good gut益生菌?有没有好心人帮我翻译!谢谢谢谢!!!只是作为参考!!!

益生菌品牌 07-03 文章编号:-20040

今天给各位分享good gut益生菌的知识,其中也会对有没有好心人帮我翻译!谢谢谢谢!!!只是作为参考!!!进行解释,如果能碰巧解决你现在面临的问题,别忘了关注本站,现在开始吧!

有益健康的英语怎么说

有益健康的英语是Itishealthytolivearegularlife.

1、起居有恒,有益健康。Itishealthytolivearegularlife.

2、多食蔬果有益健康。Itisgoodforone’shealthtoeatplentyofvegetablesandfruits.

3、源于远非有益健康的物质的臭味。Odoursoffarlesssalubriousorigin.

4、那亲切的小酒馆和有益健康的饮食。Thefriendlypubandhalesomefare.

5、有益健康的蔬菜烹调法。Healthfulmethodsofcookingvegetables.

6、食物丰盛并且有益健康。Thefoodisplentifulandverywholesome.

7、有益健康的大西洋空气。ThesalutaryAtlanticair.

8、有益健康的均衡饮食。Ahealthybalanceddiet.

9、益生菌有利于让你的肠胃恢复有益健康的菌群。Probioticshelprepopulateyourgutwiththehealthybacteria.

10、有益健康的绿叶。Healthygreenfoliage.

学习英语的好处:

走出中国这个狭小的圈子,你会发现世界上还有很多让你感到新鲜惊奇的事物,很多美好的东西等待着你去挖掘。也许你会觉得我只是在说风谅话,可是这是千真万确的。只要会说英语,别人就不会把你当井底之蛙看。你也许觉得你现在用不到英文,可是以后呢?

以后用的到怎么办?你说要翻译人才,可是并不是所有人都雇用的起你所谓的翻译人才,如果在国外生活怎么办?如果想和外国朋友聊天怎么办?向这种问题你根本就请不到你所谓的翻译人才。而且很多人觉得学英语只是为了考证,我觉得很错误。

因为英语不仅仅为的是考证考学,学好了是为自己,要是敷衍了事,可惜的只是自己。

1、学习英语可以提高自己的语言技能,增加一项语言能力。

2、学习英语有利于和外国人交朋友,聊天或者一起工作。

3、学习英语有利于了解其他国家的习俗文化等。

4、学习英语有利于找工作,例如很多外企,英语都是必修需要。

5、学习英语有利于出国学习或者旅游,至少不会迷路或者手足无措。

6、学习英语有利于看外国的原著小说或者电视电影等。

有没有好心人帮我翻译!谢谢谢谢!!!只是作为参考!!!

Thestudyfoundthatinrecentyears,duetothewidespreaduseofantibioticstoanimalsnormalintestinalfloraimbalance,drugresiduesandresistancetoanimalandhumanhealthhazardsbroughtabout.Probioticspreparationisanaturalactivityofmicrobialagents,toxic,non-drug-resistant,noresidue,noside-effectscharacteristics.Researchshowsthatprobioticshaveaverygoodanimalhealthandtreatmentofanimaldiseasesrole.

Probioticpreparationscanbeasinglestrainpreparations,itisgoodpreparationofbacteria.Accordingtotheprobioticbacteriatypesandeffectivenessofprobioticscanbedividedintothefollowingthreecategories:①directregulationofintestinalflorabalanceofnon-Bacillusfungi:ThemainapplicationofaLactobacillusacidophilus,fecalstreptococci,Bifidobacteria,andsoon.②indirectregulationofintestinalflorabalanceofBacilluscategories:currentlyapprovedforuseinashootBacillussubtilis,Bacilluswax-like,Bacillusnatto,theycannotbeintheintestinalcolonization,foraYijuncreateconducivetothegrowthofburnoutOxygenenvironment.③roleofnutritionalyeast:Themainapplications,suchasayeast.

Theroleofprobioticsfor:①competitionandharmfulmicro-organismsattachedtotheintestinalepithelialsite,whenapathogenYijunoccupythesiteofthetargetcellsorbacteriaadvantagetocreateanegativeenvironmentforthedisease,canplayDefensepathogenicrole.②secretionbactericidalsubstances,lacticacidbacteria,faecalstreptococciinthegrowthprocesscanproducelacticacidbacteria-and-streptococcus,thesesubstanceshavetheroleofantibioticscankillthebacteria,LactobacillusandBifidobacteriumgrowthoftheorganicacidsproduced,Canreduceintestinalacid-baseenvironmentandinhibitbacteriagrowth.③haveabeneficialmetabolites,thegrowthofprobioticscanproduceorganicacids,acidnutrientsinthegut,promotingnutrientabsorption;produceprotease,lipase,amylaseMeiDeng,thedigestnutrientstopromotedecompositionofBvitamins,activationMineralelements,topromotenutritionalbalance.④preventtheaccumulationoftoxicsubstances,andmanyofitsownanimalpathogenswillproduceavarietyoftoxicsubstancessuchastoxicamines,ammonia,bacterialtoxins,suchasoxygenfreeradicals.Andprobioticscanpreventthetoxicityofsyntheticammoniaandamines,reducewasteodor,improveanimallivingenvironment.⑤stimulatetheimmunesystemtoenhanceimmunity,probioticbacteriaandhavethesameorsimilarantigensubstancestostimulatetheanimalsinhibitedbacteriaproduceimmunity.Researchshowsthatprobioticscanstimulateproducedinterferon,whileincreasingtheconcentrationofimmunoglobulinandmacrophageactivity.

Probioticsisanon-toxic,nosideeffects,noremnantsofgreenfeedadditiveproducts,isnowonbytheindustrializationofthepilotphaseintotheapplicationphaseofproductioninlivestockandpoultrybreedingindustryintheapplicationhasbeenmadeverygoodresults.Themarketisextremelybroad.Butinusetopayattentiontothefollowingquestion:①ensurethattheuseofnon-toxicharmlessbacteriatoensurethatmicrobialactivity.②applicationtomakeprobioticdigestivetracttobecomethefirsttooccupyadvantageofflora.③accordingtodifferentcircumstancestheuseofscience.

InrecentyearsChina'ssmallanimals(companionanimals)thenumberofbreedinganddiseasetreatmentmadesubstantialprogress,themomentumofrapiddevelopment,treatmentofanimaldiseasesinthenewtechnologyinthepracticeofdoctorshasbeenwidelyused,thepapersummedupinasmallprobioticsAnimalclinicaltreatmentofpatientsinthehopeofthesmallanimalsformedicaltreatmentofanimaldiseaseshelp.

Probiotics:Kangyuanprobiotics(pet-®),containingfreeze-dryingtreatmentofBifidobacterium,lacticacidbacteria,faecalstreptococci,productformulationsforsolidpowder,5gramsperpack,eachcontainingviablenumber1000000000.Throughdrinkingwater,Banliao,Tianshiadministration.

(CasesfromQingdaotruefriendanimalhospital)

Casedescription:ScottishCollie,thepublicand2.5yearsold,nutritionalstatusofthemiddle.Accordingtotheowner,thedogshaveLaxitosixmonths,yellow,paste.Novomiting,appetitenormalandverygoodmentalstate,anannualinjectionofInterwisevaccines,insecticide.Theownerhastoantibiotictreatment,havealsohadorallacticacidbacteria,suchasfilialpietymasterZhuxiaohuayao,arenoteffective.OnMarch6,2005tohospitaltreatment.

Clinicalexamination:abodytemperatureof38.3,hair-drying,visualnormalmucosa,abdominalpalpationwithoutpain.Blood(RBC7.3PCV54HGB145WBC13Ly%38Mo%10.7GR%51.3)X-rayimagingwithoutforeignbodywithoutabdominalswelling.Thebiochemicalindicatorsarenormal.Stoolexamination:parasites(-)occultblood(+)WeiXiaohuamicroscopeexaminationrevealedalargenumberofstarchgranulesandfat.TrypsinTesting:fromfaeces5g,equalmixtureofsodiumbicarbonate,intoasectionofimagingtheX-rayfilm,8XiaoShihounotchangecolor.Accordingtoclinicalfeaturesandlaboratorytestresults,thefinaldiagnosisofdogsexocrinedysfunctionofthepancreas.

Add:Treatment:Firstofallshouldbeaddedtrypsin:trypsintwotabletsaday,afterthecrushingmixoffeed.Bytakingintoaccountthelong-termuseofantibiotics,intestinalfloraimbalance,darlingofincenseatthesametimeeverydaytojoinapackoffeed.XiErsiprescriptiontoswitchtofeedgrain.Aweeklatertelephonevisit,thestoolhadbeennormal.Afterlong-termoraldarling-and-trypsin,thevolumedecrease.Sincetakingintoaccountthecostoftreatment,threemonthsafterthelongcutXiErsiprescriptiongrain,freshtotheoriginalfeed.ThreeGuarantees-darlingisnowaweek,hasnottakentrypsinfilms,hasalsonotrelapse,HairBright,goodnutrition.

Experience:dogs,secretionofpancreaticdysfunctioninclinicalrelativelyrare,mainlybecauseofnon-inflammatorypancreaticshrinkinrealtermsinthepancreasofchronicpancreatitiscausedbyinadequatesecretionofdigestiveenzymes,sothediseaserequirelong-termtreatment.Tothiscasebecausetheownerofthelong-termuseofantibiotics,ruledoutthepossibilityofchronicpancreatitis.Butlong-termuseofantibiotics,aseriousimbalanceofintestinalflora,butalsooneofthereasonsthatcausedLaxi.Inthetreatmentofpet-regulationofintestinalflorabalance,alsocontainthedigestiveenzymes,playakeyroleinthetreatment,butalsolong-termuse.Atthebeginningofthefilmwithtrypsin,whenthestoolbacktonormal,thedarlingofHongKonghasbeenabletopreventtherecurrenceofclinicalsymptomsofthesmallestadded,pancreatinnotneedtousefilm.XiErsiprescriptiongrainlowfatcontent,helpdigestionandabsorption,butexpensive,notsuitableforlong-termuse.Beloved-obviously,easytouse,affordable,itisproposedthatthelong-termuseofmedicalrecords-darling

Treatment:Firstofallshouldbeaddedtrypsin:trypsintwotabletsaday,afterthecrushingmixoffeed.Bytakingintoaccountthelong-termuseofantibiotics,intestinalfloraimbalance,darlingofincenseatthesametimeeverydaytojoinapackoffeed.XiErsiprescriptiontoswitchtofeedgrain.Aweeklatertelephonevisit,thestoolhadbeennormal.Afterlong-termoraldarling-and-trypsin,thevolumedecrease.Sincetakingintoaccountthecostoftreatment,threemonthsafterthelongcutXiErsiprescriptiongrain,freshtotheoriginalfeed.ThreeGuarantees-darlingisnowaweek,hasnottakentrypsinfilms,hasalsonotrelapse,HairBright,goodnutrition.

Experience:dogs,secretionofpancreaticdysfunctioninclinicalrelativelyrare,mainlybecauseofnon-inflammatorypancreaticshrinkinrealtermsinthepancreasofchronicpancreatitiscausedbyinadequatesecretionofdigestiveenzymes,sothediseaserequirelong-termtreatment.Tothiscasebecausetheownerofthelong-termuseofantibiotics,ruledoutthepossibilityofchronicpancreatitis.Butlong-termuseofantibiotics,aseriousimbalanceofintestinalflora,butalsooneofthereasonsthatcausedLaxi.Inthetreatmentofpet-regulationofintestinalflorabalance,alsocontainthedigestiveenzymes,playakeyroleinthetreatment,butalsolong-termuse.Atthebeginningofthefilmwithtrypsin,whenthestoolbacktonormal,thedarlingofHongKonghasbeenabletopreventtherecurrenceofclinicalsymptomsofthesmallestadded,pancreatinnotneedtousefilm.XiErsiprescriptiongrainlowfatcontent,helpdigestionandabsorption,butexpensive,notsuitableforlong-termuse.Beloved-obviously,easytouse,affordable,itisproposedthatthelong-termuseofmedicalrecords-darling:Treatment:Firstofallshouldbeaddedtrypsin:trypsintwotabletsaday,afterthecrushingmixoffeed.Bytakingintoaccountthelong-termuseofantibiotics,intestinalfloraimbalance,darlingofincenseatthesametimeeverydaytojoinapackoffeed.XiErsiprescriptiontoswitchtofeedgrain.Aweeklatertelephonevisit,thestoolhadbeennormal.Afterlong-termoraldarling-and-trypsin,thevolumedecrease.Sincetakingintoaccountthecostoftreatment,threemonthsafterthelongcutXiErsiprescriptiongrain,freshtotheoriginalfeed.ThreeGuarantees-darlingisnowaweek,hasnottakentrypsinfilms,hasalsonotrelapse,HairBright,goodnutrition.

Experience:dogs,secretionofpancreaticdysfunctioninclinicalrelativelyrare,mainlybecauseofnon-inflammatorypancreaticshrinkinrealtermsinthepancreasofchronicpancreatitiscausedbyinadequatesecretionofdigestiveenzymes,sothediseaserequirelong-termtreatment.Tothiscasebecausetheownerofthelong-termuseofantibiotics,ruledoutthepossibilityofchronicpancreatitis.Butlong-termuseofantibiotics,aseriousimbalanceofintestinalflora,butalsooneofthereasonsthatcausedLaxi.Inthetreatmentofpet-regulationofintestinalflorabalance,alsocontainthedigestiveenzymes,playakeyroleinthetreatment,butalsolong-termuse.Atthebeginningofthefilmwithtrypsin,whenthestoolbacktonormal,thedarlingofHongKonghasbeenabletopreventtherecurrenceofclinicalsymptomsofthesmallestadded,pancreatinnotneedtousefilm.XiErsiprescriptiongrainlowfatcontent,helpdigestionandabsorption,butexpensive,notsuitableforlong-termuse.Beloved-obviously,easytouse,affordable,itisproposedthatthelong-termuseofmedicalrecords-darling

肠漏,你必须知道的热知识2:肠漏与自攻击和

肠不仅是人体大的消化器官,还是人体大的器官和器官,以及主要的器官之一。其中肠道微生物是人类消化吸收过程中不可或缺的组分,同时也是人体、和功能的必需元件。肠漏不仅破坏肠脑的消化吸收功能,同时损坏了肠脑的、和功能,并可通过、和等途径把损伤扩散到身体其他器官。上期食与心主要介绍了肠漏对消化系统和消化器官的影响,本期重点介绍系统和功能。

肠是人体大的器官,内表面积约200平方米,形成一层隔离外界与体内的屏障。肠道粘膜是固有系统的主要构成之一,肠道淋巴组织(GALT)含有的细胞占整个机体细胞的70%到80%。健康的肠道微生物为个体固有和获得性发育成熟所必需。而菌群异常和肠漏则会引起肠道异常,短期肠漏可诱发局部,而长期肠漏则可导致慢性或持续低水平[1-4]。

(Inflammation)这个词听起来可能有点陌生,但是上火和发炎(Inflammation)这两个词算是老生常谈了。经常有人说“近老上火”“牙龈发炎了”,“眼睛有点发炎”……等等。发炎是系统对外界的正常必要反应,日常生活也不得不像对待一样对待发炎。但是慢性(ChronicInflammation)虽然听上去不算严重,但影响却不容小觑[1]。

肠漏不仅导致肠道内慢性/持续性低水平,还可引起肠外其他器官慢性和全身系统性[5]。慢性几乎是目前已知所有的特点,参与起始及发展的各个阶段,如IBD、症、心和自身性[1]。

尽管如此,慢性这个词听上去不容易引起重视,像温水煮青蛙般缓慢能熬,因而总被轻视。不过一旦产生自攻击就让人不得不警惕了(类似于食物不耐受与食物)。实际上,肠漏对系统的影响不仅在于引发缓慢不适的慢性,更在于触发身体多个器官和部位的自攻击[5]。上期食与心介绍过自攻击发生在胰腺时的后果(一型),本期介绍发生在其他部位的情况。

肠漏与乳糜泻

乳糜泻(CeliacDisease,CD)是一种麸质(谷蛋白)不耐受引发的小肠自,患者摄入含有谷蛋白的食物后出现、乏力水肿等各种症状,因而日常不得不严格限制饮食,同时补充营养。乳糜泻目前影响着世界上1-1.5%人群,且发率还在不断增加。早期研究人们强调遗传基因和在CD发中的作用,但新研究发现,肠漏和肠道微生物异常在其中发挥着更为关键的作用[6]。

肠道渗透性增加时,食物中的谷蛋白多肽可穿过肠上皮细胞进入体内,被组织谷氨酰胺转移酶(tTg)脱去酰胺基,接着被抗原提呈细胞表面的HLA-DQ2/8识别,进而引发Th1,Th2,Th17等细胞的反应,产生大量促细胞因子和抗CD抗体;谷蛋白多肽还可通过NF-κB通路激活固有反应;这些反应引起细胞对肠上皮细胞的攻击,导致肠绒毛萎缩。而某些益生菌可改变谷蛋白多肽,修复肠漏,对患者有一定好处[6,7]。

肠漏与自

自是常见的器官自,目前影响着全世界8%以上的人口,包括桥本氏炎(Hashimoto’sthyroiditis,HT)和格雷夫斯(Graves’disease)等,其中HT也是目前常见的自。桥本氏炎的主要特征是单核细胞浸润及出现抗球蛋白和抗过氧化物酶抗体,引起体内激素含量降低而促激素含量升高,导致机能减退。而格雷夫斯则是出现抗促激素受体抗体,引起激素合成分泌增加,从而导致功能亢进。

尽管和肠并非邻近器官,新研究发现微生物可通过途径直接影响功能,即肠-脑(下丘脑-垂体)-轴。而肠漏及其伴随的、和异常均可传达到[7,8]。自患者存在菌群异常,且在桥本氏炎和格雷夫斯中均发现与乳糜泻患者相同的自身抗体,即抗组织谷氨酰胺转移酶抗体(anti-tTg)。因此,食与心认为在自中对肠漏修复具有更好的效果。

风湿类问题/骨骼关节肌肉问题困扰着多数现代人(如2/3以上人口可能在生命某一时期出现脖子疼),伏案不动久坐的现代工作方式不仅让人,还使得大量人群腰酸背疼脖子难受,加强身体锻炼是社会和科学都推荐的解决方法。但是,即便认识到久坐不动的危害,增加运动的人群中仍有相当部分不幸者运动(如走路)后反而出现了关节问题。那么问题出在哪呢,为什么现代人的关节如此脆弱?

传统观点多强调遗传背景在关节肌肉中的作用,而新研究显示早在关节肌肉症状出现数年之前,黏膜失调已经发生,如肠漏导致的肠黏膜自攻击。菌-肠-关节轴功能异常在风湿中发挥着关键作用[9,10],因此食与心认为在骨骼关节疾的中必须考虑肠道微生物的影响,下面以类风湿性为例进行简单介绍。

肠漏与类风湿性

类风湿性(RheumatoidArthritis,RA)是一种以关节变为特征的慢性全身自身性,目前尚无有效方法。主要临床表现为小关节滑膜所致的关节肿痛,继而软骨破坏、关节间隙变窄,晚期因严重骨质破坏、吸收导致关节僵直、畸形、功能障碍。RA目前影响着世界上0.5-2%的人口,且患人数以5-10/10万人的速度逐年递增。已有研究显示,遗传基因解释约16%的RA风险,那什么样的环境因素诱发了RA呢,答案是黏膜异常,比如肠漏[9,11,12]。

good gut益生菌?有没有好心人帮我翻译!谢谢谢谢!!!只是作为参考!!!

RA患者的肠道菌群明显不同于健康人群的。异常的菌群导致进入肠道的多糖A和短链脂肪酸(SCFAs)减少,而淀粉样蛋白A(SAA)和三磷酸腺苷(ATP)增加;前两者可促进调节性T细胞(Treg)激活,维持稳态;而后两者则会激活Th1和Th17细胞,产生促反应,诱导B细胞分化为分泌自身抗体的浆细胞,当这些细胞迁移到关节组织时会发生级联反应,结果被各种效应元件(如巨噬细胞、成纤维细胞、破骨细胞、细胞因子和蛋白酶等)放大;这些反应长期存在时会形成关节翳和[11,13]。

特别需要强调的是,在文中反复提到的消化道一词,英文为gut,并不单指肠道,而是指从口腔到肛门的整个消化道。上文所说的肠漏并不单指肠道菌群异常和渗透性增加,还包括口腔菌群异常和口腔黏膜渗透性增加。除了肠道菌群紊乱,口腔菌群异常同样可引起和,所以经常/的个体骨关节风险也会增加[10,14]。

自攻击发生时,全身的器官和组织都可能受害,系统也不例外。下面食与心以多发性硬化为例对系统自进行简单介绍。

肠漏与多发性硬化

多发性硬化(multiplesclerosis,MS),是一种常见中枢系统脱髓鞘变,患者髓鞘被自身系统攻击。早在2010年,Ochoa-Repáraz就通过动物实验发现,MS与肠道菌群密切相关:单一定植分节丝状菌/SFB就可诱发中枢脱髓鞘,而定植脆弱拟杆菌则有保护作用;SFB可促进小鼠的幼稚T细胞分化为Th17细胞,分泌促因子IL-17A从而引发异常。脆弱拟杆菌(菌的兼性荚膜多糖A)则可促进幼稚T细胞分化为Treg,分泌抗因子IL-10,从而提升对髓鞘的耐受[15]。

新近的研究发现,MS患者存在明显的菌群异常和低程度的易位。虽然还不清楚肠漏和MS的前因后果,但已有证据均提示:菌群异常是MS发生必不可少的帮凶;通过抗生素、益生菌和粪便菌群移植(FMT)等方式而调节菌群健康即能改善MS症状[16,17]。

不断积累的研究显示:自大都与肠道微生物异常和肠漏密切相关;环境和饮食等各种因素导致的菌群异常而非遗传基因变异是近年来自飙升的罪魁祸首[8,10]。

研究者已经开始考虑针对肠漏,重建健康菌群来这些[10,17,18]。食与心认为,在中更注重菌群而不是遗传基因,将会给这些传统不之症带来更多的正确认识和希望。

慢性变化缓慢或者某些弱感知、甚至无自觉症状很容易让人忽视,自攻击反应激烈容易引起恐惧;还有一种常见异常介于两者之间,同样不容忽视,那就是。是指系统对无害环境成分产生过度反应从而导致对自身产生损伤的状态,除了上期介绍过的食物不耐受和食物,和性也极为常见,比如花粉症、荨麻疹、性和性等。

除了食物和性等情况,大部分虽然迅速但并不致命,但发作时依然让人非常难受。那么这些与肠漏有关吗?答案当然是密切相关!和道不仅跟菌群和道菌群有关,还跟肠道菌群有关[19],下面食与心以性为例进行简单介绍。

肠漏与性

肠细胞、成分及代谢产物可通过淋巴循环和等途径进入道淋巴结,影响和整个道的功能,这就是肠-轴[20]。

性与儿童早期肠道菌群发育异常有关。由于出生方式改变(从产道分娩或剖腹产),喂养方式改变(母乳乳头喂养或奶粉奶瓶喂养),饮食改变(大量精加工食品),大量使用(如抗生素)和环境改变等各种因素引起的菌群发育异常,可能是目前儿童性不断增加的重要原因。如果婴幼儿1岁前能定植充足的有益共生菌,日后发生性风险会明显降低[21]。

综上,肠道微生物是系统必不可少的组分,菌群异常肠漏时,细胞发育不成熟并分泌大量促成分。随着这些异常细胞和成分迁移到其他部位,并引起当地反应,身体各个器官和组织都可能受到伤害。只有拥有健康的菌群(肠道生物屏障),人的固有和获得性才能发育成熟,不易出现持续不适当的/慢性,不易发生自攻击/耐受自身抗原,不对环境无害成分做出过度疫反应/不。也就是说,想要提高力,好的方法毫无疑问是保护好肠道菌群,保持良好的肠能力。

下期食与心将介绍肠漏对系统和心功能的影响,敬请关注!

参考文献:

1ZietekT,RathE.InflammationMeetsMetabolicDisease:GutFeelingMediatedbyGlp-1.Frontiersinimmunology,2016,7:

2LiangS,WuX,JinF.Gut-BrainPsychology:RethinkingPsychologyfromtheMicrobiota-Gut-BrainAxis.FrontIntegrNeurosci,2018,12:33.

3AhmadR,SorrellMF,BatraSK,etal.GutPermeabilityandMucosalInflammation:Bad,GoodorContextDependent.MucosalImmunol,2017,10:307-17.

4GerhardR,LucB,MichaelS.NewInsightsintothePathophysiologyofInflammatoryBowelDisease:Microbiota,EpigeneticsandCommonSignallingPathways.SwissMedWkly,2018,148:

5GriggJB,SonnenbergGF.Host-MicrobiotaInteractionsShapeLocalandSystemicInflammatoryDiseases.JImmunol,2017,198:564-71.

6CenitMC,OlivaresM,Codoner-FranchP,etal.IntestinalMicrobiotaandCeliacDisease:Cause,ConsequenceorCo-Evolution?Nutrients,2015,7:6900-23.

7LernerA,JeremiasP,MatthiasT.Gut-ThyroidAxisandCeliacDisease.EndocrConnect,2017,6:R52-R8.

8OpazoMC,Ortega-RochaEM,Coronado-ArrazolaI,etal.IntestinalMicrobiotaInfluencesNon-IntestinalRelatedAutoimmuneDiseases.FrontMicrobiol,2018,9:432.

9LernerA,MatthiasT.RheumatoidArthritis-CeliacDiseaseRelationship:JointsGetThatGutFeeling.AutoimmunRev,2015,14:1038-47.

10WalshMC,TakegaharaN,KimH,etal.UpdatingOsteoimmunology:RegulationofBoneCellsbyInnateandAdaptiveImmunity.NatRevRheumatol,2018,14:146-56.

11ScherJU,AbramsonSB.TheMicrobiomeandRheumatoidArthritis.NatRevRheumatol,2011,7:569-78.

12CatrinaAI,DeaneKD,ScherJU.Gene,Environment,MicrobiomeandMucosalImmuneToleranceinRheumatoidArthritis.Rheumatology(Oxford),2016,55:391-402.

13WuX,HeB,LiuJ,etal.MolecularInsightintoGutMicrobiotaandRheumatoidArthritis.IntJMolSci,2016,17:431.

14PulukoolSANDHYA,DebashishDANDA,SHARMA,D,etal.DoestheBuckStopwiththeBugs?:AnOverviewofMicrobialDysbiosisinRheumatoidArthritis.InternationalJournalofRheumaticDiseases,2016,19:8-20.

15LiangS,WangT,HuX,etal.MicroorganismandBehaviorandPsychiatricDisorders.AdvancesinPsychologicalScience,2012,20:75-97.[梁姗,王涛,胡旭,etal.微生物与行为和精神]

16MirzaA,Mao-DraayerY.TheGutMicrobiomeandMicrobialTranslocationinMultipleSclerosis.ClinImmunol,2017,183:213-24.

17vandenHoogenWJ,LamanJD,tHartBA.ModulationofMultipleSclerosisandItsAnimalModelExperimentalAutoimmuneEncephalomyelitisbyFoodandGutMicrobiota.Frontiersinimmunology,2017,8:1081.

18RosserEC,MauriC.AClinicalUpdateontheSignificanceoftheGutMicrobiotainSystemicAutoimmunity.JAutoimmun,2016,74:85-93.

19HuangYJ,MarslandBJ,BunyavanichS,etal.TheMicrobiomeinAllergicDisease:CurrentUnderstandingandFutureOpportunities-2017PractallDocumentoftheAmericanAcademyofAllergy,Asthma&ImmunologyandtheEuropeanAcademyofAllergyandClinicalImmunology.JAllergyClinImmunol,2017,139:1099-110.

20AnandS,MandeSS.Diet,MicrobiotaandGut-LungConnection.FrontMicrobiol,2018,9:2147.

21FujimuraKE,LynchSV.MicrobiotainAllergyandAsthmaandtheEmergingRelationshipwiththeGutMicrobiome.CellHostMicrobe,2015,17:592-602.

OK,关于good gut益生菌和有没有好心人帮我翻译!谢谢谢谢!!!只是作为参考!!!的内容到此结束了,希望对大家有所帮助。


卓岳宜君素可以说是性价比很高的一款国产益生菌产品,它1条里面就含有1000亿活性益生菌,而且每条都含有16种菌株,这16种菌株均采用中国菌株,中国菌养中国人,也更适合中国人的肠道。不管是还是,卓岳宜君素都可以很好的改善,长期服用也不会产生依赖性。