• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

人类大脑如何应对衰老。

How the human brain responds to aging.

作者信息

Samorajski T

出版信息

J Am Geriatr Soc. 1976 Jan;24(1):4-11. doi: 10.1111/j.1532-5415.1976.tb03246.x.

DOI:10.1111/j.1532-5415.1976.tb03246.x
PMID:172540
Abstract

The characteristic morphologic changes frequently observed in the brain of an old adult include a decrease in weight and volume, a change in the pattern of cerebral cortical convolutions, and an increase in ventricular size. Cell loss varies from region to region in the brain, and may be intensified in Alzheimer's disease and other disorders associated with senile dementia. Among the neuroglial cells, the microglia undergo the most significant changes with age. Although senile brain disease previously has been regarded as secondary to atherosclerosis, recent neuropathologic studies indicate that only 30 to 40 percent of senile brain disease arises from cerebrovascular pathologic lesions. The dilemma remains, however, of how much of the deterioration observed in the aged is related to disease and how much to senescence. The interaction between gene expression and environmental conditions in aging is another important question for the geriatrician. Progress in the control and treatment of disorders associated with old age depends upon further research into the mechanisms that underlie the process of aging in the brain.

摘要

在老年人脑中经常观察到的特征性形态学变化包括重量和体积减小、大脑皮质褶皱模式改变以及脑室大小增加。脑内不同区域的细胞损失情况各不相同,在阿尔茨海默病和其他与老年痴呆相关的疾病中可能会加剧。在神经胶质细胞中,小胶质细胞随年龄增长发生的变化最为显著。尽管老年脑疾病以前被认为是动脉粥样硬化的继发疾病,但最近的神经病理学研究表明,只有30%至40%的老年脑疾病源自脑血管病理病变。然而,一个难题仍然存在,即观察到的老年人脑功能衰退有多少与疾病有关,又有多少与衰老有关。基因表达与衰老过程中的环境条件之间的相互作用是老年医学专家面临的另一个重要问题。与老年相关疾病的控制和治疗进展取决于对大脑衰老过程潜在机制的进一步研究。

相似文献

1
How the human brain responds to aging.人类大脑如何应对衰老。
J Am Geriatr Soc. 1976 Jan;24(1):4-11. doi: 10.1111/j.1532-5415.1976.tb03246.x.
2
Variations in the size of the human brain. Influence of age, sex, body length, body mass index, alcoholism, Alzheimer changes, and cerebral atherosclerosis.人类大脑大小的变化。年龄、性别、身长、体重指数、酗酒、阿尔茨海默病变化及脑动脉粥样硬化的影响。
Acta Neurol Scand Suppl. 1985;102:1-94.
3
[Quantitative and topical problems of cerebral aging].[脑老化的定量与局部问题]
Verh Dtsch Ges Pathol. 1968;52:179-203.
4
Morphological changes in Alzheimer's disease-senile dementia: ultrastructural changes and quantitative studies.阿尔茨海默病-老年性痴呆的形态学变化:超微结构变化与定量研究。
Res Publ Assoc Res Nerv Ment Dis. 1979;57:99-105.
5
Age, senile dementia and ventricular enlargement.年龄、老年痴呆与脑室扩大。
J Neurol Neurosurg Psychiatry. 1981 Jul;44(7):631-5. doi: 10.1136/jnnp.44.7.631.
6
The pathology of dementia.痴呆的病理学
Br J Psychiatry. 1975;Spec No 9:110-8.
7
Clinical and pathological features of diffuse cortical Lewy body disease (Lewy body dementia).
Brain. 1987 Oct;110 ( Pt 5):1131-53. doi: 10.1093/brain/110.5.1131.
8
Neuropathology of dementia.痴呆的神经病理学
Neurol Clin. 1986 May;4(2):355-68.
9
[General neuropathology of senile and degenerative cerebral disorders].[老年和退行性脑疾病的一般神经病理学]
Verh Dtsch Ges Pathol. 1968;52:32-64.
10
Alzheimer's disease in late-life dementia: a minor toxic consequence of devastating cerebrovascular dysfunction.老年痴呆症在晚期痴呆症中:是严重脑血管功能障碍的一种轻微毒性后果。
Med Hypotheses. 2008;70(4):866-75. doi: 10.1016/j.mehy.2007.07.027. Epub 2007 Sep 6.

引用本文的文献

1
Oligodendroglia in Ageing and Age-Dependent Neurodegenerative Diseases.衰老及年龄相关性神经退行性疾病中的少突胶质细胞
Adv Neurobiol. 2025;43:363-405. doi: 10.1007/978-3-031-87919-7_13.
2
Bioenergetic Impairment in the Neuro-Glia-Vascular Unit: An Emerging Physiopathology during Aging.神经-胶质-血管单元中的生物能量损伤:衰老过程中一种新出现的病理生理学现象。
Aging Dis. 2021 Dec 1;12(8):2080-2095. doi: 10.14336/AD.2021.04017. eCollection 2021 Dec.
3
Annexin A3 as a Marker Protein for Microglia in the Central Nervous System of Rats. annexin A3 作为大鼠中枢神经系统中小胶质细胞的标记蛋白。
Neural Plast. 2021 Jun 10;2021:5575090. doi: 10.1155/2021/5575090. eCollection 2021.
4
Microglia senescence occurs in both substantia nigra and ventral tegmental area.小胶质细胞衰老在黑质和腹侧被盖区均有发生。
Glia. 2020 Nov;68(11):2228-2245. doi: 10.1002/glia.23834. Epub 2020 Apr 10.
5
Old age increases microglial senescence, exacerbates secondary neuroinflammation, and worsens neurological outcomes after acute traumatic brain injury in mice.老年会增加小胶质细胞衰老,加剧继发性神经炎症,并使小鼠急性创伤性脑损伤后的神经学结果恶化。
Neurobiol Aging. 2019 May;77:194-206. doi: 10.1016/j.neurobiolaging.2019.02.010. Epub 2019 Feb 20.
6
Pain: The Neglect Issue in Old People's Life.疼痛:老年人生活中的被忽视问题。
Open Access Maced J Med Sci. 2018 Sep 20;6(9):1773-1778. doi: 10.3889/oamjms.2018.335. eCollection 2018 Sep 25.
7
Microglial pathology.小胶质细胞病理学。
Acta Neuropathol Commun. 2014 Sep 26;2:142. doi: 10.1186/s40478-014-0142-6.
8
Aging reduces glial uptake and promotes extracellular accumulation of Aβ from a lentiviral vector.衰老会减少神经胶质细胞摄取,并促进慢病毒载体中外泌体 Aβ 的积累。
Front Aging Neurosci. 2014 Aug 15;6:210. doi: 10.3389/fnagi.2014.00210. eCollection 2014.
9
Microglial dysfunction in brain aging and Alzheimer's disease.脑老化和阿尔茨海默病中的小胶质细胞功能障碍。
Biochem Pharmacol. 2014 Apr 15;88(4):594-604. doi: 10.1016/j.bcp.2014.01.008. Epub 2014 Jan 18.
10
Calcium dysregulation and neuroinflammation: discrete and integrated mechanisms for age-related synaptic dysfunction.钙稳态失调与神经炎症:与年龄相关的突触功能障碍的离散和整合机制。
Ageing Res Rev. 2013 Sep;12(4):982-95. doi: 10.1016/j.arr.2013.05.008. Epub 2013 Jun 8.