This work is licensed under the Creative Commons Attribution 4.0 International License.
Stansfeld SA, Matheson MP. Noise pollution: non-auditory effects on health. Br Med Bull 2003;68:243–57. doi: 10.1093/bmb/ldg033StansfeldSAMathesonMPNoise pollution: non-auditory effects on health2003682435710.1093/bmb/ldg033Open DOISearch in Google Scholar
Babisch W. Stress hormones in the research on cardiovascular effects of noise. Noise Health 2003;5:1–11. PMID: 12631430BabischWStress hormones in the research on cardiovascular effects of noise20035111PMID: 12631430Search in Google Scholar
Ahmed SM, Abdelrahman SA, Hassan EZ. Effect of low frequency noise on fundic mucosa of adult male albino rats and the role of vitamin E supplementation (histological and immunohistochemical study). J Clin Exp Pathol 2015;5:1000256. doi: 10.4172/21610681.1000256AhmedSMAbdelrahmanSAHassanEZEffect of low frequency noise on fundic mucosa of adult male albino rats and the role of vitamin E supplementation (histological and immunohistochemical study)20155100025610.4172/21610681.1000256Open DOISearch in Google Scholar
Fonseca J, Martins-dos-Santos J, Oliveira P, Laranjeira N, Aguas A, Castelo-Branco N. Noise-induced gastric lesions: a light and electron microscopy study of the rat gastric wall exposed to low frequency noise. Arq Gastroenterol 2012;49:82–8. doi: 10.1590/s0004-28032012000100014FonsecaJMartins-dos-SantosJOliveiraPLaranjeiraNAguasACastelo-BrancoNNoise-induced gastric lesions: a light and electron microscopy study of the rat gastric wall exposed to low frequency noise20124982810.1590/s0004-28032012000100014Open DOISearch in Google Scholar
Cui B, Gai Z, She X, Wang R, Xi Z. Effects of chronic noise on glucose metabolism and gut microbiota–host inflammatory homeostasis in rats. Sci Rep 2016;6:36693. doi: 10.1038/srep36693CuiBGaiZSheXWangRXiZEffects of chronic noise on glucose metabolism and gut microbiota–host inflammatory homeostasis in rats201663669310.1038/srep36693Open DOISearch in Google Scholar
Pascuan CG, Uran SL, Gonzalez-Murano MR, Wald MR, Guelman LR, Genaro AM. Immune alterations induced by chronic noise exposure: comparison with restraint stress in BALB/c and C57Bl/6 mice . J I m mun o to x i co l 2 0 1 4 ; 1 1 : 7 8 – 8 3 . do i : 10.3109/1547691X.2013.800171PascuanCGUranSLGonzalez-MuranoMRWaldMRGuelmanLRGenaroAMImmune alterations induced by chronic noise exposure: comparison with restraint stress in BALB/c and C57Bl/6 mice10.3109/1547691X.2013.80017110.3109/1547691X.2013.800171Search in Google Scholar
Zheng KC, Ariizumi M. Modulations of immune functions and oxidative status induced by noise stress. J Occup Health 2007;49:32–8. doi: 10.1539/joh.49.32ZhengKCAriizumiMModulations of immune functions and oxidative status induced by noise stress20074932–810.1539/joh.49.32Open DOISearch in Google Scholar
Barbaresco GQ, Reis AV, Lopes GD, Boaventura LP, Castro AF, Vilanova TC, Da Cunha Junior EC, Pires KC, Pôrto Filho R, Pereira BB. Effects of environmental noise pollution on perceived stress and cortisol levels in street vendors. J Toxicol Environ Health A 2019;82:331–7. doi: 10.1080/15287394.2019.1595239BarbarescoGQReisAVLopesGDBoaventuraLPCastroAFVilanovaTCDaCunha Junior ECPiresKCPôrtoFilho RPereiraBBEffects of environmental noise pollution on perceived stress and cortisol levels in street vendors201982331710.1080/15287394.2019.1595239Open DOISearch in Google Scholar
Rabat A, Bouyer JJ, George O, Le Moal M, Mayo W. Chronic exposure of rats to noise: relationship between long-term memory deficits and slow wave sleep disturbances. Behav Brain Res 2006;171:303–12. doi: 10.1016/j.bbr.2006.04.007RabatABouyerJJGeorgeOLeMoal MMayoWChronic exposure of rats to noise: relationship between long-term memory deficits and slow wave sleep disturbances20061713031210.1016/j.bbr.2006.04.007Open DOISearch in Google Scholar
Koh SM, Dixon JB. Preparation and application of organo-minerals as sorbents of phenol, benzene and toluene. Appl Clay Sci 2001;18:111–22. doi: 10.1016/S0169-1317(00)00040-5KohSMDixonJBPreparation and application of organo-minerals as sorbents of phenol, benzene and toluene2001181112210.1016/S0169-1317(00)00040-5Open DOISearch in Google Scholar
Auvinen J, Wirtanen L. The influence of photocatalytic interior paints on indoor air quality. Atmos Environ 2008;42:4101–12. doi: 10.1016/j. atmosenv.2008.01.031AuvinenJWirtanenLThe influence of photocatalytic interior paints on indoor air quality20084241011210.1016/j.atmosenv.2008.01.031Open DOISearch in Google Scholar
Barzegar A, Mortazavi B, Asilian H, Kazemian H. Catalytic degradation of toluene by manganese oxide catalyst loaded on a natural zeolite support. Sci J Rev 2014;3:345–52.BarzegarAMortazaviBAsilianHKazemianHCatalytic degradation of toluene by manganese oxide catalyst loaded on a natural zeolite support2014334552Search in Google Scholar
Shangol AB, Mortazavi SB, Asilian H, Kazemian H. Elimination of toluene vapours using natural zeolite treated by copper oxide. J Kermanshah Univ Med Sci 2013;17(7):e74461.ShangolABMortazaviSBAsilianHKazemianHElimination of toluene vapours using natural zeolite treated by copper oxide2013177e74461Search in Google Scholar
Joshi DR, Adhikari N. An overview on common organic solvents and their toxicity. J Pharm Res Int 2019;28:1–18. doi: 10.9734/JPRI/2019/ v28i330203JoshiDRAdhikariNAn overview on common organic solvents and their toxicity20192811810.9734/JPRI/2019/v28i330203Open DOISearch in Google Scholar
Kodavanti PR, Royland JE, Moore-Smith DA, Besas J, Richards JE, Beasley TE, Evansky P, Bushnell PJ. Acute and subchronic toxicity of inhaled toluene in male Long–Evans rats: oxidative stress markers in brain. Neurotoxicology 2015;51:10–19. doi: 10.1016/j. neuro.2015.09.001KodavantiPRRoylandJEMoore-SmithDABesasJRichardsJEBeasleyTEEvanskyPBushnellPJAcute and subchronic toxicity of inhaled toluene in male Long–Evans rats: oxidative stress markers in brain201551101910.1016/j.neuro.2015.09.00126343380Open DOISearch in Google Scholar
Win-Shwe TT, Fujimaki H. Neurotoxicity of toluene. Toxicol Lett 2010;198:93–9. doi: 10.1016/j.toxlet.2010.06.022Win-ShweTTFujimakiHNeurotoxicity of toluene201019893910.1016/j.toxlet.2010.06.02220599484Open DOISearch in Google Scholar
Bowen SE, Hannigan JH. Developmental toxicity of prenatal exposure to toluene. AAPS J 2006;8:E419–24. doi: 10.1007/BF02854915BowenSEHanniganJHDevelopmental toxicity of prenatal exposure to toluene20068E4192410.1007/BF02854915323156016808045Open DOISearch in Google Scholar
Taş U, Ekici F, Koç F, Söğüt E, Ayan M, Kuloglu T, Arici A, Özyurt B. Acute cardiotoxic effects of high dose toluene: an experimental study. Anadolu Kardiyol Derg 2013;13:3–8. doi: 10.5152/akd.2013.001TaşUEkiciFKoçFSöğütEAyanMKulogluTAriciAÖzyurtBAcute cardiotoxic effects of high dose toluene: an experimental study2013133810.5152/akd.2013.00123070630Open DOISearch in Google Scholar
Kanter M. Thymoquinone attenuates lung injury induced by chronic toluene exposure in rats. Toxicol Ind Health 2011;27:387–95. doi: 10.1177/0748233710387630KanterMThymoquinone attenuates lung injury induced by chronic toluene exposure in rats2011273879510.1177/074823371038763021088054Open DOISearch in Google Scholar
Abouee-Mehrizi A, Rasoulzadeh Y, Mehdipour A, Alihemmati A, Rahimi E. Hepatotoxic effects caused by simultaneous exposure to noise and toluene in New Zealand white rabbits: a biochemical and histopathological study. Ecotoxicology 2021;30:154–63. doi: 10.1007/ s10646-020-02288-zAbouee-MehriziARasoulzadehYMehdipourAAlihemmatiARahimiEHepatotoxic effects caused by simultaneous exposure to noise and toluene in New Zealand white rabbits: a biochemical and histopathological study2021301546310.1007/s10646-020-02288-z33083967Open DOISearch in Google Scholar
Gupta RC, editor. Veterinary Toxicology: Basic and Clinical Principles. 2nd ed. Cambridge (MA): Academic Press, 2012.GuptaRCCambridge (MA)Academic Press2012Search in Google Scholar
Cobo P, Murillo-Cuesta S, Cediel R, Moreno A, Lorenzo-García P, Varela-Nieto I. Design of a reverberant chamber for noise exposure experiments with small animals. Appl Acoust 2009;70:1034–40. doi: 10.1016/j.apacoust.2009.03.005CoboPMurillo-CuestaSCedielRMorenoALorenzo-GarcíaPVarela-NietoIDesign of a reverberant chamber for noise exposure experiments with small animals20097010344010.1016/j.apacoust.2009.03.005Open DOISearch in Google Scholar
Moreno A, Ruiz J, de la Colina C. Re-visiting Bolt’s criterion for homogeneous distribution of normal frequencies in rectangular enclosures. In: Comunicacion presentada en los siguientes congresos: II Congreso Iberoamericano de Acustica. XXXI Congreso Nacional de Acustica – TecniAcustica 2000. II Jornadas Iberoamericanas de Ultrasonidos. II Congreso Iberico de Acustica. EAA Symposium on Architectural Acoustics. Madrid, 2000. p. 1–6.MorenoARuizJdela Colina CRe-visiting Bolt’s criterion for homogeneous distribution of normal frequencies in rectangular enclosuresMadrid20001–6Search in Google Scholar
Win-Shwe TT, Kunugita N, Nakajima D, Yoshida Y, Fujimaki H. Developmental stage-specific changes in immunological biomarkers in male C3H/HeN mice after early life toluene exposure. Toxicol Lett 2012;208:133–41. doi: 10.1016/j.toxlet.2011.10.015Win-ShweTTKunugitaNNakajimaDYoshidaYFujimakiHDevelopmental stage-specific changes in immunological biomarkers in male C3H/HeN mice after early life toluene exposure20122081334110.1016/j.toxlet.2011.10.01522057034Open DOISearch in Google Scholar
Fujimaki H, Yamamoto S, Hojo R, Sato F, Kunugita N, Arashidani K. Effect of long-term exposure to low-level toluene on airway inflammatory response in mice. Toxicol Lett 2007;168:132–9. doi: 10.1016/j.toxlet.2006.11.008FujimakiHYamamotoSHojoRSatoFKunugitaNArashidaniKEffect of long-term exposure to low-level toluene on airway inflammatory response in mice2007168132910.1016/j.toxlet.2006.11.00817174043Open DOISearch in Google Scholar
Loganathan S, Srinivasan S, Wankhar W, Chodhary AK, Rathinasamy S. Noise exposure effect on selective inflammatory markers of Wistar albino rats immune organs and role of Scoparia dulcis. J Biol Active Products Nat 2017;7:294–310. doi: 10.1080/22311866.2017.1334587LoganathanSSrinivasanSWankharWChodharyAKRathinasamySNoise exposure effect on selective inflammatory markers of Wistar albino rats immune organs and role of Scoparia dulcis2017729431010.1080/22311866.2017.1334587Open DOISearch in Google Scholar
Hou N, Zhang X, Zhao L, Zhao X, Li Z, Song T, Huang C. A novel chronic stress-induced shift in the Th1 to Th2 response promotes colon cancer growth. Biochem Biophys Res Commun 2013;439:471–6. doi: 10.1016/j.bbrc.2013.08.101HouNZhangXZhaoLZhaoXLiZSongTHuangCA novel chronic stress-induced shift in the Th1 to Th2 response promotes colon cancer growth2013439471–610.1016/j.bbrc.2013.08.10124036270Open DOISearch in Google Scholar
Sundareswaran L, Srinivasan S, Wankhar W, Sheeladevi R. Effect of Scoparia dulcis on noise stress induced adaptive immunity and cytokine response in immunized Wistar rats. J Ayurveda Integr Med 2017;8:13–9. doi: 10.1016/j.jaim.2016.10.004SundareswaranLSrinivasanSWankharWSheeladeviREffect of Scoparia dulcis on noise stress induced adaptive immunity and cytokine response in immunized Wistar rats2017813–910.1016/j.jaim.2016.10.004537748728161157Open DOISearch in Google Scholar
Kim A, Sung JH, Bang JH, Cho SW, Lee J, Sim CS. Effects of self-reported sensitivity and road-traffic noise levels on the immune system. PLoS One 2017;12:e0187084. doi: 10.1371/journal.pone.0187084KimASungJHBangJHChoSWLeeJSimCSEffects of self-reported sensitivity and road-traffic noise levels on the immune system201712e018708410.1371/journal.pone.0187084566221329084230Open DOISearch in Google Scholar
Piggott JJ, Townsend CR, Matthaei CD. Reconceptualizing synergism and antagonism among multiple stressors. Ecol Evol 2015;5:1538–47. doi: 10.1002/ece3.1465PiggottJJTownsendCRMatthaeiCDReconceptualizing synergism and antagonism among multiple stressors2015515384710.1002/ece3.1465439518225897392Open DOISearch in Google Scholar
Demır M, Cicek M, Eser N, Yoldaş A, Sısman T. Effects of acute toluene toxicity on different regions of rabbit brain. Anal Cell Pathol 2017;2805370. doi: 10.1155/2017/2805370DemırMCicekMEserNYoldaşASısmanTEffects of acute toluene toxicity on different regions of rabbit brain2017280537010.1155/2017/2805370538521328458992Open DOISearch in Google Scholar
Tas U, Ogeturk M, Meydan S, Kus I, Kuloglu T, Ilhan N, Kose E, Sarsilmaz M. Hepatotoxic activity of toluene inhalation and protective role of melatonin. Toxicol Ind Health 2011;27:465–73. doi: 10.1177/0748233710389853TasUOgeturkMMeydanSKusIKulogluTIlhanNKoseESarsilmazMHepatotoxic activity of toluene inhalation and protective role of melatonin2011274657310.1177/074823371038985321343225Open DOISearch in Google Scholar
Frenzilli G, Ryskalin L, Ferrucci M, Cantafora E, Chelazzi S, Giorgi FS, Lenzi P, Scarcelli V, Frati A, Biagioni F, Gambardella S, Fallen A, Fornai F. Loud noise exposure produces DNA, neurotransmitter and morphological damage within specific brain areas. Front Neurosci 2017;11:49. doi: 10.3389/fnana.2017.00049FrenzilliGRyskalinLFerrucciMCantaforaEChelazziSGiorgiFSLenziPScarcelliVFratiABiagioniFGambardellaSFallenAFornaiFLoud noise exposure produces DNA, neurotransmitter and morphological damage within specific brain areas2017114910.3389/fnana.2017.00049548344828694773Open DOISearch in Google Scholar
Gröschel M, Basta D, Ernst A, Mazurek B, Szczepek AJ. Acute noise exposure is associated with intrinsic apoptosis in murine central auditory pathway. Front Neurosci 2018;12:312. doi: 10.3389/fnins.2018.00312GröschelMBastaDErnstAMazurekBSzczepekAJAcute noise exposure is associated with intrinsic apoptosis in murine central auditory pathway20181231210.3389/fnins.2018.00312595410329867323Open DOISearch in Google Scholar
Abu-Amara TM, Abdelhay WM, Elsharawy AF, Mohamed LS, Mourad SE, Abdelghany AH, Taha NM. Effect of crowding stress on lung and heart of the adult albino rats and the possible protective role of sulpiride. Egypt J Hosp Med 2014;57:580–97. doi: 10.12816/008490Abu-AmaraTMAbdelhayWMElsharawyAFMohamedLSMouradSEAbdelghanyAHTahaNMEffect of crowding stress on lung and heart of the adult albino rats and the possible protective role of sulpiride2014575809710.12816/008490Open DOISearch in Google Scholar
Gannouni N, Mhamdi A, El May M, Tebourbi O, Rhouma KB. Morphological changes of adrenal gland and heart tissue after varying duration of noise exposure in adult rat. Noise Health 2014;16:416–21. doi: 10.4103/1463-1741.144424GannouniNMhamdiAElMay MTebourbiORhoumaKBMorphological changes of adrenal gland and heart tissue after varying duration of noise exposure in adult rat2014164162110.4103/1463-1741.14442425387538Open DOISearch in Google Scholar
Xue L, Zhang D, Wang T, Shou X. Effects of high frequency noise on female rat’s multi-organ histology. Noise Health 2014;16:213–7. doi: 10.4103/1463-1741.137048XueLZhangDWangTShouXEffects of high frequency noise on female rat’s multi-organ histology201416213710.4103/1463-1741.13704825033787Open DOISearch in Google Scholar
Assunta C, Ilaria S, Gianfranco T, Teodorico C, Carmina S, Anastasia S, Roberto G, Francesco T, Valeria RM. Noise and cardiovascular effects in workers of the sanitary fixtures industry. Int J Hyg Environ Health 2015;218:163–8. doi: 10.1016/j.ijheh.2014.09.007AssuntaCIlariaSGianfrancoTTeodoricoCCarminaSAnastasiaSRobertoGFrancescoTValeriaRMNoise and cardiovascular effects in workers of the sanitary fixtures industry2015218163810.1016/j.ijheh.2014.09.00725455423Open DOISearch in Google Scholar
Zymantiene J, Zelvyte R, Pampariene I, Aniuliene A, Juodziukyniene N, Kantautaite J, Oberauskas V. Effects of long-term construction noise on health of adult female Wistar rats. Pol J Vet Sci 2017;20:155–65. doi: 10.1515/pjvs-2017-0020ZymantieneJZelvyteRPamparieneIAniulieneAJuodziukynieneNKantautaiteJOberauskasVEffects of long-term construction noise on health of adult female Wistar rats201720155–6510.1515/pjvs-2017-002028525342Open DOISearch in Google Scholar
Da Fonseca J, Dos Santos JM, Branco NC, Alves-Pereira M, Grande N, Oliveira P, Martins AP. Noise-induced gastric lesions: a light and scanning electron microscopy study of the alterations of the rat gastric mucosa induced by low frequency noise. Cent Eur J Public Health 2006;14:35–8. doi: 10.21101/cejph.a3362DaFonseca JDosSantos JMBrancoNCAlves-PereiraMGrandeNOliveiraPMartinsAPNoise-induced gastric lesions: a light and scanning electron microscopy study of the alterations of the rat gastric mucosa induced by low frequency noise20061435810.21101/cejph.a336216705880Open DOISearch in Google Scholar
Naeimi N, Adeli HR, Zare K. Study of toluene effect on blood parameters and spleen tissue in NMRI albino male mice. JNKUMS 2017;8:481–95. doi: 10.18869/acadpub.jnkums.8.3.481NaeimiNAdeliHRZareKStudy of toluene effect on blood parameters and spleen tissue in NMRI albino male mice201784819510.18869/acadpub.jnkums.8.3.481Open DOISearch in Google Scholar
Voloshin VN, Koveshnikov VG, Voloshina IS. Morphology of the spleen in adult albino rats after whole-body exposure to low-level of toluene. Int J Anat Res 2014;2:421–30.VoloshinVNKoveshnikovVGVoloshinaISMorphology of the spleen in adult albino rats after whole-body exposure to low-level of toluene2014242130Search in Google Scholar
Farzadinia P, Bigdeli M, Akbarzadeh S, Mohammadi M, Daneshi A, Bargahi A. Effect of noise pollution on testicular tissue and hormonal assessment in rat. Andrologia 2016;48:957–61. doi: 10.1111/and.12524FarzadiniaPBigdeliMAkbarzadehSMohammadiMDaneshiABargahiAEffect of noise pollution on testicular tissue and hormonal assessment in rat2016489576110.1111/and.1252426762793Open DOISearch in Google Scholar
Kaiser K, Devito J, Jones CG, Marentes A, Perez R, Umeh L, Weickum RM, McGovern KE, Wilson EH, Saltzman W. Effects of anthropogenic noise on endocrine and reproductive function in White’s treefrog, Litoria caerulea. Conserv Physiol 2015;3(1):cou061. doi: 10.1093/conphys/cou061KaiserKDevitoJJonesCGMarentesAPerezRUmehLWeickumRMMcGovernKEWilsonEHSaltzmanWEffects of anthropogenic noise on endocrine and reproductive function in White’s treefrog, Litoria caerulea201531cou06110.1093/conphys/cou061477848627293682Open DOISearch in Google Scholar
Münzel T, Daiber A, Steven S, Tran LP, Ullmann E, Kossmann S, Schmidt FP, Oelze M, Xia N, Li H, Pinto A, Wild P, Pies K, Schmidt ER, Rapp S, Kröller-Schön S. Effects of noise on vascular function, oxidative stress, and inflammation: mechanistic insight from studies in mice. Eur Heart J 2017;38:2838–49. doi: 10.1093/eurheartj/ehx081MünzelTDaiberAStevenSTranLPUllmannEKossmannSSchmidtFPOelzeMXiaNLiHPintoAWildPPiesKSchmidtERRappSKröller-SchönSEffects of noise on vascular function, oxidative stress, and inflammation: mechanistic insight from studies in mice20173828384910.1093/eurheartj/ehx081583745928329261Open DOISearch in Google Scholar
Espinoza MB, Aedo JE, Zuloaga R, Valenzuela C, Molina A, Valdés JA. Cortisol induces reactive oxygen species through a membrane glucocorticoid receptor in rainbow trout myotubes. J Cell Biochem 2017;118:718–25. doi: 10.1002/jcb.25676EspinozaMBAedoJEZuloagaRValenzuelaCMolinaAValdésJACortisol induces reactive oxygen species through a membrane glucocorticoid receptor in rainbow trout myotubes20171187182510.1002/jcb.2567627564718Open DOISearch in Google Scholar
Flaherty RL, Owen M, Fagan-Murphy A, Intabli H, Healy D, Patel A, Allen MC, Patel BA, Flint MS. Glucocorticoids induce production of reactive oxygen species/reactive nitrogen species and DNA damage through an iNOS mediated pathway in breast cancer. Breast Cancer Res 2017;19:35. doi: 10.1186/s13058-017-0823-8FlahertyRLOwenMFagan-MurphyAIntabliHHealyDPatelAAllenMCPatelBAFlintMSGlucocorticoids induce production of reactive oxygen species/reactive nitrogen species and DNA damage through an iNOS mediated pathway in breast cancer2017193510.1186/s13058-017-0823-8536611428340615Open DOISearch in Google Scholar
Redza-Dutordoir M, Averill-Bates DA. Activation of apoptosis signalling pathways by reactive oxygen species. Biochim Biophys Acta 2016;1863:2977–92. doi: 10.1016/j.bbamcr.2016.09.012Redza-DutordoirMAverill-BatesDAActivation of apoptosis signalling pathways by reactive oxygen species2016186329779210.1016/j.bbamcr.2016.09.01227646922Open DOISearch in Google Scholar
Ko EY, Cho SH, Kwon SH, Eom CY, Jeong MS, Lee W, Kim SY, Heo SJ, Ahn G, Lee KP, Jeon YJ, Kim KN. The roles of NF-κB and ROS in regulation of pro-inflammatory mediators of inflammation induction in LPS-stimulated zebrafish embryos. Fish Shellfish Immunol 2017;68:525–9. doi: 10.1016/j.fsi.2017.07.041KoEYChoSHKwonSHEomCYJeongMSLeeWKimSYHeoSJAhnGLeeKPJeonYJKimKNThe roles of NF-κB and ROS in regulation of pro-inflammatory mediators of inflammation induction in LPS-stimulated zebrafish embryos201768525910.1016/j.fsi.2017.07.04128743626Open DOISearch in Google Scholar
Curtin NM, Mills KH, Connor TJ. Psychological stress increases expression of IL-10 and its homolog IL-19 via β-adrenoceptor activation: Reversal by the anxiolytic chlordiazepoxide. Brain Behav Immun 2009;23:371–9. doi: 10.1016/j.bbi.2008.12.010CurtinNMMillsKHConnorTJPsychological stress increases expression of IL-10 and its homolog IL-19 via β-adrenoceptor activation: Reversal by the anxiolytic chlordiazepoxide200923371910.1016/j.bbi.2008.12.01019159673Open DOISearch in Google Scholar
Téllez-Martínez D, Batista-Duharte A, Silva VP, Fuentes DP, Ferreira LS, Polesi MC, Costa CB, Carlos IZ. Adaptive stress response induced by toluene increases Sporothrix schenckii virulence and host immune response. bioRxiv 2019:539775. doi: 10.1101/539775Téllez-MartínezDBatista-DuharteASilvaVPFuentesDPFerreiraLSPolesiMCCostaCBCarlosIZAdaptive stress response induced by toluene increases Sporothrix schenckii virulence and host immune response201953977510.1101/539775Open DOISearch in Google Scholar
Kasten KR, Muenzer JT, Caldwell CC. Neutrophils are significant producers of IL-10 during sepsis. Biochem Biophys Res Commun 2010;393:28–31. doi: 10.1016/j.bbrc.2010.01.066KastenKRMuenzerJTCaldwellCCNeutrophils are significant producers of IL-10 during sepsis2010393283110.1016/j.bbrc.2010.01.066283035620097159Open DOISearch in Google Scholar
Said EA, Dupuy FP, Trautmann L, Zhang Y, Shi Y, El-Far M, Hill BJ, Noto A, Ancuta P, Peretz Y, Fonseca SG, Van Grevenynghe J, Boulassel MR, Bruneau J, Shoukry NH, Routy J-P, Douek DC, Haddad EK, Sekaly R-P. Programmed death-1–induced interleukin-10 production by monocytes impairs CD4+ T cell activation during HIV infection. Nat Med 2010;16:452–9. doi: 10.1038/nm.2106SaidEADupuyFPTrautmannLZhangYShiYEl-FarMHillBJNotoAAncutaPPeretzYFonsecaSGVanGrevenynghe JBoulasselMRBruneauJShoukryNHRoutyJ-PDouekDCHaddadEKSekalyR-PProgrammed death-1–induced interleukin-10 production by monocytes impairs CD4+ T cell activation during HIV infection201016452910.1038/nm.2106422913420208540Open DOISearch in Google Scholar