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补充富含鱼油的ω-3多不饱和脂肪酸可减轻糖尿病介导的大鼠肌肉萎缩。

Attenuation of diabetes-mediated muscle atrophy in rats by fish oil enriched omega-3 polyunsaturated fatty acids supplementation.

作者信息

Liu Shing-Hwa, Lin Wei-Hsuan, Tzeng Huei-Ping, Chiang Meng-Tsan

机构信息

Institute of Toxicology, National Taiwan University, Taipei, Taiwan.

Department of Pediatrics, College of Medicine and Hospital, National Taiwan University, Taipei, Taiwan.

出版信息

J Food Drug Anal. 2023 Aug 31;31(3):458-472. doi: 10.38212/2224-6614.3468.

Abstract

Diabetes is associated with an increased risk of muscle wasting/atrophy, which adversely affects quality of life. We hypothesized that long term supplementation of fish oil may have protective effects against sarcopenia or muscle atrophy in streptozotocin (STZ) and high-fat (HF) diet-induced diabetic rat model. Wistar rats at age of 7 weeks were injected with saline or STZ to induce hyperglycemia. After one week, they were fed on a normal control diet or HF diet with/without supplementation of fish oil for 18 weeks. Feeding diabetic rats with a fish oil-enriched diet alleviated body weight loss and the impaired glucose tolerance using OGTT test. Although fish oil did not improve the decreased muscle mass, the muscle atrophy induced by diabetes was attenuated by fish oil in gastrocnemius, soleus, tibialis anterior, and extensor digitorum longus muscles. Fish oil supplementation reversed the decreased expression of phospho (p)-AKT, pmTOR, and p-p70s6k, which are molecules related to protein synthesis. Besides, protein degradation-related signaling pathways were inhibited by fish oil, such as increasing p-FoxO1 and decreasing Atrogin-1 and MURF1 protein expression. Fish oil down-regulated the expression of autophagy-related molecules including ATG5, p62, and LC3B II/I ratio, which may result in less muscle atrophy. Inflammation-related signaling regulators including TNF-α, NF-κB, AGEs, and RAGE were suppressed by fish oil supplementation as well. Moreover, the down-regulated p-AMPKα, SIRT1, and PGC-1 in diabetic rats were counteracted by fish oil, which may improve mitochondrial function and further block FoxO action. These data suggest that long-term fish oil supplementation exerts protective effects against diabetes-induced muscle atrophy, which may in turn ameliorate insulin resistance and impaired glucose tolerance.

摘要

糖尿病与肌肉消耗/萎缩风险增加相关,这会对生活质量产生不利影响。我们推测,长期补充鱼油可能对链脲佐菌素(STZ)和高脂(HF)饮食诱导的糖尿病大鼠模型中的肌肉减少症或肌肉萎缩具有保护作用。7周龄的Wistar大鼠注射生理盐水或STZ以诱导高血糖。一周后,它们被喂食正常对照饮食或添加/不添加鱼油的HF饮食18周。用富含鱼油的饮食喂养糖尿病大鼠可减轻体重减轻,并通过口服葡萄糖耐量试验(OGTT)改善受损的葡萄糖耐量。虽然鱼油没有改善肌肉质量的下降,但糖尿病诱导的肌肉萎缩在腓肠肌、比目鱼肌、胫骨前肌和趾长伸肌中被鱼油减轻。补充鱼油可逆转与蛋白质合成相关分子磷酸化(p)-AKT、磷酸化mTOR和磷酸化p70s6k的表达下降。此外,与蛋白质降解相关的信号通路被鱼油抑制,例如增加p-FoxO1并降低Atrogin-1和MURF1蛋白表达。鱼油下调包括ATG5、p62和LC3B II/I比率在内的自噬相关分子的表达,这可能导致较少的肌肉萎缩。补充鱼油也抑制了包括TNF-α、NF-κB、晚期糖基化终末产物(AGEs)和晚期糖基化终末产物受体(RAGE)在内的炎症相关信号调节因子。此外,糖尿病大鼠中下调的磷酸化腺苷酸活化蛋白激酶α(p-AMPKα)、沉默信息调节因子1(SIRT1)和过氧化物酶体增殖物激活受体γ共激活因子1(PGC-1)被鱼油抵消,这可能改善线粒体功能并进一步阻断FoxO的作用。这些数据表明,长期补充鱼油对糖尿病诱导的肌肉萎缩具有保护作用,这反过来可能改善胰岛素抵抗和受损的葡萄糖耐量。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4928/10629917/8545b35d742c/jfda-31-03-458f1.jpg

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