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Could androgens maintain specific domains of mental health in aging men by preserving hippocampal neurogenesis

Could androgens maintain specific domains of mental health in aging men by preserving hippocampal neurogenesis
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摘要 Interest surrounds the role of sex-hormones in regulating brain function outside of reproductive behaviour. Declining androgen production in aging males has been associated with cognitive impairment, depression and increased risk of developing Alzheimer's disease. Indication for testosterone replacement therapy is based on biochemically determined low circulating testosterone combined with manifest symptoms. However, which aspects of age-related cognitive decline are attributable to low circulating testosterone remain ambiguous. Studies examining cognition in aging men receiving testosterone replacement therapy have yielded equivocal results. The exact role of testosterone in maintaining cognitive function and the underlying neural mechanisms are largely unknown, though it would appear to be domain specific. Cladty in this area will provide clinical direction toward addressing an increasing healthcare burden of mental health decline coincident with increasing longevity. The premise that androgens contribute to maintaining aspects of mental health in aging men by preserving hippocampal neurogenesis will be used as a forum in this review to discuss current knowledge and the need for further studies to better define testosterone replacement strategies for aging male health. Interest surrounds the role of sex-hormones in regulating brain function outside of reproductive behaviour. Declining androgen production in aging males has been associated with cognitive impairment, depression and increased risk of developing Alzheimer's disease. Indication for testosterone replacement therapy is based on biochemically determined low circulating testosterone combined with manifest symptoms. However, which aspects of age-related cognitive decline are attributable to low circulating testosterone remain ambiguous. Studies examining cognition in aging men receiving testosterone replacement therapy have yielded equivocal results. The exact role of testosterone in maintaining cognitive function and the underlying neural mechanisms are largely unknown, though it would appear to be domain specific. Cladty in this area will provide clinical direction toward addressing an increasing healthcare burden of mental health decline coincident with increasing longevity. The premise that androgens contribute to maintaining aspects of mental health in aging men by preserving hippocampal neurogenesis will be used as a forum in this review to discuss current knowledge and the need for further studies to better define testosterone replacement strategies for aging male health.
出处 《Neural Regeneration Research》 SCIE CAS CSCD 2012年第28期2227-2239,共13页 中国神经再生研究(英文版)
基金 supported by a National Health and Medical Research Council (Australia) postdoctoral fellowship
关键词 ANDROGEN hippocampus NEUROGENESIS AGING cognition male TESTOSTERONE androgen hippocampus neurogenesis aging cognition male testosterone
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  • 1Smith GD, Hart C, Watt G, Hole D, Hawthorne V. Individual social class, area-based deprivation, cardiovascular risk factors and mortality: the Renfrew and Paisley Study. J Epidemiol Community Health 1998; 52: 399-405.
  • 2Denton M, Waiters V. Gender differences in structural and behavioural determinants of health: an analysis of the social production of health. Soc Sci Med 1999; 48: 1221-35.
  • 3Denton M, Prus S, Waiters V. Gender differences in health: a Canadian study of the psychosocial, structural and behavioural determinants of health. Soc Sci Med 2004; 58: 2585-600.
  • 4Joffe M. Infertility and environmental pollutants. Br Med Bull 2003; 68: 47-70.
  • 5De Falco T, Capel B. Gonad morphogenesis in vertebrates: divergent means to a convergent end. Ann Rev Cell Biol 2009; 25: 457-82.
  • 6Dewing P, Shi T, Horvath S, Vilain E. Sexually dimorphic gene expression in mouse brain precedes gonadal differentiation. Brain Res Mol Brain Res 2003; 118: 82-90.
  • 7Arnold Ap, Xu J, Grisham W, Chen X, Kim Y, et al. Minireview: sex chromosomes and brain sexual differentiation. Endocrinology 2004; 145: 1057-62.
  • 8Goldman-Johnson DR, Stanley EG, de Kretser DM, Morrison JR. Evidence that androgens regulate early developmental events, prior to sexual differentiation. Endocrinology 2007; 149: 5-14.
  • 9Skuse DH, James RH, Bishop DV, Coppin B, Dalton P, et al. Evidence from Turner's syndrome of an imprinted X-linked locus affecting cognitive function. Nature 1997; 387: 705-8.
  • 10Davies W, Isles A, Smith R, Karunadasa D, Burrmann D, et aL Xlr3b is a new imprinted candidate for X-linked parent-of-origin effects on cognitive function in mice. Nat Genet 2005; 37: 625-9.

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