Trehalose as a potential therapeutic agent in different diseases

Danijela Stevanovic, Vladimir Trajković, Ljubica Vučićević
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Abstract

Trehalose is a natural, non-reducing disaccharide synthesized in some bacteria, fungi, plants, and insects. Due to its advantageous physical and chemical properties, trehalose can stabilize proteins and membranes, and protect cells from desiccation, heating, and freezing. Vertebrates do not synthesize trehalose, but the beneficial effects of trehalose have been demonstrated in numerous diseases as it eliminates aggregates, misfolded proteins, and damaged organelles, and reduces hyperinflammation and oxidative stress. Trehalose induces autophagy through nuclear translocation and activation of transcription factor EB (TFEB) in an mTOR-independent manner, but increases the expression of SQSTM1/p62 and has antioxidant properties in an autophagy-independent manner. Furthermore, trehalose induces apoptosis in tumor cells by increasing membrane fluidity through the activation of caspase 3, 6 and the JNK (c-Jun N-terminal kinase) pathway. Overall, in this review, previous knowledge on the therapeutic potential of trehalose in various diseases such as dry eye syndrome, neurodegenerative diseases, and tumors, was summarized, focusing on the underlying molecular mechanisms.
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海藻糖是一种潜在的治疗多种疾病的药物
海藻糖是一种天然的非还原性双糖,由一些细菌、真菌、植物和昆虫合成。由于海藻糖具有良好的物理和化学特性,它可以稳定蛋白质和细胞膜,保护细胞免受干燥、加热和冷冻。脊椎动物不能合成海藻糖,但海藻糖的有益作用已经在许多疾病中得到证实,因为它可以消除聚集体、错误折叠的蛋白质和受损的细胞器,并减少过度炎症和氧化应激。海藻糖通过核易位和转录因子EB (TFEB)的激活诱导自噬,以mtor独立的方式,但增加SQSTM1/p62的表达,并以自噬独立的方式具有抗氧化特性。此外,海藻糖通过激活caspase 3,6和JNK (c-Jun n -末端激酶)途径,通过增加膜流动性诱导肿瘤细胞凋亡。综上所述,本文综述了海藻糖在干眼综合征、神经退行性疾病和肿瘤等多种疾病中的治疗潜力,重点讨论了其潜在的分子机制。
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审稿时长
4 weeks
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