Zhu Xiongwei, Lee Hyoung-gon, Perry George, Smith Mark A
Department of Pathology, Case Western Reserve University, 2103 Cornell Road, Cleveland, OH 44106, USA.
Biochim Biophys Acta. 2007 Apr;1772(4):494-502. doi: 10.1016/j.bbadis.2006.10.014. Epub 2006 Oct 27.
Given the relative modality of single-insult models to accurately reflect Alzheimer disease pathogenesis, based on studies on mitogenic and oxidative stress signaling pathways, we proposed a two-hit hypothesis 2 years ago stating that both oxidative stress and mitogenic dysregulation are necessary and sufficient to cause the disease and suggested that it may be a common mechanism for other neurodegenerative diseases as well (X. Zhu, A.K. Raina, G. Perry, M.A. Smith, Alzheimer's disease: the two-hit hypothesis, Lancet Neurol. 3 (2004) 219-226). Recent developments in the field confirm some important predictions of the hypothesis and shed new lights on potential mechanisms regarding how steady state may be achieved in sporadic AD cases and therefore, in our opinion, strengthen the hypothesis, which will be the focus of this review.
鉴于单次损伤模型在准确反映阿尔茨海默病发病机制方面的相对局限性,基于对有丝分裂原和氧化应激信号通路的研究,我们在两年前提出了双打击假说,指出氧化应激和有丝分裂原失调都是引发该疾病的必要且充分条件,并认为这可能也是其他神经退行性疾病的共同机制(X.朱、A.K.雷纳、G.佩里、M.A.史密斯,《阿尔茨海默病:双打击假说》,《柳叶刀神经病学》,2004年,第3卷,第219 - 226页)。该领域的最新进展证实了该假说的一些重要预测,并为散发性阿尔茨海默病病例如何实现稳态的潜在机制提供了新线索,因此,我们认为这强化了该假说,而这将是本综述的重点。