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Main Authors: Tahan Zadeh, Navid, Knop, Mirjam, Ulrich, Lisa Marie, Bruchhaus, Iris, Lang, Roman, Lüersen, Kai, Rimbach, Gerald, Roeder, Thomas
Format: Artículo científico
Language:en
Published: Nutrients 2025
Subjects:
Online Access:https://pubmed.ncbi.nlm.nih.gov/41097142/
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author Tahan Zadeh, Navid
Knop, Mirjam
Ulrich, Lisa Marie
Bruchhaus, Iris
Lang, Roman
Lüersen, Kai
Rimbach, Gerald
Roeder, Thomas
author_facet Tahan Zadeh, Navid
Knop, Mirjam
Ulrich, Lisa Marie
Bruchhaus, Iris
Lang, Roman
Lüersen, Kai
Rimbach, Gerald
Roeder, Thomas
Tahan Zadeh, Navid
Knop, Mirjam
Ulrich, Lisa Marie
Bruchhaus, Iris
Lang, Roman
Lüersen, Kai
Rimbach, Gerald
Roeder, Thomas
collection PubMed - marine biology
contents Sex-Specific Lifespan Extension and Anti-Obesogenic Effects of Extract Through Tor Signaling Modulation in . Tahan Zadeh, Navid Knop, Mirjam Ulrich, Lisa Marie Bruchhaus, Iris Lang, Roman Lüersen, Kai Rimbach, Gerald Roeder, Thomas Animals Longevity Plant Extracts Female Male Signal Transduction Chenopodiaceae TOR Serine-Threonine Kinases Drosophila Proteins Sex Factors Drosophila Drosophila melanogaster Diet, High-Fat : Some marine plants and algae are known to exert health benefits. However, the long-term effects and underlying mechanisms of these health benefits are still poorly understood. For this reason, we have investigated an extract from the marsh samphire for its life-prolonging potential. : We investigated the effect of an aqueous extract of (SEE) on the lifespan of several wild-type strains of . In addition, we used deficient flies to elucidate the mechanism of the life-prolonging effects. Finally, we comprehensively phenotyped the treated animals. : Supplementing a standard diet with SEE extended the lifespan of different laboratory strains by up to a third (37% in and 19% in ). A total of 0.05% of SEE were ineffective, whereas 0.2% induced robust lifespan prolongation. This effect was strictly sex-specific, as the SEE application was completely ineffective in males, while prolonging life in females. We found that the body fat content of SEE-treated female flies was lower compared to controls. The extract also positively impacted the lifespan of flies fed a high-fat diet but not a high-sugar diet. SEE exhibited a lipase-inhibitory activity in vitro. Moreover, SEE counteracted aging-associated loss of intestinal barrier integrity. The sex-specific lifespan extensions induced by the SEE entirely depended on functional Tor signaling in the flies. Tissue-specific silencing of the Tor signaling pathway in different cellular compartments of the intestine reduced, but did not altogether abolish, the lifespan-prolonging effect in females. : SEE is a promising candidate for a health-promoting intervention, as it induces lifespan-prolonging and anti-obesogenic effects in a sex-specific manner. These effects depend on functional Tor and partially on FoxO signaling. Future studies should identify the active compounds in the extract.
format Artículo científico
id pubmed_41097142
institution PubMed
language en
publishDate 2025
publisher Nutrients
record_format pubmed
spellingShingle Sex-Specific Lifespan Extension and Anti-Obesogenic Effects of Extract Through Tor Signaling Modulation in .
Tahan Zadeh, Navid
Knop, Mirjam
Ulrich, Lisa Marie
Bruchhaus, Iris
Lang, Roman
Lüersen, Kai
Rimbach, Gerald
Roeder, Thomas
Animals
Longevity
Plant Extracts
Female
Male
Signal Transduction
Chenopodiaceae
TOR Serine-Threonine Kinases
Drosophila Proteins
Sex Factors
Drosophila
Drosophila melanogaster
Diet, High-Fat
Sex-Specific Lifespan Extension and Anti-Obesogenic Effects of Extract Through Tor Signaling Modulation in . Tahan Zadeh, Navid Knop, Mirjam Ulrich, Lisa Marie Bruchhaus, Iris Lang, Roman Lüersen, Kai Rimbach, Gerald Roeder, Thomas Animals Longevity Plant Extracts Female Male Signal Transduction Chenopodiaceae TOR Serine-Threonine Kinases Drosophila Proteins Sex Factors Drosophila Drosophila melanogaster Diet, High-Fat : Some marine plants and algae are known to exert health benefits. However, the long-term effects and underlying mechanisms of these health benefits are still poorly understood. For this reason, we have investigated an extract from the marsh samphire for its life-prolonging potential. : We investigated the effect of an aqueous extract of (SEE) on the lifespan of several wild-type strains of . In addition, we used deficient flies to elucidate the mechanism of the life-prolonging effects. Finally, we comprehensively phenotyped the treated animals. : Supplementing a standard diet with SEE extended the lifespan of different laboratory strains by up to a third (37% in and 19% in ). A total of 0.05% of SEE were ineffective, whereas 0.2% induced robust lifespan prolongation. This effect was strictly sex-specific, as the SEE application was completely ineffective in males, while prolonging life in females. We found that the body fat content of SEE-treated female flies was lower compared to controls. The extract also positively impacted the lifespan of flies fed a high-fat diet but not a high-sugar diet. SEE exhibited a lipase-inhibitory activity in vitro. Moreover, SEE counteracted aging-associated loss of intestinal barrier integrity. The sex-specific lifespan extensions induced by the SEE entirely depended on functional Tor signaling in the flies. Tissue-specific silencing of the Tor signaling pathway in different cellular compartments of the intestine reduced, but did not altogether abolish, the lifespan-prolonging effect in females. : SEE is a promising candidate for a health-promoting intervention, as it induces lifespan-prolonging and anti-obesogenic effects in a sex-specific manner. These effects depend on functional Tor and partially on FoxO signaling. Future studies should identify the active compounds in the extract.
title Sex-Specific Lifespan Extension and Anti-Obesogenic Effects of Extract Through Tor Signaling Modulation in .
topic Animals
Longevity
Plant Extracts
Female
Male
Signal Transduction
Chenopodiaceae
TOR Serine-Threonine Kinases
Drosophila Proteins
Sex Factors
Drosophila
Drosophila melanogaster
Diet, High-Fat
url https://pubmed.ncbi.nlm.nih.gov/41097142/