脂褐素在神经元老化和疾病中的作用。

Normale und pathologische Anatomie Pub Date : 1976-01-01
P Glees, M Hasan
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引用次数: 0

摘要

脂褐素神经元内积累的增加与衰老过程有关,积累程度与实足年龄之间存在显著的线性相关性。年龄色素可溶于极性和非极性溶剂;颜料是自动荧光的,用PAS、苏丹黑B、尼罗河蓝锇酸和三铁氰化技术染色。是否所有表现出这些特性的色素都是相同的,或者至少是密切相关的,而不考虑周围的组织、动物种类和个体的年龄,这是有争议的。在幼龄和老年动物以及受到实验压力、饮食和环境干扰的个体中,色素形成已被证明。动物电镜研究表明,单个脂褐素颗粒的精细结构具有相当大的变异性,但被单位膜包围的“透明液泡”的存在是老年人神经元脂褐素的特征之一。最近,利用冷冻蚀刻技术的电子显微镜提供了令人信服的证据,反驳了先前的观点,即朗讯液泡是在显微镜检查组织准备过程中溶解和去除的脂质物质的残留物。这些液泡也在新鲜冷冻的材料中得到证实,这些材料以前没有固定或浸泡过。空泡化的色素颗粒在大鼠脑后区域比在其他区域更早出现(Hasan和Heyder 1974)。色素沉积的时间序列存在区域差异。
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Lipofuscin in neuronal aging and diseases.

The increasing intraneuronal accumulation of lipofuscin has been linked to the aging process by a striking linear correlation between the degree of accumulation and chronological age. It has been established that age pigments are soluble in polar and nonpolar solvents; the pigment is autofluorescent and stains with PAS, Sudan black B, Nile blue osmic acid and ferric ferricyanide techniques. Whether all pigments exhibiting these properties are identical, or at least closely related, regardless of the surrounding tissue, animal species and age of the individual, is debatable. Pigment formation has been demonstrated in young and aged animals as well as in individual subjected to experimental stress and to dietetic and environmental interference. Electron microscopic studies in animals have shown a considerable variability in the fine structure of individual lipofuscin granules but the presence of "lucent vacuoles" surrounded by a unit membrane is one of the characteristic features of neuronal lipofuscin in the aged. Recently, electron microscopy, utilizing the freeze-etching technique, has provided convincing evidence which disproves the earlier view that lucent vacuoles are the remnant of lipid material dissolved and removed during the preparation of the tissues for microscopic examination. These vacuoles have also been demonstrated in freshly frozen material not previously fixed or immersed. Vacuolated pigment granules occur earlier in the area postrema than in other regions of the rat brain (Hasan and Heyder 1974). Regional differences in the time sequence of pigment deposition are present.

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