Neurosteroids: Biosynthesis and function of these novel neuromodulators

被引:634
作者
Compagnone, NA
Mellon, SH [1 ]
机构
[1] Univ Calif San Francisco, Dept Obstet Gynecol & Reprod Sci, Ctr Reprod Sci, San Francisco, CA 94143 USA
[2] Univ Calif San Francisco, Metab Res Unit, San Francisco, CA 94143 USA
关键词
D O I
10.1006/frne.1999.0188
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Over the past decade, it has become clear that the brain is a steroidogenic organ. The steroids synthesized by the brain and nervous system, given the name neurosteroids, have a wide variety of diverse functions. In general, they mediate their actions, not through classic steroid hormone nuclear receptors, but through ion-gated neurotransmitter receptors. This paper summarizes what is known about the biosynthesis of neurosteroids, the enzymes mediating these reactions, their localization during development and in the adult, and their function and mechanisms of action in the developing and adult central and peripheral nervous systems. The expression of the steroidogenic enzymes is developmentally regulated, with some enzymes being expressed only during development, while others are expressed during development and in the adult. These enzymes are expressed in both neurons and glia, suggesting that these two cell types must work in concert to produce the appropriate active neurosteroid. The functions attributed to specific neurosteroids include modulation of GABA(A), and NMDA function, modulation of sigma receptor function, regulation of myelinization, neuroprotection, and growth of axons and dendrites. Neurosteroids have also been shown to modulate expression of particular subunits of GABA(A) and NMDA receptors, providing additional sites at which these compounds can regulate neural function. The pharmacological properties of specific neurosteroids are described, and potential uses of neurosteroids in specific neuropathologies and during normal aging in humans are also discussed. (C) 2000 Academic Press.
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页码:1 / 56
页数:56
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共 276 条
  • [1] New 17-hydroxysteroid dehydrogenases - Molecular and cell biology of the type IV porcine and human enzymes
    Adamski, J
    Carstensen, J
    Husen, B
    Kaufmann, M
    deLaunoit, Y
    Leenders, F
    Markus, M
    Jungblut, PW
    [J]. BASIS FOR CANCER MANAGEMENT, 1996, 784 : 124 - 136
  • [2] NEUROSTEROID METABOLISM - 7-ALPHA-HYDROXYLATION OF DEHYDROEPIANDROSTERONE AND PREGNENOLONE BY RAT-BRAIN MICROSOMES
    AKWA, Y
    MORFIN, RF
    ROBEL, P
    BAULIEU, EE
    [J]. BIOCHEMICAL JOURNAL, 1992, 288 : 959 - 964
  • [3] AKWA Y, 1993, BIOCHEM J, V291, P952
  • [4] CLONING AND TISSUE DISTRIBUTION OF THE HUMAN 11-BETA-HYDROXYSTEROID DEHYDROGENASE TYPE-2 ENZYME
    ALBISTON, AL
    OBEYESEKERE, VR
    SMITH, RE
    KROZOWSKI, ZS
    [J]. MOLECULAR AND CELLULAR ENDOCRINOLOGY, 1994, 105 (02) : R11 - R17
  • [5] STRUCTURAL AND BIOCHEMICAL-PROPERTIES OF CLONED AND EXPRESSED HUMAN AND RAT STEROID 5-ALPHA-REDUCTASES
    ANDERSSON, S
    RUSSELL, DW
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (10) : 3640 - 3644
  • [6] DELETION OF STEROID 5-ALPHA-REDUCTASE 2-GENE IN MALE PSEUDOHERMAPHRODITISM
    ANDERSSON, S
    BERMAN, DM
    JENKINS, EP
    RUSSELL, DW
    [J]. NATURE, 1991, 354 (6349) : 159 - 161
  • [7] [Anonymous], 1991, Reproductive endocrinology: physiology pathophysiology and clinical management
  • [8] Anson LC, 1998, J NEUROSCI, V18, P581
  • [9] Cytochrome b5 augments the 17,20-lyase activity of human P450c17 without direct electron transfer
    Auchus, RJ
    Lee, TC
    Miller, WL
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (06) : 3158 - 3165
  • [10] BALLABIO A, 1995, METABOLIC MOL BASES, P2999