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我们都在变老,原因如下。

We are all aging, and here's why.

作者信息

Shinde Atharva, Deore Gargi, Navsariwala Kedar P, Tabassum Heena, Wani Minal

机构信息

Dr. D. Y. Patil Biotechnology and Bioinformatics Institute Dr. D. Y. Patil Vidyapeeth Pune Maharashtra India.

出版信息

Aging Med (Milton). 2022 Oct 3;5(3):211-231. doi: 10.1002/agm2.12223. eCollection 2022 Sep.

Abstract

Here, through this review, we aim to serve this purpose by first discussing the statistics and aging demographics, including the life expectancy of the world and India, along with the gender life expectancy gap observed throughout the world, followed by explaining the hallmarks and integral causes of aging, along with the role played by senescent cells in controlling inflammation and the effect of senescence associated secretory phenotype on longevity. A few of the molecular pathways which are crucial in modulating the process of aging, such as the nutrient-sensing mTOR pathway, insulin signaling, Nrf2, FOXO, PI3-Akt, Sirtuins, and AMPK, and their effects are also covered in paramount detail. A diverse number of ingenious research methodologies are used in the modern era of longevity exploration. We have attempted to cover these methods under the umbrella of three broad categories: in vitro, in vivo, and in silico techniques. The drugs developed to attenuate the aging process, such as rapamycin, metformin, resveratrol, etc. and their interactions with the above-mentioned molecular pathways along with their toxicity have also been reviewed in detail.

摘要

在此,通过本综述,我们旨在实现这一目的,首先讨论统计学和老龄化人口统计学,包括世界和印度的预期寿命,以及全球观察到的性别预期寿命差距,接着解释衰老的标志和内在原因,以及衰老细胞在控制炎症中的作用和衰老相关分泌表型对寿命的影响。一些在调节衰老过程中至关重要的分子途径,如营养感知mTOR途径、胰岛素信号传导、Nrf2、FOXO、PI3-Akt、沉默调节蛋白和AMPK及其作用也进行了极为详细的阐述。在现代长寿探索时代使用了多种巧妙的研究方法。我们试图将这些方法归纳为三大类:体外、体内和计算机模拟技术。还详细综述了为减缓衰老过程而开发的药物,如雷帕霉素、二甲双胍、白藜芦醇等,以及它们与上述分子途径的相互作用及其毒性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f9d6/9549314/a8b40a88bb17/AGM2-5-211-g013.jpg

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