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垃圾食品对食物驱动行为和伏隔核谷氨酸可塑性的影响;钙通透性 AMPA 受体募集机制的研究进展。

Effects of junk-food on food-motivated behavior and nucleus accumbens glutamate plasticity; insights into the mechanism of calcium-permeable AMPA receptor recruitment.

机构信息

Department of Pharmacology, University of Michigan, Ann Arbor, MI, 48109, USA.

Department of Pharmacology, University of Michigan, Ann Arbor, MI, 48109, USA; Psychology Department (Biopsychology) University of Michigan, Ann Arbor, MI, 48109, USA.

出版信息

Neuropharmacology. 2024 Jan 1;242:109772. doi: 10.1016/j.neuropharm.2023.109772. Epub 2023 Oct 26.

Abstract

In rats, eating obesogenic diets increases calcium-permeable AMPA receptor (CP-AMPAR) transmission in the nucleus accumbens (NAc) core, and enhances food-motivated behavior. Interestingly, these diet-induced alterations in NAc transmission are pronounced and sustained in obesity-prone (OP) male rats and absent in obesity-resistant (OR) populations. However, effects of diet manipulation on food motivation, and the mechanisms underlying this NAc plasticity in OPs is unknown. Using male selectively-bred OP and OR rats, we assessed food-motivated behavior following ad lib access to chow (CH), junk-food (JF), or 10d of JF followed by a return to chow diet (JF-Dep). Motivation for food was greater in OP than OR rats, as expected. However, JF-Dep only produced enhancements in food-seeking in OP groups, while continuous JF access reduced food-seeking in both OPs and ORs. Additionally, optogenetic, chemogenetic, and pharmacological approaches were used to examine NAc CP-AMPAR recruitment following diet manipulation and ex vivo treatment of brain slices. Reducing excitatory transmission in the NAc was sufficient to recruit CP-AMPARs to synapses in OPs, but not ORs. In OPs, JF-induced increases in CP-AMPARs occurred in mPFC-, but not BLA-to-NAc inputs. Together results show that diet differentially affects behavioral and neural plasticity in obesity susceptible populations. We also identify conditions for acute recruitment of NAc CP-AMPARs; these results suggest that synaptic scaling mechanisms contribute to NAc CP-AMPAR recruitment. Overall, this work helps elucidate how diet interacts with obesity susceptibility to influence food-motivated behavior and extends our fundamental understanding of NAc CP-AMPAR recruitment.

摘要

在大鼠中,进食致肥胖饮食会增加伏隔核(NAc)核心中的钙通透性 AMPA 受体(CP-AMPAR)传递,并增强食物动机行为。有趣的是,这些 NAc 传递的饮食诱导变化在肥胖易感(OP)雄性大鼠中明显且持续存在,而在肥胖抵抗(OR)人群中则不存在。然而,饮食干预对食物动机的影响,以及这种 NAc 可塑性的机制在 OPs 中尚不清楚。使用雄性选择性繁殖的 OP 和 OR 大鼠,我们评估了在随意进食标准饲料(CH)、垃圾食品(JF)或 10 天后返回标准饲料饮食(JF-Dep)后,食物动机行为。正如预期的那样,OP 大鼠的食物动机比 OR 大鼠更强。然而,JF-Dep 仅在 OP 组中增强了食物寻求,而连续 JF 摄入降低了 OPs 和 ORs 的食物寻求。此外,还使用光遗传学、化学遗传学和药理学方法来研究饮食干预和脑片离体处理后 NAc 的 CP-AMPAR 募集。减少 NAc 中的兴奋性传递足以在 OPs 中募集 CP-AMPAR,但在 ORs 中则不行。在 OPs 中,JF 诱导的 CP-AMPAR 增加发生在 mPFC-,而不是 BLA-到 NAc 的输入。总之,这些结果表明,饮食以不同的方式影响肥胖易感人群的行为和神经可塑性。我们还确定了急性募集 NAc CP-AMPAR 的条件;这些结果表明,突触缩放机制有助于 NAc CP-AMPAR 的募集。总的来说,这项工作有助于阐明饮食如何与肥胖易感性相互作用,影响食物动机行为,并扩展我们对 NAc CP-AMPAR 募集的基本理解。

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