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        神經(jīng)激素與嚙齒類動(dòng)物的社會(huì)識(shí)別研究進(jìn)展

        2017-05-30 13:02:01王智
        安徽農(nóng)業(yè)科學(xué) 2017年30期
        關(guān)鍵詞:雌激素催產(chǎn)素

        王智

        摘要綜述了催產(chǎn)素(OT)、精氨酸加壓素(AVP)、性激素(包括雌激素、孕酮、雄性激素)這些神經(jīng)激素與嚙齒類動(dòng)物的社會(huì)識(shí)別關(guān)系的研究進(jìn)展。

        關(guān)鍵詞神經(jīng)激素;社會(huì)識(shí)別;催產(chǎn)素;精氨酸加壓素;雌激素

        中圖分類號(hào)Q958.1文獻(xiàn)標(biāo)識(shí)碼

        A文章編號(hào)0517-6611(2017)30-0117-05

        AbstractThe research progresses on the correlations between oxytocin(OT),arginine vasopression(AVP),sex hormones (including estrogen,progesterone,androgenic hormones)and the social recognition of rodents were reviewed.

        Key wordsNeurohormone;Social recognition;Oxytocin;Argininevasopressin;Estrogen

        社會(huì)識(shí)別(Social recognition,SR)是指動(dòng)物在遇到熟悉的同種個(gè)體后調(diào)整其自身行為,以便恰當(dāng)互作、形成等級(jí)和其他社會(huì)關(guān)系[1-3],它是社會(huì)生活和所有社會(huì)行為的基礎(chǔ)。親緣識(shí)別(Kinrecognition)、配偶關(guān)系建立(Pairbonding)、領(lǐng)域防衛(wèi)(Domaindefense)和優(yōu)勢(shì)地位(Dominance hierarchies)的建立等都依靠于個(gè)體長(zhǎng)期對(duì)熟悉的、曾遇到過的同種個(gè)體能加以分辨的能力[4]。除了長(zhǎng)期社會(huì)識(shí)別[5-7]外,嚙齒類動(dòng)物也形成暫時(shí)的短期記憶[8]。因此,社會(huì)識(shí)別是社會(huì)關(guān)系的基礎(chǔ)。社會(huì)識(shí)別不同于其他類型的學(xué)習(xí)和記憶,它是一種特殊類型的記憶,能被大腦中不同的解剖和神經(jīng)化學(xué)環(huán)路調(diào)控[9]。此外,動(dòng)物通過社會(huì)識(shí)別就不會(huì)將精力投入到探究以前遇到過的對(duì)己無(wú)害的個(gè)體上,而是花費(fèi)時(shí)間在與群體活動(dòng)相關(guān)的行為上。因此,個(gè)體的社會(huì)識(shí)別和記憶對(duì)于動(dòng)物的繁殖和物種生存至為關(guān)鍵。人類和非人靈長(zhǎng)類主要依靠視覺和聽覺信息進(jìn)行個(gè)體識(shí)別,而對(duì)于大多數(shù)非靈長(zhǎng)類哺乳動(dòng)物,聽覺和視覺信號(hào)雖然對(duì)社會(huì)識(shí)別也有重要影響,但社會(huì)識(shí)別的最主要信息來源是嗅覺或信息素信號(hào)[10-12]。大量研究表明,社會(huì)識(shí)別受到包括催產(chǎn)素(Oxytocin,OT)、精氨酸加壓素(Arginine vasopressin,AVP)、雌激素(Estrogen)等神經(jīng)激素的調(diào)節(jié)。筆者綜述了幾種主要的神經(jīng)激素與社會(huì)識(shí)別的關(guān)系,以揭示社會(huì)識(shí)別的神經(jīng)內(nèi)分泌機(jī)制,為進(jìn)一步研究學(xué)習(xí)、記憶及更復(fù)雜的社會(huì)行為提供理論基礎(chǔ)。

        1與社會(huì)識(shí)別有關(guān)的神經(jīng)肽

        1.1催產(chǎn)素(Oxytocin,OT)催產(chǎn)素(OT)涉及各種社會(huì)行為的調(diào)節(jié),包括社會(huì)識(shí)別[13]。對(duì)雄性大鼠全身給藥的早期研究產(chǎn)生了2種沖突的結(jié)果:首次暴露于青春期大鼠后施以O(shè)T拮抗劑[14]和低劑量的OT[15-16],在2次試驗(yàn)的適應(yīng)范式中雄性大鼠均表現(xiàn)出社會(huì)記憶的易化作用;較高的OT非生理劑量則會(huì)損害社會(huì)記憶[14,17]。這些沖突的結(jié)果被歸因于OT分子的不同部分對(duì)社會(huì)記憶的相反效應(yīng)[18]。盡管如此,仍很難解釋這些全身給藥的藥物穿過血腦屏障的有限程度能對(duì)行為產(chǎn)生多大的影響[19]。對(duì)雌性大鼠的腦室內(nèi)施以O(shè)T拮抗劑后其社會(huì)識(shí)別被損害,但注入OT則未被損害[20]。相似地,在雄性大鼠和青春期大鼠相遇后,對(duì)其腦室內(nèi)施以低劑量的OT,發(fā)現(xiàn)120 min后的第2次相遇時(shí)雄性大鼠減少了對(duì)青春期大鼠的探究,這種效應(yīng)可被OT拮抗劑的協(xié)同施與所逆轉(zhuǎn)[21]。這些研究支持OT對(duì)雄性和雌性大鼠社會(huì)識(shí)別的易化作用,也表明超過生理基準(zhǔn)的OT不會(huì)增強(qiáng)社會(huì)識(shí)別。

        此后的OT基因敲除(OT knockout,OTKO)小鼠研究表明,OT對(duì)于熟悉性識(shí)別(Familiarity recognition)是必需的[13,16,19]。與野生型小鼠不同,OTKO小鼠對(duì)重復(fù)出現(xiàn)的同種個(gè)體未表現(xiàn)出適應(yīng),在不適應(yīng)期對(duì)新的刺激小鼠也沒有表現(xiàn)出更多探究[16,19]。OTKO小鼠在社會(huì)分辨試驗(yàn)中也不能區(qū)分熟悉個(gè)體和陌生個(gè)體[13]。這些轉(zhuǎn)基因小鼠的社會(huì)識(shí)別能被在暴露于同種個(gè)體前對(duì)其側(cè)腦室注射OT而得到糾正[17]。因此,這些結(jié)果表明OT對(duì)社會(huì)記憶的效應(yīng)不是鞏固或回想,而是起初的獲得。

        對(duì)OT受體基因敲除(OTR knockout,OTRKO)小鼠的研究表明,小鼠的社會(huì)識(shí)別依靠OT對(duì)

        內(nèi)側(cè)杏仁核(Medial amygdale,MeA)的OTR的作用[17,22]。在嚙齒類動(dòng)物體內(nèi),

        MeA是來自主嗅球和副嗅球系統(tǒng)的社會(huì)相關(guān)嗅覺傳入的集中位點(diǎn)[23-26]。在OTKO小鼠的MeA注射OT會(huì)恢復(fù)其社會(huì)識(shí)別[16]。相似地,施以O(shè)T拮抗劑[16]或OTR的反義DNA于MeA則會(huì)損害野生型小鼠的社會(huì)識(shí)別功能[22]。OT作用于其他腦區(qū)(如嗅球、內(nèi)側(cè)視葉前區(qū))似乎也對(duì)社會(huì)識(shí)別有調(diào)節(jié)作用,OT/OTR作用于MeA似乎對(duì)于熟悉性的識(shí)別是必需的[3]。

        1.2加壓素(Argininevasopressin,AVP)

        AVP與OT一樣,在各種社會(huì)行為中起重要作用[13],包括社會(huì)識(shí)別[24,27-28]。低劑量AVP的全身給藥不能改善社會(huì)識(shí)別,而OT卻能改善社會(huì)識(shí)別[15],表明二者在社會(huì)記憶中發(fā)揮的作用不同。AVP對(duì)社會(huì)識(shí)別的作用在雄性中似乎比雌性要大。

        研究表明,MeA作為雌激素,對(duì)社會(huì)識(shí)別效應(yīng)有特定的作用位點(diǎn)[29]。側(cè)隔(Lateral septum,LS)被認(rèn)為是介導(dǎo)社會(huì)識(shí)別的首要的大腦結(jié)構(gòu)。草原田鼠(Microtus ochrogaster)的V1aR基因插入到大鼠側(cè)隔或V1aR在LS的過量表達(dá)都會(huì)改善社會(huì)識(shí)別[30-31]。

        在選擇探究同種青春期動(dòng)物和空籠時(shí),V1bRKO動(dòng)物表現(xiàn)出對(duì)同種青春期動(dòng)物興趣的減少。AVP注入嗅球(Olfactory bulb,OB)能改善大鼠的社會(huì)識(shí)別[32],在OB局部注入V1R拮抗劑或靶向V1aR mRNA的小干擾RNA或OB的AVP能細(xì)胞的破壞會(huì)損壞大鼠的社會(huì)識(shí)別[33]。AVP介導(dǎo)的社會(huì)識(shí)別中,LS、OB、MeA都參與其中。

        多次適應(yīng)試驗(yàn)中,V1bRKO小鼠仍能區(qū)分熟悉和不熟悉的同種個(gè)體[34]。關(guān)于V1aRKO小鼠的研究發(fā)現(xiàn),LS的V1aR涉及社會(huì)識(shí)別,而且LS的V1aR表達(dá)對(duì)AVP涉及的社會(huì)識(shí)別是必需的[31,35]。

        2與社會(huì)識(shí)別有關(guān)的性激素

        2.1雌激素(Estrogens)雌性嚙齒類動(dòng)物的激素水平隨動(dòng)情周期的變化與其在社會(huì)識(shí)別范式中的表現(xiàn)相關(guān),表明雌性動(dòng)物的性激素參與社會(huì)識(shí)別[1,36]。性激素通過調(diào)節(jié)OT和AVP系統(tǒng)來影響社會(huì)識(shí)別[1,37]。雌性動(dòng)物在其繁殖活躍期的社會(huì)識(shí)別似乎變得更容易[38]。卵巢切除大鼠的社會(huì)識(shí)別記憶損害可以通過雌激素和孕酮的急性處理而逆轉(zhuǎn)[39-40],同樣情形的小鼠也可以通過雌激素的急性和慢性處理而恢復(fù)[41],這都表明雌激素在社會(huì)識(shí)別中的關(guān)鍵作用。芳香化酶基因敲除(Aromatase knock out,ArKO)小鼠在適應(yīng)/去適應(yīng)范式中社會(huì)識(shí)別的損害[42-43]可通過聯(lián)合施予雌二醇和雄激素二氫睪酮而逆轉(zhuǎn),這也表明了雌激素對(duì)社會(huì)識(shí)別的調(diào)控作用[42]。雌激素的作用受不同的受體介導(dǎo)。雌激素靶向受體主要有2個(gè)經(jīng)典的雌激素受體α(Estrogen receptors alpha,ERα)和雌激素受體β(Estrogen receptors beta,ERβ)及至少一個(gè)G蛋白偶聯(lián)受體等。ER影響雄性小鼠的長(zhǎng)期社會(huì)識(shí)別,而非短期社會(huì)識(shí)別。遺傳學(xué)和藥理學(xué)研究也支持這一論點(diǎn),即ERα和ERβ經(jīng)由長(zhǎng)期的基因組作用而涉及社會(huì)識(shí)別[44]。試驗(yàn)前48 h對(duì)小鼠以ERα 或 ERβ激動(dòng)劑進(jìn)行全身給藥后發(fā)現(xiàn),動(dòng)物的社會(huì)識(shí)別得到改善[37,45],但ERα激動(dòng)劑的作用效果更快(40 min內(nèi))[37,46]。ERαKO、ERβKO和OTKO小鼠在適應(yīng)/去適應(yīng)范式中表現(xiàn)出不能適應(yīng)重復(fù)暴露的同種個(gè)體,熟悉小鼠被新的小鼠替代后,受試動(dòng)物也不能對(duì)其表現(xiàn)出去適應(yīng)[19]。隨后的社會(huì)辨別范式中,ERαKO雌性小鼠和OTKO雌性小鼠的社會(huì)辨別能力被完全損害,而ERβKO小鼠保留了某些程度的社會(huì)辨別能力[13,47],這表明ERα對(duì)社會(huì)識(shí)別是必需的,而ERβ可能通過作用于任務(wù)的其他方面(如競(jìng)爭(zhēng)動(dòng)機(jī))調(diào)節(jié)前者[48-49]。SanchezAndrade 等[44]以麻醉的動(dòng)物作為刺激鼠的研究發(fā)現(xiàn),雄性和雌性的ERβKO小鼠的社會(huì)識(shí)別均未受到損害,這也證實(shí)了ERβ對(duì)小鼠的社會(huì)識(shí)別不是必需的。一些研究表明,ERα可能對(duì)于雌性動(dòng)物社會(huì)識(shí)別的所有方面都是必需的,但對(duì)雄性可能僅僅易化社會(huì)記憶的保持[13,19,44,50]。實(shí)際上,ERβ似乎起輕微的易化作用,這種作用僅在更富有挑戰(zhàn)的試驗(yàn)條件下發(fā)揮,如果社會(huì)刺激不易得到,試驗(yàn)鼠不能進(jìn)行氣味標(biāo)記[51],因?yàn)樵诖碳らg隔期間試驗(yàn)鼠和刺激鼠在有孔的容器內(nèi)社會(huì)氣味不能得到保留[13,19,44]。

        雌激素對(duì)社會(huì)識(shí)別的作用可通過調(diào)節(jié)OT和OTR產(chǎn)生來解釋。雌激素促進(jìn)OT和OTR mRNA的合成。OT和OTR的mRNA水平隨動(dòng)情周期而波動(dòng),與雌激素的循環(huán)水平相一致[52-53]。卵巢切除的動(dòng)物,其OT和OTR水平有所降低。大鼠的雌激素可直接調(diào)節(jié)OT產(chǎn)生[54],施以雌激素可增加下丘腦室旁核(PVN)內(nèi)涉及OT產(chǎn)生的神經(jīng)元電興奮性[55]。PVN處的OT產(chǎn)生伴有ERβ的高度表達(dá)[56],因此認(rèn)為ERβ調(diào)節(jié)OT產(chǎn)生[57]。 相應(yīng)地,施予雌激素給ERβKO雄性[58]和雌性小鼠[57]不能誘導(dǎo)PVN處OT表達(dá),而PVN處的OT及其mRNA基線水平仍然維持正常水平[57]。OT的基線水平可以解釋ERβKO小鼠社會(huì)識(shí)別僅受到部分損害[13]。此外,對(duì)于野生型小鼠,以ERβ調(diào)節(jié)的OT若處于基線水平以上,則會(huì)增強(qiáng)其社會(huì)辨別能力[13]。

        雌激素也調(diào)節(jié)MeA處OTR的密度和OTR基因的表達(dá)。雌激素對(duì)OTR的調(diào)節(jié)是通過MeA處高度表達(dá)ERα進(jìn)行的[56],這對(duì)于誘發(fā)OTR是必需的[59]。相反地,即使ERβ在MeA處有高度表達(dá),但其對(duì)OTR基因的轉(zhuǎn)錄也不是必需的[57]。OT依賴MeA處的ERα而非ERβ發(fā)揮作用,這解釋了在社會(huì)辨別范式中ERαKO小鼠的社會(huì)識(shí)別受到完全損害而ERβKO小鼠僅受到部分損害的原因[13]。帶短發(fā)夾RNA(shRNA)的雌性大鼠其杏仁核處ERα表達(dá)的減少,在適應(yīng)/去適應(yīng)范式中會(huì)選擇性地?fù)p害社會(huì)識(shí)別。這些雌性大鼠重復(fù)暴露于刺激鼠后沒有表現(xiàn)出對(duì)同種個(gè)體探究的減少,新個(gè)體取代熟悉個(gè)體后其社會(huì)探究也未發(fā)生變化[29]??偟膩碚f,ERα可能通過調(diào)節(jié)MeA處OT/OTR的產(chǎn)生是小鼠和大鼠的社會(huì)識(shí)別所必需的,而ERβ似乎在其中起易化作用。

        研究表明,PPT(Propyl pyrazole triol,一種ER激動(dòng)劑)能增強(qiáng)卵巢切除小鼠的社會(huì)識(shí)別,而2,3-雙(4-羥苯基)丙腈(DPN,一種ERβ激動(dòng)劑)則輕微損害社會(huì)識(shí)別[46]。這些快速效應(yīng)表明,雌激素能通過非基因組的作用機(jī)制來影響社會(huì)識(shí)別。與長(zhǎng)期研究結(jié)果相似,這些結(jié)果也驗(yàn)證了ERα在改善社會(huì)識(shí)別上的重要性高于ERβ。17β-雌二醇、PPT、DPN和G1的這些快速效應(yīng)似乎不是專門針對(duì)社會(huì)記憶的,因?yàn)檫@些激動(dòng)劑也能快速增強(qiáng)物體位置范式(Object location paradigm)中動(dòng)物的非社會(huì)物體識(shí)別能力和空間學(xué)習(xí)能力[46]??紤]到在施予PPT和DPN給卵巢切除小鼠40 min內(nèi),動(dòng)物海馬區(qū)的樹突棘密度受到影響,這可能就是雌激素通過調(diào)節(jié)海馬的細(xì)胞信號(hào)轉(zhuǎn)導(dǎo),從而快速影響動(dòng)物學(xué)習(xí)。雌激素的非基因組方式是通過細(xì)胞內(nèi)及與膜結(jié)合的雌激素受體激活涉及記憶形成和突觸可塑化的細(xì)胞內(nèi)信號(hào)級(jí)聯(lián)放大來發(fā)揮作用的,如絲裂原活化蛋白激酶(MAPK)依賴通路[60]。Phan等[46]研究表明17β-雌二醇在海馬內(nèi)的呈遞快速改善了小鼠的社會(huì)識(shí)別和物體定位學(xué)習(xí),表明海馬涉及雌激素在這些學(xué)習(xí)范式中的效應(yīng),社會(huì)識(shí)別的增強(qiáng)擴(kuò)展到其他學(xué)習(xí)范式。

        目前,ERα和ERβ發(fā)生作用的大腦位點(diǎn)尚不清楚。Spiteri等[29]研究表明,經(jīng)由RNA干擾的雌性大鼠后背杏仁核(MePDA)中ERα的表達(dá)減少會(huì)抑制社會(huì)識(shí)別,而下丘腦腹內(nèi)側(cè)核(VMN)的ERα減少則不會(huì)影響社會(huì)識(shí)別。這說明社會(huì)識(shí)別是受杏仁核的ERα調(diào)控的,雌激素效應(yīng)可能通過OT發(fā)揮作用。研究發(fā)現(xiàn),與低社會(huì)性的小鼠相比,高社會(huì)性的雄性小鼠在PVN處有較多的OT和AVP的mRNA,MeA處有較多的OTR、V1a R和ERα的mRNA,OTR和V1aR的mRNA與MeA處的ERα的mRNA高度相關(guān),OT和AVP的mRNA與PVN處的ERβ高度相關(guān),表明OT和AVP系統(tǒng)受雌激素受體高度調(diào)控[61]。以上發(fā)現(xiàn)支持Choleris 等[19]提出的4基因的“微網(wǎng)”模型,認(rèn)為4個(gè)基因在2個(gè)腦區(qū)的組合活性構(gòu)成雌激素調(diào)節(jié)依賴于OT的小鼠社會(huì)識(shí)別的基礎(chǔ)。雌激素通過ERβ控制PVN處的OT產(chǎn)生,雌激素通過ERα調(diào)控OTR基因在MeA的表達(dá),而MeA處是社會(huì)相關(guān)的嗅覺信息處理部位[23,25,62-63]。

        2.2孕酮(Progesterone)

        孕酮一直被認(rèn)為是“雌性的”激素,在雄性動(dòng)物中含量較少,只有遇到緊急事件時(shí)雄性動(dòng)物的孕酮含量才有所上升。Wagner[64]研究表明孕酮及其受體在雄性動(dòng)物的行為和生理中起重要的替補(bǔ)作用。Auger等[65]研究發(fā)現(xiàn)孕酮受體幾乎存在于終紋床核(Bed nucleus of the stria terminalis,BNST)和MeA內(nèi)的每個(gè)AVP免疫反應(yīng)細(xì)胞內(nèi)。這種共存有調(diào)控BNST和MeA內(nèi)AVP的功能,因?yàn)樵型獣?huì)導(dǎo)致這些細(xì)胞內(nèi)的AVP免疫反應(yīng)標(biāo)記的抑制,而且這些細(xì)胞的2個(gè)投射位點(diǎn)側(cè)隔(LS)和側(cè)韁(Lateral habenula,LH)的相應(yīng)標(biāo)記也被抑制[66],而LS是涉及社會(huì)識(shí)別調(diào)控的重要位點(diǎn),所以孕酮可能經(jīng)由抑制AVP的表達(dá)而損害社會(huì)識(shí)別。Bychowski等[67]認(rèn)為用孕酮處理雄性大鼠會(huì)導(dǎo)致其社會(huì)識(shí)別受到顯著損害,而且孕酮可能作用于孕酮受體以損害社會(huì)識(shí)別,因?yàn)樵型荏w拮抗劑RU-486會(huì)抑制孕酮對(duì)社會(huì)識(shí)別的損害,特定的孕酮激動(dòng)劑R5020也會(huì)使社會(huì)識(shí)別受到損害。Bychowski等[68]研究發(fā)現(xiàn),將AVP注入側(cè)隔解除了由孕酮導(dǎo)致的社會(huì)辨別損害。盡管目前尚不明確孕酮與AVP的作用機(jī)制,但這些研究表明孕酮在調(diào)節(jié)雄性動(dòng)物大腦內(nèi)的社會(huì)識(shí)別上起著重要作用。孕酮引起的社會(huì)記憶損害在人類已有體現(xiàn),外源性孕酮暴露會(huì)損害女性回憶社會(huì)相關(guān)刺激的能力(如人臉)[69]。孕酮似乎干擾社會(huì)識(shí)別記憶的形成,而不妨礙一般的非空間記憶或嗅覺功能。孕酮在雄性系統(tǒng)中有重要功能,這種功能對(duì)于介導(dǎo)社會(huì)互作是有益的[67]。

        2.3雄性激素

        雄性激素也涉及調(diào)控社會(huì)識(shí)別。Bluthe等[70-71]研究發(fā)現(xiàn)睪酮對(duì)大鼠長(zhǎng)期的社會(huì)識(shí)別效應(yīng)。性腺完整的雄性大鼠在首次暴露于刺激鼠后表現(xiàn)出30~60 min適應(yīng)。雌性和閹割的雄性大鼠在首次暴露于刺激鼠后表現(xiàn)出顯著的適應(yīng)反應(yīng)(長(zhǎng)達(dá)2~3 h)[8,71]。因此,可能性腺完整的雄性動(dòng)物對(duì)熟悉個(gè)體的識(shí)別能力相對(duì)較低。閹割的雄性動(dòng)物在手術(shù)后第1周內(nèi)表現(xiàn)出暫時(shí)的社會(huì)識(shí)別記憶損害,但到手術(shù)后2~3周其社會(huì)識(shí)別能力完全恢復(fù)[70-72]。但是,手術(shù)后的閹割大鼠與性腺完整大鼠在隔日測(cè)試時(shí),其社會(huì)識(shí)別并無(wú)不同[70,72]。從性腺完整大鼠與雄性閹割大鼠對(duì)刺激鼠或刺激鼠的氣味線索(污染的草墊、尿液)重復(fù)暴露的反應(yīng)可證實(shí)閹割的雄性大鼠社會(huì)識(shí)別受損。在社會(huì)暴露10 min后,性腺完整大鼠對(duì)刺激鼠及其氣味線索的社會(huì)探究都表現(xiàn)出顯著下降,而閹割雄性大鼠僅對(duì)刺激鼠表現(xiàn)出探究減少,對(duì)熟悉刺激鼠或陌生刺激鼠的氣味線索均未表現(xiàn)出探究減少[73]。閹割對(duì)動(dòng)物社會(huì)識(shí)別的效應(yīng)取決于閹割后的測(cè)試時(shí)間[72]和閹割后被測(cè)試的次數(shù)[71]。雄激素受體通過發(fā)育方式單獨(dú)介導(dǎo)效應(yīng)似乎不可能,因?yàn)橐訟R拮抗劑氟他米特(Flutamide)每日進(jìn)行產(chǎn)前暴露,對(duì)雄性大鼠沒有效果[74]。大量研究表明,睪酮對(duì)社會(huì)識(shí)別的效應(yīng)實(shí)際上也是通過雌激素機(jī)制來調(diào)節(jié)的。將雄性小鼠的cyp19基因突變(此基因編碼芳香化酶,芳香化酶可將睪酮通過芳香化轉(zhuǎn)化為雌二醇),動(dòng)物在適應(yīng)/去適應(yīng)范式中的社會(huì)識(shí)別被損害[42]。此外,芳香化酶敲除(ArKO)的雄性小鼠其社會(huì)識(shí)別的損害是由于基因敲除的引發(fā)性和非組織效應(yīng),因?yàn)橐源贫己投洳G酮(2種睪酮代謝物)聯(lián)合處理成年小鼠,其社會(huì)識(shí)別得到恢復(fù)[2]。此外,相對(duì)于野生雄性小鼠,ArKO雄性小鼠即使增加睪酮注射量,它們的社會(huì)識(shí)別仍會(huì)被損害[75]。因此,可能是睪酮-AR作用損害社會(huì)識(shí)別或是雌二醇對(duì)雄性小鼠的社會(huì)識(shí)別起重要作用。目前,關(guān)于AR在社會(huì)識(shí)別中所起的作用研究甚少。Karlsson 等[76]研究發(fā)現(xiàn),雄性小鼠神經(jīng)系統(tǒng)中的AR對(duì)雌性同種個(gè)體的社會(huì)記憶是不需要的,但它們對(duì)雄性刺激鼠卻是關(guān)鍵。今后應(yīng)開展對(duì)睪酮-AR及其與雌激素關(guān)系的進(jìn)一步研究,闡明它們?cè)诖笫蠛托∈笊鐣?huì)識(shí)別中的機(jī)制。

        迄今為止,已知睪酮會(huì)調(diào)控AVP[77-79]。雄性大鼠大腦比雌性有更高的AVP表達(dá)[80-81]。AVP介導(dǎo)雄性動(dòng)物中雄激素對(duì)社會(huì)識(shí)別的效應(yīng)。依賴于睪酮的AVP神經(jīng)元所在腦區(qū)(如BNST、MeA),其AVP纖維投射到LS,LS內(nèi)的AVP作用對(duì)于雄性的社會(huì)識(shí)別是必需的[82-85]。雄性大鼠中,睪酮可逆轉(zhuǎn)由于閹割造成的幾個(gè)邊緣腦區(qū)AVP表達(dá)減少[86]。雌性大鼠和閹割的雄性大鼠其社會(huì)識(shí)別不依賴于AVP,因?yàn)槭┯鐰VP或其拮抗劑對(duì)大鼠的社會(huì)識(shí)別無(wú)影響[27]。此外,雄性閹割大鼠的社會(huì)識(shí)別對(duì)AVP的依賴可通過睪酮處理得到補(bǔ)救[27,79],小鼠情況與大鼠類似[71]??傊?,雄性大鼠和小鼠的社會(huì)識(shí)別以依賴于睪酮(和雌激素)的方式通過AVP介導(dǎo)。研究表明,睪酮對(duì)AVP產(chǎn)生的調(diào)控效應(yīng)至少部分可能是通過其轉(zhuǎn)化為雌激素的,因?yàn)橐源贫迹ǚ嵌洳G酮)處理會(huì)逆轉(zhuǎn)雄性閹割大鼠AVP水平的減少[87-88]。此外,ArKO小鼠也表現(xiàn)出在LS、MeA、BNST和視上核的AVP免疫反應(yīng)活性減少[42-43]。Scordalakes等[89]對(duì)ERαKO小鼠的研究表明,ERα連同AR會(huì)提高邊緣系統(tǒng)的AVP表達(dá)水平。小鼠的雌激素誘導(dǎo)PVN處AVP減少,雌激素的這種效應(yīng)在ERβKO小鼠體內(nèi)被抑制,證實(shí)了ERβ 對(duì)OT和AVP在PVN處合成的雙重和相反作用[58]??偠灾?,雄激素在雄性動(dòng)物的社會(huì)識(shí)別中起間接作用,可能通過調(diào)節(jié)AVP和雌激素系統(tǒng)來實(shí)現(xiàn)。

        3小結(jié)與展望

        對(duì)大鼠和小鼠的大量研究支持社會(huì)識(shí)別被一個(gè)復(fù)雜的具性別依賴的OT和ATP系統(tǒng)所調(diào)控,性激素可能通過特異性激活雌激素受體而提升OT作用易化社會(huì)識(shí)別。對(duì)以依賴雄激素方式的社會(huì)識(shí)別而言,雄性動(dòng)物似乎比雌性更依賴AVP,尤其是V1aR,即使此系統(tǒng)最終由雌激素機(jī)制所介導(dǎo)。在某種程度上,涉及社會(huì)識(shí)別的特定腦區(qū)是性二態(tài)的,LS對(duì)于雄性的社會(huì)識(shí)別十分重要,MeA對(duì)雄性和雌性的社會(huì)識(shí)別都是必需的,尤其是通過非揮發(fā)性嗅覺信號(hào)進(jìn)行的社會(huì)識(shí)別[90]。社會(huì)記憶屬于記憶研究中的新興領(lǐng)域。目前,不僅涉及社會(huì)記憶獲取和鞏固的相關(guān)腦區(qū)的細(xì)胞機(jī)制尚不明確,而且控制社會(huì)識(shí)別記憶形成及社會(huì)記憶的最大持續(xù)時(shí)間的細(xì)胞機(jī)制也不明確。少數(shù)研究表明,調(diào)控學(xué)習(xí)與記憶的突觸可塑性的最知名受體——N-甲基-D-天冬氨酸受體(N-methyl-D-aspartate receptor,NMDA受體)的其中2個(gè)亞單位——NR2B和NR2A對(duì)社會(huì)識(shí)別記憶的不同影響:NR2B在前腦的過量表達(dá)會(huì)增強(qiáng)不同品系和動(dòng)物的社會(huì)識(shí)別記憶[91],而NR2A的過量表達(dá)則會(huì)損害小鼠的長(zhǎng)期社會(huì)識(shí)別和非社會(huì)嗅覺記憶[92]。

        總而言之,神經(jīng)激素通過神經(jīng)內(nèi)分泌水平和基因水平影響動(dòng)物和人類的社會(huì)識(shí)別,而且這些神經(jīng)激素之間互有交叉,特定的腦區(qū)或器官對(duì)其發(fā)揮作用具有重要影響。對(duì)于生活在社會(huì)群體的人類和其他動(dòng)物而言,社會(huì)識(shí)別是社會(huì)認(rèn)知發(fā)展的重要組成部分。Skuse等[93]研究發(fā)現(xiàn), 孤獨(dú)者譜系障礙(Autism spectrum disorders,ASD)患者的OT受體上一個(gè)普通SNP(rs237887)與先證者、父母和同胞的面部識(shí)別記憶強(qiáng)烈相關(guān),提示OXTR在調(diào)控社會(huì)識(shí)別上的保守作用通過進(jìn)化從嚙齒類的嗅覺記憶跨越到人類視覺記憶,超越感覺界限。Strauss等[94]研究發(fā)現(xiàn),精神分裂癥低水平的社會(huì)認(rèn)知水平與精神分裂癥血漿中減少的催產(chǎn)素水平顯著相關(guān)。這些都表明對(duì)社會(huì)識(shí)別近因機(jī)制的理解不僅有助于從整體上闡明社會(huì)行為,也將為高度性二態(tài)的異常社會(huì)失調(diào)(如ASD)的發(fā)展和調(diào)控提供視角[95],進(jìn)而揭示與人類認(rèn)知相關(guān)疾病的機(jī)制,增強(qiáng)這些疾病治療的可能。

        參考文獻(xiàn)

        [1]

        CHOLERIS E,KAVALIERS M,PFAFF D W.Functional genomics of social recognition[J].J Neuroendocrinol,2004,16(4):383-389.

        [2] PIERMAN S,DOUHARD Q,BAKKER J.Evidence for a role of early oestrogens in the central processing of sexually relevant olfactory cues in female mice[J].Eur J Neurosci,2008,27(2):423-431.

        [3] CHOLERIS E,CLIPPERTONALLEN A E,PHAN A,et al.Neuroendocrinology of social information processing in rats and mice[J].Front neuroendocrinol,2009,30(4):442-459.

        [4] FERGUSON J N,YOUNG L J,INSEL T R.The neuroendocrine basis of social recognition[J].Front neuroendocrino,2002,23(2):200-224.

        [5] KABA H,ROSSER A,KEVERNE B.Neural basis of olfactory memory in the context of pregnancy block[J].Neuroscience,1989,32(3):657-662.

        [6] DEMAS G E,WILLIAMS J M,NELSON R J.Amygdala but not hippocampal lesions impair olfactory memory for mate in prairie voles (Microtus ochrogaster)[J].Am J Physiol,1997,273(5Pt2):1683-1689.

        [7] KEVERNE E B.Vomeronasal/accessory olfactory system and pheromonal recognition[J].Chem Senses,1998,23(4):491-494.

        [8] THOR D H,HOLLOWAY W J.Anosmia and play fighting behavior in prepubescent male and female rats[J].Physiol Behav,1982,29(2):281-285.

        [9] BIELSKY I F,YOUNG L J.Oxytocin,vasopressin,and social recognition in mammals[J].Peptides,2004,25(9):1565-1574.

        [10] POPIK P,VETULANI J,BISAGA A,et al.Recognition cue in the rat's social memory paradigm[J].J Basic Clin Physiol Pharmacol,1991,2(4):315-327.

        [11] SPEHR M,SPEHR J,UKHANOV K,et al.Parallel processing of social signals by the mammalian main and accessory olfactory systems[J].Cell Mol Life Sci,2006,63(13):1476-1484.

        [12] BRENNAN P A,KENDRICK K M.Mammalian social odours:Attraction and individual recognition[J].Philos Trans R Soc Lond B Biol Sci,2006,361(1476):2061-2078.

        [13] DONALDSON Z R,YOUNG L J.Oxytocin,vasopressin,and the neurogenetics of sociality[J].Science,2008,322(5903):900-904.

        [14] POPIK P,VETULANI J.Opposite action of oxytocin and its peptide antagonists on social memory in rats[J].Neuropeptides,1991,18(1):23-27.

        [15] POPIK P,VETULANI J,VAN REE J M.Low doses of oxytocin facilitate social recognition in rats[J].Psychopharmacology (Berl),1992,106(1):71-74.

        [16] POPIK P,VETULANI J,VAN REE J M.Low doses of oxytocin facilitate social recognition in rats[J].Psychopharmacology,1992,106(1):71-74.

        [17] DANTZER R,BLUTHE R M,KOOB G F,et al.Modulation of social memory in male rats by neurohypophyseal peptides[J].Psychopharmacology,1987,91(3):363-368.

        [18] POPIK P,VETULANI J,VAN REE J M.Facilitation and attenuation of social recognition in rats by different oxytocinrelated peptides[J].Eur J Pharmacol,1996,308(2):113-116.

        [19] POPIK P,VAN REE J M.Neurohypophyseal peptides and social recognition in rats[J].Prog Brain Res,1998,119:415-436.

        [20] ENGELMANN M,EBNER K,WOTJAK C T,et al.Endogenous oxytocin is involved in shortterm olfactory memory in female rats[J].Behav Brain Res,1998,90(1):89-94.

        [21] BENELLI A,BERTOLINI A,POGGIOLI R,et al.Polymodal doseresponse curve for oxytocin in the social recognition test[J].Neuropeptides,1995,28(4):251-255.

        [22] CHOLERIS E,LITTLE S R,MONG J A,et al.Microparticlebased delivery of oxytocin receptor antisense DNA in the medial amygdala blocks social recognition in female mice[J].Proc Natl Acad Sci USA,2007,104(11):4670-4675.

        [23] DULAC C,TORELLO A T.Molecular detection of pheromone signals in mammals:From genes to behaviour[J].Nat Rev Neurosci,2003,4(7):551-562.

        [24] BIELSKY I F,HU S B,SZEGDA K L,et al.Profound impairment in social recognition and reduction in anxietylike behavior in vasopressin V1a receptor knockout mice[J].Neuropsychopharmacology,2004,29(3):483-493.

        [25] KANG N,BAUM M J,CHERRY J A.A direct main olfactory bulb projection to the ‘vomeronasal amygdala in female mice selectively responds to volatile pheromones from males[J].Eur J Neurosci,2009,29(3):624-634.

        [26] JOHNSTON R E,PENG A.Memory for individuals:Hamsters (Mesocricetus auratus) require contact to develop multicomponent representations (concepts) of others[J].Journal of comparative psychology,2008,122(2):121-131.

        [27] BLUTHE R M,SCHOENEN J,DANTZER R.Androgendependent vasopressinergic neurons are involved in social recognition in rats[J].Brain Res,1990,519(1/2):150-157.

        [28] POPIK P,VOS P E,VAN REE J M.Neurohypophyseal hormone receptors in the septum are implicated in social recognition in the rat[J].Behav Pharmacol,1992,3(4):351-358.

        [29] SPITERI T,MUSATOV S,OGAWA S,et al.The role of the estrogen receptor alpha in the medial amygdala and ventromedial nucleus of the hypothalamus in social recognition,anxiety and aggression[J].Behav Brain Res,2010,210(2):211-220.

        [30] LANDGRAF R,F(xiàn)RANK E,ALDAG J,et al.Viral vectormediated gene transfer of the vole V1a vasopressin receptor in the rat septum:Improved social discrimination and active social behavior[J].The European journal of neuroscience.2003,18(2):403-411.

        [31] BIELSKY I F,HU S B,REN X,et al.The V1a vasopressin receptor is necessary and sufficient for normal social recognition:A gene replacement study[J].Neuron,2005,47(4):503-513.

        [32] DLUZEN D E,MURAOKA S,ENGELMANN M,et al.The effects of infusion of arginine vasopressin,oxytocin,or their antagonists into the olfactory bulb upon social recognition responses in male rats[J].Peptides,1998,19(6):999-1005.

        [33] TOBIN V A,HASHIMOTO H,WACKER D W,et al.An intrinsic vasopressin system in the olfactory bulb is involved in social recognition[J].Nature,2010,464(7287):413-417.

        [34] WERSINGER S R,KELLIHER K R,ZUFALL F,et al.Social motivation is reduced in vasopressin 1b receptor null mice despite normal performance in an olfactory discrimination task[J].Horm Behav,2004,46(5):638-645.

        [35] LANDGRAF R,GERSTBERGER R,MONTKOWSKI A,et al.V1 vasopressin receptor antisense oligodeoxynucleotide into septum reduces vasopressin binding,social discrimination abilities,and anxietyrelated behavior in rats[J].J Neurosci,1995,15(6):4250-4258.

        [36] CLIPPERTONALLEN A E,LEE A W,REYES A,et al.Oxytocin,vasopressin and estrogen receptor gene expression in relation to social recognition in female mice[J].Physiol Behav,2012,105(4):915-924.

        [37] CHOLERIS E,CLIPPERTON A E,PHAN A,et al.Estrogen receptor beta agonists in neurobehavioral investigations[J].Curr Opin Investig Drugs,2008,9(7):760-773.

        [38] WALMER D K,WRONA M A,HUGHES C L,et al.Lactoferrin expression in the mouse reproductive tract during the natural estrous cycle:correlation with circulating estradiol and progesterone[J].Endocrinology,1992,131(3):1458-1466.

        [39] HLINAK Z.Social recognition in ovariectomized and estradioltreated female rats[J].Horm Behav,1993,27(2):159-166.

        [40] SPITERI T,AGMO A.Ovarian hormones modulate social recognition in female rats[J].Physiol Behav,2009,98(1/2):247-250.

        [41] TANG A C,NAKAZAWA M,ROMEO R D,et al.Effects of longterm estrogen replacement on social investigation and social memory in ovariectomized C57BL/6 mice[J].Horm Behav,2005,47(3):350-357.

        [42] PIERMAN S,SICA M,ALLIERI F,et al.Activational effects of estradiol and dihydrotestosterone on social recognition and the argininevasopressin immunoreactive system in male mice lacking a functional aromatase gene[J].Horm Behav,2008,4(1):98-106.

        [43] PLUMARI L,VIGLIETTIPANZICA C,ALLIERI F,et al.Changes in the argininevasopressin immunoreactive systems in male mice lacking a functional aromatase gene[J].J Neuroendocrinol,2002,14(12):971-978.

        [44] SANCHEZANDRADE G,KENDRICK K M.Roles of alpha and betaestrogen receptors in mouse social recognition memory:Effects of gender and the estrous cycle[J].Horm Behav,2011,59(1):114-122.

        [45] CLIPPERTONALLEN A E,LEE A W,REYES A,et al.Oxytocin,vasopressin and estrogen receptor gene expression in relation to social recognition in female mice[J].Physiol Behav,2012,105(4):915-924.

        [46] PHAN A,LANCASTER K E,ARMSTRONG J N,et al.Rapid effects of estrogen receptor alpha and beta selective agonists on learning and dendritic spines in female mice[J].Endocrinology,2011,152(4):1492-1502.

        [47] CHOLERIS E,VALSECCHI P,WANG Y,et al.Social learning of a food preference in male and female Mongolian gerbils is facilitated by the anxiolytic,chlordiazepoxide[J].Pharmacol Biochem Behav,1998,60(2):575-584.

        [48] OGAWA S,CHOLERIS E,PFAFF D.Genetic influences on aggressive behaviors and arousability in animals[J].Ann N Y Acad Sci,2004,1036:257-266.

        [49] CLIPPERTON A A,CRAGG C L,WOOD A J,et al.Agonistic behavior in males and females:Effects of an estrogen receptor beta agonist in gonadectomized and gonadally intact mice[J].Psychoneuroendocrinology,2010,35(7):1008-1022.

        [50] IMWALLE D B,SCORDALAKES E M,RISSMAN E F.Estrogen receptor alpha influences socially motivated behaviors[J].Horm Behav,2002,42(4):484-491.

        [51] INSEL T R,F(xiàn)ERNALD R D.How the brain processes social information:Searching for the social brain[J].Annu Rev Neurosci,2004,27:697-722.

        [52] HO M L,LEE J N.Ovarian and circulating levels of oxytocin and arginine vasopressin during the estrous cycle in the rat[J].Acta Endocrinol (Copenh),1992,126(6):530-534.

        [53] SARKAR D K,F(xiàn)RAUTSCHY S A,MITSUGI N.Pituitary portal plasma levels of oxytocin during the estrous cycle,lactation,and hyperprolactinemia[J].Ann N Y Acad Sci,1992,652:397-410.

        [54] DELLOVADE T L,ZHU Y S,PFAFF D W.Thyroid hormones and estrogen affect oxytocin gene expression in hypothalamic neurons[J].J Neuroendocrinol,1999,11(1):1-10.

        [55] AKAISHI T,SAKUMA Y.Estrogen excites oxytocinergic,but not vasopressinergic cells in the paraventricular nucleus of female rat hypothalamus[J].Brain Res,1985,335(2):302-305.

        [56] MITRA S W,HOSKIN E,YUDKOVITZ J,et al.Immunolocalization of estrogen receptor beta in the mouse brain:Comparison with estrogen receptor alpha[J].Endocrinology,2003,144(5):2055-2067.

        [57] PATISAUL H B,SCORDALAKES E M,YOUNG L J,et al.Oxytocin,but not oxytocin receptor,is rRegulated by oestrogen receptor beta in the female mouse hypothalamus[J].J Neuroendocrinol,2003,15(8):787-793.

        [58] NOMURA M,MCKENNA E,KORACH K S,et al.Estrogen receptorbeta regulates transcript levels for oxytocin and arginine vasopressin in the hypothalamic paraventricular nucleus of male mice[J].Brain Res Mol Brain Res,2002,109(1/2):84-94.

        [59] YOUNG L J,WANG Z,DONALDSON R,et al.Estrogen receptor alpha is essential for induction of oxytocin receptor by estrogen[J].Neuroreport,1998,9(5):933-936.

        [60] THOMAS G M,HUGANIR R L.MAPK cascade signalling and synaptic plasticity[J].Nat Rev Neurosci,2004,5(3):173-183.

        [61] MURAKAMI G,HUNTER R G,F(xiàn)ONTAINE C,et al.Relationships among estrogen receptor,oxytocin and vasopressin gene expression and social interaction in male mice[J].Eur J Neurosci,2011,34(3):469-477.

        [62] BEAUCHAMP G K,YAMAZAKI K.Chemical signalling in mice[J].Biochem Soc Trans,2003,31(Pt1):147-151.

        [63] JOHNSTON R E.Chemical communication in rodents:From pheromones to individual recognition[J].Journal of mammalogy,2003,84(4):1141-1162.

        [64] WAGNER C K.The many faces of progesterone:A role in adult and developing male brain[J].Front neuroendocrinol,2006,27(3):340-359.

        [65] AUGER C J,DE VRIES G J.Progestin receptor immunoreactivity within steroidresponsive vasopressinimmunoreactive cells in the male and female rat brain[J].J Neuroendocrinol,2002,14(7):561-567.

        [66] AUGER C J,VANZO R J.Progesterone treatment of adult male rats suppresses arginine vasopressin expression in the bed nucleus of the stria terminalis and the centromedial amygdala[J].J Neuroendocrinol,2006,18(3):187-194.

        [67] BYCHOWSKI M E,AUGER C J.Progesterone impairs social recognition in male rats[J].Horm Behav,2012,61(4):598-604.

        [68] BYCHOWSKI M E,MENA J D,AUGER C J.Vasopressin infusion into the lateral septum of adult male rats rescues progesteroneinduced impairment in social recognition[J].Neuroscience,2013,246:52-58.

        [69] VAN WINGEN G,VAN BROEKHOVEN F,VERKES R J,et al.How progesterone impairs memory for biologically salient stimuli in healthy young women[J].J Neurosci,2007,27(42):11416-11423.

        [70] BLUTHE R M,DANTZER R.Role of the vomeronasal system in vasopressinergic modulation of social recognition in rats[J].Brain Res,1993,604(1/2):205-210.

        [71] BLUTHE R M,GHEUSI G,DANTZER R.Gonadal steroids influence the involvement of arginine vasopressin in social recognition in mice[J].Psychoneuroendocrinology,1993,18(4):323-335.

        [72] BLUTHE R M,DANTZER R.Social recognition does not involve vasopressinergic neurotransmission in female rats[J].Brain Res,1990,535(2):301-304.

        [73] SAWYER T F,HENGEHOLD A K,PEREZ W A.Chemosensory and hormonal mediation of social memory in male rats[J].Behav Neurosci,1984,98(5):908-913.

        [74] AXELSON J F,SMITH M,DUARTE M.Prenatal flutamide treatment eliminates the adult male rat's dependency upon vasopressin when forming socialolfactory memories[J].Horm Behav,1999,36(2):109-118.

        [75] FISHER C R,GRAVES K H,PARLOW A F,et al.Characterization of mice deficient in aromatase (ArKO) because of targeted disruption of the cyp19 gene[J].Proc Natl Acad Sci USA,1998,95(12):6965-6970.

        [76] KARLSSON S A,STUDER E,KETTUNEN P,et al.Neural androgen receptors modulate gene expression and social recognition but not social investigation[J].Front Behav Neurosci,2016,10:41.

        [77] DE VRIES G J,BUIJS R M,SLUITER A A.Gonadal hormone actions on the morphology of the vasopressinergic innervation of the adult rat brain[J].Brain Res,1984,298(1):141-145.

        [78] SZOT P,DORSA D M.Differential timing and sexual dimorphism in the expression of the vasopressin gene in the developing rat brain[J].Brain Res Dev Brain Res,1993,73(2):177-183.

        [79] WANG Z,BULLOCK N A,DE VRIES G J.Sexual differentiation of vasopressin projections of the bed nucleus of the stria terminals and medial amygdaloid nucleus in rats[J].Endocrinology,1993,132(6):2299-2306.

        [80] MAYES C R,WATTS A G,MCQUEEN J K,et al.Gonadal steroids influence neurophysin Ⅱ distribution in the forebrain of normal and mutant mice[J].Neuroscience,1988,25(3):1013-1022.

        [81] DE VRIES G J,RISSMAN E F,SIMERLY R B,et al.A model system for study of sex chromosome effects on sexually dimorphic neural and behavioral traits[J].J Neurosci,2002,22(20):9005-9014.

        [82] POPIK P,VAN REE J M.Social transmission of flavored tea preferences:facilitation by a vasopressin analog and oxytocin[J].Behav Neural Biol,1993,59(1):63-68.

        [83] EVERTS H G,DE RUITER A J,KOOLHAAS J M.Differential lateral septal vasopressin in wildtype rats:Correlation with aggression[J].Horm Behav,1997,31(2):136-144.

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