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Long-Lasting Metabolic Imbalance Related to Obesity Alters Olfactory Tissue Homeostasis and Impairs Olfactory-Driven Behaviors

机译:与肥胖有关的持久代谢不平衡改变嗅觉组织稳态并削弱嗅觉驱动的行为

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摘要

Obesity is associated with chronic food intake disorders and binge eating. Food intake relies on the interaction between homeostatic regulation and hedonic signals among which, olfaction is a major sensory determinant. However, its potential modulation at the peripheral level by a chronic energy imbalance associated to obese status remains a matter of debate. We further investigated the olfactory function in a rodent model relevant to the situation encountered in obese humans, where genetic susceptibility is juxtaposed on chronic eating disorders. Using several olfactory-driven tests, we compared the behaviors of obesity-prone Sprague-Dawley rats (OP) fed with a high-fat/high-sugar diet with those of obese-resistant ones fed with normal chow. In OP rats, we reported 1) decreased odor threshold, but 2) poor olfactory performances, associated with learning/memory deficits, 3) decreased influence of fasting, and 4) impaired insulin control on food seeking behavior. Associated with these behavioral modifications, we found a modulation of metabolism-related factors implicated in 1) electrical olfactory signal regulation (insulin receptor), 2) cellular dynamics (glucorticoids receptors, pro- and antiapoptotic factors), and 3) homeostasis of the olfactory mucosa and bulb (monocarboxylate and glucose transporters). Such impairments might participate to the perturbed daily food intake pattern that we observed in obese animals
机译:肥胖与慢性食物摄入障碍和狂犬病有关。食物摄入量依赖于稳态调节与蜂窝的相互作用,其中嗅觉是主要的感官决定簇。然而,它通过与肥胖状态相关的慢性能量不平衡在外围级别的潜在调制仍然是辩论问题。我们进一步调查了与肥胖人类遇到的啮齿动物模型中的啮齿动物模型中的嗅觉功能,其中遗传易感性并列在慢性饮食障碍上。使用几种嗅觉驱动的测试,比较了肥胖的俯卧型Sprague-Dawley大鼠(OP)的行为与高脂肪/高糖饮食的饮食,抗肥胖的抗饮食喂养了正常的食物。在OP大鼠中,我们报告1)减少气味阈值,但是2)与学习/记忆缺陷的差的嗅觉性能,3)减少禁食的影响,4)胰岛素对食物寻求行为的影响受损。与这些行为修饰相关联,我们发现一种涉及的代谢相关因素的调节,其中包括1)电嗅觉信号调节(胰岛素受体),2)蜂窝动力学(葡萄糖糖激素受体,胰腺炎受体,胰腺炎,抗透露因子),以及3)嗅觉的稳态粘膜和灯泡(单羧酸盐和葡萄糖转运蛋白)。这些损害可能参与我们在肥胖动物中观察到的扰动日常食物摄入模式

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