Abstract

Severalreports havestatedthe 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 studyaimedtoprovide insights into TASE and athymol-mediated multifactorial therapeutic approach in a scopolamine-induced Alzheimer's disease (AD) mouse model. TASE and thymol supplementation significantly reduced oxidative stress markers suchas brain glutathione, hydrogen peroxide, and malondialdehyde in mouse whole brain homogenates. Tumor necrosis factor-alpha was significantly downregulated, whereas theelevation 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 Aβ 1-42 peptides was observed in thebrainsofTASE- 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 actas natural therapeutic agentsforthetreatmentof neurodegenerative disorders, suchas AD.

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