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红松精油可促进 SH-SY5Y 神经母细胞瘤细胞摄取葡萄糖和增殖。

Pinus koraiensis essential oil enhances glucose uptake and proliferation in SH-SY5Y neuroblastoma cells.

机构信息

Department of Biotechnology, College of Life and Health Sciences, Hoseo University, Baebang, Asan, 31499, South Korea.

出版信息

Sci Rep. 2024 Nov 4;14(1):26630. doi: 10.1038/s41598-024-78357-8.

Abstract

Aromatherapy using essential oils (EOs) is well known for its beneficial effects on mental health and neuroprotection. However, the significant molecular mechanisms have not yet been identified. Recent studies have identified a decrease in glucose uptake as a common feature across various neurodegenerative diseases (NDDs), leading to mitochondrial dysfunction and excessive autophagy. This suggests that glucose may serve not only as an energy source but also as a therapeutic target for NDDs. Using SH-SY5Y neuroblast-like cells and the glucose uptake inhibitor BAY-876, we demonstrated that glucose depletion promoted autophagy. To discover the potential therapeutics that modulate glucose metabolism, we obtained EO from Pinus koraiensis Siebold & Zucc. (PKSZ) using steam distillation. PKSZ-EO upregulated mRNA expression of SLC2A2, SLC2A3, and SLC2A4, leading to increased glucose uptake in SH-SY5Y cells. Furthermore, PKSZ-EO protected SH-SY5Y cells from BAY-876-induced mitochondrial dysfunction, cytostasis, autophagy, and inflammation. Using gas chromatography-mass spectrometry, we confirmed the high levels of α-pinene, an inducer of GLUT4 expression, in PKSZ-EO. These results suggest that PKSZ-EO exerts a protective effect against glucose depletion stress, highlighting its potential as a therapeutic agent for NDDs.

摘要

使用精油(EO)的芳香疗法因其对心理健康和神经保护的有益作用而广为人知。然而,其重要的分子机制尚未确定。最近的研究表明,葡萄糖摄取减少是各种神经退行性疾病(NDD)的共同特征,导致线粒体功能障碍和过度自噬。这表明葡萄糖不仅可以作为能量来源,还可以作为 NDD 的治疗靶点。我们使用 SH-SY5Y 神经母细胞瘤样细胞和葡萄糖摄取抑制剂 BAY-876 证明,葡萄糖耗竭会促进自噬。为了发现调节葡萄糖代谢的潜在治疗方法,我们使用水蒸气蒸馏法从红松(Pinus koraiensis Siebold & Zucc.)中提取精油(PKSZ-EO)。PKSZ-EO 上调了 SH-SY5Y 细胞中 SLC2A2、SLC2A3 和 SLC2A4 的 mRNA 表达,从而增加了葡萄糖摄取。此外,PKSZ-EO 可防止 BAY-876 诱导的 SH-SY5Y 细胞线粒体功能障碍、细胞停滞、自噬和炎症。通过气相色谱-质谱联用仪,我们证实 PKSZ-EO 中含有高水平的α-蒎烯,它可以诱导 GLUT4 表达。这些结果表明,PKSZ-EO 对葡萄糖耗竭应激具有保护作用,突出了其作为 NDD 治疗剂的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/176f/11535478/2afa181d27b6/41598_2024_78357_Fig1_HTML.jpg

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