Center for Behavioural Sciences and Mental Health, Istituto Superiore di Sanità, Viale Regina Elena 299, 00161 Rome, Italy; Program in Science of Nutrition, Metabolism, Ageing and Gender-Related Diseases, Faculty of Medicine and Surgery, Catholic University of the Sacred Heart, Largo Francesco Vito 1, 00168 Rome, Italy.
Center for Behavioural Sciences and Mental Health, Istituto Superiore di Sanità, Viale Regina Elena 299, 00161 Rome, Italy.
Clin Nutr. 2024 Oct;43(10):2236-2248. doi: 10.1016/j.clnu.2024.08.012. Epub 2024 Aug 18.
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 low-grade 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.
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.
RA prevented insulin resistance in males while protecting both males and females from WD-dependent 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-κB, GR and STAT3, that have been recently suggested to promote healthspan and longevity by modulating inflammatory and cell survival pathways.
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.
不健康的生活方式,如长期摄入西式饮食(WD),与全身炎症和氧化应激(OS)的增加有关,这种情况可能有利于衰老过程中的认知功能障碍。多酚,如迷迭香酸(RA),可以缓冲低度炎症和 OS,从而维持 WD 驱动的衰老大脑的健康,延长健康寿命。本研究旨在评估 RA 预防 WD 驱动的不健康衰老小鼠模型认知能力下降的能力,并深入了解大脑内调节的特定分子途径。
雄性和雌性 C57Bl/6N 老年小鼠分别用 RA 或载体补充 6 周。在 RA 治疗 2 周后,开始给予 WD 或对照饮食(CD)。随后,所有小鼠均在 Morris 水迷宫(MWM)中进行认知能力测试,在高架十字迷宫(EPM)中进行情绪测试。通过取血样检测血糖和血脂稳态,取出海马进行 RNAseq 转录组分析。
RA 可预防雄性胰岛素抵抗,并保护雄性和雌性免受 WD 依赖性记忆障碍的影响。在海马体中,RA 调节了雄性的 OS 途径,以及雌性的免疫和性激素相关信号级联(Lhb 和 Lhcgr 基因)。此外,RA 总体上导致了 Glp1r 的上调,Glp1r 最近被确定为预防代谢紊乱的有希望的靶点。此外,我们还发现 RA 依赖性核转录因子的富集,如 NF-κB、GR 和 STAT3,这些因子最近被建议通过调节炎症和细胞存活途径来促进健康寿命和长寿。
口服 RA 补充可能通过抗氧化和免疫调节特性促进衰老过程中的大脑和代谢可塑性,可能以性别依赖的方式影响产后激素环境。因此,作为一种保持认知功能和对抗代谢紊乱的策略,RA 的补充应该在精准医学的背景下被考虑。