(5)--5_PM2.5与不良妊娠结局.pdf
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1、Contents lists available at ScienceDirectEcotoxicology and Environmental Safetyjournal homepage: of ambient PM2.5on adverse birth outcome and potential molecularmechanismZhou Li,Yuqing Tang,Xin Song,Lissy Lazar,Zhen Li,Jinshun ZhaoDepartment of Preventative Medicine,Zhejiang Key Laboratory of Pathop
2、hysiology,Medicine School of Ningbo University,818 Fenghua Road,Ningbo,Zhejiang Province315211,Peoples Republic of ChinaA R T I C L E I N F OKeywords:PM2.5(particulate matter 2.5m inaerodynamic diameter)Prenatal exposureAdverse birth outcomeOxidative stressMitochondrial DNAEndocrine disruptionA B S
3、T R A C TPM2.5(particulate matter 2.5 m in aerodynamic diameter)refers to atmospheric particulate matter(PM)withan aerodynamic diameter of equal and less than 2.5 m that tends to be suspended for long periods of time andtravel over long distances in both outdoor and indoor atmospheres.PM2.5,along wi
4、th the toxic compoundsattached on it,may cause a wide range of disorders.The fetus is considered to be highly susceptible to a varietyof toxicants including atmospheric pollutants such as PM2.5through prenatal exposure.To better understand therelationship between maternal exposure to PM2.5and advers
5、e birth outcomes for reproduction and fetus de-velopment,we studied the published data on this issue including case-control studies,cohort studies and meta-analyses studies,and summarized the basic impact of ambient particulate matter on adverse birth outcomes.Research evidence indicates that PM2.5h
6、as a potential to induce low birth weight(LBW),preterm birth(PTB),and stillbirth.A further in-depth analysis shows that oxidative stress,DNA methylation,mitochondrial DNA(mtDNA)content alteration,and endocrine disruptions may all play an important role in PM2.5induced adverseeffects to pregnant wome
7、n and fetuses.In addition,PM2.5exposure can cause male reproductive toxicity,leadingto associated adverse pregnancy outcomes.1.IntroductionPM2.5refers to a heterogeneous mixture of substances,anthro-pogenic and naturally derived,that can include accumulated heavymetals and toxic organic pollutants,s
8、uch as polycyclic aromatic hy-drocarbons(PAHs)(Pandey et al.,2013).The health effects of PM2.5vary greatly based on its source and components.Many studies havefound that the percentages of the PM2.5constituents such as EC,Ni,andPb may vary across regions.Additionally,indoor air pollution andsmoking
9、have been identified as the main sources of overall personalPM2.5exposure for those mothers living in affected households.TheWorld Health Organization(WHO)estimated that in 2013,87%of theglobal population lived in communities that exceeded WHOs air qualityguideline of a maximum mean ambient PM2.5of
10、10g/m3(Braueret al.,2015).A fraction of the particles inhaled can not only penetrateinto the lungs gas-exchange region but also further travel through therespiratory barrier and enter the circulatory system,thereby spreadingthroughout the entire body(Wang et al.,2013).Some PM2.5metalconstituents suc
11、h as Ni and Pb have been confirmed to be embry-onically toxic and teratogenic in various animal species,and they mightalso impact human intrauterine growth(Manzo et al.,2010).Currently,household PM2.5concentrations(specifically in the kitchen area)arethe parameters most often used for evaluating emi
12、ssions to indoor ex-posure,specifically the contributions from solid cook-fuels(Smith et al.,2014).The prenatal stage of life is a very sensitive period when anyhttps:/doi.org/10.1016/j.ecoenv.2018.10.109Received 30 August 2018;Received in revised form 26 October 2018;Accepted 30 October 2018Abbrevi
13、ations:PM2.5,particulate matter 2.5 m in aerodynamic diameter;PM,particulate matter;LBW,low birth weight;PTB,preterm birth;mtDNA,mi-tochondrial DNA;PAHs,polycyclic aromatic hydrocarbons;SGA,small for gestational age;DEP,diesel exhaust particles;GD,gestational day;OR,odds ratio;TLBW,term low birth we
14、ight;BMI,body mass index;IQR,interquartile range;LCC,low concentration cut-off;RRs,relative risk;ROS,reactive oxygen species;EPFRs,environmentally persistent free radicals;8-OHdG,8-hydroxy-2deoxyguanosine;OGG1,oxoguanine glycosylase 1;PROGRESS,Programming Research in Obesity,Growth,Environment and S
15、ocial Stressors;D-loop,displacement loop;MT-RNR1,mitochondrial RNR1;BER,base excision repair;NER,nucleotide excision repair;APEX1,AP endonuclease 1;ERCC14,Excision repair complementing factors 1 and 4;CLOCK,circadian locomotor output cycles kaput;NPAS2,neuronal PASdomain-containing protein 2;CRY12,c
16、rypto chrome circadian clock 1 or 2;PER13,period circadian clock 1,2 or 3;ENVIRONAGE,environmental influence onearly aging;EDCs,Endocrine-disrupting chemicals;POPs,Persistent organic pollutants;hCG,Human chorionic gonadotropin;3-HSD1,3-Hhydroxysteroid de-hydrogenase;SD,Sprague Dawley;LDH,lactate deh
17、ydrogenase;TUNEL,terminal dUTP nick-end labellingCorresponding authors.E-mail addresses:(Z.Li),(J.Zhao).Ecotoxicology and Environmental Safety 169(2019)2482540147-6513/2018 Published by Elsevier Inc.Texposure to harmful substances can adversely affect the developingfetus.Numerous studies have docume
18、nted associations between PM2.5exposure and harmful health effects including the exacerbation ofasthma(Evans et al.,2014),chronic obstructive pulmonary disease,lung cancer(Hamra et al.,2014)and cardiovascular diseases(Huttunenet al.,2012).Recent epidemiological investigations(Clemente et al.,2016a;S
19、aenen et al.,2016),covering large populations and includingboth case-control and cohort studies,have shown that PM2.5exposurecan also contribute to the incidence and development of adverse birthoutcomes,such as LBW,PTB,small for gestational age(SGA)births(Scheers and Nawrot,2011),low birth length(Ba
20、llester et al.,2010a)and head circumference(Ballester et al.,2010b),still birth(Yang et al.,2018),as well as diseases arising later in life such as pulmonary andcardiovascular disorders and even mortality(Bourdrel et al.,2017).Moreover,in animal studies,harmful effects were observed on fetalweight,e
21、arly embryonic development and the hatching process afterexposure to PM2.5and diesel exhaust particles(DEP)(Janurio et al.,2010).Another animal study demonstrated that a 24h/d exposure ofpregnant Balb/c mice to 27.5 g/m3PM2.5from the start of pregnancythrough gestational day(GD)resulted in decreased
22、 placental weight(Zhao et al.,2016).Additionally,one study(Dadvand et al.,2014)showed a strong association between exposure to particulate air pol-lutants and adverse birth outcomes during the third-trimester,but nosignificant correlation was found during the first and second trimesters.Another stud
23、y(Ballester et al.,2010b)found that exposure during thefirst trimester was most closely related to a decrease in birth weight andlength.A further study(Lee et al.,2013)found that exposure to par-ticulate matter(mainly PM2.5)and ozone air pollutants during the firsttrimester were associated with an i
24、ncreased risk of developing pre-eclampsia,gestational hypertension,and preterm delivery.These re-sults indicate that particulate matter exposure during any stage ofpregnancy may lead to adverse birth outcomes.Entry of PM2.5into pregnant womens bodies may lead to oxidativeinflammation,mitochondrial a
25、nd nuclear DNA methylation and endo-crine disruption in the placenta,thereby increasing the potential foradverse reproductive outcomes.The placenta plays a unique role in thetransfer of gases,nutrients,and waste between the mother and devel-oping child.However,the placenta has a limited capability t
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