Canet Geoffrey, Chevallier Nathalie, Zussy Charleine, Desrumaux Catherine, Givalois Laurent
Molecular Mechanisms in Neurodegenerative Dementia Laboratory, INSERM, U1198, Team Environmental Impact in Alzheimer's Disease and Related Disorders (EiAlz), Montpellier, France.
University of Montpellier, Montpellier, France.
Front Neurosci. 2018 Oct 16;12:739. doi: 10.3389/fnins.2018.00739. eCollection 2018.
Alzheimer's disease (AD) is the principal neurodegenerative pathology in the world displaying negative impacts on both the health and social ability of patients and inducing considerable economic costs. In the case of sporadic forms of AD (more than 95% of patients), even if mechanisms are unknown, some risk factors were identified. The principal risk is aging, but there is growing evidence that lifetime events like chronic stress or stress-related disorders may increase the probability to develop AD. This mini-review reinforces the rationale to consider major depressive disorder (MDD) as an important risk factor to develop AD and points the central role played by the hypothalamic-pituitary-adrenal (HPA) axis, glucocorticoids (GC) and their receptors (GR) in the etiology of MDD and AD. Several strategies directly targeting GR were tested to neutralize the HPA axis dysregulation and GC overproduction. Given the ubiquitous expression of GR, antagonists have many undesired side effects, limiting their therapeutic potential. However, a new class of molecules was developed, highly selective and acting as modulators. They present the advantage to selectively abrogate pathogenic GR-dependent processes, while retaining beneficial aspects of GR signaling. In fact, these "selective GR modulators" induce a receptor conformation that allows activation of only a subset of downstream signaling pathways, explaining their capacity to combine agonistic and antagonistic properties. Thus, targeting GR with selective modulators, alone or in association with current strategies, becomes particularly attractive and relevant to develop novel preventive and/or therapeutic strategies to tackle disorders associated with a dysregulation of the HPA axis.
阿尔茨海默病(AD)是全球主要的神经退行性病变,对患者的健康和社交能力均产生负面影响,并带来相当大的经济成本。对于散发性AD(超过95%的患者),尽管其发病机制尚不清楚,但已确定了一些风险因素。主要风险因素是衰老,但越来越多的证据表明,诸如慢性应激或与应激相关的疾病等一生经历可能会增加患AD的概率。这篇综述强化了将重度抑郁症(MDD)视为AD重要风险因素的理论依据,并指出下丘脑 - 垂体 - 肾上腺(HPA)轴、糖皮质激素(GC)及其受体(GR)在MDD和AD病因学中所起的核心作用。人们测试了几种直接针对GR的策略,以中和HPA轴失调和GC过量产生的问题。鉴于GR的广泛表达,拮抗剂具有许多不良副作用,限制了它们的治疗潜力。然而,已开发出一类新型分子,具有高度选择性且起调节剂作用。它们的优势在于能选择性消除致病性GR依赖的过程,同时保留GR信号传导的有益方面。事实上,这些“选择性GR调节剂”诱导一种受体构象,仅允许激活一部分下游信号通路,这解释了它们兼具激动和拮抗特性的能力。因此,单独或与当前策略联合使用选择性调节剂靶向GR,对于开发应对与HPA轴失调相关疾病的新型预防和/或治疗策略而言,变得极具吸引力且意义重大。