Magaña-Gómez Javier A, González-Ochoa Guadalupe, Rosas-Rodríguez Jesus A, Stephens-Camacho N Aurora, Flores-Mendoza Lilian K
Posgrado en Ciencias Biomédicas, Facultad de Ciencias Químico Biológicas, Universidad Autónoma de Sinaloa, Av. de las Américas y Josefa Ortiz, CU 80010 Culiacán, Sinaloa, Mexico.
Laboratorio Universitario de Análisis Clínicos e Investigación, Universidad de Sonora (LUACI) Departamento de Ciencias Químico-Biológicas y Agropecuarias, Campus Navojoa. Lázaro Cárdenas del Río #100, CP 85880 Navojoa, Sonora, Mexico.
Int J Mol Sci. 2024 Dec 20;25(24):13635. doi: 10.3390/ijms252413635.
Sucralose, a commonly nonnutritive sweetener used in daily products of habitual diet, is related to impairing the gut microbiome by disrupting inflammatory response, promoting weight gain by increasing adipose tissue and promoting chronic inflammatory processes. Considering the impact of sucralose in the development of metabolic diseases, in this work, we focused on the impact of sucralose on the adipocyte differentiation process to determine if sucralose can promote adipogenesis and increase adipose tissue depots in PCS 210 010 human preadipocytes cell line. Sucralose at 25 (S25) and 100 ng/µL (S100) concentrations were tested against control with no edulcorant (NS) during the adipocyte differentiation process at 48 h and 96 h. The genetic expression of adipogenesis markers such as CEBP-α, PPARγ, EBF-2, UCP-1, and lipogenesis regulator ACC was determined by qPCR. A panel of human cytokines related to inflammatory response was measured by a flow cytometer using the kit Legend Plex Human Cytokine panel of BIOLUMINEX. Our results indicate that sucralose increased the expression of white adipocyte differentiation marker CEBP-α and lipogenesis regulator ACC at 96 h before complete differentiation. Also, sucralose triggers an inflammatory response by synthesizing adiponectin, resistin, IL-6, IL-8, and Il-1B. To summarize, sucralose stimulates the expression of genes related to adipogenesis and negatively affects the secretion of inflammatory cytokines and adipokines during preadipocyte differentiation.
三氯蔗糖是一种常用于日常习惯性饮食产品中的非营养性甜味剂,它通过破坏炎症反应损害肠道微生物群,通过增加脂肪组织促进体重增加,并促进慢性炎症过程。考虑到三氯蔗糖对代谢疾病发展的影响,在这项研究中,我们重点关注三氯蔗糖对脂肪细胞分化过程的影响,以确定三氯蔗糖是否能促进PCS 210 010人前脂肪细胞系中的脂肪生成并增加脂肪组织储存。在脂肪细胞分化过程的48小时和96小时,对25(S25)和100 ng/µL(S100)浓度的三氯蔗糖与不含甜味剂的对照组(NS)进行了测试。通过qPCR测定脂肪生成标志物如CEBP-α、PPARγ、EBF-2、UCP-1和脂肪生成调节因子ACC的基因表达。使用BIOLUMINEX的Legend Plex人细胞因子检测试剂盒,通过流式细胞仪测量一组与炎症反应相关的人细胞因子。我们的结果表明,在完全分化前的96小时,三氯蔗糖增加了白色脂肪细胞分化标志物CEBP-α和脂肪生成调节因子ACC的表达。此外,三氯蔗糖通过合成脂联素、抵抗素、IL-6、IL-8和Il-1B引发炎症反应。总之,三氯蔗糖刺激前脂肪细胞分化过程中与脂肪生成相关的基因表达,并对炎症细胞因子和脂肪因子的分泌产生负面影响。