Department of Psychiatry, Psychiatric Institute, College of Medicine, University of Illinois at Chicago, Chicago, IL 60612, USA.
J Neuroendocrinol. 2012 Jan;24(1):102-16. doi: 10.1111/j.1365-2826.2011.02234.x.
Benzodiazepines remain the most frequently used psychotropic drugs for the treatment of anxiety spectrum disorders; however, their use is associated with the development of tolerance and dependence. Another major hindrance is represented by their lack of efficacy in many patients, including patients with post-traumatic stress disorder (PTSD). For these nonresponders, the use of selective serotonin reuptake inhibitors (SSRIs) has been the therapy of choice. In the past decade, clinical studies have suggested that the pharmacological action of SSRIs may include the ability of these drugs to normalise decreased brain levels of neurosteroids in patients with depression and PTSD; in particular, the progesterone derivative allopregnanolone, which potently, positively and allosterically modulates the action of GABA at GABA(A) receptors. Preclinical studies using the socially-isolated mouse as an animal model of PTSD have demonstrated that fluoxetine and congeners ameliorate anxiety-like behaviour, fear responses and aggressive behaviour expressed by such mice by increasing corticolimbic levels of allopregnanolone. This is a novel and more selective mechanism than serotonin reuptake inhibition, which, for half a century, has been considered to be the main molecular mechanism for the therapeutic action of SSRIs. Importantly, this finding may shed light on the high rates of SSRI resistance among patients with PTSD and depression, comprising disorders in which there appears to be a block in allopregnanolone synthesis. There are several different mechanisms by which such a block may occur, and SSRIs may only be corrective under some conditions. Thus, the up-regulation of allopregnanolone biosynthesis in corticolimbic neurones may offer a novel nontraditional pharmacological target for a new generation of potent nonsedating, anxiolytic medications for the treatment of anxiety, depression, and PTSD: selective brain steroidogenic stimulants.
苯二氮䓬类药物仍然是治疗焦虑谱系障碍最常用的精神药物;然而,它们的使用与耐受性和依赖性的发展有关。另一个主要障碍是它们在许多患者中,包括创伤后应激障碍(PTSD)患者中的疗效不佳。对于这些无反应者,选择性 5-羟色胺再摄取抑制剂(SSRIs)的使用一直是首选的治疗方法。在过去的十年中,临床研究表明,SSRIs 的药理作用可能包括这些药物能够使抑郁和 PTSD 患者大脑中神经甾体水平降低正常化;特别是孕激素衍生物孕烷醇酮,它能够强有力地、积极地和变构调节 GABA(A)受体上 GABA 的作用。使用社会隔离小鼠作为 PTSD 的动物模型的临床前研究表明,氟西汀和同类物通过增加皮质边缘的孕烷醇酮水平来改善这些小鼠的焦虑样行为、恐惧反应和攻击行为。这是一种比 50 年来被认为是 SSRIs 治疗作用的主要分子机制的 5-羟色胺再摄取抑制更为新颖和更具选择性的机制。重要的是,这一发现可能揭示了 PTSD 和抑郁症患者中 SSRIs 耐药率高的原因,这些障碍似乎存在孕烷醇酮合成的阻断。可能有几种不同的机制导致这种阻断,SSRIs 可能只在某些条件下具有纠正作用。因此,皮质边缘神经元中孕烷醇酮生物合成的上调可能为新一代具有非镇静、抗焦虑作用的新型非传统药理学靶标提供新的有力药物,用于治疗焦虑、抑郁和 PTSD:选择性脑甾体生成刺激剂。