Comparison of age-related inflammation and oxidative stress in two lemur species.

IF 1.7 3区 生物学 Q4 PHYSIOLOGY
Elaine E Guevara, Nicholas M Grebe, Richard R Lawler, Anne Crowley, Savannah Lo, Elise N Paietta, Janet L Huebner, Virginia B Kraus, Christine M Drea
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引用次数: 0

Abstract

Oxidative damage and inflammation are mechanisms proposed to contribute to physiological senescence. Variation in oxidative damage and inflammation may reflect differential allocation of resources to reproduction and survival, contributing to differences in species-typical longevity and resulting from distinct, evolved life-history strategies. To investigate the link between molecular processes and physiological senescence, we compared urinary biomarkers of oxidative stress (8-isoprostane and 8-OHdG) and inflammation (neopterin) in a cross-sectional sample of two species that differ in life-history schedules: the relatively fast-paced ring-tailed lemur (Lemur catta; n = 41; ages = 1-32 years) and slow-paced Coquerel's sifaka (Propithecus coquereli; n = 49; ages = 1-27 years). Consistent with a faster life-history pace, ring-tailed lemurs showed significantly higher average levels of DNA damage than did sifakas (8-OHdG: ring-tailed lemur mean: 18.6 ± 10.3 ng/mg Cr, sifaka mean 8.0 ± 9.0 ng/mg Cr, p = 0.001). Species differences in lipid damage and inflammatory biomarkers were not significant (8-isoprostane: ring-tailed lemur mean: 0.5 ± 0.3 ng/mg Cr, sifaka mean: 0.3 ± 0.2 ng/mg Cr, p = 0.11), although sifakas tended to show greater inflammation (neopterin: ring-tailed lemur mean: 0.01 ± 0.02 ng/mg Cr, sifaka mean: 0.02 ± 0.02 ng/mg Cr; p = 0.14), which may reflect health challenges faced by this species in captivity. Contrary to our predictions, neither species showed age-related change in either marker of oxidative stress. Thus, although lemurs appear not to experience an increase in the rate of oxidative damage incurred with age, we cannot exclude the possibility that accumulated damage contributes to aging. Neither lemur species exhibited age-related change in inflammation; if anything, contrary to our prediction, ring-tailed lemurs showed marginal declines in inflammation with age. This finding, consistent with a few recent studies of other non-human primates, suggests that lemurs avoid the phenomenon of "inflammaging" widely observed in humans.

两种狐猴年龄相关炎症和氧化应激的比较。
氧化损伤和炎症是引起生理性衰老的机制。氧化损伤和炎症的变化可能反映了资源在繁殖和生存方面的不同分配,导致了物种典型寿命的差异,这是由不同的、进化的生活史策略造成的。为了研究分子过程与生理衰老之间的联系,我们比较了两种不同生活史时间表物种的横截面样本中氧化应激(8-异前列腺素和8-OHdG)和炎症(新蝶呤)的尿液生物标志物:相对较快的环尾狐猴(lemur catta;n = 41;年龄= 1-32岁)和慢节奏Coquerel的狐猴(prothecus coquereli;n = 49;年龄= 1-27岁)。与更快的生活史节奏一致,环尾狐猴的平均DNA损伤水平显著高于狐猴(8-OHdG:环尾狐猴平均值:18.6±10.3 ng/mg Cr,狐猴平均值:8.0±9.0 ng/mg Cr, p = 0.001)。脂质损伤和炎症生物标志物的物种差异不显著(8-异前列腺素:环尾狐猴平均值:0.5±0.3 ng/mg Cr,狐猴平均值:0.3±0.2 ng/mg Cr, p = 0.11),尽管狐猴倾向于表现出更大的炎症(新蝶呤:环尾狐猴平均值:0.01±0.02 ng/mg Cr,狐猴平均值:0.02±0.02 ng/mg Cr;P = 0.14),这可能反映了该物种在圈养环境中面临的健康挑战。与我们的预测相反,两个物种的氧化应激标志物都没有显示出与年龄相关的变化。因此,尽管狐猴的氧化损伤率似乎没有随着年龄的增长而增加,但我们不能排除累积损伤导致衰老的可能性。两种狐猴都没有表现出与年龄相关的炎症变化;如果有什么不同的话,与我们的预测相反,环尾狐猴的炎症随着年龄的增长而略有下降。这一发现与最近对其他非人类灵长类动物的一些研究一致,表明狐猴避免了在人类中广泛观察到的“炎症”现象。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
3.90
自引率
0.00%
发文量
51
审稿时长
3.5 months
期刊介绍: The Journal of Comparative Physiology B publishes peer-reviewed original articles and reviews on the comparative physiology of invertebrate and vertebrate animals. Special emphasis is placed on integrative studies that elucidate mechanisms at the whole-animal, organ, tissue, cellular and/or molecular levels. Review papers report on the current state of knowledge in an area of comparative physiology, and directions in which future research is needed.
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