Laboratory for Proteomics and Metabolomics, Research Division, General Hospital of Mexico "Dr. Eduardo Liceaga", 06720 Mexico City, Mexico.
Clinical Nutrition Division, General Hospital of Mexico "Dr. Eduardo Liceaga", 06720 Mexico City, Mexico.
J Immunol Res. 2019 Apr 28;2019:6105059. doi: 10.1155/2019/6105059. eCollection 2019.
Sucralose is a noncaloric artificial sweetener that is widely consumed worldwide and has been associated with alteration in glucose and insulin homeostasis. Unbalance in monocyte subpopulations expressing CD11c and CD206 hallmarks metabolic dysfunction but has not yet been studied in response to sucralose. Our goal was to examine the effect of a single sucralose sip on serum insulin and blood glucose and the percentages of classical, intermediate, and nonclassical monocytes in healthy young adults subjected to an oral glucose tolerance test (OGTT). This study was a randomized, placebo-controlled clinical trial. Volunteers randomly received 60 mL water as placebo ( = 20) or 48 mg sucralose dissolved in 60 mL water ( = 25), fifteen minutes prior to an OGTT. Blood samples were individually drawn every 15 minutes for 180 minutes for quantifying glucose and insulin concentrations. Monocyte subsets expressing CD11c and CD206 were measured at -15 and 180 minutes by flow cytometry. As compared to controls, volunteers receiving sucralose exhibited significant increases in serum insulin at 30, 45, and 180 minutes, whereas blood glucose values showed no significant differences. Sucralose consumption caused a significant 7% increase in classical monocytes and 63% decrease in nonclassical monocytes with respect to placebo controls. Pearson's correlation models revealed a strong association of insulin with sucralose-induced monocyte subpopulation unbalance whereas glucose values did not show significant correlations. Sucralose ingestion decreased CD11c expression in all monocyte subsets and reduced CD206 expression in nonclassical monocytes suggesting that sucralose does not only unbalance monocyte subpopulations but also alter their expression pattern of cell surface molecules. This work demonstrates for the first time that a 48 mg sucralose sip increases serum insulin and unbalances monocyte subpopulations expressing CD11c and CD206 in noninsulin-resistant healthy young adults subjected to an OGTT. The apparently innocuous consumption of sucralose should be reexamined in light of these results.
三氯蔗糖是一种无热量的人工甜味剂,在全球范围内广泛消费,并且与葡萄糖和胰岛素稳态的改变有关。表达 CD11c 和 CD206 标志物的单核细胞亚群的失衡与代谢功能障碍有关,但尚未在对三氯蔗糖的反应中进行研究。我们的目标是研究单次三氯蔗糖摄入对健康年轻成年人口服葡萄糖耐量试验(OGTT)中血清胰岛素和血糖以及经典、中间和非经典单核细胞百分比的影响。这项研究是一项随机、安慰剂对照的临床试验。志愿者随机接受 60 毫升水作为安慰剂(=20)或 48 毫克三氯蔗糖溶解在 60 毫升水中(=25),在 OGTT 前 15 分钟。在 180 分钟内,每隔 15 分钟抽取一次血样,以定量检测葡萄糖和胰岛素浓度。在 -15 和 180 分钟时,通过流式细胞术测量表达 CD11c 和 CD206 的单核细胞亚群。与对照组相比,接受三氯蔗糖的志愿者在 30、45 和 180 分钟时血清胰岛素显著升高,而血糖值无显著差异。与安慰剂对照相比,三氯蔗糖的消耗导致经典单核细胞增加 7%,非经典单核细胞减少 63%。Pearson 相关模型显示,胰岛素与三氯蔗糖诱导的单核细胞亚群失衡密切相关,而血糖值没有显示出显著相关性。三氯蔗糖摄入降低了所有单核细胞亚群中的 CD11c 表达,并降低了非经典单核细胞中的 CD206 表达,表明三氯蔗糖不仅会使单核细胞亚群失衡,还会改变其细胞表面分子的表达模式。这项工作首次表明,48 毫克三氯蔗糖的摄入会增加血清胰岛素并使非胰岛素抵抗的健康年轻成年人 OGTT 中表达 CD11c 和 CD206 的单核细胞亚群失衡。鉴于这些结果,应重新审视看似无害的三氯蔗糖消费。