Zein nanoparticles extend lifespan in C. elegans and SAMP8 mice

Empty zein nanoparticles (NP) have been shown to lower glycemia in rats by stimulating the secretion of endogenous GLP-1. This study evaluated the effect of these nanoparticles on the lifespan of two animal models: C. elegans fed with a glucose-rich diet and the senescence accelerated mouse-prone 8 (SAMP8 mice). In C. elegans, NP increased the mean lifespan of worms by 7 days (from 17.1 for control to 24.5 days). This observation was in line with the observed significant reductions of glucose and fat contents, lipofuscin accumulation, and ROS expression. Furthermore, NP supplementation led to an upregulation of the expression of daf-16 and skn-1 genes. DAF-16 (orthologue of the FOXO family) and SKN-1 (orthologue of mammalian Nrf/CNC proteins) are implicated in activating detoxification mechanisms against oxidative damage. In SAMP8, oral administration of NP also extended the mean lifespan of mice (by 28 % compared to controls), corroborating the protective effect of these nanoparticles.

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Publication Details

Journal
International Journal of Pharmaceutics
Published
2024-10-02
DOI
https://doi.org/10.1016/j.ijpharm.2024.124798
Citations
2
Primary Topic
Genetics, Aging, and Longevity in Model Organisms
Type
article
Field-Weighted Citation Impact
0.46

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article

Zein nanoparticles extend lifespan in C. elegans and SAMP8 mice

Elena Puerta, Cristian Reboredo, Marı́a J. Ramı́rez, Juan M. Irache et al.
2 citations
International Journal of Pharmaceutics
Genetics, Aging, and Longevity in Model Organisms
0.46
article

Zein nanoparticles extend lifespan in C. elegans and SAMP8 mice

Elena Puerta, Cristian Reboredo, Marı́a J. Ramı́rez, Juan M. Irache, J.L. Vizmanos, Ana L. Martínez‐López, Carlos J. González-Navarro, Maite Solas
article en
2 citations

Abstract

Empty zein nanoparticles (NP) have been shown to lower glycemia in rats by stimulating the secretion of endogenous GLP-1. This study evaluated the effect of these nanoparticles on the lifespan of two animal models: C. elegans fed with a glucose-rich diet and the senescence accelerated mouse-prone 8 (SAMP8 mice). In C. elegans, NP increased the mean lifespan of worms by 7 days (from 17.1 for control to 24.5 days). This observation was in line with the observed significant reductions of glucose and fat contents, lipofuscin accumulation, and ROS expression. Furthermore, NP supplementation led to an upregulation of the expression of daf-16 and skn-1 genes. DAF-16 (orthologue of the FOXO family) and SKN-1 (orthologue of mammalian Nrf/CNC proteins) are implicated in activating detoxification mechanisms against oxidative damage. In SAMP8, oral administration of NP also extended the mean lifespan of mice (by 28 % compared to controls), corroborating the protective effect of these nanoparticles.

International Journal of PharmaceuticsVol. 666
Navarre Institute of Health Research (ES), Universidad de Navarra (ES)
“la Caixa” Foundation, Consejo Nacional de Ciencia y Tecnología, Universidad de Navarra, National Institutes of Health, Asociación de Amigos de la Universidad de Navarra, Office of Research Infrastructure Programs, National Institutes of Health
Openalex Percentile: Top 39%
Genetics, Aging, and Longevity in Model Organisms
0.46
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Zein nanoparticles extend lifespan in C. elegans and SAMP8 mice — Elena Puerta, Cristian Reboredo, et al. · International Journal of Pharmaceutics (2024) | TGRS Research Map | TGRS