Arizona College of Osteopathic Medicine.
College of Veterinary Medicine.
Cell Physiol Biochem. 2023 Sep 1;57(5):315-330. doi: 10.33594/000000659.
BACKGROUND/AIMS: The goal of this study was to determine the influence of high-fat high-sugar diet (Western diet) on intestinal function and subsequently to determine if there were any beneficial effects of exercise, genistein (a naturally occurring phytoestrogen) or both, on the intestine.
We measured transepithelial short circuit current (I), across freshly isolated segments of jejunum from male and female C57Bl/6J mice randomly assigned to one of the following groups for the 12-week study duration: high-fat high-sugar diet (HFS), HFS with genistein (Gen), HFS with exercise (Ex), or HFS with both genistein and exercise (Gen+Ex) and compared them to lean controls. Genistein concentration was 600 mg genistein/kg diet. Exercise comprised of moderate intensity treadmill running (150 min per week). 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 cytokine assays were performed.
Basal I was significantly decreased (by 70%, P<0.05) in HFS females and males versus leans. This decrease was partially mitigated by exercise in both sexes. In females, the HFS-induced decrease in I was attributed to a significant loss of CLC2, NKCC1 and CFTR expression whereas in males this was due to a significant loss of Na/K-ATPase, K and NKCC1 expression (indicating sex-dependent mechanisms). Exercise mitigated most of the loss of I in both sexes. Our data suggested that A2BR levels were dysregulated in HFS fed mice and that concomitant treatment with Gen or Gen+Ex prevented this disruption in females only. Inflammatory state was associated with body weight changes.
Our data suggests that the reduced basal jejunal I in HFS mice is attributed to sex-dependent mechanisms and while exercise partially mitigated this, it's mechanism of action was unclear. Improved understanding of Western diet induced intestinal dysfunctions may allow for the development of novel drug targets to treat gastrointestinal disturbances in diabetic obesity.
背景/目的:本研究旨在确定高脂肪高糖饮食(西式饮食)对肠道功能的影响,随后确定运动、染料木黄酮(一种天然植物雌激素)或两者对肠道是否有任何有益影响。
我们测量了雄性和雌性 C57Bl/6J 小鼠新鲜分离的空肠段的跨上皮短路电流(I),这些小鼠随机分配到以下研究组中的一组,为期 12 周:高脂肪高糖饮食(HFS)、HFS 加染料木黄酮(Gen)、HFS 加运动(Ex)或 HFS 加染料木黄酮和运动(Gen+Ex),并与瘦对照组进行比较。染料木黄酮浓度为 600mg 染料木黄酮/千克饮食。运动包括中等强度的跑步机跑步(每周 150 分钟)。在研究结束时,将空肠段冷冻用于测定参与分泌和吸收功能以及衰老的关键蛋白质的 Western blot,评估肠道形态,并进行血清细胞因子测定。
HFS 雌性和雄性的基础 I 显著降低(降低 70%,P<0.05),而瘦对照组则没有。这种降低在两性中都可以通过运动部分缓解。在雌性中,HFS 诱导的 I 降低归因于 CLC2、NKCC1 和 CFTR 表达的显著丧失,而在雄性中则归因于 Na/K-ATPase、K 和 NKCC1 表达的显著丧失(表明存在性别依赖性机制)。运动在两性中都缓解了大部分 I 的丧失。我们的数据表明,A2BR 水平在 HFS 喂养的小鼠中失调,而同时给予 Gen 或 Gen+Ex 仅在雌性中防止了这种破坏。炎症状态与体重变化有关。
我们的数据表明,HFS 小鼠基础空肠 I 的降低归因于性别依赖性机制,虽然运动部分缓解了这种情况,但它的作用机制尚不清楚。对西式饮食引起的肠道功能障碍的进一步了解可能为治疗糖尿病肥胖相关的胃肠道紊乱开发新的药物靶点提供依据。