老年NSY小鼠自发性淀粉样变的研究。

K Shimizu, H Morita, T Niwa, K Maeda, M Shibata, K Higuchi, T Takeda
{"title":"老年NSY小鼠自发性淀粉样变的研究。","authors":"K Shimizu,&nbsp;H Morita,&nbsp;T Niwa,&nbsp;K Maeda,&nbsp;M Shibata,&nbsp;K Higuchi,&nbsp;T Takeda","doi":"10.1111/j.1440-1827.1993.tb01135.x","DOIUrl":null,"url":null,"abstract":"<p><p>Senile Nagoya, Shibata, Yasuda (NSY) mice developed amyloidosis and died from renal failure as a result of amyloidosis. NSY mice were first reported as experimental congenital diabetic mice by Shibata et al. in 1980. This study questioned whether NSY mice died from diabetic nephropathy. The authors of the present study investigated the life span and cause of death in these mice. The life span of NSY mice was found to be 618.7 +/- 72.5 days. NSY mice that lived for more than 400 days showed rising blood urea nitrogen and large amounts of amyloid deposits in the glomerulus of the kidneys. NSY mice died of renal amyloidosis. Immunological methods revealed that AApoAII was evident in the amyloid deposits of NSY mice. Apart from the kidneys, amyloid deposition was also found in the tongue, esophagus, stomach, small intestine, large intestine, rectum, lung, heart and adrenal glands. Amyloid deposits were found to a slight degree in the liver and the spleen. The most dominant amyloid deposition in NSY mice was seen in the glomerulus of the kidneys. From the point of view of amyloid depositional distribution, NSY mice were unique compared with other spontaneous amyloid mice.</p>","PeriodicalId":75413,"journal":{"name":"Acta pathologica japonica","volume":"43 5","pages":"215-21"},"PeriodicalIF":0.0000,"publicationDate":"1993-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1111/j.1440-1827.1993.tb01135.x","citationCount":"13","resultStr":"{\"title\":\"Spontaneous amyloidosis in senile NSY mice.\",\"authors\":\"K Shimizu,&nbsp;H Morita,&nbsp;T Niwa,&nbsp;K Maeda,&nbsp;M Shibata,&nbsp;K Higuchi,&nbsp;T Takeda\",\"doi\":\"10.1111/j.1440-1827.1993.tb01135.x\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Senile Nagoya, Shibata, Yasuda (NSY) mice developed amyloidosis and died from renal failure as a result of amyloidosis. NSY mice were first reported as experimental congenital diabetic mice by Shibata et al. in 1980. This study questioned whether NSY mice died from diabetic nephropathy. The authors of the present study investigated the life span and cause of death in these mice. The life span of NSY mice was found to be 618.7 +/- 72.5 days. NSY mice that lived for more than 400 days showed rising blood urea nitrogen and large amounts of amyloid deposits in the glomerulus of the kidneys. NSY mice died of renal amyloidosis. Immunological methods revealed that AApoAII was evident in the amyloid deposits of NSY mice. Apart from the kidneys, amyloid deposition was also found in the tongue, esophagus, stomach, small intestine, large intestine, rectum, lung, heart and adrenal glands. Amyloid deposits were found to a slight degree in the liver and the spleen. The most dominant amyloid deposition in NSY mice was seen in the glomerulus of the kidneys. From the point of view of amyloid depositional distribution, NSY mice were unique compared with other spontaneous amyloid mice.</p>\",\"PeriodicalId\":75413,\"journal\":{\"name\":\"Acta pathologica japonica\",\"volume\":\"43 5\",\"pages\":\"215-21\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1993-05-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1111/j.1440-1827.1993.tb01135.x\",\"citationCount\":\"13\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Acta pathologica japonica\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1111/j.1440-1827.1993.tb01135.x\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Acta pathologica japonica","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1111/j.1440-1827.1993.tb01135.x","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 13

摘要

老年名古屋、柴田、安田(NSY)小鼠发生淀粉样变,并因淀粉样变导致肾功能衰竭而死亡。Shibata等人于1980年首次报道了NSY小鼠作为实验性先天性糖尿病小鼠。本研究质疑NSY小鼠是否死于糖尿病肾病。本研究的作者调查了这些小鼠的寿命和死亡原因。NSY小鼠的寿命为618.7±72.5天。存活超过400天的NSY小鼠表现出血液尿素氮升高和肾小球大量淀粉样蛋白沉积。NSY小鼠死于肾淀粉样变。免疫学方法显示,AApoAII在NSY小鼠淀粉样蛋白沉积中明显存在。除了肾脏外,舌头、食道、胃、小肠、大肠、直肠、肺、心脏和肾上腺也发现了淀粉样蛋白沉积。肝脏和脾脏有轻微的淀粉样蛋白沉积。NSY小鼠中最主要的淀粉样蛋白沉积见于肾小球。从淀粉样蛋白沉积分布来看,NSY小鼠与其他自发性淀粉样蛋白小鼠相比具有独特性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Spontaneous amyloidosis in senile NSY mice.

Senile Nagoya, Shibata, Yasuda (NSY) mice developed amyloidosis and died from renal failure as a result of amyloidosis. NSY mice were first reported as experimental congenital diabetic mice by Shibata et al. in 1980. This study questioned whether NSY mice died from diabetic nephropathy. The authors of the present study investigated the life span and cause of death in these mice. The life span of NSY mice was found to be 618.7 +/- 72.5 days. NSY mice that lived for more than 400 days showed rising blood urea nitrogen and large amounts of amyloid deposits in the glomerulus of the kidneys. NSY mice died of renal amyloidosis. Immunological methods revealed that AApoAII was evident in the amyloid deposits of NSY mice. Apart from the kidneys, amyloid deposition was also found in the tongue, esophagus, stomach, small intestine, large intestine, rectum, lung, heart and adrenal glands. Amyloid deposits were found to a slight degree in the liver and the spleen. The most dominant amyloid deposition in NSY mice was seen in the glomerulus of the kidneys. From the point of view of amyloid depositional distribution, NSY mice were unique compared with other spontaneous amyloid mice.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信