Université de Rouen Normandie, INSERM UMR 1073 "Nutrition, Inflammation and Microbiota-Gut-Brain Axis", 76183 Rouen, France.
Institute for Research and Innovation in Biomedicine (IRIB), Université de Rouen Normandie, 76183 Rouen, France.
Nutrients. 2022 Aug 31;14(17):3607. doi: 10.3390/nu14173607.
The role of microbiota in eating disorders has recently emerged. Previous data reported that lipopolysaccharides induce anorexia and a decrease of body weight through the activation of toll-like receptor 4 (TLR4). In the activity-based anorexia (ABA) mouse model, an increase of TLR4 expression in intestinal epithelial cells (IEC) has been described. We thus aimed to characterize the role of TLR4 in IEC in the ABA model in male and female mice. For this purpose, Vill-Cre-TLR4 LoxP, which are depleted for TLR4 in IEC in response to 4-OH tamoxifen, were submitted (ABA) or not (CT) to the ABA procedure that combined free access to a running wheel and progressive time-limited access to food. We thus compared CT and ABA TLR4 mice to CT and ABA TLR4 mice. In response to the ABA model, TLR4 male and female mice exhibited a body weight loss associated to a decrease of lean mass. In TLR4 male mice, body weight loss was delayed and less pronounced compared to TLR4 male mice. We did not observe a difference of body weight loss in female mice. The body composition remained unchanged between TLR4 and TLR4 mice in both sexes. In both sexes, ABA TLR4 mice exhibited an increase of food-anticipatory activity, as well as an increase of immobility time during the open field test. However, female TLR4 mice showed a decrease of the time spent at the centre and an increase of the time spent at the periphery of the open field area, whereas we did not observe differences in the male mice. In conclusion, the invalidation of TLR4 in IEC modified the response to the ABA model in a sex-dependent manner. Further studies should decipher the underlying mechanisms.
微生物群在进食障碍中的作用最近已经显现出来。以前的数据表明,脂多糖通过激活 Toll 样受体 4(TLR4)诱导厌食和体重下降。在基于活动的厌食症(ABA)小鼠模型中,已经描述了肠上皮细胞(IEC)中 TLR4 表达的增加。因此,我们旨在描述 TLR4 在 ABA 模型中 IEC 中的作用在雄性和雌性小鼠中。为此,使用了 Vill-Cre-TLR4 LoxP,它可以响应 4-OH 他莫昔芬在 IEC 中耗尽 TLR4,然后将其提交(ABA)或不提交(CT)ABA 程序,该程序结合了自由访问跑步轮和渐进限时访问食物。因此,我们比较了 CT 和 ABA TLR4 小鼠与 CT 和 ABA TLR4 小鼠。在对 ABA 模型的反应中,TLR4 雄性和雌性小鼠表现出体重减轻,与瘦体重减少有关。与 TLR4 雄性小鼠相比,TLR4 雄性小鼠的体重减轻延迟且不那么明显。我们没有观察到雌性小鼠体重减轻的差异。在两性中,TLR4 和 TLR4 小鼠的身体成分保持不变。在两性中,ABA TLR4 小鼠表现出食物预期活动增加,以及在开阔场测试中不动时间增加。然而,雌性 TLR4 小鼠表现出中心停留时间减少和外周停留时间增加,而我们没有观察到雄性小鼠的差异。总之,TLR4 在 IEC 中的无效性以性别依赖的方式改变了对 ABA 模型的反应。进一步的研究应该阐明潜在的机制。