Ceftriaxone reverses diet-induced deficits in goal-directed control.

IF 3.5 3区 医学 Q2 NEUROSCIENCES
Psychopharmacology Pub Date : 2024-10-01 Epub Date: 2024-06-01 DOI:10.1007/s00213-024-06621-w
Benjamin-Israel Moke, Megan L Shipman, Simon Lui, Laura Corbit
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引用次数: 0

Abstract

Rationale: Obesity is associated with numerous health risks and ever-increasing rates are a significant global concern. However, despite weight loss attempts many people have difficulty maintaining weight loss. Previous studies in animals have shown that chronic access to an obesogenic diet can disrupt goal-directed behavior, impairing the ability of animals to flexibly adjust food-seeking behavior following changes in the value of earned outcomes. Changes in behavioral control have been linked to disruption of glutamate transmission in the dorsal medial striatum (DMS), a region critical for the acquisition and expression of goal-directed behavior.

Objectives: The goal of this study was to test whether ceftriaxone, a beta-lactam antibiotic shown elsewhere to upregulate the expression of the glutamate transporter GLT-1, would improve goal-directed control following long-term exposure to an obesogenic diet.

Methods: Male and female rats were given access to either standard chow or chow plus sweetened condensed milk (SCM) for 6 weeks. Access to SCM was ended and rats received daily injections of either ceftriaxone or saline for 6 days. Rats were then trained to press a lever to earn a novel food reward and, finally, were assessed for sensitivity to outcome devaluation. Histological analyses examined changes to GLT-1 protein levels and morphological changes to astrocytes, within the DMS.

Results: We found that ceftriaxone robustly restored goal-directed behavior in animals following long-term exposure to SCM. While we did not observe changes in protein levels of GLT-1 in the DMS, we observed that SCM induced changes in the morphology of astrocytes in the DMS, and that ceftriaxone mitigated these changes.

Conclusions: These results demonstrate that long-term access to a SCM diet impairs goal-directed behavior while also altering the morphology of astrocytes in the DMS. Furthermore, these results suggest that ceftriaxone administration can reverse the impairment of goal-directed behavior potentially through its actions on astrocytes in decision-making circuitry.

Abstract Image

头孢曲松能逆转饮食引起的目标定向控制缺陷。
理由肥胖与众多健康风险相关,肥胖率的不断上升是全球关注的一个重要问题。然而,尽管很多人都尝试过减肥,但仍难以保持体重。以往的动物研究表明,长期摄入致肥饮食会扰乱目标导向行为,损害动物根据所获结果的价值变化灵活调整觅食行为的能力。行为控制的变化与背侧内侧纹状体(DMS)谷氨酸传递的中断有关,DMS是获得和表达目标导向行为的关键区域:本研究的目的是测试头孢曲松(一种β-内酰胺类抗生素)是否会改善长期暴露于肥胖饮食后的目标定向控制:方法:让雄性和雌性大鼠食用标准饲料或饲料加甜炼乳(SCM)6 周。结束食用炼乳后,大鼠每天接受头孢曲松或生理盐水注射,为期 6 天。然后训练大鼠按下杠杆以获得新的食物奖励,最后评估大鼠对结果贬值的敏感性。组织学分析检查了DMS内GLT-1蛋白水平的变化和星形胶质细胞的形态变化:结果:我们发现,头孢曲松能强有力地恢复长期暴露于单片机的动物的目标定向行为。虽然我们没有观察到 DMS 中 GLT-1 蛋白水平的变化,但我们观察到单片机诱导了 DMS 中星形胶质细胞形态的变化,而头孢曲松减轻了这些变化:这些结果表明,长期摄入单链氯化石蜡饮食会损害目标定向行为,同时也会改变 DMS 中星形胶质细胞的形态。此外,这些结果表明,服用头孢曲松可能会通过其对决策回路中的星形胶质细胞的作用来逆转目标定向行为的损害。
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来源期刊
Psychopharmacology
Psychopharmacology 医学-精神病学
CiteScore
7.10
自引率
5.90%
发文量
257
审稿时长
2-4 weeks
期刊介绍: Official Journal of the European Behavioural Pharmacology Society (EBPS) Psychopharmacology is an international journal that covers the broad topic of elucidating mechanisms by which drugs affect behavior. The scope of the journal encompasses the following fields: Human Psychopharmacology: Experimental This section includes manuscripts describing the effects of drugs on mood, behavior, cognition and physiology in humans. The journal encourages submissions that involve brain imaging, genetics, neuroendocrinology, and developmental topics. Usually manuscripts in this section describe studies conducted under controlled conditions, but occasionally descriptive or observational studies are also considered. Human Psychopharmacology: Clinical and Translational This section comprises studies addressing the broad intersection of drugs and psychiatric illness. This includes not only clinical trials and studies of drug usage and metabolism, drug surveillance, and pharmacoepidemiology, but also work utilizing the entire range of clinically relevant methodologies, including neuroimaging, pharmacogenetics, cognitive science, biomarkers, and others. Work directed toward the translation of preclinical to clinical knowledge is especially encouraged. The key feature of submissions to this section is that they involve a focus on clinical aspects. Preclinical psychopharmacology: Behavioral and Neural This section considers reports on the effects of compounds with defined chemical structures on any aspect of behavior, in particular when correlated with neurochemical effects, in species other than humans. Manuscripts containing neuroscientific techniques in combination with behavior are welcome. We encourage reports of studies that provide insight into the mechanisms of drug action, at the behavioral and molecular levels. Preclinical Psychopharmacology: Translational This section considers manuscripts that enhance the confidence in a central mechanism that could be of therapeutic value for psychiatric or neurological patients, using disease-relevant preclinical models and tests, or that report on preclinical manipulations and challenges that have the potential to be translated to the clinic. Studies aiming at the refinement of preclinical models based upon clinical findings (back-translation) will also be considered. The journal particularly encourages submissions that integrate measures of target tissue exposure, activity on the molecular target and/or modulation of the targeted biochemical pathways. Preclinical Psychopharmacology: Molecular, Genetic and Epigenetic This section focuses on the molecular and cellular actions of neuropharmacological agents / drugs, and the identification / validation of drug targets affecting the CNS in health and disease. We particularly encourage studies that provide insight into the mechanisms of drug action at the molecular level. Manuscripts containing evidence for genetic or epigenetic effects on neurochemistry or behavior are welcome.
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