炎症
氧化应激
热休克蛋白
老化
医学
免疫系统
生理学
休克(循环)
抗体
热休克蛋白70
全身炎症
免疫学
内科学
生物
生物化学
基因
作者
Janet E. Alexander,Alison Colyer,Richard Haydock,Michael G. Hayek,JeanSoon Park
出处
期刊:The Journals of Gerontology
[Oxford University Press]
日期:2017-11-06
卷期号:73 (6): 720-728
被引量:43
标识
DOI:10.1093/gerona/glx182
摘要
As in human populations, advances in nutrition and veterinary care have led to an increase in the lifespan of companion animals. Detrimental physiological changes occurring later in life must be understood before interventions can be made to slow or reduce them. One important aspect of human aging is upregulation of the inflammatory response and increase in oxidative damage resulting in pathologies linked to chronic inflammation. To determine whether similar processes occur in the aging dog, changes in markers of inflammation and oxidative stress were investigated in 80 Labrador retrievers from adulthood to the end of life. Serum levels of immunoglobulin M (p < .001) and 8-hydroxy-2-deoxyguanosine (p < .001) increased with age, whereas no effect of age was detected for immunoglobulin G or C-reactive protein unless the last year of life was included in the analysis (p = .002). Baseline levels of heat shock protein 70 decreased with age (p < .001) while those after exposure to heat stress were maintained (p = .018). However, when excluding final year of life data, a decline in the heat shock protein 70 response after heat stress was observed (p = .004). These findings indicate that aging dogs undergo changes similar to human inflammaging and offer the possibility of nutritional or pharmacological intervention to delay or reduce these effects.
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