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Prune Consumption Attenuates Proinflammatory Cytokine Secretion and Alters Monocyte Activation in Postmenopausal Women: Secondary Outcome Analysis of a 12-Mo Randomized Controlled Trial: The Prune Study.
Damani, Janhavi J; Oh, Ester S; De Souza, Mary Jane; Strock, Nicole Ca; Williams, Nancy I; Nakatsu, Cindy H; Lee, Hang; Weaver, Connie; Rogers, Connie J.
Afiliación
  • Damani JJ; The Intercollege Graduate Degree Program in Integrative and Biomedical Physiology, Huck Institutes of the Life Sciences, The Pennsylvania State University, University Park, PA, United States.
  • Oh ES; Department of Nutritional Sciences, The Pennsylvania State University, University Park, PA, United States; Division of Renal Diseases and Hypertension, University of Colorado Anschutz Medical Campus, Aurora, CO, United States.
  • De Souza MJ; Department of Kinesiology, The Pennsylvania State University, University Park, PA, United States.
  • Strock NC; Department of Kinesiology, The Pennsylvania State University, University Park, PA, United States.
  • Williams NI; Department of Kinesiology, The Pennsylvania State University, University Park, PA, United States.
  • Nakatsu CH; Department of Agronomy, Purdue University, West Lafayette, IN, United States.
  • Lee H; Biostatistics Center, Massachusetts General Hospital and Harvard Medical School, Boston, MA, United States.
  • Weaver C; School of Exercise and Nutritional Sciences, San Diego State University, San Diego, CA, United States.
  • Rogers CJ; Department of Nutritional Sciences, The Pennsylvania State University, University Park, PA, United States; Center for Molecular Immunology and Infectious Disease, The Pennsylvania State University, University Park, PA, United States; Department of Nutritional Sciences, University of Georgia, Athens,
J Nutr ; 2023 Nov 19.
Article en En | MEDLINE | ID: mdl-37984741
ABSTRACT

BACKGROUND:

Proinflammatory cytokines are implicated in the pathophysiology of postmenopausal bone loss. Clinical studies demonstrate that prunes prevent bone mineral density loss; however, the mechanism underlying this effect is unknown.

OBJECTIVE:

We investigated the effect of prune supplementation on immune, inflammatory, and oxidative stress markers.

METHODS:

A secondary analysis was conducted in the Prune Study, a single-center, parallel-arm, 12-mo randomized controlled trial of postmenopausal women (55-75 y old; n = 235 recruited; n = 183 completed) who were assigned to 1 of 3 groups "no-prune" control, 50 g prune/d and 100 g prune/d groups. At baseline and after 12 mo of intervention, blood samples were collected to measure serum high-sensitivity C-reactive protein (hs-CRP), serum total antioxidant capacity (TAC), plasma 8-isoprostane, proinflammatory cytokines [interleukin (IL)-1ß, IL-6, IL-8, monocyte chemoattractant protein-1, and tumor necrosis factor (TNF)-α] concentrations in plasma and lipopolysaccharide (LPS)-stimulated peripheral blood mononuclear cells (PBMCs) culture supernatants, and the percentage and activation of circulating monocytes, as secondary outcomes.

RESULTS:

Prune supplementation did not alter hs-CRP, TAC, 8-isoprostane, and plasma cytokine concentrations. However, percent change from baseline in circulating activated monocytes was lower in the 100 g prune/d group compared with the control group (mean ± SD, -1.8% ± 4.0% in 100 g prune/d compared with 0.1% ± 2.9% in control; P < 0.01). Furthermore, in LPS-stimulated PBMC supernatants, the percent change from baseline in TNF-α secretion was lower in the 50 g prune/d group compared with the control group (-4.4% ± 43.0% in 50 g prune/d compared with 24.3% ± 70.7% in control; P < 0.01), and the percent change from baseline in IL-1ß, IL-6, and IL-8 secretion was lower in the 100 g prune/d group compared with the control group (-8.9% ± 61.6%, -4.3% ± 75.3%, -14.3% ± 60.8% in 100 g prune/d compared with 46.9% ± 107.4%, 16.9% ± 70.6%, 39.8% ± 90.8% in control for IL-1ß, IL-6, and IL-8, respectively; all P < 0.05).

CONCLUSIONS:

Dietary supplementation with 50-100 g prunes for 12 mo reduced proinflammatory cytokine secretion from PBMCs and suppressed the circulating levels of activated monocytes in postmenopausal women. This trial was registered at clinicaltrials.gov as NCT02822378.
Palabras clave

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: J Nutr Año: 2023 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: J Nutr Año: 2023 Tipo del documento: Article País de afiliación: Estados Unidos