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限制硫氨基酸通过增强肌肉中的脂肪氧化来提高小鼠的运动能力。

Sulfur Amino Acid Restriction Enhances Exercise Capacity in Mice by Boosting Fat Oxidation in Muscle.

作者信息

Mann Charlotte G, MacArthur Michael R, Zhang Jing, Gong Songlin, AbuSalim Jenna E, Hunter Craig J, Lu Wenyun, Agius Thomas, Longchamp Alban, Allagnat Florent, Rabinowitz Joshua, Mitchell James R, De Bock Katrien, Mitchell Sarah J

机构信息

Department of Health Sciences and Technology, ETH Zurich, Zurich 8092, Switzerland.

Department of Chemistry, Princeton University, Princeton, NJ 08544, USA.

出版信息

bioRxiv. 2024 Jul 1:2024.06.27.601041. doi: 10.1101/2024.06.27.601041.

Abstract

Dietary restriction of the sulfur-containing amino acids methionine and cysteine (SAAR) improves body composition, enhances insulin sensitivity, and extends lifespan; benefits seen also with endurance exercise. Yet, the impact of SAAR on skeletal muscle remains largely unexplored. Here we demonstrate that one week of SAAR in sedentary, young, male mice increases endurance exercise capacity. Indirect calorimetry showed that SAAR increased lipid oxidation at rest and delayed the onset of carbohydrate utilization during exercise. Transcriptomic analysis revealed increased expression of genes involved in fatty acid catabolism especially in glycolytic muscle following SAAR. These findings were functionally supported by increased fatty acid circulatory turnover flux and muscle β-oxidation. Reducing lipid uptake from circulation through endothelial cell (EC)-specific CD36 deletion attenuated the running phenotype. Mechanistically, VEGF-signaling inhibition prevented exercise increases following SAAR, without affecting angiogenesis, implicating noncanonical VEGF signaling and EC CD36-dependent fatty acid transport in regulating exercise capacity by influencing muscle substrate availability.

摘要

限制含硫氨基酸甲硫氨酸和半胱氨酸(SAAR)的饮食可改善身体组成、增强胰岛素敏感性并延长寿命;耐力运动也有类似益处。然而,SAAR对骨骼肌的影响在很大程度上仍未得到探索。在此,我们证明,久坐不动的年轻雄性小鼠进行一周的SAAR饮食可提高其耐力运动能力。间接测热法表明,SAAR增加了静息时的脂质氧化,并延迟了运动期间碳水化合物利用的起始。转录组分析显示,SAAR后,尤其是在糖酵解肌肉中,参与脂肪酸分解代谢的基因表达增加。脂肪酸循环周转通量和肌肉β-氧化增加从功能上支持了这些发现。通过内皮细胞(EC)特异性缺失CD36减少循环中的脂质摄取,减弱了跑步表型。从机制上讲,VEGF信号抑制可防止SAAR后运动能力的提高,而不影响血管生成,这表明非经典VEGF信号和EC CD36依赖性脂肪酸转运通过影响肌肉底物可用性来调节运动能力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a353/11244859/d1c5014993a5/nihpp-2024.06.27.601041v1-f0001.jpg

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