle. Circ Res 96: 838-846, 2005. DOI |
33 | Hardie, D.G. Mini review: the AMP-activated protein kinase cascade: the key sensor of cellular energy status. Endocrinol. 144: 5179-5183, 2003. DOI |
34 | Stapleton, D., Mitchelhill, K.I., Gao, G., Widmer, J., Michell, B.J., The, T., House, C.M., Fernandez, C.S., Cox, T., Witters, L.A., Kemp, B.E. Mammalian AMP-activated protein kinase subfamily. J Biol Chem. 271: 611-614, 1996. DOI |
35 | Winder, W.W., Thomson, D.M. Cellular energy sensing and signaling by AMP-activated protein kinase. Cell Biochem Biophys. 47: 332-347, 2007. DOI |
36 | Choi, H.C. AMP-activated protein kinase Activating Agent and Its Implication. Endocrinol Metab. 27(2):109-115, 2012. DOI |
37 | Boudeau, J., Sapkota, G., Alessi, D.R. LKB1, a protein kinase regulating cell proliferation and polarity. FEBS Lett. 546: 159-165, 2003. DOI |