Dichloromethane extracts of propolis protect cell from oxygen-glucose deprivation-induced oxidative stress via reducing apoptosis

References

• Heineke J, Kempf T, Kraft T, Hilfiker A, Morawietz H, Scheubel RJ, etal. Downregulation of cytoskeletal muscle LIM protein by nitric oxide: impact on cardiac myocyte hypertrophy. Circulation. 2003; 107: 1424–32.
   Google Scholar
• Ashafaq M, Khan MM, Shadab Raza S, Ahmad A, Khuwaja G, Javed H, etal. S-allyl cysteine mitigates oxidative damage and improves neurologic deficit in a rat model of focal cerebral ischemia. Nutr Res. 2012; 32: 133–43.
   Google Scholar
• Patten RD, Pourati I, Aronovitz MJ, Baur J, Celestin F, Chen X, etal. 17beta-estradiol reduces cardiomyocyte apoptosis in vivo and in vitro via activation of phospho-inositide-3 kinase/Akt signaling. Circulation Res. 2004; 95: 692–9.
   Google Scholar
• Strelau J, Sullivan A, Bottner M, Lingor P, Falkenstein E, Suter-Crazzolara C, etal. Growth/differentiation factor-15/macrophage inhibitory cytokine-1 is a novel trophic factor for midbrain dopaminergic neurons in vivo. J Neurosci. 2000; 20: 8597–603.
   Google Scholar
• Allen CL, Bayraktutan U. Oxidative stress and its role in the pathogenesis of ischaemic stroke. Int J Stroke. 2009; 4: 461–70.
   Google Scholar
• Rodrigo R, Fernandez-Gajardo R, Gutierrez R, Matamala JM, Carrasco R, Miranda-Merchak A, etal. Oxidative stress and pathophysiology of ischemic stroke: novel therapeutic opportunities. CNS Neurol Disord Drug Targets. 2013; 12: 698–714.
   Google Scholar
• Apel K, Hirt H. Reactive oxygen species: metabolism, oxidative stress, and signal transduction. Ann Rev Plant Biol. 2004; 55: 373–99.
   PubMed Web of Science ®Google Scholar
• Lee BI, Chan PH, Kim GW. Metalloporphyrin-based superoxide dismutase mimic attenuates the nuclear translocation of apoptosis-inducing factor and the subsequent DNA fragmentation after permanent focal cerebral ischemia in mice. Stroke. 2005; 36: 2712–7.
   Google Scholar
• Lauffenburger JC, Farley JF, Gehi AK, Rhoney DH, Brookhart MA, Fang G. Effectiveness and safety of dabigatran and warfarin in real-world US patients with non-valvular atrial fibrillation: a retrospective cohort study. J Am Heart Assoc. 2015; 4: e001798.
   Google Scholar
• Burdock GA. Review of the biological properties and toxicity of bee propolis (propolis). Food Chem Toxicol. 1998; 36: 347–63.
   Google Scholar
• Teixeira EW, Negri G, Meira RM, Message D, Salatino A. Plant origin of green propolis: bee behavior, plant anatomy and chemistry. Evid Based Complement Alternat Med. 2005; 2: 85–92.
   Google Scholar
• Kosalec I, Bakmaz M, Pepeljnjak S, Vladimir-Knezevic S. Quantitative analysis of the flavonoids in raw propolis from northern Croatia. Acta Pharm. 2004; 54: 65–72.
   Google Scholar
• Salatino A, Fernandes-Silva CC, Righi AA, Salatino ML. Propolis research and the chemistry of plant products. Nat Prod Rep. 2011; 28: 925–36.
   Google Scholar
• Alencar SM, Oldoni TL, Castro ML, Cabral IS, Costa-Neto CM, Cury JA, etal. Chemical composition and biological activity of a new type of Brazilian propolis: red propolis. J Ethnopharmacol. 2007; 113: 278–83.
   Google Scholar
• Campo Fernandez M, Cuesta-Rubio O, Rosado Perez A, Montes De Oca Porto R, Marquez Hernandez I, Piccinelli AL, etal. GC-MS determination of isoflavonoids in seven red Cuban propolis samples. J Agric Food Chem. 2008; 56: 9927–32.
   Google Scholar
• Li Y, Chen M, Xuan H, Hu F. Effects of encapsulated propolis on blood glycemic control, lipid metabolism, and insulin resistance in type 2 diabetes mellitus rats. Evid Based Complement Alternat Med. 2012; 2012: 981896.
   Google Scholar
• Zhu W, Li YH, Chen ML, Hu FL. Protective effects of Chinese and Brazilian propolis treatment against hepatorenal lesion in diabetic rats. Hum Exp Toxicol. 2011; 30: 1246–55.
   Google Scholar
• Hu F, Hepburn HR, Li Y, Chen M, Radloff SE, Daya S. Effects of ethanol and water extracts of propolis (bee glue) on acute inflammatory animal models. J Ethnopharmacol. 2005; 100: 276–83.
   Google Scholar
• Ahn MR, Kunimasa K, Ohta T, Kumazawa S, Kamihira M, Kaji K, etal. Suppression of tumor-induced angiogenesis by Brazilian propolis: major component artepillin C inhibits in vitro tube formation and endothelial cell proliferation. Cancer Lett. 2007; 252: 235–43.
   Google Scholar
• Altug ME, Serarslan Y, Bal R, Kontas T, Ekici F, Melek IM, etal. Caffeic acid phenethyl ester protects rabbit brains against permanent focal ischemia by antioxidant action: a biochemical and planimetric study. Brain Res. 2008; 1201: 135–42.
   Google Scholar
• Drago L, De Vecchi E, Nicola L, Gismondo MR. In vitro antimicrobial activity of a novel propolis formulation (actichelated propolis). J Appl Microbiol. 2007; 103: 1914–21.
   Google Scholar
• Shimizu T, Hino A, Tsutsumi A, Park YK, Watanabe W, Kurokawa M. Anti-influenza virus activity of propolis in vitro and its efficacy against influenza infection in mice. Antivir Chem Chemother. 2008; 19: 7–13.
   Google Scholar
• Silici S, Koc NA, Ayangil D, Cankaya S. Antifungal activities of propolis collected by different races of honeybees against yeasts isolated from patients with superficial mycoses. J Pharmacolog Sci. 2005; 99: 39–44.
   Web of Science ®Google Scholar
• Grunberger D, Banerjee R, Eisinger K, Oltz EM, Efros L, Caldwell M, etal. Preferential cytotoxicity on tumor cells by caffeic acid phenethyl ester isolated from propolis. Experientia. 1988; 44: 230–2.
   Google Scholar
• Su KY, Hsieh CY, Chen YW, Chuang CT, Chen CT, Chen YL. Taiwanese green propolis and propolin G protect the liver from the pathogenesis of fibrosis via eliminating TGF-beta-induced Smad2/3 phosphorylation. J Agric Food Chem. 2014; 62: 3192–3201.
   PubMed Web of Science ®Google Scholar
• Shi H, Yang H, Zhang X, Yu LL. Identification and quantification of phytochemical composition and anti-inflammatory and radical scavenging properties of methanolic extracts of Chinese propolis. J Agric Food Chem. 2012; 60: 12403–10.
   Google Scholar
• Sun LP, Chen AL, Hung HC, Chien YH, Huang JS, Huang CY, etal. Chrysin: a histone deacetylase 8 inhibitor with anticancer activity and a suitable candidate for the standardization of Chinese propolis. J Agric Food Chem. 2012; 60: 11748–58.
   Google Scholar
• Petrishchev NN, Vlasov TD. [Endothelium function in ischemia-reperfusion (a literature review)]. Ross Fiziol Zh Im I M Sechenova. 2000; 86: 148–63.
   Google Scholar
• Stephens FB, Constantin-Teodosiu D, Greenhaff PL. New insights concerning the role of carnitine in the regulation of fuel metabolism in skeletal muscle. J Physiol. 2007; 581: 431–44.
   Google Scholar
• Broughton BR, Reutens DC, Sobey CG. Apoptotic mechanisms after cerebral ischemia. Stroke. 2009; 40: e331–9.
   Google Scholar
• Delorenzo RJ, Sun DA, Deshpande LS. Cellular mechanisms underlying acquired epilepsy: the calcium hypothesis of the induction and maintainance of epilepsy. Pharmacol Ther. 2005; 105: 229–66.
   Google Scholar
• Schild L, Reiser G. Oxidative stress is involved in the permeabilization of the inner membrane of brain mitochondria exposed to hypoxia/reoxygenation and low micromolar Ca2+. FEBS J. 2005; 272: 3593–601.
   Google Scholar
• Sanderson TH, Reynolds CA, Kumar R, Przyklenk K, Huttemann M. Molecular mechanisms of ischemia-reperfusion injury in brain: pivotal role of the mitochondrial membrane potential in reactive oxygen species generation. Mol Neurobiol. 2013; 47: 9–23.
   Google Scholar