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乳清分离蛋白包封虾青素纳米乳剂更有效地减轻地塞米松诱导的小鼠骨骼肌萎缩。

Whey Protein Isolate-Encapsulated Astaxanthin Nanoemulsion More Effectively Mitigates Skeletal Muscle Atrophy in Dexamethasone-Induced Mice.

作者信息

Huan Yuchen, Yue Han, Song Yanli, Zhang Wenmei, Wei Biqian, Tang Qingjuan

机构信息

College of Food Science and Engineering, Ocean University of China, Qingdao 266400, China.

Department of Emergency, Tongji Hospital, Tongji University School of Medicine, Shanghai 200065, China.

出版信息

Nutrients. 2025 Feb 20;17(5):750. doi: 10.3390/nu17050750.

Abstract

BACKGROUND

Skeletal muscle, as the largest organ in the body and the main protein pool, is crucial for various physiological processes, but atrophy of skeletal muscle can result from glucocorticoids, including dexamethasone, or from aging. Astaxanthin (AST) is a ketocarotenoid with a variety of physiological activities. However, the clinical application of AST is hampered by its strong hydrophobicity, intense off-flavors, and susceptibility to oxidation.

METHODS

In this study, we prepared whey protein isolate (WPI)-encapsulated AST nanoemulsion (WPI-AST, W-A) and investigated its alleviating effects on dexamethasone-induced skeletal muscle atrophy.

RESULTS

The optimal concentration of astaxanthin was determined to be 30 mg/mL with an oil/water ratio of 1:5. The W-A was a typical oil-in-water (O/W) emulsion with a particle size of about 110 nm. The bioaccessibility of astaxanthin was significantly improved, with the off-flavors of astaxanthin effectively masked. After oral administration, the W-A further ameliorated skeletal muscle atrophy by inhibiting skeletal muscle catabolism, promoting skeletal muscle production, and inhibiting mitochondrial autophagy compared with the same dose of WPI and AST. In addition to this, the W-A further improved the glycometabolism of skeletal muscle by reducing the expression of Foxo3 and increasing the expression of PGC-1α.

CONCLUSIONS

In conclusion, the W-A nanoemulsion demonstrated good therapeutic value in alleviating skeletal muscle atrophy.

摘要

背景

骨骼肌作为人体最大的器官和主要的蛋白质库,对各种生理过程至关重要,但糖皮质激素(包括地塞米松)或衰老可导致骨骼肌萎缩。虾青素(AST)是一种具有多种生理活性的酮类胡萝卜素。然而,AST的强疏水性、强烈的异味和易氧化性阻碍了其临床应用。

方法

在本研究中,我们制备了乳清蛋白分离物(WPI)包裹的AST纳米乳剂(WPI-AST,W-A),并研究了其对糖皮质激素诱导的骨骼肌萎缩的缓解作用。

结果

确定虾青素的最佳浓度为30mg/mL,油/水比为1:5。W-A是一种典型的水包油(O/W)乳剂,粒径约为110nm。虾青素的生物可及性显著提高,虾青素的异味被有效掩盖。口服给药后,与相同剂量的WPI和AST相比,W-A通过抑制骨骼肌分解代谢、促进骨骼肌生成和抑制线粒体自噬进一步改善了骨骼肌萎缩。除此之外,W-A通过降低Foxo3的表达和增加PGC-1α的表达进一步改善了骨骼肌的糖代谢。

结论

总之,W-A纳米乳剂在缓解骨骼肌萎缩方面显示出良好的治疗价值。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ffc1/11901752/1a4ce136c8e2/nutrients-17-00750-g001.jpg

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