Do Rego Jean Luc, Tremblay Yves, Luu-The Van, Repetto Emanuela, Castel Hélène, Vallarino Mauro, Bélanger Alain, Pelletier Georges, Vaudry Hubert
INSERM U413, Laboratory of Cellular and Molecular Neuroendocrinology, European Institute for Peptide Research (IFRMP 23), University of Rouen, Mont-Saint-Aignan, France.
J Neurochem. 2007 Jan;100(1):251-68. doi: 10.1111/j.1471-4159.2006.04209.x. Epub 2006 Oct 31.
It is now clearly established that the brain has the capability of synthesizing various biologically active steroids including 17-hydroxypregnenolone (17OH-Delta(5)P), 17-hydroxyprogesterone (17OH-P), dehydroepiandrosterone (DHEA) and androstenedione (Delta(4)). However, the presence, distribution and activity of cytochrome P450 17alpha-hydroxylase/C17, 20-lyase (P450(C17)), a key enzyme required for the conversion of pregnenolone (Delta(5)P) and progesterone (P) into these steroids, are poorly documented. Here, we show that P450(C17)-like immunoreactivity is widely distributed in the frog brain and pituitary. Prominent populations of P450(C17)-containing cells were observed in a number nuclei of the telencephalon, diencephalon, mesencephalon and metencephalon, as well as in the pars distalis and pars intermedia of the pituitary. In the brain, P450(C17)-like immunoreactivity was almost exclusively located in neurons. In several hypothalamic nuclei, P450(C17)-positive cell bodies also contained 3beta-hydroxysteroid dehydrogenase-like immunoreactivity. Incubation of telencephalon, diencephalon, mesencephalon, metencephalon or pituitary explants with [(3)H]Delta(5)P resulted in the formation of several tritiated steroids including 17OH-Delta(5)P, 17OH-P, DHEA and Delta(4). De novo synthesis of C(21) 17-hydroxysteroids and C(19) ketosteroids was reduced in a concentration-dependent manner by ketoconazole, a P450(C17) inhibitor. This is the first detailed immunohistochemical mapping of P450(C17) in the brain and pituitary of any vertebrate. Altogether, the present data provide evidence that CNS neurons and pituitary cells can synthesize androgens.
现已明确证实,大脑具有合成多种生物活性甾体的能力,这些甾体包括17 - 羟孕烯醇酮(17OH - Δ⁵P)、17 - 羟孕酮(17OH - P)、脱氢表雄酮(DHEA)和雄烯二酮(Δ⁴)。然而,细胞色素P450 17α - 羟化酶/C17,20 - 裂解酶(P450(C17))作为将孕烯醇酮(Δ⁵P)和孕酮(P)转化为这些甾体所需的关键酶,其存在、分布和活性的相关记录却很少。在此,我们表明P450(C17)样免疫反应性广泛分布于蛙脑和垂体中。在端脑、间脑、中脑和后脑的多个核团以及垂体远侧部和中间部中观察到大量含P450(C17)的细胞。在脑中,P450(C17)样免疫反应性几乎仅位于神经元中。在几个下丘脑核团中,P450(C17)阳性细胞体还含有3β - 羟类固醇脱氢酶样免疫反应性。用[³H]Δ⁵P孵育端脑、间脑、中脑、后脑或垂体外植体,会导致形成多种氚标记的甾体,包括17OH - Δ⁵P、17OH - P、DHEA和Δ⁴。酮康唑是一种P450(C17)抑制剂,它以浓度依赖的方式降低了C₂₁ 17 - 羟甾体和C₁₉酮甾体的从头合成。这是在任何脊椎动物的脑和垂体中对P450(C1)进行的首次详细免疫组织化学定位。总之,目前的数据提供了中枢神经系统神经元和垂体细胞能够合成雄激素的证据。