Unraveling cysteine deficiency-associated rapid weight loss

Alan Varghese, Ivan Gusarov, Begona Gamallo-Lana, Daria Dolgonos, Yatin Mankan, Ilya Shamovsky, Mydia Phan, Rebecca Jones, Maria Gomez-Jenkins, Eileen White, Rui Wang, Drew Jones, Thales Papagiannakopoulos, Michael E. Pacold, Adam C Mar, Dan R Littman, Evgeny Nudler
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Abstract

Forty percent of the US population and 1 in 6 individuals worldwide are obese, and the incidence of this disease is surging globally1,2. Various dietary interventions, including carbohydrate and fat restriction, and more recently amino acid restriction, have been explored to combat this epidemic3-6. We sought to investigate the impact of removing individual amino acids on the weight profiles of mice. Compared to essential amino acid restriction, induction of conditional cysteine restriction resulted in the most dramatic weight loss, amounting to 20% within 3 days and 30% within one week, which was readily reversed. This weight loss occurred despite the presence of substantial cysteine reserves stored in glutathione (GSH) across various tissues7. Further analysis demonstrated that the weight reduction primarily stemmed from an increase in the utilization of fat mass, while locomotion, circadian rhythm and histological appearance of multiple other tissues remained largely unaffected. Cysteine deficiency activated the integrated stress response (ISR) and NRF2-mediated oxidative stress response (OSR), which amplify each other, leading to the induction of GDF15 and FGF21, hormones associated with increased lipolysis, energy homeostasis and food aversion8-10. We additionally observed rapid tissue coenzyme A (CoA) depletion, resulting in energetically inefficient anaerobic glycolysis and TCA cycle, with sustained urinary excretion of pyruvate, orotate, citrate, α-ketoglutarate, nitrogen rich compounds and amino acids. In summary, our investigation highlights that cysteine restriction, by depleting GSH and CoA, exerts a maximal impact on weight loss, metabolism, and stress signaling compared to other amino acid restrictions. These findings may pave the way for innovative strategies for addressing a range of metabolic diseases and the growing obesity crisis.
解读半胱氨酸缺乏症相关的快速体重减轻
美国有 40% 的人肥胖,全球每 6 个人中就有 1 人肥胖,而且肥胖症的发病率在全球急剧上升1,2。为了应对这一流行病,人们探索了各种饮食干预措施,包括限制碳水化合物和脂肪,以及最近的限制氨基酸3-6。我们试图研究去除个别氨基酸对小鼠体重曲线的影响。与限制必需氨基酸相比,诱导条件性半胱氨酸限制导致的体重减轻最为显著,3 天内体重减轻 20%,一周内体重减轻 30%,而且很容易逆转。尽管各组织的谷胱甘肽(GSH)中储存了大量的半胱氨酸,但体重仍出现了下降7。进一步分析表明,体重减轻主要源于脂肪利用率的提高,而运动、昼夜节律和其他多个组织的组织学外观基本未受影响。半胱氨酸缺乏激活了综合应激反应(ISR)和 NRF2 介导的氧化应激反应(OSR),这两种反应相互放大,导致诱导 GDF15 和 FGF21,这些激素与脂肪分解增加、能量平衡和食物厌恶有关8-10。此外,我们还观察到组织辅酶 A(CoA)迅速耗竭,导致无氧糖酵解和 TCA 循环能量效率低下,丙酮酸、乳清酸、柠檬酸、α-酮戊二酸、富氮化合物和氨基酸持续排出尿液。总之,我们的研究强调,与其他氨基酸限制相比,半胱氨酸限制通过消耗 GSH 和 CoA,对体重减轻、新陈代谢和应激信号转导产生了最大的影响。这些发现可能会为解决一系列代谢性疾病和日益严重的肥胖危机的创新策略铺平道路。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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