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Causal Link between n-3 Polyunsaturated Fatty Acid Deficiency and Motivation Deficits

机译:N-3多不饱和脂肪酸缺乏和动机缺陷之间的因果关系

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摘要

Reward-processing impairment is a common symptomatic dimension of several psychiatric disorders. However, whether the underlying pathological mechanisms are common is unknown. Herein, we asked if the decrease in the n-3 polyunsaturated fatty acid (PUFA) lipid species, consistently described in these pathologies, could underlie reward-processing deficits. We show that reduced n-3 PUFA biostatus in mice leads to selective motivational impairments. Electrophysiological recordings revealed increased collateral inhibition of dopamine D2 receptor-expressing medium spiny neurons (D2-MSNs) onto dopamine D1 receptor-expressing MSNs in the nucleus accumbens, a main brain region for the modulation of motivation. Strikingly, transgenically preventing n-3 PUFA deficiency selectively in D2-expressing neurons normalizes MSN collateral inhibition and enhances motivation. These results constitute the first demonstration of a causal link between a behavioral deficit and n-3 PUFA decrease in a discrete neuronal population and suggest that lower n-3 PUFA biostatus in psychopathologies could participate in the etiology of reward-related symptoms.
机译:奖励处理障碍是几种精神疾病的常见症状。但是,潜在的病理机制是否常见是未知的。在此,我们询问N-3多不饱和脂肪酸(PUFA)脂质物种的降低是否始终描述于这些病理学中,可以提高奖励处理缺陷。我们表明,小鼠中的N-3 Pufa Biostatus降低导致选择性励志障碍。电生理记录揭示了多巴胺D2受体表达培养基刺(D2-MSNS)对核心腺中的多巴胺D1受体 - 表达MSN的增加的抵押品抑制,是用于调节动机的主要脑区。尖锐的是,在D2表达神经元中有选择性地重原预防N-3 PUFA缺乏,使MSN抵押品抑制标准化并增强动机。这些结果构成了行为缺陷和N-3 PUFA之间存在离散神经元群体之间的因果关系的第一次演示,并表明PSPockologies的低N-3 Pufa Biostatus可以参与奖励相关症状的病因。

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  • 来源
    《Cell metabolism》 |2020年第4期|共25页
  • 作者单位

    Univ Bordeaux NutriNeuro Bordeaux INP INRAE F-33000 Bordeaux France;

    Univ Bordeaux NutriNeuro Bordeaux INP INRAE F-33000 Bordeaux France;

    Univ Bordeaux NutriNeuro Bordeaux INP INRAE F-33000 Bordeaux France;

    Univ Bordeaux NutriNeuro Bordeaux INP INRAE F-33000 Bordeaux France;

    Univ Bordeaux NutriNeuro Bordeaux INP INRAE F-33000 Bordeaux France;

    Univ Bordeaux NutriNeuro Bordeaux INP INRAE F-33000 Bordeaux France;

    Univ Bordeaux NutriNeuro Bordeaux INP INRAE F-33000 Bordeaux France;

    Univ Bordeaux NutriNeuro Bordeaux INP INRAE F-33000 Bordeaux France;

    IMG Pharma Biotech SL Res Dept BIC Bizkaia 612 Derio 48160 Spain;

    Univ Bordeaux NutriNeuro Bordeaux INP INRAE F-33000 Bordeaux France;

    Univ Bourgogne Franche Comte Ctr Sci Gout &

    Alimentat INRAE AgroSup Dijon CNRS F-21000 Dijon;

    Univ Bourgogne Franche Comte Ctr Sci Gout &

    Alimentat INRAE AgroSup Dijon CNRS F-21000 Dijon;

    Univ Bourgogne Franche Comte Ctr Sci Gout &

    Alimentat INRAE AgroSup Dijon CNRS F-21000 Dijon;

    Univ Bordeaux NutriNeuro Bordeaux INP INRAE F-33000 Bordeaux France;

    Univ Bordeaux NutriNeuro Bordeaux INP INRAE F-33000 Bordeaux France;

    Massachusetts Gen Hosp Lab Lipid Med &

    Technol Boston MA 02114 USA;

    Univ Bordeaux NutriNeuro Bordeaux INP INRAE F-33000 Bordeaux France;

    Univ Bourgogne Franche Comte Ctr Sci Gout &

    Alimentat INRAE AgroSup Dijon CNRS F-21000 Dijon;

    IMG Pharma Biotech SL Res Dept BIC Bizkaia 612 Derio 48160 Spain;

    Univ Bourgogne Franche Comte Ctr Sci Gout &

    Alimentat INRAE AgroSup Dijon CNRS F-21000 Dijon;

    Univ Bordeaux NutriNeuro Bordeaux INP INRAE F-33000 Bordeaux France;

    Univ Guelph Dept Human Hlth &

    Nutr Sci 50 Stone Rd E Guelph ON N1G 2W1 Canada;

    Univ Bordeaux NutriNeuro Bordeaux INP INRAE F-33000 Bordeaux France;

    Univ Bordeaux NutriNeuro Bordeaux INP INRAE F-33000 Bordeaux France;

    Univ Bordeaux NutriNeuro Bordeaux INP INRAE F-33000 Bordeaux France;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 内分泌腺疾病及代谢病;
  • 关键词

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