Rastgoo Samira, Pourvali Katayoun, Raeissadat Seyed Ahmad, Eslamian Ghazaleh, Zand Hamid
Department of Cellular and Molecular Nutrition, Faculty of Nutrition and Food Technology, National Nutrition and Food Technology Research Institute, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Physical Medicine and Rehabilitation Department, Shahid Modarres Hospital, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Front Immunol. 2025 May 12;16:1570441. doi: 10.3389/fimmu.2025.1570441. eCollection 2025.
Immunosenescence is an important factor in the impaired immune response in older adults and plays a significant role in the development of biological aging. Targeting immunosenescence could present a novel pharmacological approach to mitigating aging and age-related diseases. We aimed to investigate the effect of N-acetylcysteine (NAC) and vitamin D (Vit-D) on the senescence of peripheral blood mononuclear cells (PBMCs).
This randomized clinical trial was conducted on older adults with Vit-D deficiency. Eligible participants were randomly assigned to one of four groups to receive either (A) 1000 IU of Vit-D daily (D1) (B), 1000 IU of Vit-D plus 600 mg of NAC daily (D1N) (C), 5000 IU of Vit-D daily (D5), or (D) 5000 IU of Vit-D plus 600 mg of NAC daily (D5N) for 8 weeks. Senescence-associated beta-galactosidase (SA-β-gal) staining, expression of senescence-related genes, and serum inflammatory factors were measured at baseline and after 8 weeks.
After the intervention, supplementation with D5N and D5 significantly downregulated , interleukin-6 (), and tumor necrosis factor-α () expression and decreased SA-β-gal activity compared to the D1 group. Additionally, co-administration of NAC with 1000 IU of Vit-D significantly downregulated transcripts in PBMCs compared to Vit-D 1000 IU alone. No significant differences were observed between the groups in serum IL-6, C-reactive protein (CRP), or the neutrophil-to-lymphocyte ratio (NLR) after the intervention.
The loading dose of Vit-D significantly attenuates senescence in PBMCs of older adults. However, co-administration of NAC with both the standard and loading doses of Vit-D further enhances these beneficial effects.
https://irct.behdasht.gov.ir, identifier IRCT20230508058120N1.
免疫衰老是老年人免疫反应受损的一个重要因素,在生物衰老的发展过程中起着重要作用。针对免疫衰老可能会提供一种减轻衰老和与年龄相关疾病的新型药理学方法。我们旨在研究N-乙酰半胱氨酸(NAC)和维生素D(Vit-D)对外周血单个核细胞(PBMC)衰老的影响。
本随机临床试验针对维生素D缺乏的老年人开展。符合条件的参与者被随机分配到四组之一,分别接受:(A)每日1000 IU维生素D(D1);(B)每日1000 IU维生素D加600 mg NAC(D1N);(C)每日5000 IU维生素D(D5);或(D)每日5000 IU维生素D加600 mg NAC(D5N),为期8周。在基线和8周后测量衰老相关β-半乳糖苷酶(SA-β-gal)染色、衰老相关基因的表达以及血清炎症因子。
干预后,与D1组相比,补充D5N和D5显著下调白细胞介素-6(IL-6)和肿瘤坏死因子-α(TNF-α)的表达,并降低SA-β-gal活性。此外,与单独使用1000 IU维生素D相比,NAC与1000 IU维生素D联合使用显著下调PBMC中TNF-α转录本。干预后,各组之间血清IL-6、C反应蛋白(CRP)或中性粒细胞与淋巴细胞比值(NLR)未观察到显著差异。
维生素D的负荷剂量显著减轻老年人PBMC的衰老。然而,NAC与标准剂量和负荷剂量的维生素D联合使用可进一步增强这些有益效果。