Are gonadal steroid hormones involved in disorders of brain aging?

被引:19
作者
Azcoitia, I
DonCarlos, LL
Garcia-Segura, LM
机构
[1] CSIC, Inst Cajal, E-28002 Madrid, Spain
[2] Univ Complutense Madrid, Fac Biol, Dept Biol Celular, E-28040 Madrid, Spain
[3] Loyola Univ, Stritch Sch Med, Dept Cell Biol Neurobiol & Anat, Maywood, IL 60153 USA
关键词
estradiol; neurodegenerative diseases; neuroprotection; progesterone; testosterone;
D O I
10.1046/j.1474-9728.2003.00013.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Human aging is associated with a decrease of circulating gonadal steroid hormones. Since these hormones act as trophic factors for neurones and glia, it is possible that the decrease in sex steroid levels may contribute to the increased risk of neurodegenerative disorders with advanced age. Sex steroids are neuroprotective in several animal models of central and peripheral neurodegenerative diseases, and clinical data suggest that these hormones may reduce the risk of neural pathology in aged humans. Potential therapeutic approaches for aged-associated neural disorders may emerge from studies conducted to understand the mechanisms of action of sex steroids in the nervous system of aged animals. Alterations in the endogenous capacity of the aged brain to synthesize and metabolize sex steroids, as well as possible aged-associated modifications in the signalling of sex steroid receptors in the nervous system, are important areas for future investigation.
引用
收藏
页码:31 / 37
页数:7
相关论文
共 105 条
  • [1] Different modes of hippocampal plasticity in response to estrogen in young and aged female rats
    Adams, MM
    Shah, RA
    Janssen, WGM
    Morrison, JH
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (14) : 8071 - 8076
  • [2] GONADAL-STEROID INDUCTION OF STRUCTURAL SEX-DIFFERENCES IN THE CENTRAL NERVOUS-SYSTEM
    ARNOLD, AP
    GORSKI, RA
    [J]. ANNUAL REVIEW OF NEUROSCIENCE, 1984, 7 : 413 - 442
  • [3] Azcoitia I, 1999, J NEUROSCI RES, V58, P815, DOI 10.1002/(SICI)1097-4547(19991215)58:6<815::AID-JNR8>3.0.CO
  • [4] 2-R
  • [5] Brain aromatase is neuroprotective
    Azcoitia, I
    Sierra, A
    Veiga, S
    Honda, S
    Harada, N
    Garcia-Segura, LM
    [J]. JOURNAL OF NEUROBIOLOGY, 2001, 47 (04): : 318 - 329
  • [6] Baulieu EE, 2001, INT REV NEUROBIOL, V46, P1
  • [7] Dehydroepiandrosterone (DHEA), DHEA sulfate, and aging:: Contribution of the DHEAge Study to a sociobiomedical issue
    Baulieu, EE
    Thomas, G
    Legrain, S
    Lahlou, N
    Roger, M
    Debuire, B
    Faucounau, V
    Girard, L
    Hervy, MP
    Latour, F
    Leaud, MC
    Mokrane, A
    Pitti-Ferrandi, H
    Trivalle, C
    de Lacharrière, O
    Nouveau, S
    Rakoto-Arison, B
    Souberbielle, JC
    Raison, J
    Le Bouc, Y
    Raynaud, A
    Girerd, X
    Forette, F
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (08) : 4279 - 4284
  • [8] The tyrosine kinase and mitogen-activated protein kinase pathways mediate multiple effects of estrogen in hippocampus
    Bi, RF
    Broutman, G
    Foy, MR
    Thompson, RF
    Baudry, M
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (07) : 3602 - 3607
  • [9] Birkhäuser M, 2002, MATURITAS, V41, pS3
  • [10] Prenatal immune challenge disrupts sensorimotor gating in adult rats:: Implications for the etiopathogenesis of schizophrenia
    Borrell, J
    Vela, JM
    Arévalo-Martin, A
    Molina-Holgado, E
    Guaza, C
    [J]. NEUROPSYCHOPHARMACOLOGY, 2002, 26 (02) : 204 - 215