期刊文献+

Expression of Clock genes in the pineal glands of newborn rats with hypoxic-ischemic encephalopathy 被引量:1

Expression of Clock genes in the pineal glands of newborn rats with hypoxic-ischemic encephalopathy
下载PDF
导出
摘要 Clock genes are involved in circadian rhythm regulation, and surviving newborns with hypoxic-ischemic encephalopathy may present with sleep-wake cycle reversal. This study aimed to determine the expression of the clock genes Clock and Bmall, in the pineal gland of rats with hypoxic-ischemic brain damage. Results showed that levels of Clock mRNA v^re not significantly changed within 48 hours after cerebral hypoxia and ischemia. Expression levels of CLOCK and BMAL1 protein were significantly higher after 48 hours. The levels of Bmall mRNA reached a peak at 36 hours, but were significantly reduced at 48 hours. Experimental findings indicate that Clock and Bmall genes were indeed expressed in the pineal glands of neonatal rats. At the initial stage (within 36 hours) of hypoxic-ischemic brain damage, only slight changes in the expression levels of these two genes were detected, followed by significant changes at 36-48 hours. These changes may be associated with circadian rhythm disorder induced by hypoxic-ischemic brain damage. Clock genes are involved in circadian rhythm regulation, and surviving newborns with hypoxic-ischemic encephalopathy may present with sleep-wake cycle reversal. This study aimed to determine the expression of the clock genes Clock and Bmall, in the pineal gland of rats with hypoxic-ischemic brain damage. Results showed that levels of Clock mRNA v^re not significantly changed within 48 hours after cerebral hypoxia and ischemia. Expression levels of CLOCK and BMAL1 protein were significantly higher after 48 hours. The levels of Bmall mRNA reached a peak at 36 hours, but were significantly reduced at 48 hours. Experimental findings indicate that Clock and Bmall genes were indeed expressed in the pineal glands of neonatal rats. At the initial stage (within 36 hours) of hypoxic-ischemic brain damage, only slight changes in the expression levels of these two genes were detected, followed by significant changes at 36-48 hours. These changes may be associated with circadian rhythm disorder induced by hypoxic-ischemic brain damage.
出处 《Neural Regeneration Research》 SCIE CAS CSCD 2012年第28期2221-2226,共6页 中国神经再生研究(英文版)
基金 supported by grants from the Foundation for Advancing Medical Sciences of the Health Department, Jiangsu Province, No. Z200519 the Project for Social Development of Suzhou, No. SSZ0230
关键词 brain hypoxia cerebral ischemia neonatal rats pineal gland CLOCK Bmall MRNA PROTEIN BRAIN neural regeneration brain hypoxia cerebral ischemia neonatal rats pineal gland Clock Bmall mRNA protein brain neural regeneration
  • 相关文献

参考文献29

  • 1de Vries LS, Jongmans MJ. Long-term outcome after neonatal hypoxic-ischaemic encephalopathy. Arch Dis Child Fetal Neonatal Ed. 2010;95(3):F220-224.
  • 2Perlman M, Shah PS. Hypoxic-ischemic encephalopathy: challenges in outcome and prediction. J Pediatr. 2011 ;158 (2 Suppl):e51-54.
  • 3Kommedal S, B6dis G, Matkovits A, et al. Expression pattern of clock under acute phase-delay of the light/dark cycle in the chicken pineal model. Gen Comp Endocrinol. 2011;172(1):170-172.
  • 4Okano T, Yamamoto K, Okano K, et al. Chicken pineal clock genes: implication of BMAL2 as a bidirectional regulator in circadian clock oscillation. Genes Cells. 2001;6(9):825-836.
  • 5Shearman LP, Sriram S, Weaver DR, et al. Interacting molecular loops in the mammalian circadian clock. Science. 2000;288 (5468):1013-1019.
  • 6Asher G, Schibler U. Crosstalk between components of circadian and metabolic cycles in mammals. Cell Metab. 2011 ;13(2):125-137.
  • 7Bellet MM, Sassone-Corsi P. Mammalian circadian clock and metabolism - the epigenetic link. J Cell Sci. 2010;123 (Pt 22):3837-3848.
  • 8Simonneaux V, Poirel V J, Garidou ML, et al. Daily rhythm and regulation of clock gene expression in the rat pineal gland. Brain Res Mol Brain Res. 2004; 120(2):164-172.
  • 9Bustos DM, Bailey M J, Sugden D, et al. Global daily dynamics of the pineal transcriptome. Cell Tissue Res. 2011 ;344(1):1-11.
  • 10Klein DC, Bailey M J, Carter DA, et al. Pineal function: impact of microarray analysis. Mol Cell Endocrinol. 2010;314(2):170-183.

同被引文献1

引证文献1

二级引证文献4

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部