| Literature DB >> 33815875 |
Serafino Teseo1,2, Benjamin Houot1, Kaiye Yang3, Véronique Monnier1, Guangrong Liu3, Hervé Tricoire1.
Abstract
In the last decades, the strong increase in the proportion of older people worldwide, and the increased prevalence of age associated degenerative diseases, have put a stronger focus on aging biology. In spite of important progresses in our understanding of the aging process, an integrative view is still lacking and there is still need for efficient anti-aging interventions that could improve healthspan, reduce incidence of age-related disease and, eventually, increase the lifespan. Interestingly, some compounds from traditional medicine have been found to possess anti-oxidative and anti-inflammatory properties, suggesting that they could play a role as anti-aging compounds, although in depth in vivo investigations are still scarce. In this study we used one the major aging model organisms, Drosophila melanogaster, to investigate the ability of four herb extracts (HEs: Dendrobium candidum, Ophiopogon japonicum, Ganoderma sinense and Panax notoginseng) widely used in traditional Chinese medicine (TCM) to slow down aging and improve healthspan of aged animals. Combining multiple approaches (stress resistance assays, lifespan and metabolic measurements, functional heart characterizations and behavioral assays), we show that these four HEs provide in vivo protection from various insults, albeit with significant compound-specific differences. Importantly, extracts of P. notoginseng and G. sinense increase the healthspan of aging animals, as shown by increased activity during aging and improved heart function. In addition, these two compounds also provide protection in a Drosophila model of Huntington's disease (HD), suggesting that, besides their anti-aging properties in normal individuals, they could be also efficient in the protection against age-related diseases. copyright:Entities:
Keywords: Aging; Drosophila; ER stress; Ganoderma sinense; Huntington disease; Panax notoginseng; heart aging; oxidative stress
Year: 2021 PMID: 33815875 PMCID: PMC7990376 DOI: 10.14336/AD.2020.0714-1
Source DB: PubMed Journal: Aging Dis ISSN: 2152-5250 Impact factor: 6.745