Kim Yoo-Hee, Phuong Nguyen, Hoang Nguyen Minh Anh, Kim Hye-Jin, Baik Moo-Yeol, Koh Young Ho
Ilsong Institute of Life Science, Hallym University, Seoul 07247, Republic of Korea.
Department of Biomedical Gerontology, Hallym University, Chuncheon 24252, Republic of Korea.
Nutrients. 2025 Jun 19;17(12):2044. doi: 10.3390/nu17122044.
: This study investigated whether enzymatic hydrolysis enhances the cognitive benefits of HongJam (steamed mature silkworms) and explored the underlying mechanisms. A marker compound of enzyme-treated HongJam was also identified to support quality control. : Mice were supplemented with Golden Silk HongJam (GS) or its enzyme hydrolysates (GS-EHS). Behavioral tests showed both improved fear-aggravated memory, with GS-EHS producing similar or greater effects at lower doses. GS-EHS activated the cyclic AMP response element binding protein/brain-derived neurotrophic factor signaling pathway and mitigated scopolamine-induced mitochondrial dysfunction by enhancing mitochondrial complex activity and ATP production. It also increased esterase activity, reduced reactive oxygen species, and modulated programmed cell death by suppressing apoptosis while promoting autophagy and unfolded protein response pathways. These changes led to reduced endoplasmic reticulum stress and neuroinflammation. Mass spectrometry identified glycine-tyrosine dipeptide as a potential bioactive marker. : GS-EHS enhances cognitive function by improving mitochondrial activity, reducing oxidative stress, and regulating programmed cell death. Enzymatic hydrolysis appears to increase the bioavailability of active compounds, making GS-EHS effective at lower doses. The glycine-tyrosine dipeptide may serve as a marker compound for standardizing GS-EHS based on its cognitive-enhancing properties.
本研究调查了酶解是否能增强红僵蚕(蒸熟的成熟蚕)的认知益处,并探索其潜在机制。还鉴定了酶处理红僵蚕的一种标记化合物以支持质量控制。
小鼠补充了金丝红僵蚕(GS)或其酶水解产物(GS-EHS)。行为测试表明,二者均改善了恐惧加剧记忆,GS-EHS在较低剂量下产生相似或更大的效果。GS-EHS激活了环磷酸腺苷反应元件结合蛋白/脑源性神经营养因子信号通路,并通过增强线粒体复合物活性和ATP生成减轻了东莨菪碱诱导的线粒体功能障碍。它还增加了酯酶活性,减少了活性氧,并通过抑制凋亡同时促进自噬和未折叠蛋白反应途径来调节程序性细胞死亡。这些变化导致内质网应激和神经炎症减轻。质谱分析确定甘氨酰-酪氨酸二肽为潜在的生物活性标记物。
GS-EHS通过改善线粒体活性、减少氧化应激和调节程序性细胞死亡来增强认知功能。酶解似乎提高了活性化合物的生物利用度,使GS-EHS在较低剂量下也有效。基于其认知增强特性,甘氨酰-酪氨酸二肽可作为标准化GS-EHS的标记化合物。