雄激素在运动神经元中的生理病理作用

A. Poletti
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摘要

雄激素受体在70年代被纯化在80年代被克隆。它是类固醇受体超家族的一员,在雄激素依赖或敏感组织中介导雄激素的最重要作用。大脑的一些生理功能在两性中受到不同的控制,雄激素在性别分化过程中起着特定的作用,并参与成年期男性性行为的维持。当雄激素受体发生突变时,由于靶细胞中雄激素功能的丧失,雄激素受体可能会影响许多雄激素调节的活动。然而,在一种特殊类型的突变的情况下,通常存在于其n端的聚谷氨酰胺束的伸长,雄激素受体变得神经毒性并诱导脊髓中大量运动神经元的细胞死亡,这些运动神经元表达非常高水平的这种蛋白质。在这里,我们将简要讨论雄激素受体介导的雄激素活性在大脑中的最重要作用,以及雄激素受体突变可能导致脊髓和球性肌萎缩症(SBMA)神经退行性变的机制。
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THE PHYSIOPATHOLOGICAL ROLES OF ANDROGENS IN MOTONEURONS
The androgen receptor has been purified in the ‘70s and cloned in the ‘80s. It is a member of the steroid receptor superfamily and mediated the most important effects of androgen in androgen dependent or sensitive tissues. Several physiological function of the brain are differentially controlled in the two sexes and androgens play specific role in the processes of sexual differentiation and it is involved in the maintenance of male sex behaviour in adulthood. When mutated, the androgen receptor may impact on many of these androgen-regulated activities because of a loss of androgenic function in target cells. However, in the case of a peculiar type of mutation, the elongation of the polyglutamine tract normally present in its N-terminus, the androgen receptor becomes neurotoxic and induces cells death of a number of motoneurons in the spinal cord, which express very high level of this protein. Here, we will briefly discuss the most important actions of androgen receptor-mediated androgen activity in the brain and the mechanisms by which the mutant androgen receptor may lead to neurodegeneration in Spinal and Bulbar Muscular Atrophy (SBMA).
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