Martini L, Celotti F, Melcangi R C
Istituto di Endocrinologia, Università degli Studi di Milano, Italy.
Cell Mol Neurobiol. 1996 Jun;16(3):271-82. doi: 10.1007/BF02088095.
This paper summarizes the most recent data obtained in the authors' laboratory on the metabolism of testosterone and progesterone in neurons and in the glia. 1. The activities of 5 alpha-reductase (the enzyme that converts testosterone into dihydrotestosterone; DHT) and of 3 alpha-hydroxy steroid dehydrogenase (the enzyme that converts DHT into 5 alpha-androstane-3 alpha, 17 beta-diol; 3 alpha-diol) were first evaluated in primary cultures of neurons, oligodendrocytes, and type-1 and type-2 astrocytes, obtained from the fetal or neonatal rat brain. The formation of DHT and 3 alpha-diol was evaluated incubating the different cultures with labeled testosterone or labeled DHT as substrates. The results obtained indicate that the formation of DHT takes place preferentially in neurons; however, also type-2 astrocytes and oligodendrocytes possess considerable 5 alpha-reductase activity. A completely different localization was observed for 3 alpha-hydroxysteroid dehydrogenase; the formation of 3 alpha-diol appears to be prevalently, if not exclusively, present in type-1 astrocytes; 3 alpha-diol is formed in very low yields by neurons, type-2 astrocytes, and oligodendrocytes. Moreover, the results indicate that, in type 1 astrocytes, both 5 alpha-reductase and 3 alpha-HSD are stimulated by coculture with neurons and by the addition of neuron-conditioned medium, suggesting that secretory products released by neurons might intervene in the control of glial cell function. 2. Subsequently it was shown that, similarly to what happens when testosterone is used as the substrate, 5 alpha-reductase, which metabolizes progesterone into 5 alpha-pregnane-3,20-dione, (DHP), shows a significantly higher activity in neurons than in glial cells; however, also type-1 and type-2 astrocytes as well as oligodendrocytes possess some ability to 5 alpha-reduce progesterone. On the contrary, 3 alpha-hydroxysteroid dehydrogenase, the enzyme which converts DHP into 5 alpha-pregnane-3 alpha-ol-20-one (THP), appears to be present mainly in type-1 astrocytes; much lower levels of this enzyme are present in neurons and in type-2 astrocytes. At variance with the previous results obtained using androgens as precursors, oligodendrocytes show considerable 3 alpha-hydroxysteroid dehydrogenase activity, even if this is statistically lowe than that present in type-1 astrocytes. The existence of isoenzymatic forms of the enzymes involved in androgen and progesterone metabolism is discussed.
本文总结了作者实验室最近获得的关于神经元和神经胶质细胞中睾酮和孕酮代谢的最新数据。1. 首先在从胎鼠或新生鼠脑获得的原代神经元、少突胶质细胞、1型和2型星形胶质细胞培养物中,评估了5α-还原酶(将睾酮转化为二氢睾酮;DHT的酶)和3α-羟基类固醇脱氢酶(将DHT转化为5α-雄甾烷-3α,17β-二醇;3α-二醇的酶)的活性。用标记的睾酮或标记的DHT作为底物孵育不同培养物,评估DHT和3α-二醇的形成。获得的结果表明,DHT的形成优先发生在神经元中;然而,2型星形胶质细胞和少突胶质细胞也具有相当的5α-还原酶活性。对于3α-羟基类固醇脱氢酶观察到完全不同的定位;3α-二醇的形成似乎主要(如果不是唯一)存在于1型星形胶质细胞中;神经元、2型星形胶质细胞和少突胶质细胞形成3α-二醇的产量非常低。此外,结果表明,在1型星形胶质细胞中,5α-还原酶和3α-HSD都受到与神经元共培养以及添加神经元条件培养基的刺激,这表明神经元释放的分泌产物可能参与神经胶质细胞功能的控制。2. 随后表明,与以睾酮为底物时的情况类似,将孕酮代谢为5α-孕烷-3,20-二酮(DHP)的5α-还原酶在神经元中的活性明显高于神经胶质细胞;然而,1型和2型星形胶质细胞以及少突胶质细胞也具有一定的5α-还原孕酮的能力。相反,将DHP转化为5α-孕烷-3α-醇-20-酮(THP)的3α-羟基类固醇脱氢酶似乎主要存在于1型星形胶质细胞中;该酶在神经元和2型星形胶质细胞中的水平要低得多。与先前使用雄激素作为前体获得的结果不同,少突胶质细胞显示出相当的3α-羟基类固醇脱氢酶活性,即使在统计学上低于1型星形胶质细胞中的活性。讨论了参与雄激素和孕酮代谢的酶的同工酶形式的存在。