4.5 Article

Differential menopause-versus aging-induced changes in oxidative stress and circadian rhythm gene markers

期刊

MECHANISMS OF AGEING AND DEVELOPMENT
卷 164, 期 -, 页码 41-48

出版社

ELSEVIER IRELAND LTD
DOI: 10.1016/j.mad.2017.04.002

关键词

Biology of aging; Gender differences; Genomics; Oxidative stress; Senescence

资金

  1. Fundacion Patrimonio Comunal Olivarero
  2. Junta de Andalucia (Consejeria de Salud, Consejeria de Agricultura y Pesca, Consejeria de Innovacion, Ciencia y Empresa)
  3. Diputaciones de Jaen y Cordoba, Centro de Excelencia en Investigation sobre Aceite de Oliva y Salud
  4. Ministerio de Medio Ambiente, Medio Rural y Marino, Gobierno de Esparia
  5. Ministerio de Ciencia e Innovacion [AGL2009-122270]
  6. Ministerio de Economia y Competitividad [AGL2012/39615, PIE14/00005, PIE 14/00031, SAF2014-52480-R, FIS PI13/00185, PI13/00619]
  7. Consejeria de Economia, Innovacion y Ciencia, Proyectos de Investigation de Excelencia, Junta de Andalucia [AGR922]
  8. Consejeria de Salud, Junta de Andalucia [PI0193/09, PI-0058/10]
  9. Consejeria de Innovacion Ciencia y Empresa [CVI-7450]
  10. Fondo Europeo de Desarrollo Regional (FEDER)
  11. ISCIII [CP14/00114]

向作者/读者索取更多资源

Menopause is characterized by the depletion of estrogen that has been proposed to cause oxidative stress. Circadian rhythm is an internal biological clock that controls physiological processes. It was analyzed the gene expression in peripheral blood mononuclear cells and the lipids and glucose levels in plasma of a subgroup of 17 pre-menopausal women, 19 men age-matched as control group for the pre-menopausal women, 20 postmenopausal women and 20 men age-matched as control group for the post-menopausal women; all groups were matched by body mass index. Our study showed a decrease in the expression of the oxidative stress-related gene GPX1, and an increase in the expression of SOD1 as consequence of menopause. In addition, we found that the circadian rhythm-related gene PER2 decreased as consequence of menopause. On the other hand, we observed a decrease in the expression of the oxidative stress-related gene GPX4 and an increase in the expression of CAT as a consequence of aging, independently of menopause. Our results suggest that the menopause-induced oxidative stress parallels a disruption in the circadian clock in women, and part of the differences in oxidative stress observed between pre- and post-menopausal women was due to aging, independent of menopause.

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