Beneficial effects of a combined lifestyle intervention for older people in a long-term-care facility on redox balance and endothelial function.

Aging Caloric restriction Mitochondrial function Oxidants Physical activity Psychological intervention

Journal

Heliyon
ISSN: 2405-8440
Titre abrégé: Heliyon
Pays: England
ID NLM: 101672560

Informations de publication

Date de publication:
30 Aug 2024
Historique:
received: 15 02 2024
revised: 28 06 2024
accepted: 05 08 2024
medline: 2 9 2024
pubmed: 2 9 2024
entrez: 2 9 2024
Statut: epublish

Résumé

It has recently been highlighted how a short healthy life-style program (LSP) can improve the functional outcomes of older people admitted to a Long-Term Care (LTC) facility. Although it is known that life-style medicine-based interventions can exert anti-aging effects through the modulation of oxidative stress and mitochondrial function, the mechanisms underlying the aforementioned effects have not been clarified, yet. For this reason, in this study, the outcomes were focused on the investigation of the possible mechanisms underlying the benefits of a short LSP in older people. This was achieved by examining circulating markers of oxidative stress and immunosenescence, such as Tymosin β (Tβ4), before and after LSP and the effects of plasma of older people undergone or not LSP on endothelial cells. Fifty-four older people were divided into two groups (n = 27 each): subjects undergoing LSP and subjects not undergoing LSP (control). The LSP consisted of a combination of caloric restriction, physical activity, and psychological intervention and lasted 3 months. Plasma samples were taken before (T0) and after LSP (T1) and were used to measure thiobarbituric acid reactive substances (TBARS), 8-hydroxy-2-deoxyguanosine (8OHdG), 8-Isoprostanes (IsoP), glutathione (GSH), superoxide dismutase (SOD) activity and Tβ4. In addition, plasma was used to stimulate human vascular endothelial cells (HUVEC), which were examined for cell viability, mitochondrial membrane potential, reactive oxygen species (ROS) and mitochondrial ROS (MitoROS) release. At T1, in LSP group we did not detect the increase of plasma TBARS and IsoP, which was observed in control. Also, plasma levels of 8OHdG were lower in LSP group vs control. In addition, LSP group only showed an increase of plasma GSH and SOD activity. Moreover, plasma levels of Tβ4 were more preserved in LSP group. Finally, at T1, in HUVEC treated with plasma from LSP group only we found an increase of the mitochondrial membrane potential and a reduction of ROS and MitoROS release in comparison with T0. The results of this study showed that a short LSP in older persons exerts antiaging effects by modulating oxidative stress also at cellular levels. Implications of those findings could be related to both prognostic and therapeutic strategies, which could be pursued as antiaging methods.

Identifiants

pubmed: 39220897
doi: 10.1016/j.heliyon.2024.e35850
pii: S2405-8440(24)11881-6
pmc: PMC11363854
doi:

Types de publication

Journal Article

Langues

eng

Pagination

e35850

Informations de copyright

© 2024 Published by Elsevier Ltd.

Déclaration de conflit d'intérêts

The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

Elena Grossini (E)

Laboratory of Physiology, Department of Translational Medicine, Università del Piemonte Orientale, 28100 Novara, Italy.

Sakthipryian Venkatesan (S)

Laboratory of Physiology, Department of Translational Medicine, Università del Piemonte Orientale, 28100 Novara, Italy.

Mohammad Mostafa Ola Pour (MMO)

Laboratory of Physiology, Department of Translational Medicine, Università del Piemonte Orientale, 28100 Novara, Italy.

Andrea Conti (A)

Department of Translational Medicine, Università del Piemonte Orientale, 28100 Novara, Italy.
Doctoral Program in Food, Health, and Longevity, Università del Piemonte Orientale, 28100 Novara, Italy.

Diego Concina (D)

Department of Translational Medicine, Università del Piemonte Orientale, 28100 Novara, Italy.
Doctoral Program in Food, Health, and Longevity, Università del Piemonte Orientale, 28100 Novara, Italy.
Anteo Impresa Sociale, 13900 Biella, Italy.

Annalisa Opizzi (A)

Department of Translational Medicine, Università del Piemonte Orientale, 28100 Novara, Italy.
Doctoral Program in Food, Health, and Longevity, Università del Piemonte Orientale, 28100 Novara, Italy.
Anteo Impresa Sociale, 13900 Biella, Italy.

Agatino Sanguedolce (A)

Department of Translational Medicine, Università del Piemonte Orientale, 28100 Novara, Italy.

Carmela Rinaldi (C)

Education and Research area, Health Professions' Direction, Maggiore Della Carità Hospital, Novara, Italy.

Sophia Russotto (S)

Department of Translational Medicine, Università del Piemonte Orientale, 28100 Novara, Italy.
Doctoral Program in Sports and Health - Patient Safety line, Universitas Miguel Hernandez, Alicante, Spain.
Residency Program of Psychiatry, Università del Piemonte Orientale, Novara, Italy.

Carla Maria Gramaglia (CM)

Department of Translational Medicine, Università del Piemonte Orientale, 28100 Novara, Italy.

Patrizia Zeppegno (P)

Department of Translational Medicine, Università del Piemonte Orientale, 28100 Novara, Italy.

Massimiliano Panella (M)

Department of Translational Medicine, Università del Piemonte Orientale, 28100 Novara, Italy.

Classifications MeSH