Fractions of Adenopus breviflorus Extract Modulate Calcium-induced Mitochondrial Permeability Transition Pore Opening in Rat Liver

Angelova, P. R., and Abramov, A. P., 2018. Role of mitochondrial ROS in the brain: from physiology to neurodegeneration. FEBS Lett. 592 (5), 692-702.10.1002/1873-3468.12964Search in Google Scholar

Bernardi, P. 2013. The mitochondrial permeability transition pore: A mystery solved? Front. Physiol. 4, 9510.3389/fphys.2013.00095Search in Google Scholar

Calzia, D., Oneto, M., Caicci, F., Bianchini, P., Ravera, S., Bartolucci, M., Diaspro, A., Degan, P., Manni, L., Traverso, C, E., and Panfoli, I., 2015. Effect of polyphenolic phytochemicals on ectopic oxidative phosphorylation in rod outer segments of bovine retina. Br. J Pharmacol. 172, 3890 – 3903.10.1111/bph.13173Search in Google Scholar

Chin, D., Huebbe, P., Pallauf, K., and Rimbach, G., 2013. Neuroprotective properties of curcumin in Alzheimer’s diseasemerits and limitations. Curr. Med. Chem. 20, 3955-398510.2174/09298673113209990210Open DOISearch in Google Scholar

Crompton, M., 1999. The mitochondrial permeability transition pore and its role in cell death. Biochem. J. 341, 233-249.10.1042/bj3410233Search in Google Scholar

Elujoba, A. A., Olagbenle, S. O., and Adesina, S. K., 1985. Antiimplantation activity of the fruit of Lagenaria breviflora Robert. J. Ethnopharmacol. 13, 281-288.10.1016/0378-8741(85)90073-XOpen DOISearch in Google Scholar

Elustondo, P. A., Nichols, M., Negoda, A., Thirumaran, A., Zakharian, E., Robertoson, G. S., and Pavlov, E. V., 2016. Mitochondrial permeability transition pore induction is linked to the formation of the complex of ATPasee C-Subunit polyhydroxybutyrate and inorganic polyphosphate. Cell Death Dis., 2, 1-9.10.1038/cddiscovery.2016.70513718627924223Search in Google Scholar

Federico, A., Cardaioli, E., Da Pozzo, P., Formichi, P., Gallus, G, N., and Radi, E., 2012. Mitochondria, Oxidatiive Stress and Neurodegeneration. J. Neurol. Sci. 322 (1-2), 254-262.10.1016/j.jns.2012.05.03022669122Search in Google Scholar

Fulda, S., 2010. Modulation of Apoptosis by Natural Products for Cancer Therapy. Planta Med. 76, 1075-1079.10.1055/s-0030-124996120486070Search in Google Scholar

Fulda, S., 2016. Regulation of necroptosis signalling and cell death by reactive oxygen species. Biol. Chem. 397 (7), 657–66010.1515/hsz-2016-010226918269Search in Google Scholar

Fulda, S., Galluzzi, L., and Kroemer, G., 2010. Targeting mitochondrial for cancer therapy. Nature Rev. 9, 447-464.10.1038/nrd3137Search in Google Scholar

Gorlach, A., Bertram, K., Hudecova, S., and Krizanova, O., 2015. Calcium and ROS: A mutual interplay. Redox Biol. 6, 260-271.10.1016/j.redox.2015.08.010Search in Google Scholar

Halestrap, A. P., 2009. What is the mitochondrial permeability transition pore. J. Mol. Cel. Cardio. 41 (2), 821-821.10.1016/j.yjmcc.2009.02.021Search in Google Scholar

Hroudova, J., Singh, N., and Fisar, Z., 2014. Mitochondrial Dysfunctions in Neurodegenerative Diseases: Relevance to Alzheimer’s Disease. Biomed. Res. Int. Vol. 2014, Article ID 175062 1-9.10.1155/2014/175062Search in Google Scholar

Johnson, D., and Lardy, H., 1967. Isolation of Liver and Kidney mitochondria. Methods in Enzymol. 10: 94-96.10.1016/0076-6879(67)10018-9Search in Google Scholar

Khan, N., Adhami, V. M., and Mukhtar, H., 2010. Apoptosis by dietary agents for prevention and treatment of prostate cancer. Endo Related Cancer17, 39-52.10.1677/ERC-09-0262Search in Google Scholar

Kipp, J. L., and Ramirez, V. D., 2001. Effect of estradiol, diethylstibestrol and resveratrol on F0F1-ATPase activity from mitochondrial preparations of heart, liver and brain. Endocrine, 15(2), 165-175.10.1385/ENDO:15:2:165Search in Google Scholar

Lapidus, R, G., and Sokolove, P. M., 1992. Inhibition by spermine of the inner membrane permeability transition of isolated rat heart mitochondria. FEBS Lett. 313 (3), 314-318.10.1016/0014-5793(92)81217-AOpen DOISearch in Google Scholar

Lapidus, R, G., and Sokolove, P. M., 1993. Spermine Inhibition of the permeability transition of isolated rat liver mitochondria: An investigation of mechanisms. Biochem. Biophys. J. 64, 246-25310.1006/abbi.1993.1507Open DOISearch in Google Scholar

Lardy, H. A., and Wellman, H., 1953. The catalytical effect of 2, 4-dinitrophenol on adenosine triphosphatase and soluble enzymes. J. Biol. Chem. 201, 357-37010.1016/S0021-9258(18)71378-1Search in Google Scholar

Lemasters, J. J., Theruvath, T. P., Zhong, and Nieminen, A. 2009. Biochim. Biophys. Bioenerg. 1787 (11), 1395-1401.10.1016/j.bbabio.2009.06.009Search in Google Scholar

Lowry, O. H., Rosebrough, N. J., Farr, A. I., and Randall, R. J., 1951. Protein Measurements with the Folin-phenol reagent. J. Biol. Chem. 193, 260-265.10.1016/S0021-9258(19)52451-6Search in Google Scholar

Madreiter-Sokolowski, C. T., Sokolowski, A. A., Graier, W. F., 2017. Dosis Facot Sanitatem-Concentration-dependent effects of Resveratrol on mitochondria. Nutrients, 9 (10), 111710.3390/nu9101117569173329027961Search in Google Scholar

Man, S., Gao, W., Zhang, Y., Huang, L., Liu, C., 2010. Chemical Study and medical application of saponins as anti-cancer agents. Fitoterapia, 81(7), 703-71410.1016/j.fitote.2010.06.00420550961Search in Google Scholar

Martin, K. R. 2006 Targeting Apoptosis with Dietary Bioactive Agents. Exp. Biol. Med., 231, 117-129.10.1177/153537020623100201Search in Google Scholar

McBride, H. M., Neuspiel, M., and Wasiak, S., 2006. Mitochondria: More than just a powerhouse. Curr. Biol., 16(14), R551-R560.10.1016/j.cub.2006.06.05416860735Open DOISearch in Google Scholar

NIH., Guide for the care and use of Laboratory Animals. NIH Publication 1985, No. 85-123, National Institutes of Health, U.S. Department of Health Education and Welfare, Bethesda, USA.Search in Google Scholar

Oyedeji, T. A., Akintehinse, T., Avan, E. D., Soremekun, O. O., Solomon, O. E., and Olorunsogo, O. O., 2017. Extracts of Adenopus breviflorus induce opening of Rat Liver Mitochondrial Membrane Permeability Transition Pore. Biokemistri. 29 (4), 140-145.Search in Google Scholar

Perez-Hernandez, J., Zaldvar-Machorro, V. J., Villanueva-Porras, D., Vega-Avila, E., and Chavarria, A., 2016. A Potential Alternative against Neurodegenerative Diseases: Phytodrugs. Oxid. Med. Cell. Longevity, Volume 2016, Article ID 8378613, pp 1-19.10.1155/2016/8378613473680126881043Search in Google Scholar

Qiu, Y., Yu, T., Wang, W., Pan, K., Shi, D., and Sun, H., 2014. Curcumin-induced melanoma cell death is associated with mitochondrial permeability transition pore (mPTP) opening. Biochem. Biophys. Res. Commun. 448, 15-21.10.1016/j.bbrc.2014.04.02424735534Search in Google Scholar

Rao, V. K., Carlson, E. A., and Yan, S. S., 2014. Mitochondrial permeability transition pore is a potential drug target for neurodegeration. Biochim. Biophys. Act. 1842(8), 1267-1272.10.1016/j.bbadis.2013.09.003Search in Google Scholar

Rasola, A., and Bernardi, P., 2014 The mitochondrial permeability transition pore and its adaptive responses in tumour cells. Cell. Calcium, 56 (6), 437-445.10.1016/j.ceca.2014.10.003427431425454774Open DOISearch in Google Scholar

Rottenberg, H., Hoek, J, B., 2017. The path from mitochondrial ROS to aging runs through the mitochondrial permeability transition pore. Aging Cell, 16, 943-955.10.1111/acel.12650559568228758328Open DOISearch in Google Scholar

Ruberto, G., Baratta, M. T., Deans, S. G., and Dorman, H. J. D., 2000. Antioxidant and antimicrobial Activity of Foeniculum vulgare and Crithmum maritimum essential oils. Planta Medica. 66(8), 687-693.10.1055/s-2000-977311199122Search in Google Scholar

Schwarz, M., Miguel, A., Navarro, A., and Gross, A., 2007. Mitochondrial carriers and pores: key regulators of the mitochondrial apoptotic program? Apoptosis12, 869-87610.1007/s10495-007-0748-217453157Open DOISearch in Google Scholar

Sowndhararajan, K., and Kim, S., 2017. Neuroprotective and cognitive Enhancement Potentials of Angelica gigas Nakai Root: A review. Sci. Pharm., 85 (21), 1-11.10.3390/scipharm85020021548992528452965Search in Google Scholar

Sun, N., Youle, R. J., and Finkel, T., 2016. The mitochondrial Basis of Aging. Mol. Cell. 61, 654-666.10.1016/j.molcel.2016.01.028477917926942670Search in Google Scholar

Wang, X., 2001. The expanding role of mitochondria in apoptosis. Genes Dev. 15, 2922-2933.Search in Google Scholar

Zheng, J., and Ramirez, V. D., 2000. Inhibition of mitochondrial proton F0F1-ATPase/ATP synthase by polyphenolic phytochemicals. Br. J. Pharmacol. 13(5), 1115-1123.10.1038/sj.bjp.0703397157215810882397Search in Google Scholar