Translocator protein (18 kDa) (TSPO) as a therapeutic target for anxiety and neurologic disorders

被引:45
|
作者
Nothdurfter, Caroline [1 ,2 ]
Baghai, Thomas C. [1 ]
Schuele, Cornelius [3 ]
Rupprecht, Rainer [1 ,2 ]
机构
[1] Univ Regensburg, Dept Psychiat & Psychotherapy, D-93053 Regensburg, Germany
[2] Max Planck Inst Psychiat, D-80804 Munich, Germany
[3] Univ Munich, Dept Psychiat & Psychotherapy, D-80336 Munich, Germany
关键词
TSPO; Neurosteroid; Anxiety disorder; GABA(A) receptor; Neuroregeneration; PERIPHERAL BENZODIAZEPINE-RECEPTOR; NEUROACTIVE STEROIDS; ANXIOLYTIC ETIFOXINE; CHOLESTEROL-BINDING; NERVOUS-SYSTEM; PANIC DISORDER; MESSENGER-RNA; EXPRESSION; STRESS; STEROIDOGENESIS;
D O I
10.1007/s00406-012-0352-5
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
The translocator protein (18kD) (TSPO) plays a crucial role for the synthesis of neurosteroids by promoting the transport of cholesterol to the inner mitochondrial membrane, which is the rate-limiting step in neurosteroidogenesis. Neurosteroids are allosteric modulators of GABA(A) receptor function, which plays an important role in the pathophysiology of anxiety disorders. The TSPO ligand XBD173 enhances GABAergic neurotransmission by promoting neurosteroidogenesis without direct effects at the GABAA receptor. In humans, XBD173 shows potent antipanic efficacy without sedation and withdrawal after 7 days of treatment. XBD173 therefore appears to be a promising compound for rapid anxiolytic efficacy with a favorable side-effect profile. Furthermore, TSPO ligands show neuroprotective and antiinflammatory effects in experimental models of peripheral neuropathies and traumatic brain injury. These compounds might therefore also be valuable for the treatment of neurologic diseases with inflammation-related pathophysiology.
引用
收藏
页码:S107 / S112
页数:6
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