Western diet-induced cognitive and metabolic dysfunctions in aged mice are prevented by rosmarinic acid in a sex-dependent fashion

被引:3
|
作者
Giona, Letizia [1 ,2 ]
Musillo, Chiara [1 ]
De Cristofaro, Gaia [1 ]
Ristow, Michael [3 ]
Zarse, Kim [3 ]
Siems, Karsten [4 ]
Tait, Sabrina [5 ]
Cirulli, Francesca [1 ]
Berry, Alessandra [1 ]
机构
[1] Ist Super Sanita, Ctr Behav Sci & Mental Hlth, Viale Regina Elena 299, I-00161 Rome, Italy
[2] Univ Cattolica Sacro Cuore, Fac Med & Surg, Program Sci Nutr Metab Ageing & Gender Related Dis, Largo Francesco Vito 1, I-00168 Rome, Italy
[3] Charite Univ Med Berlin, Inst Expt Endocrinol & Diabetol, D-10117 Berlin, Germany
[4] AnalytiCon Discovery GmbH, D-14473 Potsdam, Germany
[5] Ist Super Sanita, Ctr Gender Specif Med, Viale Regina Elena 299, I-00161 Rome, Italy
基金
瑞士国家科学基金会; 欧盟地平线“2020”;
关键词
Rosmarinic acid; Metabolic syndrome; Aging; Cognitive dysfunction; Mouse; Sex differences; OXIDATIVE STRESS; NEUROPEPTIDE-S; MOUSE MODEL; HIPPOCAMPAL; EVOLUTIONARY; SENSITIVITY; RESISTANCE; DELETION; HORMONES;
D O I
10.1016/j.clnu.2024.08.012
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
Background & aims: Unhealthy lifestyles, such as chronic consumption of a Western Diet (WD), have been associated with increased systemic inflammation and oxidative stress (OS), a condition that may favour cognitive dysfunctions during aging. Polyphenols, such as rosmarinic acid (RA) may buffer lowgrade inflammation and OS, characterizing the aging brain that is sustained by WD, promoting healthspan. The aim of this study was to evaluate the ability of RA to prevent cognitive decline in a mouse model of WD-driven unhealthy aging and to gain knowledge on the specific molecular pathways modulated within the brain. Methods: Aged male and female C57Bl/6N mice were supplemented either with RA or vehicle for 6 weeks. Following 2 weeks on RA they started being administered either with WD or control diet (CD). Successively all mice were tested for cognitive abilities in the Morris water maze (MWM) and emotionality in the elevated plus maze (EPM). Glucose and lipid homeostasis were assessed in trunk blood while the hippocampus was dissected out for RNAseq transcriptomic analysis. Results: RA prevented insulin resistance in males while protecting both males and females from WDdependent memory impairment. In the hippocampus, RA modulated OS pathways in males and immune- and sex hormones-related signalling cascades (Lhb and Lhcgr genes) in females. Moreover, RA overall resulted in an upregulation of Glp1r, recently identified as a promising target to prevent metabolic derangements. In addition, we also found an RA-dependent enrichment in nuclear transcription factors, such as NF-KB, GR and STAT3, that have been recently suggested to promote healthspan and longevity by modulating inflammatory and cell survival pathways. Conclusions: Oral RA supplementation may promote brain and metabolic plasticity during aging through antioxidant and immune-modulating properties possibly affecting the post-reproductive hormonal milieu in a sex-dependent fashion. Thus, its supplementation should be considered in the context of precision medicine as a possible strategy to preserve cognitive functions and to counteract metabolic derangements.
引用
收藏
页码:2236 / 2248
页数:13
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