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How Klingler's dissection permits exploration of brain structural connectivity? An electron microscopy study of human white matter

机译:克林格勒的解剖方法如何探索大脑的结构连通性?人类白质的电子显微镜研究

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The objective of this study is to explore histological and ultrastructural changes induced by Klingler's method. Five human brains were prepared. First, the effects of freezing-defrosting on white matter were explored with optical microscopy on corpus callosum samples of two brains; one prepared in accordance with the description of Klingler (1956) and the other without freezing-defrosting. Then, the combined effect of formalin fixation and freezing-defrosting was explored with transmission electron microscopy (EM) on samples of cingulum from one brain: samples from one hemisphere were fixed in paraformaldehyde-glutaraldehyde (para/gluta), other samples from the other hemisphere were fixed in formalin; once fixed, half of the samples were frozen-defrosted. Finally, the effect of dissection was explored from three formalin-fixed brains: one hemisphere of each brain was frozen-defrosted; samples of the corpus callosum were dissected before preparation for scanning EM. Optical microscopy showed enlarged extracellular space on frozen samples. Transmission EM showed no significant alteration of white matter ultrastructure after formalin or para/gluta fixation. Freezing-defrosting created extra-axonal lacunas, larger on formalin-fixed than on para/gluta-fixed samples. In all cases, myelin sheaths were preserved, allowing maintenance of axonal integrity. Scanning EM showed the destruction of most of the extra-axonal structures after freezing-defrosting and the preservation of most of the axons after dissection. Our results are the first to highlight the effects of Klingler's preparation and dissection on white matter ultrastructure. Preservation of myelinated axons is a strong argument to support the reliability of Klingler's dissection to explore the structure of human white matter.
机译:这项研究的目的是探讨克林格勒方法引起的组织学和超微结构变化。准备了五个人脑。首先,利用光学显微镜对两个大脑的call体样品进行了冻融解冻对白质的影响。一种是按照Klingler(1956)的描述制备的,另一种是不进行冷冻除霜的。然后,用透射电子显微镜(EM)研究了福尔马林固定和冷冻-解冻对一个大脑的扣带样品的联合作用:一个半球的样品固定在低聚甲醛-戊二醛(para / gluta)中,另一半固定在另一个半球固定在福尔马林中;固定后,将一半样品冷冻解冻。最后,从三个福尔马林固定的大脑中探索解剖的效果:每个大脑的一个半球被冷冻解冻;在准备扫描EM之前,解剖scanning体样品。光学显微镜显示冷冻样品上的细胞外空间增大。透射电镜显示福尔马林或对/谷氨酰胺固定后白质超微结构无明显改变。冷冻-解冻产生了轴突外空隙,福尔马林固定的样本比对/谷氨酰胺固定的样本更大。在所有情况下,髓鞘均得以保留,从而可维持轴突的完整性。扫描电镜显示冷冻-解冻后大多数轴突外结构被破坏,解剖后大部分轴突被保留。我们的结果首次强调了克林格勒的制备和解剖对白质超微结构的影响。髓鞘轴突的保存是一个强有力的论据,可以支持克林格勒解剖的可靠性,以探索人类白质的结构。

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