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神经突变大鼠“抖抖”、“震颤”及“抖抖 - 震颤”双突变体(自发性癫痫大鼠,SER)的中枢神经系统病理学。SER中临床和神经病理学表型的加剧。

CNS pathology in the neurological mutant rats zitter, tremor and zitter-tremor double mutant (spontaneously epileptic rat, SER). Exaggeration of clinical and neuropathological phenotypes in SER.

作者信息

Kondo A, Nagara H, Akazawa K, Tateishi J, Serikawa T, Yamada J

机构信息

Department of Neuropathology, Faculty of Medicine, Kyushu University, Japan.

出版信息

Brain. 1991 Apr;114 ( Pt 2):979-99. doi: 10.1093/brain/114.2.979.

Abstract

The pathological alterations in the central nervous system (CNS) were examined in three kinds of mutant rat; the zitter (zi/zi; Zi), the tremor rat (tm/tm; Tm) and the spontaneously epileptic rat (SER) which is a double mutant carrying both zitter and tremor genes. Two major alterations demonstrated in these mutants were hypomyelination and vacuolation or spongy degeneration. Hypomyelination was observed predominantly in SER and to a lesser extent in Zi, and was accompanied by a redundant or aberrant myelin sheath formation in addition to a decreased number of myelinated fibres. This appeared to be related to the occurrence of tremor. There was no abnormality in the structure of the myelin lamellae and oligodendrocytes or any destruction of myelin sheaths by phagocytic cells. The number of radial components in CNS myelin was increased almost equally in Zi, Tm and SER. Vacuolation was prominent in SER and Tm, especially in the brainstem and thalamus. Zi also developed mild vacuolation with advancing age. Vacuolation seemed to be related to the epileptic phenomena in SER and Tm. Vacuoles consisted mainly of swollen astrocytic processes and enlargement of the extracellular space, as well as occasional enlargement of periaxonal spaces. Thus both pathological findings--the hypomyelination derived from the zitter mutation with tremor, and the vacuolation from the tremor mutation with epileptic symptoms--were mutually exaggerated in SER. It is postulated that the two different genetic loci with zi and tm mutations interact and synergistically reinforce each other both clinically and pathologically in SER.

摘要

在三种突变大鼠中检查了中枢神经系统(CNS)的病理改变,即颤抖大鼠(zi/zi;Zi)、震颤大鼠(tm/tm;Tm)和自发性癫痫大鼠(SER,一种携带颤抖和震颤基因的双突变体)。在这些突变体中发现的两个主要改变是髓鞘形成不足以及空泡化或海绵状变性。髓鞘形成不足主要在SER中观察到,在Zi中程度较轻,并且除了有髓纤维数量减少外,还伴有多余或异常的髓鞘形成。这似乎与震颤的发生有关。髓鞘板层和少突胶质细胞的结构没有异常,也没有吞噬细胞对髓鞘的任何破坏。CNS髓鞘中放射状成分的数量在Zi、Tm和SER中几乎同等增加。空泡化在SER和Tm中很明显,尤其是在脑干和丘脑。Zi随着年龄增长也出现轻度空泡化。空泡化似乎与SER和Tm中的癫痫现象有关。空泡主要由肿胀的星形胶质细胞突起、细胞外间隙扩大以及偶尔的轴周间隙扩大组成。因此,两种病理表现——源自伴有震颤的颤抖突变的髓鞘形成不足,以及源自伴有癫痫症状的震颤突变的空泡化——在SER中相互加剧。据推测,带有zi和tm突变的两个不同基因位点在SER中在临床和病理上相互作用并协同增强。

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