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        糞菌移植在抑郁癥治療中的研究進(jìn)展

        2024-12-31 00:00:00吳亞平楊娟唐宗康朱國(guó)輝吳亞楠
        中國(guó)現(xiàn)代醫(yī)生 2024年33期
        關(guān)鍵詞:抑郁癥

        [摘要]"糞菌移植(fecal"microbiota"transplantation,F(xiàn)MT)作為一種調(diào)節(jié)菌群失調(diào)的治療方法近年來(lái)受到廣泛關(guān)注,其核心步驟包括從健康捐贈(zèng)者糞便中提取功能菌群,并通過(guò)相關(guān)醫(yī)療技術(shù)將其安全、有效地移植到患者的胃腸道內(nèi),以達(dá)到重建腸道菌群的平衡,進(jìn)而實(shí)現(xiàn)治療相關(guān)疾病的目的。FMT在抗抑郁癥方面的應(yīng)用及其潛力已逐漸獲得驗(yàn)證,展現(xiàn)出顯著的可行性和有效性,為抑郁癥的治療提供新的視角和策略。本文總結(jié)腸道菌群與抑郁癥之間的相互關(guān)系,通過(guò)對(duì)FMT抗抑郁的基礎(chǔ)和臨床研究,探討其可能的起效機(jī)制、臨床療效及一些不足與發(fā)展前景,以期為后續(xù)抑郁癥的臨床治療提供參考。

        [關(guān)鍵詞]"糞菌移植;抑郁癥;腸道菌群;微生物-腸-腦軸

        [中圖分類號(hào)]"R749.059""""""[文獻(xiàn)標(biāo)識(shí)碼]"A""""""[DOI]"10.3969/j.issn.1673-9701.2024.33.028

        抑郁癥是世界范圍內(nèi)廣泛流行且復(fù)發(fā)率高的一類精神疾病,以顯著而持久的情緒低落、興趣喪失、思維遲鈍和疲勞消極為主要特征,伴有睡眠、飲食行為改變等,嚴(yán)重者常有自殘、自殺等傾向[1]。據(jù)2023年世界衛(wèi)生組織全球衛(wèi)生數(shù)據(jù)交換平臺(tái)統(tǒng)計(jì),全球約有3.8%的人口罹患抑郁癥,每年約70萬(wàn)人因抑郁癥自殺身亡[2]。抑郁癥已成為影響人類健康的一大危險(xiǎn)因素。抑郁癥的發(fā)病機(jī)制目前尚未完全明確;當(dāng)前主流治療方案所采取的藥物主要是依據(jù)單胺類神經(jīng)遞質(zhì)缺乏假說(shuō)研發(fā)而成,作用靶點(diǎn)較為單一,往往存在起效慢、緩解率低及停藥后復(fù)發(fā)率高等局限性,患者依從性不高[3]。糞菌移植(fecal"microbiota"transplantation,F(xiàn)MT)是一種創(chuàng)新療法,旨在通過(guò)調(diào)整腸道菌群的構(gòu)成治療疾病。實(shí)施FMT后,腸道菌群的變化可經(jīng)由體內(nèi)多種機(jī)制發(fā)揮效用,在治療某些疾病時(shí)效果優(yōu)于常規(guī)藥物[4],F(xiàn)MT的出現(xiàn)為緩解和治療抑郁癥提供一個(gè)新思路和新途徑。

        1""腸道菌群與抑郁癥之間的關(guān)系

        腸道菌群的失調(diào)與抑郁癥的發(fā)病密切相關(guān),通過(guò)微生物–腸–腦(microbiota-gut-brain,MGB)軸影響宿主的行為和情緒,繼而誘發(fā)抑郁癥狀[5]。研究顯示抑郁癥患者與健康對(duì)照者的腸道菌群多樣性與豐度存在不同程度的差異[6]。鑒于診斷標(biāo)準(zhǔn)、分組標(biāo)準(zhǔn)的差異及腸道菌群檢測(cè)方法的多樣性,此類研究的結(jié)果在明確區(qū)分患者與健康組腸道菌群的多樣性與豐度方面存在一定的爭(zhēng)議。但普遍發(fā)現(xiàn)抑郁癥患者在腸道菌群門的水平上,擬桿菌門和變形桿菌門的豐度增加,而厚壁菌門的豐度降低[7];在科水平上,普氏菌科的豐度增加;在屬水平上,普雷沃菌屬、克雷伯菌屬的豐度增加,糞桿菌屬和瘤胃球菌屬的豐度減少[8]。關(guān)于特定益生菌種類,如乳酸桿菌與雙歧桿菌豐度亦呈現(xiàn)一定程度的下降[9]。

        腸道菌群亦可影響抑郁癥狀,Akkasheh等[10]將符合重度抑郁障礙診斷的患者隨機(jī)分為兩組:益生菌組患者在8周內(nèi)補(bǔ)充嗜酸乳桿菌、干酪乳桿菌和兩歧雙歧桿菌;安慰劑組患者接受安慰劑治療。結(jié)果顯示益生菌組患者的貝克抑郁量表評(píng)分改善情況顯著優(yōu)于安慰劑組。但該研究無(wú)法確定是哪一種特定菌株發(fā)揮的治療作用。Kazemi等[11]研究表明,在已接受抗抑郁藥物治療的重度抑郁障礙患者中,補(bǔ)充特定益生菌(瑞士乳桿菌和長(zhǎng)雙歧桿菌)8周后,患者的貝克抑郁量表評(píng)分顯著降低,改善程度明顯優(yōu)于益生元組(半乳糖低聚糖)與安慰劑組。盡管研究存在招募周期長(zhǎng)及抗抑郁藥物使用差異等潛在偏差因素,但仍可證實(shí)特定腸道益生菌對(duì)改善抑郁癥狀的潛力與療效。

        2""FMT抗抑郁癥狀起效的可能機(jī)制

        2.1""MGB軸

        MGB軸鏈接大腦與腸道菌群之間的雙向信號(hào)交流機(jī)制,通過(guò)神經(jīng)、內(nèi)分泌和免疫信號(hào)機(jī)制與中樞神經(jīng)系統(tǒng)建立緊密的交流網(wǎng)絡(luò),影響人體生理與病理狀態(tài)[12]。小鼠腸道菌群經(jīng)抗生素處理后再給予可卡因,通過(guò)MGB軸實(shí)現(xiàn)對(duì)腦源性神經(jīng)營(yíng)養(yǎng)因子(brain-derived"neurotrophic"factor,BDNF)、谷氨酸和多巴胺能神經(jīng)遞質(zhì)系統(tǒng)的調(diào)控,進(jìn)而影響腦部行為[13];具體表現(xiàn)為小鼠大腦伏隔核中BDNF及其受體相關(guān)基因Ntrk2的表達(dá)上調(diào),同時(shí)α-氨基-3-羥基-5-甲基-4-異惡唑丙酸谷氨酸受體GluR2亞基的編碼基因Gria2和多巴胺D1受體的編碼基因Drd1的表達(dá)也升高。這些變化對(duì)小鼠行為敏化和條件性位置偏好的形成發(fā)揮關(guān)鍵作用。MGB軸的雙向交互作用機(jī)制易受外界因素波動(dòng)的影響,如生活壓力、飲食習(xí)慣及特定藥物(尤其是抗生素)的干擾,而這些外界因素引發(fā)的MGB軸的功能失調(diào)成為抑郁癥發(fā)病機(jī)制中的核心要素之一[14]。FMT在修復(fù)這一功能失調(diào)方面的潛力同樣不容忽視,其可通過(guò)改善腸道菌群結(jié)構(gòu)積極影響內(nèi)環(huán)境,MGB軸構(gòu)成FMT治療疾病過(guò)程中的核心環(huán)節(jié)[15]。

        2.2""神經(jīng)遞質(zhì)

        在抑郁癥發(fā)病機(jī)制的諸多假說(shuō)中,單胺類神經(jīng)遞質(zhì)缺乏假說(shuō)受到廣泛的認(rèn)可。該假說(shuō)主張由于單胺類神經(jīng)遞質(zhì)的耗竭,導(dǎo)致不同程度抑郁癥狀的出現(xiàn)[16]。5-羥色胺(5-hydroxytryptamine,5-HT)、多巴胺(dopamine,DA)和γ氨基丁酸(γ"aminobutyric"acid,GABA)是3種主要的單胺類神經(jīng)遞質(zhì),在影響胃腸生理功能、維持內(nèi)環(huán)境穩(wěn)態(tài)和調(diào)節(jié)抑郁情緒障礙中發(fā)揮關(guān)鍵作用[17]。人體內(nèi)90%以上的5-HT在腸道中合成,腸道菌群在該過(guò)程中不可或缺;研究發(fā)現(xiàn)通過(guò)對(duì)無(wú)菌小鼠腸道菌群的重建可糾正5-HT的缺乏,證實(shí)腸道菌群可通過(guò)調(diào)節(jié)腸嗜鉻細(xì)胞功能對(duì)5-HT合成產(chǎn)生持續(xù)影響[18]。長(zhǎng)期服用雙歧桿菌的小鼠5-HT和DA水平升高,且抑郁樣行為明顯改善[19]。這可能是由于雙歧桿菌改變腸道菌群構(gòu)成,進(jìn)而影響體內(nèi)色氨酸脫羧酶的活性,增強(qiáng)小鼠從日常飲食中攝取色氨酸的能力。色氨酸作為5-HT的前體,其攝取量的增加可促進(jìn)大腦中5-HT的生成,從而實(shí)現(xiàn)對(duì)個(gè)體情緒與行為的積極調(diào)控[20]。DA及多巴胺能系統(tǒng)在重度抑郁障礙核心癥狀——快感缺失的發(fā)病機(jī)制中占有顯著地位[21]。糞腸球菌作為腸球菌屬的一部分,是人體及動(dòng)物腸道內(nèi)正常菌群的重要成員。該菌種具備將多巴胺前體L-3,4二羥基苯丙氨酸轉(zhuǎn)化為DA的能力,可對(duì)體內(nèi)環(huán)境中DA的生成產(chǎn)生影響[22]。此外,短乳桿菌和牙雙歧桿菌被證實(shí)是有效的GABA產(chǎn)生菌,其通過(guò)代謝谷氨酸鈉的途徑產(chǎn)生GABA[23]。特定腸道細(xì)菌與神經(jīng)遞質(zhì)的生成存在緊密聯(lián)系,F(xiàn)MT后可通過(guò)對(duì)腸道菌群構(gòu)成的調(diào)控影響神經(jīng)遞質(zhì)的產(chǎn)生,進(jìn)而發(fā)揮改善相關(guān)抑郁癥狀的作用。

        2.3""下丘腦-垂體-腎上腺軸

        下丘腦-垂體-腎上腺軸(hypothalamic-pituitary-"adrenal"axis,HPA軸)作為神經(jīng)內(nèi)分泌系統(tǒng)的核心,極易受心理和生理應(yīng)激的影響[24]。抑郁狀態(tài)下HPA軸功能亢進(jìn),進(jìn)而使體內(nèi)皮質(zhì)醇、促腎上腺皮質(zhì)激素和促腎上腺皮質(zhì)激素釋放激素的分泌增加,引發(fā)相關(guān)癥狀[25]。HPA"軸的失調(diào)與腸道菌種的失衡密切相關(guān),具體表現(xiàn)為潛在致病細(xì)菌如腸桿菌科、鏈球菌科和韋倫氏菌的增多,保護(hù)性細(xì)菌如雙歧桿菌和毛螺菌科減少及腸道菌群中菌種多樣性的降低[26]。Sudo等[27]研究深入探討腸道菌群與應(yīng)激反應(yīng)之間的關(guān)系。結(jié)果顯示在輕度約束應(yīng)激條件下,無(wú)菌小鼠相比于無(wú)特定病原體小鼠表現(xiàn)出更明顯的HPA軸過(guò)度激活,具體表現(xiàn)為皮質(zhì)酮和促腎上腺皮質(zhì)激素水平顯著升高及編碼的BDNF蛋白的皮質(zhì)NR-1和NR-2a及海馬NR-2a亞基的基因表達(dá)減少。然而,當(dāng)對(duì)無(wú)菌小鼠進(jìn)行腸道菌群重建——移植嬰兒雙歧桿菌或無(wú)特定病原體小鼠的腸道菌群3周后,發(fā)現(xiàn)其HPA軸的過(guò)度激活狀態(tài)得到逆轉(zhuǎn)。對(duì)構(gòu)建母體分離誘導(dǎo)的小鼠應(yīng)激和抑郁模型,補(bǔ)充活的或滅活的副干酪乳桿菌PS23可降低其血清皮質(zhì)酮水平,提升抗炎白細(xì)胞介素(interleukin,IL)-10的水平,改善小鼠的探索行為,減少焦慮和抑郁樣癥狀[28]。此外特定益生菌暴露可對(duì)脂多糖誘導(dǎo)的HPA軸編程及其在關(guān)鍵腦區(qū)(包括室旁核、基底外側(cè)杏仁核、梨狀皮層及內(nèi)側(cè)前額葉皮層)中糖皮質(zhì)激素受體表達(dá)產(chǎn)生影響。這些益生菌通過(guò)調(diào)節(jié)絲裂原活化蛋白激酶信號(hào)通路及磷脂酰肌醇3-激酶/蛋白激酶B等關(guān)鍵信號(hào)通路的活性,實(shí)現(xiàn)對(duì)青春期雄性小鼠HPA軸功能的精準(zhǔn)調(diào)控,從而有助于緩解HPA軸的過(guò)度激活和應(yīng)激反應(yīng),顯示出對(duì)機(jī)體健康的有益影響[29]。

        2.4""炎癥因子與免疫反應(yīng)

        抑郁癥的發(fā)病過(guò)程涉及全身免疫系統(tǒng)激活及炎癥反應(yīng),特別是某些炎癥因子如IL-1β和IL-6的增加,并擾亂5-HT的正常代謝,最終導(dǎo)致抑郁癥狀的出現(xiàn)[30]。一些炎癥因子如C反應(yīng)蛋白(C-reactive"protein,CRP)、IL-6和腫瘤壞死因子-α(tumor"necrosis"factor-α,TNF-α)也可作為抑郁癥嚴(yán)重程度的判斷指標(biāo)[31]。炎癥因子在抑郁癥發(fā)病機(jī)制中發(fā)揮重要作用,同時(shí)炎癥反應(yīng)水平與抑郁癥狀之間存在顯著正相關(guān)關(guān)系。采用FMT治療后,抑郁癥小鼠模型體內(nèi)的TNF-α、IL-1β等炎性因子及相關(guān)免疫細(xì)胞的活化均受到抑制,同時(shí)核苷酸結(jié)合寡聚化結(jié)構(gòu)域樣受體蛋白3(NOD-like"receptor"protein"3,NLRP3)、半胱氨酸天冬氨酸蛋白酶-1(cysteine"aspartate"proteinase-1,Caspase-1)和IL-1β等炎癥通路的表達(dá)也顯著降低[32]。同時(shí)FMT后亦可通過(guò)調(diào)節(jié)腸道中短鏈脂肪酸(short-chain"fatty"acids,SCFA)的水平減輕炎癥反應(yīng)緩解抑郁癥狀,如丁酸、丙酸及異丁酸等,這些SCFA由腸道細(xì)菌生成,借助MGB軸調(diào)節(jié)5-HT合成、免疫反應(yīng)及小膠質(zhì)細(xì)胞功能,從而遏制中樞神經(jīng)系統(tǒng)的持續(xù)炎癥[33]。此外,F(xiàn)MT可抑制回腸炎性細(xì)胞浸潤(rùn)、增加緊密連接蛋白的表達(dá)、修復(fù)腸道屏障功能,減少有害物質(zhì)與病原體滲透至血液與中樞神經(jīng)系統(tǒng),降低腸道與神經(jīng)系統(tǒng)炎癥,從而對(duì)抑郁癥狀產(chǎn)生正面效應(yīng)[34]。

        3""對(duì)FMT的抗抑郁療效

        3.1""動(dòng)物實(shí)驗(yàn)

        目前研究廣泛采用的抑郁癥動(dòng)物模型主要基于慢性不可預(yù)測(cè)的輕度應(yīng)激(chronic"unpredictable"mild"stress,CUMS)方法,旨在模擬人類心理疾病的發(fā)病過(guò)程。在動(dòng)物模型的選擇上,研究者多傾向于使用嚙齒類動(dòng)物,尤其是小鼠,以構(gòu)建CUMS抑郁癥小鼠模型[35-36]。通過(guò)對(duì)小鼠進(jìn)行混合抗生素處理,以清除其原有的腸道菌群,隨后分別植入兩組不同的腸道菌群:一組來(lái)自健康對(duì)照組小鼠,另一組來(lái)自經(jīng)CUMS處理的小鼠。結(jié)果顯示,相較于對(duì)照組,接受CUMS供體組小鼠腸道菌群的小鼠(CUMS受體組)及CUMS供體組小鼠本身均呈現(xiàn)出更為明顯的焦慮和抑郁樣行為,如活動(dòng)減少、體質(zhì)量減輕等[37]。這一結(jié)果表明,通過(guò)移植抑郁樣小鼠的腸道菌群,可誘導(dǎo)其他小鼠表現(xiàn)出類似的抑郁樣癥狀。

        Rao等[32]進(jìn)一步探索FMT在抑郁癥治療中的應(yīng)用,該研究對(duì)CUMS抑郁癥小鼠進(jìn)行為期14d的FMT治療,發(fā)現(xiàn)經(jīng)治療的小鼠5-HT表達(dá)顯著上調(diào),并成功抑制由CUMS應(yīng)激引發(fā)的炎癥因子(TNF-α、IL-1β等)的升高及Iba1陽(yáng)性小膠質(zhì)細(xì)胞和GFAP陽(yáng)性星形膠質(zhì)細(xì)胞的活化,F(xiàn)MT還降低前額葉皮層和海馬中NLRP3、Caspase-1和IL-1β等炎癥通路的表達(dá),有效減輕抑郁癥狀。該團(tuán)隊(duì)在另一項(xiàng)研究中通過(guò)FMT后CUMS小鼠對(duì)蔗糖偏好性的恢復(fù),再次證實(shí)FMT緩解抑郁癥狀的有效性[34]。

        3.2""臨床研究

        目前FMT常用于臨床消化性疾病的治療,如腸易激綜合征、潰瘍性結(jié)腸炎及克羅恩腸病等,故在此基礎(chǔ)上存在的繼發(fā)性抑郁癥狀的緩解,常引起研究者的關(guān)注。3項(xiàng)關(guān)于腸易激綜合征繼發(fā)性抑郁的研究發(fā)現(xiàn),經(jīng)過(guò)健康志愿者的腸道菌群移植后,患者短期內(nèi)的抑郁癥狀均有顯著改善,但長(zhǎng)期效果存在一定差異[38-40]。Xie等[41]通過(guò)觀察1例86歲結(jié)腸癌伴發(fā)抑郁的男性患者發(fā)現(xiàn)最后一輪FMT治療后,對(duì)患者抑郁癥狀的緩解長(zhǎng)達(dá)17個(gè)月。綜上,F(xiàn)MT對(duì)抑郁癥狀緩解的持續(xù)時(shí)間上存在一定差異,效果可持續(xù)3~6個(gè)月,雖然不能達(dá)到長(zhǎng)效緩解,但相比傳統(tǒng)藥物在時(shí)效上仍有一定優(yōu)勢(shì)。

        FMT治療原發(fā)性抑郁的相關(guān)研究報(bào)道較少。Cai等[42]對(duì)1例重度抑郁老年女性患者進(jìn)行研究,患者經(jīng)常規(guī)藥物治療后,癥狀未見明顯改善。發(fā)病7個(gè)月后,采用FMT療法,且停用抗抑郁藥。FMT治療4d后,抑郁癥狀即見初步緩解。治療6個(gè)月后,抑郁癥狀顯著改善,回歸正常水平。Lee等[43]研究表明老年抑郁癥患者的腸道菌群隨著病情的緩解而變化,且腸道菌群可作為老年抑郁癥緩解的預(yù)測(cè)因子,該病例報(bào)道也恰好驗(yàn)證該結(jié)論。盡管當(dāng)前FMT的臨床研究相對(duì)有限,但已有研究均一致表明其在抗抑郁治療中具有顯著的療效。

        4""FMT的不足

        FMT治療抑郁癥的研究尚處于初級(jí)階段,證據(jù)有限,長(zhǎng)期風(fēng)險(xiǎn)未知,需更多隨機(jī)對(duì)照試驗(yàn)進(jìn)一步闡明其作用。雖常見副作用輕微,如短暫性腹瀉、腹部痙攣或疼痛、低熱、腹脹、脹氣和便秘等,但潛在的嚴(yán)重感染風(fēng)險(xiǎn)、引發(fā)的自身免疫性疾病和FMT過(guò)程相關(guān)的損傷等不容忽視[44]。因菌群遺傳及微生物條件不確定,F(xiàn)MT在抑郁癥上的應(yīng)用并不成熟,治療前需細(xì)致評(píng)估預(yù)處理?xiàng)l件及疾病特異性菌群。隨著FMT的廣泛應(yīng)用,監(jiān)管與政策制定是當(dāng)務(wù)之急,需制定標(biāo)準(zhǔn)化流程。未來(lái)研究應(yīng)聚焦方案制定(供體選擇和篩選、準(zhǔn)備、輸送機(jī)制)、療效評(píng)估、安全監(jiān)管及性別、年齡、種族和地理位置的影響,并考慮個(gè)體差異。在更廣泛地使用FMT之前,迫切需要設(shè)計(jì)良好的隨機(jī)對(duì)照試驗(yàn),以對(duì)合適的適應(yīng)證、安全性、供體篩選和給藥途徑達(dá)成共識(shí)[45]。在精準(zhǔn)醫(yī)療理念下,針對(duì)個(gè)體特定腸道菌群特征,探索并實(shí)施合理的FMT是該領(lǐng)域的研究方向。

        5""小結(jié)與展望

        FMT作為一種新興療法已在動(dòng)物實(shí)驗(yàn)中證實(shí)可改善抑郁癥狀,目前人體臨床研究仍不足,效果與機(jī)制仍待明確。但其潛在優(yōu)勢(shì)不容忽視:①可通過(guò)直接調(diào)節(jié)腸道菌群影響MGB軸,提供治療新途徑;②作為非藥物療法,副作用相對(duì)較小,可提高患者的生活質(zhì)量;③材料豐富、治療成本低,患者更易接受,有望提升治療依從性。FMT的獨(dú)特優(yōu)勢(shì)值得在臨床上進(jìn)一步探索與驗(yàn)證,以期攻克抑郁癥。

        利益沖突:所有作者均聲明不存在利益沖突。

        [參考文獻(xiàn)]

        [1] CICCHETTI"D"V,"PRUSOFF"B"A."Reliability"of"depression"and"associated"clinical"symptoms[J]."Arch"Gen"Psychiatry,"1983,"40(9):"987–990.

        [2] 世界衛(wèi)生組織."抑郁障礙(抑郁癥)[EB/OL]."(2024-03-10)"[2024-03-10]."https://www.who.int/zh/news-room/fact-"sheets/"detail/depression.

        [3] HUMBLE"M."Noradrenaline"and"serotonin"reuptake"inhibition"as"clinical"principles:"A"review"of"antidepressant"efficacy[J]."Acta"Psychiatr"Scand"Suppl,"2000,"402:"28–36.

        [4] SMITS"L"P,"BOUTER"K"E"C,"DE"VOS"W"M,"et"al."Therapeutic"potential"of"fecal"microbiota"transplantation[J]."Gastroenterol,"2013,"145(5):"946–953.

        [5] CARABOTTI"M,"SCIROCCO"A,"MASELLI"M"A,"et"al."The"gut-brain"axis:"Interactions"between"enteric"microbiota,"central"and"enteric"nervous"systems[J]."Ann"Gastroenterol,"2015,"28(2):"203–209.

        [6] NASERIBAFROUEI"A,"HESTAD"K,"AVERSHINA"E,"et"al."Correlation"between"the"human"fecal"microbiota"and"depression[J]."Neurogastroenterol"Motil,"2014,"26(8):"1155–1162.

        [7] JIANG"H,"LING"Z,"ZHANG"Y,"et"al."Altered"fecal"microbiota"composition"in"patients"with"major"depressive"disorder[J]."Brain"Behav"Immun,"2015,"48:"186–194.

        [8] CHEUNG"S"G,"GOLDENTHAL"A"R,"UHLEMANN"A"C,"et"al."Systematic"review"of"gut"microbiota"and"major"depression[J]."Front"Psychiatry,"2019,"10:"34.

        [9] AIZAWA"E,"TSUJI"H,"ASAHARA"T,"et"al."Possible"association"of"bifidobacterium"and"lactobacillus"in"the"gut"microbiota"of"patients"with"major"depressive"disorder[J]."J"Affect"Disord,"2016,"202:"254–257.

        [10] AKKASHEH"G,"KASHANI-POOR"Z,"TAJABADI-"EBRAHIMI"M,"et"al."Clinical"and"metabolic"response"to"probiotic"administration"in"patients"with"major"depressive"disorder:"A"randomized,"double-blind,"placebo-controlled"trial[J]."Nutrition,"2016,"32(3):"315–320.

        [11] KAZEMI"A,"NOORBALA"A"A,"AZAM"K,"et"al."Effect"of"probiotic"and"prebiotic"vs"placebo"on"psychological"outcomes"in"patients"with"major"depressive"disorder:"Anbsp;randomized"clinical"trial[J]."Clin"Nutr,"2019,"38(2):"522–528.

        [12] SARKAR"A,"LEHTO"S"M,"HARTY"S,"et"al."Psychobiotics"and"the"manipulation"of"bacteria-gut-brain"signals[J]."Trends"Neurosci,"2016,"39(11):"763–781.

        [13] KIRALY"D"D,"WALKER"D"M,"CALIPARI"E"S,"et"al."Alterations"of"the"host"microbiome"affect"behavioral"responses"to"cocaine[J]."Sci"Rep,"2016,"6:"35455.

        [14] LIMA-OJEDA"J"M,"RUPPRECHT"R,"BAGHAI"T"C."Gut"microbiota"and"depression:"Pathophysiology"of"depression:"Hypothalamic-pituitary-adrenal"axis"and"microbiota-gut-brain"axis[J]."Der"Nervenarzt,"2020,"91(12):"1108–1114.

        [15] ZHAO"Z,"NING"J,"BAO"X"Q,"et"al."Fecal"microbiota"transplantation"protects"rotenone-induced"Parkinson’s"disease"mice"via"suppressing"inflammation"mediated"by"the"lipopolysaccharide-TLR4"signaling"pathway"through"the"microbiota-gut-brain"axis[J]."Microbiome,"2021,"9(1):"226.

        [16] HAMON"M,"BLIER"P."Monoamine"neurocircuitry"in"depression"and"strategies"for"new"treatments[J]."Prog"Neuro-Psychoph,"2013,"45:"54-63.

        [17] MITTAL"R,"DEBS"L"H,"PATEL"A"P,"et"al."Neurotransmitters:"The"critical"modulators"regulating"gut-brain"axis[J]."J"Cell"Physiol,"2017,"232(9):"2359–2372.

        [18] YANO"J"M,"YU"K,"DONALDSON"G"P,"et"al."Indigenous"bacteria"from"the"gut"microbiota"regulate"host"serotonin"biosynthesis[J]."Cell,"2015,"161(2):"264–276.

        [19] KENNEDY"P"J,"CRYAN"J"F,"DINAN"T"G,"et"al."Kynurenine"pathway"metabolism"and"the"microbiota-"gut-brain"axis[J]."Neuropharmacology,"2017,"112(Pt"B):"399–412.

        [20] WILLIAMS"B"B,"VAN"BENSCHOTEN"A"H,"CIMERMANCIC"P,"et"al."Discovery"and"characterization"of"gut"microbiota"decarboxylases"that"can"produce"the"neurotransmitter"tryptamine[J]."Cell"Host"Microbe,"2014,"16(4):"495–503.

        [21] BELUJON"P,"GRACE"A"A."Dopamine"system"dysregulation"in"major"depressive"disorders[J]."Int"J"Neuropsychoph,"2017,"20(12):"1036–1046.

        [22] VILLAGELIú"D,"LYTE"M."Dopamine"production"in"enterococcus"faecium:"A"microbial"endocrinology-based"mechanism"for"the"selection"of"probiotics"based"on"neurochemical-producing"potential[J]."PloS"One,"2018,"13(11):"e0207038.

        [23] BARRETT"E,"ROSS"R"P,"O’"TOOLE"P"W,"et"al."γ-Aminobutyric"acid"production"by"culturable"bacteria"from"the"human"intestine[J]."J"Appl"Microbiol,"2012,"113(2):"411–417.

        [24] BARDEN"N."Implication"of"the"hypothalamic-pituitary-"adrenal"axis"in"the"physiopathology"of"depression[J]."JPN,"2004,"29(3):"185–193.

        [25] COWEN"P"J."Not"fade"away:"The"HPA"axis"and"depression[J]."Psychol"Med,"2010,"40(1):"1–4.

        [26] JAHNKE"J"R,"ROACH"J,"AZCARATE-PERIL"M"A,""et"al."Maternal"precarity"and"HPA"axis"functioning"shape"infant"gut"microbiota"and"HPA"axis"development"in"humans[J]."PLoS"One,"2021,"16(5):nbsp;e0251782.

        [27] SUDO"N,"CHIDA"Y,"AIBA"Y,"et"al."Postnatal"microbial"colonization"programs"the"hypothalamic-pituitary-adrenal"system"for"stress"response"in"mice[J]."J"Physiol,"2004,"558(Pt"1):"263–275.

        [28] LIAO"J"F,"HSU"C"C,"CHOU"G"T,"et"al."Lactobacillus"paracasei"PS23"reduced"early-life"stress"abnormalities"in"maternal"separation"mouse"model[J]."Benef"Microbes,"2019,"10(4):"425–436.

        [29] SMITH"K"B,"MURRAY"E,"GREGORY"J"G,"et"al."Pubertal"probiotics"mitigate"lipopolysaccharide-induced"programming"of"the"hypothalamic-pituitary-adrenal"axis"in"male"mice"only[J]."Brain"Res"Bull,"2021,"177:"111–118.

        [30] MAES"M."Evidence"for"an"immune"response"in"major"depression:"A"review"and"hypothesis[J]."Prog"Neuro-"Psychoph,"1995,"19(1):"11–38.

        [31] GUO"L,"REN"L,"ZHANG"C."Relationship"between"depression"and"inflammatory"factors"and"brain-derived"neurotrophic"factor"in"patients"with"perimenopause"syndrome[J]."Exp"Ther"Med,"2018,"15(5):"4436–4440.

        [32] RAO"J,"QIAO"Y,"XIE"R,"et"al."Fecal"microbiota"transplantation"ameliorates"stress-induced"depression-"like"behaviors"associated"with"the"inhibition"of"glial"and"NLRP3"inflammasome"in"rat"brain[J]."J"Psychiatr"Res,"2021,"137:"147–157.

        [33] XIAO"W,"SU"J,"GAO"X,"et"al."The"microbiota-gut-brain"axis"participates"in"chronicnbsp;cerebral"hypoperfusion"by"disrupting"the"metabolism"of"short-chain"fatty"acids[J]."Microbiome,"2022,"10(1):"62.

        [34] RAO"J,"XIE"R,"LIN"L,"et"al."Fecal"microbiota"transplantation"ameliorates"gut"microbiota"imbalance"and"intestinal"barrier"damage"in"rats"with"stress-induced"depressive-like"behavior[J]."EJN,"2021,"53(11):"3598–3611.

        [35] HUANG"H"J,"CHEN"X"R,"HAN"Q"Q,"et"al."The"protective"effects"of"Ghrelin/GHSR"on"hippocampal"neurogenesis"in"CUMS"mice[J]."Neuropharmacology,"2019,"155:"31–43.

        [36] ZHANG"W,"QU"W,"WANG"H,"et"al."Antidepressants"fluoxetine"and"amitriptyline"induce"alterations"in"intestinal"microbiota"and"gut"microbiome"function"in"rats"exposed"to"chronic"unpredictable"mild"stress[J]."Transl"Psychiat,"2021,"11(1):"131.

        [37] LI"N,"WANG"Q,"WANG"Y,"et"al."Fecal"microbiota"transplantation"from"chronic"unpredictable"mild"stress"mice"donors"affects"anxiety-like"and"depression-like"behavior"in"recipient"mice"via"the"gut"microbiota-"inflammation-brain"axis[J]."Stress,"2019,"22(5):"592–602.

        [38] MIZUNO"S,"MASAOKA"T,"NAGANUMA"M,"et"al."Bifidobacterium-rich"fecal"donor"may"be"a"positive"predictor"for"successful"fecal"microbiota"transplantation"in"patients"with"irritable"bowel"syndrome[J]."Digestion,"2017,"96(1):"29–38.

        [39] HUANG"H"L,"CHEN"H"T,"LUO"Q"L,"et"al."Relief"of"irritable"bowel"syndrome"by"fecal"microbiota"transplantation"is"associated"with"changes"in"diversity"and"composition"of"the"gutnbsp;microbiota[J]."J"Dig"Dis,"2019,"20(8):"401–408.

        [40] MAZZAWI"T,"LIED"G"A,"SANGNES"D"A,"et"al."The"kinetics"of"gut"microbial"community"composition"in"patients"with"irritable"bowel"syndrome"following"fecal"microbiota"transplantation[J]."PLoS"One,"2018,"13(11):"e0194904.

        [41] XIE"W"R,"YANG"X"Y,"XIA"H"H"X,"et"al."Hair"regrowth"following"fecal"microbiota"transplantation"in"an"elderly"patient"with"alopecia"areata:"A"case"report"and"review"of"the"literature[J]."WJCC,"2019,"7(19):"3074–3081.

        [42] CAI"T,"SHI"X,"YUAN"L"Z,"et"al."Fecal"microbiota"transplantation"in"an"elderly"patient"with"mental"depression[J]."Int"Psychogeriatr,"2019,"31(10):"1525–1526.

        [43] LEE"S"M,"DONG"T"S,"KRAUSE-SORIO"B,"et"al."The"intestinal"microbiota"as"a"predictor"for"antidepressant"treatment"outcome"in"geriatric"depression:"A"prospective"pilot"study[J]."Int"Psychogeriatr,"2022,"34(1):"33–45.

        [44] WANG"S,"XU"M,"WANG"W,"et"al."Systematic"review:"Adverse"events"of"fecal"microbiota"transplantation[J]."PLoS"One,"2016,"11(8):"e0161174.

        [45] BOWMAN"K"A,"BROUSSARD"E"K,"SURAWICZ"C"M."Fecal"microbiota"transplantation:"Current"clinical"efficacy"and"future"prospects[J]."Clin"Exp"Gastroenter,"2015,"8:"285–291.

        (收稿日期:2024–07–08)

        (修回日期:2024–11–07)

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