Systematic review and technological prospection: ethyl ferulate, a phenylpropanoid with antioxidant and neuroprotective actions

References

• Oliveira CMB, Sakata RK, Issy AM, et al. Citocinas e Dor. Rev Bras Anestesiol. 2011;61:255–265.
   PubMedGoogle Scholar
• Dinarello CA. Historical Review of Cytokines. Eur J Immunol. 2007;37:S34–S5.
   PubMed Web of Science ®Google Scholar
• Vogt T. Phenylpropanoid Biosynthesis. Mol Plant. 2010;03:2–18.
   Google Scholar
• Sá RCS, Andrade LN, Oliveira RRB, et al. A review on anti-inflammatory activity of phenylpropanoids found in essential oils. Mol. 2014;19:1459–1480.
   PubMed Web of Science ®Google Scholar
• Korkina LG. Phenylpropanoids as naturally occurring antioxidants: from plant defense to human health. Cel Mol Biol. 2007;53:15–25.
   Web of Science ®Google Scholar
• Zhang L, Al-Suwayeh SA, Hsiehc P, et al. A comparison of skin delivery of ferulic acid and its derivatives: evaluation of their efficacy and safety. Internat J Pharmaceut. 2010;399:44–47.
   PubMed Web of Science ®Google Scholar
• Nenadis N, Zhang H, Tsimidou MZ. Structure-antioxidant activity relationship of ferulic acid derivatives: effect of carbon side chain characteristic groups. J Agric Food Chem. 2003;51:1874–1875.
   PubMed Web of Science ®Google Scholar
• Sultana R. Ferulic acid ethyl ester as a potential therapy in neurodegenerative disorders. Biochim Biophy Acta. 2012;1822:748–752.
   PubMed Web of Science ®Google Scholar
• Islam S, Yoshida H, Matsuki N, et al. Antioxidant, free radical–scavenging, and NF-κB–inhibitory activities of phytosteryl ferulates: structure–activity studies. J Pharmacol Sci. 2009;111:328–329.
   PubMed Web of Science ®Google Scholar
• Bolling BW, Ji LL, Lee C, et al. Dietary supplementation of ferulic acid and ferulic acid ethyl ester induces quinone reductase and glutathione-S-transferase in rats. Food Chem. 2011;124:1–6.
   Web of Science ®Google Scholar
• Calabrese V, Calafato S, Puleo E, et al. Redox regulation of cellular stress response by ferulic acid ethyl ester in human dermal fibroblasts: role of vitagenes. Clin Dermatol. 2008;26:358–363.
   PubMed Web of Science ®Google Scholar
• Abdul HM, Butterfield DA. Protection against amyloid beta-peptide (1–42)-induced loss of phospholipid asymmetry in synaptosomal membranes by tricyclodecan-9-xanthogenate (D609) and ferulic acid ethyl ester: implications for Alzheimer’s disease. Biochim Biophy Acta. 2005;1741:140–148.
   PubMed Web of Science ®Google Scholar
• Perluigi M, Joshi G, Sultana R, et al. In vivo protective effects of ferulic acid ethyl ester against amyloid-beta peptide 1–42-induced oxidative stress. J Neurosci Res. 2006;84:418–426.
   PubMed Web of Science ®Google Scholar
• Nazaré AC, Faria CMQG, Chiari BG, et al. Ethyl ferulate, a component with anti-inflammatory properties for emulsion-based creams. Mol. 2014;19:8124–8139.
   PubMed Web of Science ®Google Scholar
• Cunha FVM, Gomes BS, Sousa Neto B, et al. Ferulic acid ethyl ester diminished Complete Freund’s Adjuvant-induced incapacitation through antioxidant and anti-inflammatory activity. Naunyn-Schmiedeberg’s Arch Pharmacol. 2016;389:117–130.
   Google Scholar
• Scapagnini G, Butterfield A, Colombrita C, et al. Ethyl ferulate, a lipophilic polyphenol, induces HO-1 and protects rat neurons against oxidative stress. Antioxid Redox Signal. 2004;6:811–817.
   PubMed Web of Science ®Google Scholar
• Sultana R, Ravagna A, Mohmmad-Abdul H, et al. Ferulic acid ethyl ester protects neurons against amyloid β-peptide(1–42)-induced oxidative stress and neurotoxicity: relationship to antioxidant activity. J Neurochem. 2005;92:749–758.
   PubMed Web of Science ®Google Scholar
• Joshi G, Perluigi M, Sultana R, et al. In vivo protection of synaptosomes by ferulic acid ethyl ester (FAEE) from oxidative stress mediated by 2,2-azobis(2-amidino-propane) dihydrochloride (AAPH) or Fe2+/H2O2: insight into mechanisms of neuroprotection and relevance to oxidative stress-related neurodegenerative disorders. Neurochem Int. 2006;48:318–319.
   PubMed Web of Science ®Google Scholar
• Feng Y, Yw LU, Ph XU, et al. Caffeic acid phenethyl ester and its related compounds limit the functional alterations of the isolated mouse brain and liver mitochondria submitted to in vitro anoxia–reoxygenation: relationship to their antioxidant activities. Biochim Biophy Acta. 2008;1780:659–672.
   PubMed Web of Science ®Google Scholar
• Garrido J, Gaspar A, Garrido M, et al. Alkyl esters of hydroxycinnamic acids with improved antioxidant activity. Biochim. 2012;94:961–966.
   PubMed Web of Science ®Google Scholar
• Kikuzaki H, Hisamoto M, Hirose K, et al. Antioxidant properties of ferulic acid and its related compounds. J Agric Food Chem. 2002;50:2161–2167.
   PubMed Web of Science ®Google Scholar
• Di Domenico F, Perluigi M, Foppoli C, et al. Protective effect of ferulic acid ethyl ester against oxidative stress mediated by UVB irradiation in human epidermal melanocytes. Free Radic Res. 2009;43:365–375.
   PubMed Web of Science ®Google Scholar
• Cloquenet B, Couteau C, Paparis E, et al. Interest of ferulic acid ethyl ester in photoprotective creams: measure of efficacy by in vitro method. Nat Prod Res. 2008;22:1467–1471.
   PubMed Web of Science ®Google Scholar
• Tsai YC, Lee YM, Hsu CH, et al. The effect of ferulic acid ethyl ester on leptin-induced proliferation and migration of aortic smooth muscle cells. Experiment Mol Med. 2015;47:1–9.
   Web of Science ®Google Scholar
• Gulçin I. Antioxidant activity of food constituents-an overview. Arch Toxicol. 2012;86:345–346.
   PubMed Web of Science ®Google Scholar
• Bursal E, Köksal E, Gülçin I, et al. Antioxidant activity and polyphenol content of cherry stem (Cerasus avium L.) determined by LC-MS/MS. Food Res Internat. 2013;51:66–68.
   Web of Science ®Google Scholar
• Nguyen T, Nioi P, Pickett CB. Oxidative stress signaling pathway and its activation by the Nrf2 - antioxidant response element. J Biol Chem. 2009;284:13291–13295.
   PubMed Web of Science ®Google Scholar
• Brigelius-Flohé R, Kipp AP. Physiological functions of GPx2 and its role in inflammation-triggered carcinogenesis. Annuals New York Academ Sci. 2012;1259:19–25.
   PubMed Web of Science ®Google Scholar
• Wojtunik-Kulesza KA, Oniszczuka A, Oniszczuk T, et al. The influence of common free radicals and antioxidants on development of Alzheimer’s disease. Biomed Pharmacoth. 2016;78:39–49.
   PubMed Web of Science ®Google Scholar
• Chen X, Guo C, Kong J. Oxidative stress in neurodegenerative diseases. Neural Regen Res. 2012;7:376–385.
   PubMed Web of Science ®Google Scholar
• Federico A, Cardaioli E, Da Pozzo P, et al. Mitochondria, oxidative stress and neurodegeneration. J Neurologic Sci. 2012;322:254–255.
   PubMed Web of Science ®Google Scholar
• Niedzielska E, Smaga I, Gawlik M, et al. Oxidative stress in neurodegenerative diseases. Mol Neurobiol. 2016;53:4094–4125.
   PubMed Web of Science ®Google Scholar
• Surh Y. NF-κB and Nrf2 as potential chemopreventive targets of some anti-inflammatory and antioxidative phytonutrients with anti-inflammatory and antioxidative activities. Asia Pacific J Clinic Nutrit. 2008;17:269–272.
   PubMed Web of Science ®Google Scholar
• Banerjee R. Redox outside the box: linking extracellular redox remodeling with intracellular redox metabolism. J Biol Chem. 2012;287:4397–4402.
   PubMed Web of Science ®Google Scholar
• Lugrin J, Rosenblatt-Velin N, Parapanov R, et al. The role of oxidative stress during inflammatory processes. Bio Chem. 2014;395:203–227.
   PubMed Web of Science ®Google Scholar
• Morgan MJ, Liu Z. Crosstalk of reactive oxygen species and NF-ҝB signaling. Cell Res. 2011;23:102–112.
   Google Scholar
• Li W, Khor TO, Xu C, et al. Activation of Nrf2-antioxidant signaling attenuates NF ҝB-inflammatory response and elicits apoptosis. Biochem Pharmacol. 2008;76:1485–1489.
   PubMed Web of Science ®Google Scholar
• Wardyn JD, Ponsford AH, Sanderson CM. Dissecting molecular cross-talk between Nrf2 and NF-ҝB response pathways. Biochem Soc Trans. 2015;43:621–625.
   PubMed Web of Science ®Google Scholar
• Fisch C, Block J, Sandner P. Chinese university patents: quantity, quality, and the role of subsidy programs. SSRN Working Paper; 2014.
   Google Scholar
• Qiu R, Wang J, Parkin KL. Isolation and identification of cytoprotective agents from nonpolar extracts of buckwheat flour. Food Res Internat. 2014;66:86–92.
   Web of Science ®Google Scholar
• Shahidi F, Chandrasekara A. Hydroxycinnamates and their in vitro and in vivo antioxidant activities. Phytochem Rev. 2010;9:147–170.
   Web of Science ®Google Scholar
• Fisch CO, Hassel TM, Sandner PG, et al. University patenting: a comparison of 300 leading universities worldwide. J Technol Transf. 2015;40:318–334.
   Web of Science ®Google Scholar