Thymol in Trachyspermum ammi seed extract exhibits neuroprotection, learning, and memory enhancement in scopolamine-induced Alzheimer's disease mouse model

被引:8
作者
Timalsina, Binod [1 ]
Haque, Md Nazmul [1 ,2 ]
Choi, Ho Jin [1 ]
Dash, Raju [1 ]
Moon, Il Soo [1 ,3 ]
机构
[1] Dongguk Univ, Dept Anat, Coll Med, Gyeongju, South Korea
[2] Patuakhali Sci & Technol Univ, Dept Fisheries Biol & Genet, Patuakhali, Bangladesh
[3] Dongguk Univ, Dept Anat, Coll Med, Gyeongju 38066, South Korea
基金
新加坡国家研究基金会;
关键词
Alzheimer's disease; neurogenesis; neuroprotection; Scopolmaine; thymol; Trachyspermum ammi; ADULT NEUROGENESIS; PROGENITOR CELLS; AMYLOID-BETA; BRAIN; PLASTICITY; PROTEIN; PROLIFERATION; HIPPOCAMPUS; OLIGOMERS; MODULATOR;
D O I
10.1002/ptr.7777
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Several reports have stated the neuroprotective and learning/memory effects of Tachyspermum ammi seed extract (TASE) and its principal component thymol; however, little is known about its underlying molecular mechanisms and neurogenesis potential. This study aimed to provide insights into TASE and a thymol-mediated multifactorial therapeutic approach in a scopolamine-induced Alzheimer's disease (AD) mouse model. TASE and thymol supplementation significantly reduced oxidative stress markers such as brain glutathione, hydrogen peroxide, and malondialdehyde in mouse whole brain homogenates. Tumor necrosis factor-alpha was significantly downregulated, whereas the elevation of brain-derived neurotrophic factor and phospho-glycogen synthase kinase-3 beta (serine 9) enhanced learning and memory in the TASE- and thymol-treated groups. A significant reduction in the accumulation of A beta 1-42 peptides was observed in the brains of TASE- and thymol-treated mice. Furthermore, TASE and thymol significantly promoted adult neurogenesis, with increased doublecortin positive neurons in the subgranular and polymorphic zones of the dentate gyrus in treated-mice. Collectively, TASE and thymol could potentially act as natural therapeutic agents for the treatment of neurodegenerative disorders, such as AD.
引用
收藏
页码:2811 / 2826
页数:16
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