衰老小鼠的实用病理学。

Pathobiology of aging & age related diseases Pub Date : 2011-01-01 Epub Date: 2011-06-01 DOI:10.3402/pba.v1i0.7202
Christina Pettan-Brewer, Piper M Treuting
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引用次数: 107

摘要

年老的老鼠会有一部分病变,这是器官功能逐渐衰退的一部分,这就是衰老的定义。在试验、换笼或体检期间,研究人员、饲养人员或兽医人员将注意到外部和可触及的病变。虽然这些容易观察到的病变可能引起警报,但并不是所有的病变都会造成不必要的痛苦或危及生命。在衰老研究中,老鼠被维持到接近生命终点,根据菌株和基因操作,可以超过33个月。老龄化研究具有独特的福利问题,涉及与年龄相关的衰退、衰弱、脆弱和相关的慢性疾病疼痛。一个有效的老龄化研究项目包括研究、饲养和兽医人员以及机构动物护理和使用委员会成员之间的合作和教育。这种合作对于人道地维持老年小鼠和防止因非致命疾病而过度审查至关重要。教育过程的一部分是熟悉老年小鼠在临床、尸检和组织病理学上的表现。这一基线知识对于确定人道终点、确定健康期限、确定死亡原因和干预措施的效果非常重要。本文的目的是向研究人员介绍年龄相关疾病和小鼠损伤模式,从临床表现到病理评估。为了做到这一点,我们提出并说明了在华盛顿大学维持的老化菌落亚群中常见的临床表现、尸检和组织病理学病变。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Practical pathology of aging mice.

Practical pathology of aging mice.

Practical pathology of aging mice.

Practical pathology of aging mice.

Old mice will have a subset of lesions as part of the progressive decline in organ function that defines aging. External and palpable lesions will be noted by the research, husbandry, or veterinary staff during testing, cage changing, or physical exams. While these readily observable lesions may cause alarm, not all cause undue distress or are life-threatening. In aging research, mice are maintained until near end of life that, depending on strain and genetic manipulation, can be upwards of 33 months. Aging research has unique welfare issues related to age-related decline, debilitation, fragility, and associated pain of chronic diseases. An effective aging research program includes the collaboration and education of the research, husbandry, and veterinary staff, and of the members of the institution animal care and use committee. This collaborative effort is critical to humanely maintaining older mice and preventing excessive censorship due to non-lethal diseases. Part of the educational process is becoming familiar with how old mice appear clinically, at necropsy and histopathologically. This baseline knowledge is important in making the determination of humane end points, defining health span, contributing causes of death and effects of interventions. The goal of this paper is to introduce investigators to age-associated diseases and lesion patterns in mice from clinical presentation to pathologic assessment. To do so, we present and illustrate the common clinical appearances, necropsy and histopathological lesions seen in subsets of the aging colonies maintained at the University of Washington.

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