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Cellular metabolic pathways of aging in dogs: could p53 and SIRT1 be at play?狗的衰老的细胞代谢途径:p53 和 SIRT1 是否发挥作用?
Geroscience. 2024 Apr;46(2):1895-1908. doi: 10.1007/s11357-023-00942-y. Epub 2023 Sep 28.
2
Dog Life Spans and the Evolution of Aging.狗的寿命跨度与衰老的演化。
Am Nat. 2023 Jun;201(6):E140-E152. doi: 10.1086/724384. Epub 2023 Apr 4.
3
Inflammaging in domestic dogs: basal level concentrations of IL-6, IL-1β, and TNF-α in serum of healthy dogs of different body sizes and ages.犬的炎症老化:不同体型和年龄的健康犬血清中 IL-6、IL-1β 和 TNF-α 的基础浓度。
Biogerontology. 2023 Aug;24(4):593-602. doi: 10.1007/s10522-023-10037-y. Epub 2023 May 17.
4
Exploring the role of primary fibroblast cells in comparative physiology: a historical and contemporary overview.探索原代成纤维细胞在比较生理学中的作用:历史和当代综述。
Am J Physiol Regul Integr Comp Physiol. 2023 Jul 1;325(1):R45-R54. doi: 10.1152/ajpregu.00025.2023. Epub 2023 May 15.
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A conserved MTMR lipid phosphatase increasingly suppresses autophagy in brain neurons during aging.在衰老过程中,一种保守的 MTMR 脂质磷酸酶会逐渐抑制大脑神经元中的自噬。
Sci Rep. 2022 Dec 17;12(1):21817. doi: 10.1038/s41598-022-24843-w.
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How size and genetic diversity shape lifespan across breeds of purebred dogs.体型和遗传多样性如何影响纯种犬的寿命。
Geroscience. 2023 Apr;45(2):627-643. doi: 10.1007/s11357-022-00653-w. Epub 2022 Sep 6.
7
New hallmarks of ageing: a 2022 Copenhagen ageing meeting summary.衰老的新标志:2022 年哥本哈根衰老会议总结。
Aging (Albany NY). 2022 Aug 29;14(16):6829-6839. doi: 10.18632/aging.204248.
8
From Chihuahua to Saint-Bernard: how did digestion and microbiota evolve with dog sizes.从吉娃娃到圣伯纳犬:狗的体型如何影响消化和微生物群的演变。
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重新审视家犬的“衰老标志”:文献现状。

A revisiting of "the hallmarks of aging" in domestic dogs: current status of the literature.

机构信息

Department of Biology, Colgate University, 13 Oak Dr, Hamilton, NY, 133546, USA.

出版信息

Geroscience. 2024 Feb;46(1):241-255. doi: 10.1007/s11357-023-00911-5. Epub 2023 Aug 18.

DOI:10.1007/s11357-023-00911-5
PMID:37594598
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10828135/
Abstract

A progressive decline in biological function and fitness is, generally, how aging is defined. However, in 2013, a description on the "hallmarks of aging" in mammals was published, and within it, it described biological processes that are known to alter the aging phenotype. These include genomic instability, telomere attrition, epigenetic alterations, loss of proteostasis, deregulated nutrient sensing, mitochondrial dysfunction, cellular senescence, stem cell exhaustion, altered intercellular communication (inflammation), and changes within the microbiome. This mini-review provides a detailed account of the progress on each of these hallmarks of aging in the domestic dog within the last 5 years. Additionally, when there are gaps in the literature between other mammalian species and dogs, I highlight the aging biomarkers that may be missing for dogs as aging models. I also argue for the importance of dog aging studies to include several breeds of dogs at differing ages and for age corrections for breeds with differing mean lifespans throughout.

摘要

一般来说,生物功能和适应力的逐渐下降就是衰老的定义。然而,在 2013 年,一篇关于哺乳动物“衰老标志”的描述发表了,其中描述了已知会改变衰老表型的生物学过程。这些过程包括基因组不稳定性、端粒磨损、表观遗传改变、蛋白质稳态丧失、营养感应失调、线粒体功能障碍、细胞衰老、干细胞衰竭、细胞间通讯改变(炎症)以及微生物组内的变化。这篇简要综述详细介绍了在过去 5 年内,犬类在这些衰老标志中的每一个方面的研究进展。此外,当其他哺乳动物物种和犬类之间的文献存在差距时,我强调了可能作为衰老模型的犬类所缺失的衰老生物标志物。我还主张犬类衰老研究的重要性,包括不同年龄的多个犬种,并对具有不同平均寿命的犬种进行年龄校正。