Molecular Neurobiology Unit, Experimental Neurology Fondazione Santa Lucia, Rome, Italy.
Front Endocrinol (Lausanne). 2011 Oct 19;2:55. doi: 10.3389/fendo.2011.00055. eCollection 2011.
Anxiety disorders are the most common psychiatric disorders. They are frequently treated with benzodiazepines, which are fast acting highly effective anxiolytic agents. However, their long-term use is impaired by tolerance development and abuse liability. In contrast, antidepressants such as selective serotonin reuptake inhibitors (SSRIs) are considered as first-line treatment but have a slow onset of action. Neurosteroids are powerful allosteric modulators of GABA(A) and glutamate receptors. However, they also modulate sigma receptors and they are modulated themselves by SSRIs. Both pre-clinical and clinical studies have shown that neurosteroid homeostasis is altered in depression and anxiety disorders and antidepressants may act in part through restoring neurosteroid disbalance. Moreover, novel drugs interfering with neurosteroidogenesis such as ligands of the translocator protein (18 kDa) may represent an attractive pharmacological option for novel anxiolytics which lack the unwarranted side effects of benzodiazepines. Thus, neurosteroids are important endogenous neuromodulators for the physiology and pathophysiology of anxiety and they may constitute a novel therapeutic approach in the treatment of these disorders.
焦虑障碍是最常见的精神障碍。它们通常用苯二氮䓬类药物治疗,苯二氮䓬类药物是快速起效、高效的抗焦虑药物。然而,它们的长期使用受到耐受性发展和滥用倾向的影响。相比之下,选择性 5-羟色胺再摄取抑制剂(SSRIs)等抗抑郁药被认为是一线治疗药物,但起效缓慢。神经甾体是 GABA(A)和谷氨酸受体的有效变构调节剂。然而,它们也调节 sigma 受体,并且自身受 SSRIs 调节。临床前和临床研究表明,抑郁和焦虑障碍中的神经甾体动态平衡发生改变,抗抑郁药可能部分通过恢复神经甾体失衡发挥作用。此外,干扰神经甾体生成的新型药物,如转位蛋白(18 kDa)配体,可能是一种有吸引力的药理学选择,用于治疗缺乏苯二氮䓬类药物不必要副作用的新型抗焦虑药物。因此,神经甾体是焦虑生理和病理生理学的重要内源性神经调节剂,它们可能是治疗这些疾病的一种新的治疗方法。