Laboratory of Behavioral Genetics (LGC), Brain Mind Institute, École Polytechnique Fédérale de Lausanne (EPFL), Lausanne, Switzerland.
Department of Pharmacology, Physiology, and Neuroscience, University of South Carolina School of Medicine, Columbia, United States.
Elife. 2022 Nov 8;11:e77791. doi: 10.7554/eLife.77791.
Emerging evidence is implicating mitochondrial function and metabolism in the nucleus accumbens in motivated performance. However, the brain is vulnerable to excessive oxidative insults resulting from neurometabolic processes, and whether antioxidant levels in the nucleus accumbens contribute to motivated performance is not known. Here, we identify a critical role for glutathione (GSH), the most important endogenous antioxidant in the brain, in motivation. Using proton magnetic resonance spectroscopy at ultra-high field in both male humans and rodent populations, we establish that higher accumbal GSH levels are highly predictive of better, and particularly, steady performance over time in effort-related tasks. Causality was established in experiments in rats that, first, showed that downregulating GSH levels through micro-injections of the GSH synthesis inhibitor buthionine sulfoximine in the nucleus accumbens impaired effort-based reward-incentivized performance. In addition, systemic treatment with the GSH precursor N-acetyl-cysteine increased accumbal GSH levels in rats and led to improved performance, potentially mediated by a cell-type-specific shift in glutamatergic inputs to accumbal medium spiny neurons. Our data indicate a close association between accumbal GSH levels and an individual's capacity to exert reward-incentivized effort over time. They also suggest that improvement of accumbal antioxidant function may be a feasible approach to boost motivation.
越来越多的证据表明,伏隔核中的线粒体功能和代谢与动机表现有关。然而,大脑容易受到神经代谢过程中过度氧化损伤的影响,目前尚不清楚伏隔核中的抗氧化剂水平是否有助于动机表现。在这里,我们发现谷胱甘肽(GSH)在大脑中最重要的内源性抗氧化剂在动机中起着关键作用。我们使用超高场质子磁共振波谱技术在男性人类和啮齿动物群体中进行研究,发现伏隔核中较高的 GSH 水平与更好的、特别是随着时间的推移在与努力相关的任务中稳定表现高度相关。在大鼠实验中,我们通过核内注射 GSH 合成抑制剂丁硫氨酸亚砜亚胺来降低 GSH 水平,实验结果首先确立了因果关系,结果表明这种方法损害了基于努力的奖励激励表现。此外,系统给予 GSH 前体 N-乙酰半胱氨酸增加了大鼠伏隔核中的 GSH 水平,从而提高了表现,这可能是通过谷氨酸能传入到伏隔核中间神经元的细胞类型特异性变化介导的。我们的数据表明,伏隔核中的 GSH 水平与个体随着时间推移进行奖励激励努力的能力密切相关。它们还表明,改善伏隔核中的抗氧化功能可能是提高动机的一种可行方法。