齒狀回
齒狀回 | |
---|---|
基本資訊 | |
屬於 | 顳葉 |
動脈 | 大腦後動脈 前脈絡叢動脈 |
標識字符 | |
拉丁文 | gyrus dentatus |
MeSH | D018891 |
NeuroNames | 179 |
NeuroLex ID | birnlex_1178 |
TA98 | A14.1.09.237、A14.1.09.339 |
TA2 | 5521 |
FMA | FMA:61922 |
格雷氏 | p.827 |
《神經解剖學術語》 [在維基數據上編輯] |
齒狀回(英文:Dentate gyrus,縮寫:DG)是大腦顳葉海馬結構的一部分,其中還包括海馬體和下托。齒狀回是海馬體三突觸迴路的一部分。它被認為有助於形成新的情節記憶、[1][2]自發探索新環境[2]和其他功能。[3]
值得注意的是,它是已知在許多哺乳動物(從齧齒目到靈長目動物)中具有顯着的成體神經發生率的少數幾個大腦結構之一。[4]成體神經發生可能發生的其他部位包括腦室下區、紋狀體和小腦。[5]然而,成人齒狀回中是否存在顯着的神經發生一直是一個有爭議的問題。[6][7]2019年的證據表明,成體神經發生確實發生在腦室下區和齒狀回的顆粒層下區。[8][9]
結構
[編輯]齒狀回與海馬體一樣,由三個不同的原皮層組成:外層是分子層、中間層是顆粒細胞層、內層是多態層。[10]組成海馬體的原皮層:外層是分子層,中間層是錐體層、內層是定向層。多態層也是齒狀回的門(CA4,海馬體和齒狀回的交界處)。[11][12]
顆粒層位於上面的分子層和下面的多態層(門)之間。[13]顆粒層的顆粒細胞投射出稱為苔蘚狀纖維的軸突,在CA3錐體神經元的樹突上形成興奮性突觸。顆粒細胞以層壓的方式緊密堆積在一起,抑制了神經元的興奮。[14]
顆粒細胞的一些基底樹突向上彎曲進入分子層。而大多數基底樹突則進入門。這些門樹突更短更細,側枝也更少。[15]
門中的第二種興奮性細胞類型是苔蘚細胞。[11]它沿隔顳軸廣泛投射其軸突(從隔區到顳葉),同側投射跳過細胞體附近的前1-2毫米[16]。通過隨機化它們的細胞分布來準備CA3中的一組細胞組合以用於數據檢索的作用。[17]
在門和顆粒細胞層之間是一個稱為顆粒層下區的區域,是成體神經發生的部位。[13]
齒狀回前內側的延續稱為齒狀回尾部,或Band of Giacomini。大部分齒狀回沒有暴露在腦表面,但齒狀回尾部卻暴露在表面,是鈎回下表面的重要標誌。[18]
三突觸迴路
[編輯]三突觸迴路由內嗅皮II層的興奮性細胞(主要是星狀細胞)組成,通過穿緣通路投射到齒狀回的顆粒細胞層。[19][20]齒狀回不接收來自其他皮層結構的直接輸入。[21]穿緣通路分為內側穿緣通路和外側穿緣通路,分別產生於內嗅皮質的內側和外側。內側穿緣通路突觸到顆粒細胞的近端樹突區域,而外側穿緣通路突觸到顆粒細胞的遠端樹突。齒狀回的大多數側面視圖似乎表明一個結構僅由一個實體組成,但內側運動可能提供齒狀回腹側和背側部分的證據。[22]稱為苔蘚狀纖維的顆粒細胞的軸突與CA3和CA1的錐體細胞建立興奮性突觸連接。[20]
發育
[編輯]齒狀回中的顆粒細胞的特點是它們在大腦發育過程中形成的時間較晚。在老鼠中,大約85%的顆粒細胞是在出生後產生的。[23]據推測,在人類中,顆粒細胞在妊娠第10.5至11周開始生成,並在妊娠中期、晚期、出生後直至成年的期間繼續生成。[24][25]科學家研究了在老鼠大腦發育過程中顆粒細胞的生發來源及其遷移途徑。[26]最老的顆粒細胞在海馬神經上皮的特定區域產生,並在胚胎期(E)17/18左右遷移到原始齒狀回,然後作為形成顆粒層中最外層的細胞沉澱。接着,齒狀前體細胞移出海馬神經上皮的同一區域,並保留其有絲分裂能力,侵入正在形成的齒狀回的門(核心)。從這時起,這種分散的生發基質就是顆粒細胞的來源。新生成的顆粒細胞聚集在已經開始沉澱在顆粒層中的舊細胞之下。隨着更多顆粒細胞的產生,層慢慢變厚,細胞根據年齡堆積,越老的越淺,越年輕的越深。[27]顆粒細胞前體保留在顆粒下區域,隨着齒狀回的生長逐漸變薄,但這些前體細胞保留在成年老鼠體內。這些稀疏分散的細胞不斷產生顆粒細胞神經元,[28][29]增加了神經元總數。老鼠、猴子和人類的齒狀回還有許多其他差異。老鼠的顆粒細胞只有頂端樹突,但在猴子和人類中,許多顆粒細胞有基底樹突。[30]
作用
[編輯]齒狀回被認為有助於記憶的形成,並在抑鬱症中發揮作用。
海馬體在學習和記憶中的作用已經研究了幾十年,特別是自1950年之後。根據手術結果,一名美國男性切除了大部分海馬體。[33]目前尚不清楚海馬體如何促成新記憶的形成,但在該大腦區域發生了一個稱為長時程增強作用(LTP)的過程。[34]LTP涉及在反覆刺激後持久強化突觸連接。[19]雖然齒狀回顯示LTP,但它也是哺乳動物大腦中為數不多的成體神經發生(新神經元的形成)發生的區域之一。一些研究假設新的記憶可以優先使用齒狀回新形成的顆粒細胞,這為區分相似事件的多個實例或多次訪問同一位置提供了一種潛在的機制。[35]相應地,有人提出,未成熟的新生顆粒細胞接受與來自內嗅皮層II層的軸突形成新的突觸連接,通過這種方式,首先將具有適當年齡的年輕顆粒細胞中的事件關聯起來,從而將特定的新事件群作為情景記憶來記憶。[36]通過在迷宮中的表現可以看出,增加的神經發生與改善齧齒動物的空間記憶有關,這一事實強化了這一概念。[37]
已知齒狀回用作預處理單元。雖然CA3子域參與記憶的編碼、存儲和檢索,但齒狀回在模式分離中很重要。[20]當信息通過穿緣通路進入時,齒狀回將非常相似的信息分成不同且獨特的細節。[38][39]這確保了新的記憶被單獨編碼,而無需從先前存儲的類似特徵的記憶中輸入,[13]並準備相關數據以存儲在CA3區域中。[38]模式分離提供了將一個記憶與其他存儲的記憶區分開來的能力。[40]模式分離始於齒狀回。齒狀回中的顆粒細胞使用競爭性學習處理感覺信息,並傳遞初步表示以形成位置場。[41]位置場非常具體,因為它們能夠重新映射和調整發射率以響應細微的感覺信號變化。這種特異性對於模式分離至關重要,因為它可以將記憶彼此區分開來。[40]
齒狀回顯示出一種特定形式的神經可塑性,這是由於新形成的興奮性顆粒細胞的持續整合所致。[13]
臨床意義
[編輯]記憶
[編輯]將海馬體與記憶形成聯繫起來的順行性遺忘症最突出的早期病例之一是亨利·莫萊森(匿名稱為患者H.M.,直到2008年去世)。[34]他的癲癇症通過手術切除海馬體(左右半球各有自己的海馬體)以及一些周圍組織得到治療。這種有針對性的腦組織切除使莫萊森先生無法形成新的記憶。從那時起,海馬體就被認為對記憶形成至關重要,儘管所涉及的過程尚不清楚。[34]
壓力和抑鬱
[編輯]齒狀回也可能在壓力和抑鬱中發揮作用。例如在老鼠中,已發現神經發生隨着抗抑鬱藥的長期治療而增加。[42]壓力的生理效應,通常表現為皮質醇等糖皮質激素的釋放,以及交感神經系統(自主神經系統的一個分支)的激活,已被證明可抑制靈長類動物的神經發生過程。[43]已知內源性和外源性糖皮質激素都會導致精神病和抑鬱症,[44]這意味着齒狀回的神經發生可能在調節壓力和抑鬱症狀方面發揮重要作用。[45]
血糖
[編輯]哥倫比亞大學歐文醫學中心研究人員的研究表明,血糖調節不佳會對齒狀回產生有害影響,從而導致記憶力下降。[46]
其他
[編輯]在老鼠身上看到的一些證據表明,齒狀回的神經發生隨着有氧運動而增加。[47]幾項實驗表明,當成年齧齒動物暴露於豐富的環境中時,神經發生(神經組織的發育)通常會增加。[48][49]
突觸相關蛋白DLG1(齒狀回中的一種支架蛋白質)的突變可能在精神分裂症的易感性中起作用。[50][51]
空間行為
[編輯]有研究表明,在大約90%的齒狀回細胞被破壞後,老鼠在穿過之前通過的迷宮時遇到了極大的困難。經過多次測試它們是否可以學習迷宮,結果顯示老鼠不能通過迷宮,表明它們的工作記憶嚴重受損。老鼠在放置策略方面也遇到了麻煩,因為它們無法將關於迷宮的學習信息整合到它們的工作記憶中,因此,在後來的試驗中穿過同一個迷宮時,它們無法記住它。每次老鼠進入迷宮,老鼠的表現就好像它第一次看到迷宮一樣。[52]
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外部連結
[編輯]- Slide at psycheducation.org
- Stained brain slice images which include the "Dentate gyrus" at the BrainMaps project
- McHugh TJ. Dentate Gyrus NMDA Receptors Mediate Rapid Pattern Separation in the Hippocampal Network. Science. 2007, 317 (5834): 94–99. Bibcode:2007Sci...317...94M. PMID 17556551. S2CID 18548. doi:10.1126/science.1140263. - The source of déjà vu
- NIF Search - Dentate Gyrus via the Neuroscience Information Framework
- See Altman and Bayer's work on dentate gyrus development and adult neurogenesis (頁面存檔備份,存於網際網路檔案館)
- Amaral, David G.; Scharfman, Helen E.; Lavenex, Pierre. The dentate gyrus: Fundamental neuroanatomical organization (Dentate gyrus for dummies). The Dentate Gyrus: A Comprehensive Guide to Structure, Function, and Clinical Implications. Progress in Brain Research 163. 2007: 3–790. ISBN 9780444530158. PMC 2492885 . PMID 17765709. doi:10.1016/S0079-6123(07)63001-5.