Kawamata T, Akiguchi I, Maeda K, Tanaka C, Higuchi K, Hosokawa M, Takeda T
Hyogo Institute for Aging Brain and Cognitive Disorders, Himeji, Japan.
Microsc Res Tech. 1998 Oct 1;43(1):59-67. doi: 10.1002/(SICI)1097-0029(19981001)43:1<59::AID-JEMT9>3.0.CO;2-X.
Twelve substrains of inbred senescence-accelerated mice (SAM) have been developed, among which the SAMP8 and SAMP10 strains show a significant age-related deterioration in learning and memory for passive and active avoidance tasks. These strains have, respectively, a low and high incidence of systemic senile amyloidosis. Although we found no amyloid deposits in their brain parenchyma, a variety of age-related alterations were identified, involving neurons, glia, and vessels in the brain tissues. Here we review the degenerative changes in aged SAMP8 and SAMP10 brains. These changes are generally similar to the pathology of aging human brain and may be characterized by their association with some specific glial reactions.
已经培育出了12个近交系衰老加速小鼠(SAM)亚系,其中SAMP8和SAMP10亚系在被动和主动回避任务的学习和记忆方面表现出与年龄相关的显著衰退。这些亚系分别具有低和高的系统性老年淀粉样变性发病率。虽然我们在它们的脑实质中未发现淀粉样沉积物,但已识别出多种与年龄相关的改变,涉及脑组织中的神经元、神经胶质和血管。在此,我们综述老年SAMP8和SAMP10脑的退行性变化。这些变化通常与人类衰老脑的病理学相似,并且可能以它们与某些特定神经胶质反应的关联为特征。