Carpinelli Sarah, Ahlert John, Rubin Maxwell, Aratani Alex, Smith Emma, Floyd Dana, Potter Ross M, Al-Nakkash Layla
Arizona College of Osteopathic Medicine, Midwestern University, Glendale, Arizona, United States.
College of Veterinary Medicine, Midwestern University, Glendale, Arizona, United States.
Am J Physiol Gastrointest Liver Physiol. 2025 Feb 1;328(2):G83-G93. doi: 10.1152/ajpgi.00160.2024. Epub 2024 Dec 23.
The goal of this study was to determine whether the influence of a high-fat high-sugar diet (Western diet) on intestinal function and health was reversible. We measured transepithelial short circuit current (), across freshly isolated segments of jejunum from male C57Bl/6J mice randomly assigned to one of the following groups for the study duration: high-fat high-sugar diet for 24 wk (HFHS), HFHS diet for 12 wk then switched to standard chow and water for a further 12 wk (Std), and lean controls (standard chow and water for 24 wk). At the completion of the study, segments of jejunum were frozen for Western blot determination of key proteins involved in secretory and absorptive functions, as well as senescence. Intestinal morphology was assessed. Serum and tissue assays were performed. Basal was significantly decreased (by 42%, < 0.05) in HFHS versus leans. This decrease in was fully reversed by switching to Std diet. The HFHS-induced decrease in was attributed to a significant loss of calcium-activated chloride channel (ClC2) expression. Changes in inflammatory state (TNF-α) and intestinal health [myeloperoxidase (MPO) activity] were associated with body weight changes. Our data suggests that the reduced basal jejunal in HFHS mice is reversible. Better understanding of Western diet-mediated intestinal disturbances may permit for improved treatment options for gastrointestinal abnormalities in obese individuals. Our data suggests that the reduced basal jejunal (decreased secretory function) in Western diet-fed mice is reversible. A better understanding of Western diet-mediated intestinal disturbances may permit improved treatment options for gastrointestinal abnormalities in obese individuals.
本研究的目的是确定高脂高糖饮食(西式饮食)对肠道功能和健康的影响是否可逆。我们测量了经上皮短路电流(),该电流通过雄性C57Bl/6J小鼠新鲜分离的空肠段,这些小鼠在研究期间被随机分配到以下组之一:高脂高糖饮食24周(HFHS),高脂高糖饮食12周,然后改为标准饲料和水再喂养12周(Std),以及瘦素对照组(标准饲料和水喂养24周)。在研究结束时,将空肠段冷冻用于蛋白质免疫印迹法测定参与分泌和吸收功能以及衰老的关键蛋白质。评估肠道形态。进行血清和组织检测。与瘦素对照组相比,HFHS组的基础()显著降低(降低42%,<0.05)。改为Std饮食后,的这种降低完全逆转。HFHS诱导的降低归因于钙激活氯离子通道(ClC2)表达的显著丧失。炎症状态(TNF-α)和肠道健康[髓过氧化物酶(MPO)活性]的变化与体重变化相关。我们的数据表明,HFHS小鼠空肠基础的降低是可逆的。更好地了解西式饮食介导的肠道紊乱可能有助于改善肥胖个体胃肠道异常的治疗选择。我们的数据表明,西式饮食喂养小鼠空肠基础的降低(分泌功能降低)是可逆的。更好地了解西式饮食介导的肠道紊乱可能有助于改善肥胖个体胃肠道异常的治疗选择。