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Top Voted Preprints
Q2 2023
ISSN 2817-8831
Candidate Preprints
Q2 2023
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Cognitive Rejuvenation in Old Rats by Hippocampal OSKM Gene Therapy

Cognitive Rejuvenation in Old Rats by Hippocampal OSKM Gene Therapy

Steve Horvath, Ezequiel Lacunza, Martina Canatelli Mallat, Enrique L. Portiansky, Maria D. Gallardo, Robert T. Brooke, Priscila Chiavellini, Diana C. Pasquini, Mauricio Girard, Marianne Lehmann, Qi Yan, Ake T. Lu, Amin Haghani, Juozas Gordevicius, Martin Abba, Rodolfo G. Goya

The injection of Yamanaka genes (OSKM) into the hippocampus of old rats significantly improved their spatial learning performance and potentially their spatial memory. Morphological changes were not observed in astrocytes or mature neurons, indicating the treatment caused no harmful brain changes. The analysis of differential methylation suggested a possible rejuvenation effect on the old hippocampal methylome, extending evidence that viral vector-mediated delivery of Yamanaka genes in the brain can have regenerative effects.

Q2 2023
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Regeneration leads to global tissue rejuvenation in aging sexual planarians

Regeneration leads to global tissue rejuvenation in aging sexual planarians

Xiaoting Dai, Xinghua Li, Scott Pletcher, David Paris, Leonid Kruglyak, Jacob Sobota, Longhua Guo

The research demonstrated that the sexually reproducing lineage of the planarian Schmidtea mediterranea, a freshwater species known for its remarkable regenerative capabilities, shows signs of aging. However, the process of amputation followed by regeneration reversed these aging signs, restoring youthful gene expression, stem cell states, tissue composition, and overall physiology. Findings suggest that planaria's natural age-reversal solution could offer valuable insights into anti-aging strategies for humans.

Q2 2023
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A single-cell atlas of the aging murine ovary

A single-cell atlas of the aging murine ovary

José V. V. Isola, Sarah R. Ocañas, Chase R. Hubbart, Sunghwan Ko, Samim Ali Mondal, Jessica D. Hense, Augusto Schneider, Susan Kovats, Willard M. Freeman, Michael B. Stout

Single-cell RNA sequencing was prformed on ovarian tissue from young and reproductively aged mice, revealing significant transcriptomic changes with aging. Notably, there was a doubling of immune cells, especially T and B lymphocytes, and changes in stromal fibroblasts pathways. The follicular cells exhibited increased stress response, immunogenic and fibrotic signaling with age, more in atretic granulosa cells, but also noticeable in healthy granulosa cells. Interestingly, no age-related cellular senescence was observed, raising new hypotheses for mechanisms of ovarian aging.

Q2 2023
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Initiation phase cellular reprogramming ameliorates DNA damage in the ERCC1 mouse model of premature aging

Initiation phase cellular reprogramming ameliorates DNA damage in the ERCC1 mouse model of premature aging

Patrick Treat Paine, Cheyenne Rechsteiner, Francesco Morandini, Gabriela Desdin Mico, Calida Mrabti, Alberto Parras, Amin Haghani, Robert Brooke, Steve Horvath, Andrei Seluanov, Vera Gorbunova, Alejandro Ocampo

The study examined the rejuvenating properties of cellular reprogramming in an accelerated aging mouse model. Through the process of in vivo partial cellular reprogramming, they found significant lifespan extension and restoration of aging phenotypes. Particularly, the technique effectively reversed DNA damage, stimulated DNA repair processes, and rejuvenated the epigenetic clock. Additionally, inhibiting TGFb pathway receptors produced similar benefits. The study suggests cellular reprogramming responds to aging signals and restores youthful molecular characteristics, offering potential breakthroughs in anti-aging research.

Q2 2023
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Cognitive Rejuvenation in Old Rats by Hippocampal OSKM Gene Therapy

Cognitive Rejuvenation in Old Rats by Hippocampal OSKM Gene Therapy

The injection of Yamanaka genes (OSKM) into the hippocampus of old rats significantly improved their spatial learning performance and potentially their spatial memory. Morphological changes were not observed in astrocytes or mature neurons, indicating the treatment caused no harmful brain changes. The analysis of differential methylation suggested a possible rejuvenation effect on the old hippocampal methylome, extending evidence that viral vector-mediated delivery of Yamanaka genes in the brain can have regenerative effects.

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The associations of long-term physical activity in adulthood with later biological ageing and all-cause mortality – a prospective twin study

The associations of long-term physical activity in adulthood with later biological ageing and all-cause mortality – a prospective twin study

The study investigates the association between long-term leisure-time physical activity (LTPA), biological ageing, and mortality. It seeks to understand if LTPA patterns influence biological ageing and mortality, potentially mediating the beneficial relationship between LTPA and death from all causes. It also aims to account for reverse causality and genetic/environmental factors through prevalent disease accounting and a twin study design, as some suggest that LTPA may not prevent premature mortality, but reflect underlying good health.

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Effects of antidiabetic drugs on mortality risks in individuals with type 2 diabetes: A prospective cohort study of UK Biobank participants

Effects of antidiabetic drugs on mortality risks in individuals with type 2 diabetes: A prospective cohort study of UK Biobank participants

This prospective study on a UK Biobank cohort reveals that among individuals with type 2 diabetes, those prescribed metformin or sodium glucose cotransporter 2 inhibitors (SGLT2I) have a higher survival probability compared to those using other anti-diabetic drugs. Remarkably, individuals on SGLT2I even showed increased survival compared to those without type 2 diabetes. Other anti-diabetic drugs either had a negative effect on lifespan or no significant impact.

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Initiation phase cellular reprogramming ameliorates DNA damage in the ERCC1 mouse model of premature aging

Initiation phase cellular reprogramming ameliorates DNA damage in the ERCC1 mouse model of premature aging

The study examined the rejuvenating properties of cellular reprogramming in an accelerated aging mouse model. Through the process of in vivo partial cellular reprogramming, they found significant lifespan extension and restoration of aging phenotypes. Particularly, the technique effectively reversed DNA damage, stimulated DNA repair processes, and rejuvenated the epigenetic clock. Additionally, inhibiting TGFb pathway receptors produced similar benefits. The study suggests cellular reprogramming responds to aging signals and restores youthful molecular characteristics, offering potential breakthroughs in anti-aging research.

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