日照工作的時候,我們腦部的神經細胞會產生與神經退化症狀有關連的β-amyloid (Aβ)。745Please respect copyright.PENANAO2JNqLVa7I745Please respect copyright.PENANAvIvXk4NJMg
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在睡覺尤其是深層睡眠的時候,我們腦部的神經細胞會減少產生β-amyloid (Aβ)。同時間, β-amyloid (Aβ)會從腦脊髓液轉移到血液循環系統的靜脈,離開大腦。745Please respect copyright.PENANAm5gxBxsPt4
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夜間工作而日照時間睡覺會否達到同樣效果,暫時未有人體確實數據可以證實。745Please respect copyright.PENANA6U8A8ugrRx
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(圖2)睡覺時份,位於腦脊髓液(CSF)的β-amyloid (Aβ)透過星狀細胞(astrocyte)的協助,抵達靜脈排出腦外;745Please respect copyright.PENANAnJsJqPXOcX
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另有研究指出(Ref1),部份的麻醉藥亦能促成同等效果。745Please respect copyright.PENANAvSOQOPXwfM
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淋巴系統(Lymphatic System)是排除廢物的系統,基於排除Aβ需要透過星狀細胞的幫助,學術界把整套系統命名為Glympathic system,取其Glial Cell(神經膠質細胞)及Lymphatic System(淋巴系統)的結合,雖則整個機制並沒有淋巴系統的參與(Ref5)。745Please respect copyright.PENANAqRvi3IrTcm
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年老以及神經退化症狀的患者,Glympathic system效率大幅減低,因此引致大量β-amyloid (Aβ)聚積在腦部。而大量Aβ聚積在腦部的話,亦會影響睡眠的質素,形成惡性循環(Ref6)。745Please respect copyright.PENANAmHmkIGXdff
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對比年輕人士,年老者的腦部Aβ水平平均高出17%。以同等年齡作比較的話,患有神經退化症人士的腦部Aβ水平則比健康人士平均高出31%。745Please respect copyright.PENANA1HpRNnwsnY
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(圖3)為作進一步了解睡覺與腦部Aβ水平的關係,有研究(Ref2)找來20名人士,分別嘗試進行連續31小時不准睡覺以及睡覺9小時兩種環境,繼而量度Aβ水平。745Please respect copyright.PENANAvU7pSWpTub
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兩種測驗環境之間,測試者平均相隔15日分別進行。結果得出,不論性別歲數,通宵一晚平均將會導致5%的Aβ上升。745Please respect copyright.PENANARXvHSyPdFY
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(圖4)另外,他們亦發現睡眠時數與Aβ的移除有著一定程度的正面關係。而另一研究(Ref3)找來了142名試驗者,發現睡眠質素越高的話,Aβ的移除比率亦會越大。745Please respect copyright.PENANA9CSIymi0p9
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只不過,亦有研究指出睡眠時數少於5小時或多於11的話,認知能力會有衰退傾向,但未知與Aβ是否有關。745Please respect copyright.PENANAaCdVjgYTeO
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長遠而言,通宵會導致Aβ在腦部的聚積,增加患上神經退化症狀的機會,情況許可的話,可免就則免。745Please respect copyright.PENANANtiQx3lBRL
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Ref1:https://advances.sciencemag.org/content/5/2/eaav5447745Please respect copyright.PENANABfDIkd0DmL
Ref2:https://www.pnas.org/content/115/17/4483745Please respect copyright.PENANAr8dtdMkxuJ
Ref3:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3676720/745Please respect copyright.PENANAlG7Mrxg3bm
Ref4:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4636982/745Please respect copyright.PENANAnW01xR8hrr
Ref5:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4636982/745Please respect copyright.PENANAHTZXyQ3qbi
Ref6:https://www.nature.com/articles/nrneurol.2013.269#ref-CR13