Biological effects of zinc oxide nanoparticles on inflammation
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With the rapid developments in nanotechnology, an increasing number of nanomaterials have been applied in various aspects of our lives. Recently, pharmaceutical nanotechnology with numerous advantages has growingly attracted the attention of many researchers. Zinc oxide nanoparticles (ZnO-NPs) are nanomaterials that are widely used in many fields including diagnostics, therapeutics, drug-delivery systems, electronics, cosmetics, sunscreens, coatings, ceramic products, paints, and food additives, due to their magnetic, catalytic, semiconducting, anti-cancer, anti-bacterial, anti-inflammatory, ultraviolet-protective, and binding properties. The present review focused on the recent research works concerning role of ZnO-NP on inflammation. Several studies have reported that ZnO-NP induces inflammatory reaction through the generation of reactive oxygen species by oxidative stress and production of inflammatory cytokines by activation of nuclear factor-κB (NF-B). Meanwhile, other researchers reported that ZnO-NP exhibits an anti-inflammatory effect by inhibiting the up-regulation of inflammatory cytokines and the activation of NF-κB, caspase-1, IκB kinaseβ, receptor interacting protein2, and extracellular signal-regulated kinase. Previous studies reported that size and shape of nanoparticles, surfactants used for nanoparticles protection, medium, and experimental conditions can also affect cellular signal pathway. This review indicated that the anti-inflammatory effectiveness of ZnO-NP was determined by the nanoparticle size as well as various experimental conditions. Therefore, the author suggests that pharmaceutical therapy with the ZnO-NP is one of the possible strategies to overcome the inflammatory reactions. However, further studies should be performed to maximize the anti-inflammatory effect of ZnO-NP to apply as a potential agent in biomedical applications.
Abstract
With the rapid developments in nanotechnology, an increasing number of nanomaterials have been applied in various aspects of our lives. Recently, pharmaceutical nanotechnology with numerous advantages has growingly attracted the attention of many researchers. Zinc oxide nanoparticles (ZnO-NPs) are nanomaterials that are widely used in many fields including diagnostics, therapeutics, drug-delivery systems, electronics, cosmetics, sunscreens, coatings, ceramic products, paints, and food additives, due to their magnetic, catalytic, semiconducting, anti-cancer, anti-bacterial, anti-inflammatory, ultraviolet-protective, and binding properties. The present review focused on the recent research works concerning role of ZnO-NP on inflammation. Several studies have reported that ZnO-NP induces inflammatory reaction through the generation of reactive oxygen species by oxidative stress and production of inflammatory cytokines by activation of nuclear factor-κB (NF-B). Meanwhile, other researchers reported that ZnO-NP exhibits an anti-inflammatory effect by inhibiting the up-regulation of inflammatory cytokines and the activation of NF-κB, caspase-1, IκB kinaseβ, receptor interacting protein2, and extracellular signal-regulated kinase. Previous studies reported that size and shape of nanoparticles, surfactants used for nanoparticles protection, medium, and experimental conditions can also affect cellular signal pathway. This review indicated that the anti-inflammatory effectiveness of ZnO-NP was determined by the nanoparticle size as well as various experimental conditions. Therefore, the author suggests that pharmaceutical therapy with the ZnO-NP is one of the possible strategies to overcome the inflammatory reactions. However, further studies should be performed to maximize the anti-inflammatory effect of ZnO-NP to apply as a potential agent in biomedical applications.
참고문헌 (53)
- Andoh T, "Substance P induction of itch-associated response mediated by cutaneous NK1 tachykinin receptors in mice", J Pharmacol Exp Ther, 286, pp.1140~1145 (1998)
- Babin K, "Nanoparticles enhance the ability of human neutrophils to exert phagocytosis by a Sykdependent mechanism", Biochim Biophys Acta, 1850, pp.2276~2282 (2015)
- Barton GM, "A calculated response : control of inflammation by the innate immune system", J Clin Invest, 118, pp.413~420 (2008)
- Chang H, "Involvement of MyD88 in zinc oxide nanoparticle-induced lung inflammation", Exp Toxicol Pathol, 65, pp.887~896 (2013)
- Chiang HM, "Nanoscale ZnO induces cytotoxicity and DNA damage in human cell lines and rat primary neuronal cells", J Nanosci Nanotechnol, 12, pp.2126~2135 (2012)
- Contado C, "Nanomaterials in consumer products : a challenging analytical problem", Front Chem, 3, pp.48~ (2015)
- Dizaj SM, "Antimicrobial activity of the metals and metal oxide nanoparticles", Mater Sci Eng C Mater Biol Appl, 44, pp.278~284 (2014)
- Frederickson CJ, "Loss of zinc staining from hippocampal mossy fibers during kainic acid induced seizures : a histofluorescence study", Brain Res, 446, pp.383~386 (1988)
- Frederickson CJ, "The neurobiology of zinc in health and disease", Nat Rev Neurosci, 6, pp.449~462 (2005)
- Fukui H, "Ascorbic acid attenuates acute pulmonary oxidative stress and inflammation caused by zinc oxide nanoparticles", J Occup Health, 57, pp.118~125 (2015)
- Giovanni M, "Proinflammatory responses of RAW264.7 macrophages when treated with ultralow concentrations of silver, titanium dioxide, and zinc oxide nanoparticles", J Hazard Mater, 297, pp.146~152 (2015)
- Hackenberg S, "Cytotoxic, genotoxic and pro-inflammatory effects of zinc oxide nanoparticles in human nasal mucosa cells in vitro", Toxicol In Vitro, 25, pp.657~663 (2011)
- Harhaj EW, "Deubiquitinases in the regulation of NF-κB signaling", Cell Res, 21, pp.22~39 (2011)
- Higgs GA, "Eicosanoids in inflammation", Ann Clin Res, 16, pp.287~299 (1984)
- Horie M, "Pharyngeal aspiration of metal oxide nanoparticles showed potential of allergy aggravation effect to inhaled ovalbumin", Inhal Toxicol, 27, pp.181~190 (2015)
- Huang KL, "Zinc oxide nanoparticles induce eosinophilic airway inflammation in mice", J Hazard Mater, 297, pp.304~312 (2015)
- Ilves M, "Topically applied ZnO nanoparticles suppress allergen induced skin inflammation but induce vigorous IgE production in the atopic dermatitis mouse model", Part Fibre Toxicol, 11, pp.38~ (2014)
- Jansen J, "Zinc and diabetes--clinical links and molecular mechanisms", J Nutr Biochem, 20, pp.399~417 (2009)
- Jeong HJ, "Inhibition of TNF-alpha and IL-6production by Aucubin through blockade of NF-kappaB activation RBL-2H3 mast cells", Cytokine, 18, pp.252~259 (2002)
- Jeong SH, "ZnO nanoparticles induce TNF-α expression via ROS-ERK-Egr-1 pathway in human keratinocytes", J Dermatol Sci, 72, pp.263~273 (2013)
- Kim MH, "Zinc oxide nanoparticels demoted MDM2expression to suppress TSLP-induced mast cell proliferation", J Nanosci Nanotechnol, 16, pp.2492~2498 (2016)
- Kim MH, "Zinc Oxide Nanoparticles Suppress LPSInduced NF-κB Activation by Inducing A20, a Negative Regulator of NF-κB, in RAW 264.7 Macrophages", J Nanosci Nanotechnol, 15, pp.6509~6515 (2015)
- Kim MH, "Zinc oxide nanoparticles, a novel candidate for the treatment of allergic inflammatory diseases", Eur J Pharmacol, 738, pp.31~39 (2014)
- Kumar R, "The dynamics of acute inflammation", J Theor Biol, 230, pp.145~155 (2004)
- Kumar V, "Robbins Basic Pathology" (2003), Saunders
- Kwon DJ, "Suppression of iNOS and COX-2 expression by flavokawain A via blockade of NF-κB and AP-1 activation in RAW 264.7 macrophages", Food Chem Toxicol, 58, pp.479~486 (2013)
- Li CH, "Zinc oxide nanoparticles-induced intercellular adhesion molecule 1 expression requires Rac1", Cdc42, mixed lineage kinase 3, and c-Jun N-terminal kinase activation in endothelial cells, 2012, pp.126, 162~172
- Liu J, "The toxicology of ion-shedding zinc oxide nanoparticles", Crit Rev Toxicol, 46, pp.348~384 (2016)
- Majno G, "Cells, Tissues, and Disease" (2004), Oxford University Press
- Maremanda KP, "Zinc protects cyclophosphamide-induced testicular damage in rat : Involvement of metallothionein, tesmin and Nrf2", Biochem Biophys Res Commun, 445, pp.591~596 (2014)
- Medzhitov R, "Origin and physiological roles of inflammation", Nature, 454(24), pp.428~435 (2008)
- Nakanishi W, "Bioactive nanocarbon assemblies : Nanoarchitectonics and applications", Nano Today, 9, pp.378~394 (2014)
- Pati R, "Topical application of zinc oxide nanoparticles reduces bacterial skin infection in mice and exhibits antibacterial activity by inducing oxidative stress response and cell membrane disintegration in macrophages", Nanomedicine, 10, pp.1195~1208 (2014)
- Perkins ND, "Integrating cell-signalling pathways with NF-κB and IKK function", Nat Rev Mol Cell Biol, 8, pp.49~62 (2007)
- Roy R, "Zinc oxide nanoparticles provide an adjuvant effect to ovalbumin via a Th2 response in Balb", c mice, 2014, pp.26, 159~172
- Roy R, "Mechanism of uptake of ZnO nanoparticles and inflammatory responses in macrophages require PI3K mediated MAPKs signaling", Toxicol In Vitro, 28, pp.457~467 (2013)
- Roy R, "Mechanism of uptake of ZnO nanoparticles and inflammatory responses in macrophages require PI3K mediated MAPKs signaling", Toxicol In Vitro, 28, pp.457~467 (2014)
- Seabra AB, "Biogenic synthesis of nanostructured iron compounds : applications and perspectives", IET Nanobiotechnol, 7, pp.90~99 (2013)
- Senapati VA, "ZnO nanoparticles induced inflammatory response and genotoxicity in human blood cells : A mechanistic approach", Food Chem Toxicol, 85, pp.61~70 (2015)
- Shapiro SD, "Elastin degradation by mononuclear phagocytes", Ann N Y Acad Sci, 624, pp.69~80 (1991)
- Sharma V, "Induction of oxidative stress, DNA damage and apoptosis in mouse liver after sub-acute oral exposure to zinc oxide nanoparticles", Mutat Res, 745, pp.84~91 (2012)
- Shembade N, "Inhibition of NF-kappaB signaling by A20 through disruption of ubiquitin enzyme complexes", Science, 327, pp.1135~1139 (2010)
- Skjøt-Arkil H, "Macrophage-mediated proteolytic remodeling of the extracellular matrix in atherosclerosis results in neoepitopes : a potential new class of biochemical markers", Assay Drug Dev Technol, 8, pp.542~552 (2010)
- Song YH, "Socioeconomic impact traditional Korean medicine, Pyeongwee-San (KMP6) as an anti-allergic inflammatory drug", TANG, 2, pp.e29~ (2002)
- Spencer LA, "Human eosinophils constitutively express multiple Th1, Th2, and immunoregulatory cytokines that are secreted rapidly and differentially", J Leukoc Biol, 85, pp.117~123 (2009)
- Stoehr LC, "Assessment of a panel of interleukin-8reporter lung epithelial cell lines to monitor the proinflammatory response following zinc oxide nanoparticle exposure under different cell culture conditions", Part Fibre Toxicol, 12, pp.29~ (2015)
- Stone SF, "Immune response to snake envenoming and treatment with antivenom; complement activation, cytokine production and mast cell degranulation", PLoS Negl Trop Dis, 7, pp.e2326~ (2013)
- Taniguchi N, "Proceedings of the International Conference on Production Engineering, Tokyo, PartII" (1974), Japan Society of Precision Engineering
- Tornatore L, "The nuclear factor kappa B signaling pathway : integrating metabolism with inflammation", Trends Cell Biol, 22, pp.557~566 (2012)
- Tsou TC, "Zinc oxide particles induce inflammatory responses in vascular endothelial cells via NF-κB signaling", J Hazard Mater, 183, pp.182~188 (2010)
- Wahab R, "Formation of ZnO Micro-Flowers Prepared via Solution Process and their Antibacterial Activity", Nanoscale Res Lett, 5, pp.1675~1681 (2010)
- Wahab R, "ZnO nanoparticles induced oxidative stress and apoptosis in HepG2 and MCF-7cancer cell and their antibacterial activity", Colloids Surf B Biointerfaces, 117, pp.267~276 (2014)
- Whatmore RW, "Nanotechnology--what is it? Should we be worried?", Occupational Medicine, 56, pp.295~299 (2006)
