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Peripheral nerves: a target for the action of neuroactive steroids.

机译:周围神经:神经活性类固醇作用的靶标。

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Peripheral nervous system possesses both classical and non-classical steroid receptors and consequently may represent a target for the action of neuroactive steroids. The present review summarizes the state of art of this intriguing field of research reporting data which indicate that neuroactive steroids, like for instance progesterone, dihydroprogesterone, tetrahydroprogesterone, dihydrotestosterone and 3alpha-diol, stimulate the expression of two important proteins of the myelin of peripheral nerves, the glycoprotein P0 (P0) and the peripheral myelin protein 22 (PMP22). Interestingly, the mechanisms by which neuroactive steroids exert their effects involve classical steroid receptors, like for instance progesterone and androgen receptors, in case of P0 and non-classical steroid receptors, like GABA(A) receptor, in case of PMP22. Moreover, neuroactive steroids not only control the expression of these specific myelin proteins, but also influence the morphology of myelin sheaths and axons suggesting that these molecules may represent an interesting new therapeutic approach to maintain peripheral nerve integrity during neurodegenerative events.
机译:周围神经系统同时具有经典和非经典类固醇受体,因此可能代表神经活性类固醇的作用靶标。本综述总结了这个有趣的研究报告数据的最新技术水平,这些数据表明神经活性类固醇,例如孕酮,二氢孕酮,四氢孕酮,二氢睾丸激素和3α-二醇,可以刺激周围神经髓磷脂的两种重要蛋白的表达。 ,糖蛋白P0(P0)和外周髓磷脂蛋白22(PMP22)。有趣的是,神经活性类固醇发挥作用的机制涉及经典类固醇受体(例如,对于P0为孕激素和雄激素受体)和非经典类固醇受体(例如在PMP22中为GABA(A)受体)。此外,神经活性类固醇不仅控制这些特定的髓鞘蛋白的表达,而且影响髓鞘和轴突的形态,表明这些分子可能代表了一种有趣的新治疗方法,可以在神经退行性事件中维持周围神经的完整性。

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