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Review
. 2022 Jun 11;23(12):6546.
doi: 10.3390/ijms23126546.

The Less We Eat, the Longer We Live: Can Caloric Restriction Help Us Become Centenarians?

Affiliations
Review

The Less We Eat, the Longer We Live: Can Caloric Restriction Help Us Become Centenarians?

Tamara Dakic et al. Int J Mol Sci. .

Abstract

Striving for longevity is neither a recent human desire nor a novel scientific field. The first article on this topic was published in 1838, when the average human life expectancy was approximately 40 years. Although nowadays people on average live almost as twice as long, we still (and perhaps more than ever) look for new ways to extend our lifespan. During this seemingly endless journey of discovering efficient methods to prolong life, humans were enthusiastic regarding several approaches, one of which is caloric restriction (CR). Where does CR, initially considered universally beneficial for extending both lifespan and health span, stand today? Does a lifelong decrease in food consumption represent one of the secrets of centenarians' long and healthy life? Do we still believe that if we eat less, we will live longer? This review aims to summarize the current literature on CR as a potential life-prolonging intervention in humans and discusses metabolic pathways that underlie this effect.

Keywords: caloric restriction; centenarians; health span; insulin sensitivity; longevity; metabolism; signaling pathways.

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Conflict of interest statement

The authors declare no conflict of interest. The funders had no role in the design of the study; in the collection, analyses, or interpretation of data; in the writing of the manuscript, or in the decision to publish the results.

Figures

Figure 1
Figure 1
The interplay of the major nutrient-sensing pathways (IR/IGF1, mTORC1, AMPK, sirtuins) underlying CR’s pro-longevity effects. This figure represents a simplified version of the interconnectivity between the main molecular mechanisms and their components addressed in this review. IR/IGF1R—insulin/insulin-like growth factor 1 receptor; IRS—insulin receptor substrate; PI3K—phosphoinositide 3-kinase; Akt—protein kinase B; mTORC1—mammalian target of rapamycin complex 1; S6K1—S6 kinase 1; AMPK—AMP-activated protein kinase; LKB1—liver kinase B1; Sirt—sirtuins; Foxo—forkhead box protein O.

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