Institute of Molecular and Clinical Medicine, Kunming Medical University, 1168, West Chunrong Road, Yuhua Street, Chenggong New Town, Kunming 650500, China.
J Clin Neurosci. 2012 Jul;19(7):946-9. doi: 10.1016/j.jocn.2011.12.022. Epub 2012 May 20.
Alzheimer's disease (AD) is one of the most common causes of dementia in the elderly. It is characterized by extracellular deposition of the neurotoxic peptide, amyloid-beta (Aβ) peptide fibrils, and is accompanied by extensive loss of neurons in the brains of affected individuals. However, the pathogenesis of AD is not fully understood. The aim of this review is to discuss the possible role of brain-derived neurotrophic factor (BDNF)/tropomyosin-related kinase B (TrkB) signalling in the development of AD, focusing on BDNF/TrkB signalling in the production of Aβ, tau hyperphosphorylation and cognition decline, and exploring new possibilities for AD intervention.
阿尔茨海默病(AD)是老年人中最常见的痴呆症病因之一。其特征是细胞外沉积神经毒性肽,淀粉样β(Aβ)肽原纤维,并伴有受影响个体大脑中神经元的广泛丧失。然而,AD 的发病机制尚未完全阐明。本综述的目的是讨论脑源性神经营养因子(BDNF)/原肌球蛋白相关激酶 B(TrkB)信号在 AD 发展中的可能作用,重点讨论 BDNF/TrkB 信号在 Aβ产生、tau 过度磷酸化和认知能力下降中的作用,并探索 AD 干预的新可能性。