Liere Philippe, Pianos Antoine, Oudinet Jean-Paul, Schumacher Michael, Akwa Yvette
U1195 INSERM and Université Paris Sud and Université Paris-Saclay, 80 rue du Général Leclerc, 94276 Le Kremlin-Bicêtre, France.
U1195 INSERM and Université Paris Sud and Université Paris-Saclay, 80 rue du Général Leclerc, 94276 Le Kremlin-Bicêtre, France.
Psychoneuroendocrinology. 2017 Sep;83:122-134. doi: 10.1016/j.psyneuen.2017.05.022. Epub 2017 Jun 3.
Etifoxine is indicated in humans for treating anxiety. In rodents, besides its anxiolytic-like properties, it has recently shown neuroprotective and neuroregenerative activities. It acts by enhancing GABA receptor function and by stimulating acute steroid biosynthesis via the activation of the 18-kDa translocator protein. However, the regulatory action of etifoxine on steroid production is not well characterized. In this work, we performed dose-response, acute and chronic time-course experiments on the effects of intraperitoneal injections of etifoxine on steroid levels in adult male rat brain and plasma analyzed by gas chromatography-mass spectrometry. Concentrations of pregnenolone, progesterone and its 5α-reduced metabolites were significantly increased in both tissues in response to 25 and 50mg/kg of etifoxine, as compared with vehicle controls, and reached maximal values at 0.5-1h post-injection. Daily injections of etifoxine (50mg/kg, 15days) kept them increased at day 15. Comparisons between steroidogenic tissues revealed that 1h after 50mg/kg of etifoxine treatment, levels of pregnenolone, progesterone and corticosterone were highest in adrenal glands and markedly increased together with their reduced metabolites. They were also increased by etifoxine in brain and plasma, but not in testis except for corticosterone and its metabolites. In contrast, testosterone level was significantly decreased in testis while with its 5α-reduced metabolites, it was unchanged in brain. Results demonstrate that the modulation of steroid concentrations by etifoxine is dependent on the type of steroid and on the steroidogenic organ. They further suggest that adrenal steroids upregulated by etifoxine make an important contribution to the steroids present in brain. This work provides a precise and complete view of steroids regulated by etifoxine that could be useful in therapeutic research.
依替福辛在人体中用于治疗焦虑症。在啮齿动物中,除了具有抗焦虑样特性外,它最近还表现出神经保护和神经再生活性。它通过增强GABA受体功能以及通过激活18 kDa转位蛋白来刺激急性类固醇生物合成发挥作用。然而,依替福辛对类固醇生成的调节作用尚未得到充分表征。在这项研究中,我们通过气相色谱-质谱法对成年雄性大鼠脑和血浆中类固醇水平进行了剂量反应、急性和慢性时间进程实验,以研究腹腔注射依替福辛的影响。与溶剂对照组相比,给予25和50mg/kg依替福辛后,两种组织中孕烯醇酮、孕酮及其5α-还原代谢物的浓度均显著增加,并在注射后0.5 - 1小时达到最大值。每日注射依替福辛(50mg/kg,共15天)可使它们在第15天仍保持升高。对类固醇生成组织的比较显示,在给予50mg/kg依替福辛治疗1小时后,肾上腺中孕烯醇酮、孕酮和皮质酮的水平最高,并且与其还原代谢物一起显著增加。它们在脑和血浆中也被依替福辛升高,但在睾丸中除皮质酮及其代谢物外没有变化。相比之下,睾丸中的睾酮水平显著降低,而其5α-还原代谢物在脑中没有变化。结果表明,依替福辛对类固醇浓度的调节取决于类固醇的类型和类固醇生成器官。它们进一步表明,依替福辛上调的肾上腺类固醇对脑中存在的类固醇有重要贡献。这项工作提供了依替福辛调节类固醇的精确而完整的观点,这可能对治疗研究有用。