以细胞衰老为中心的综合方法来理解机体衰老。

Q3 Medicine
Rohit Sharma, Bhawna Diwan
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引用次数: 1

摘要

老龄化仍然是老年人发病率和死亡率上升的根本原因。尽管研究仍在继续,但对衰老的分子机制和影响的综合和全面的理解仍然是难以捉摸的。这在生物老年学中提出了一个重大挑战,因此,旨在整合衰老的多面性以识别和开发成功的治疗靶点的新策略是非常需要的。目前,细胞衰老、免疫衰老和肠道菌群失调是已知的关键衰老调节因子。然而,可以设想一种以细胞衰老为中心的综合观点,该观点与免疫衰老和肠道微生物群失调的看似不同的过程有关,这意味着对衰老的理解更具包容性和针对性。本文讨论了细胞衰老的新证据和意义,如-à-vis免疫衰老和肠道微生物群失调在潜在抗衰老疗法的发展中。这些个体调节剂之间的潜在联系和机制已被审议,以提供对生物衰老更连贯和切实的理解。作者强调,衰老应在这些过程的综合范围内进行研究,这可能最终有助于设计出一种具有明确治疗目标的新的包容和巩固的衰老理论。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A Cellular Senescence-Centric Integrated Approach to Understanding Organismal Aging.

Aging remains the fundamental cause of the increased rate of morbidity and mortality in the elderly. Despite continuing research, an integrative and holistic understanding of the molecular mechanisms and effects of aging is still elusive. This presents a major challenge in biogerontology, and therefore novel strategies aimed at integrating the multifaceted nature of aging for the identification and development of successful therapeutic targets are highly desirable. At present, cellular senescence, immunosenescence, and gut microbiota dysbiosis are key known modulators of aging. However, a cellular senescence-centric integrative view that relates to the seemingly distinct processes of immunosenescence and gut microbiota dysbiosis can be envisaged, which implies a more inclusive and targetable understanding of aging. The present manuscript discusses the emerging evidence and significance of cellular senescence vis-à-vis immunosenescence and gut microbiota dysbiosis in the development of potential anti-aging therapies. Underlying interconnections and mechanisms amongst these individual modulators have been deliberated to present a more coherent and tangible understanding of biological aging. It is emphasized that aging be studied within the integrative purview of these processes that may ultimately help devise a new inclusive and consolidated theory of aging with well-defined therapeutic targets.

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来源期刊
Current aging science
Current aging science Medicine-Geriatrics and Gerontology
CiteScore
3.90
自引率
0.00%
发文量
40
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