Literature DB >> 11299324

Involvement of calcium-calmodulin protein kinase but not mitogen-activated protein kinase in light-induced phase delays and Per gene expression in the suprachiasmatic nucleus of the hamster.

S Yokota 1, M Yamamoto, T Moriya, M Akiyama, K Fukunaga, E Miyamoto, S Shibata.   

Abstract

It is known that Ca(2+)-dependent phosphorylation of cAMP response element binding protein (CREB) and the rapid induction of mPer1 and mPer2, mouse period genes in the suprachiasmatic nucleus (SCN) are associated with light-induced phase shifting. The CREB/CRE transcriptional pathway has been shown to be activated by calcium/calmodulin dependent kinase II (CaMKII) and mitogen-activated protein kinase (MAPK); however, there is a lack of evidence concerning whether the activation of CaMKII and/or MAPK elicited by photic stimuli are associated with the change in Per gene expression and behavioral phase shifting. In this experiment, we found there was an inhibitory effect by KN93, CaMKII inhibitor, on hamster Per1 and Per2 expression in the SCN and on phase delays in wheel running rhythm induced by light pulses. PD98059 and U0126, MAPK kinase inhibitors, however, affected neither light-induced Per1 and Per2 expression nor behavioral phase delays, even though PD98059 attenuated the light-induced phosphorylation of MAPK in the SCN. The present findings demonstrate that the light-induced activation of CaMKII plays an important role in the induction of Per1 and Per2 mRNA in the hamster SCN as well as phase shifting. These results suggest that gated induction of Per1 and/or Per2 genes through CaMKII-CREB/CRE accompanied with photic stimuli may be a critical step in phase shifting.

Entities:  

Mesh:

Substances:

Year:  2001        PMID: 11299324     DOI: 10.1046/j.1471-4159.2001.00270.x

Source DB:  PubMed          Journal:  J Neurochem        ISSN: 0022-3042            Impact factor:   5.372


  20 in total

1.  Phase resetting light pulses induce Per1 and persistent spike activity in a subpopulation of biological clock neurons.

Authors:  Sandra J Kuhlman; Rae Silver; Joseph Le Sauter; Abel Bult-Ito; Douglas G McMahon
Journal:  J Neurosci       Date:  2003-02-15       Impact factor: 6.167

2.  Circadian and photic regulation of phosphorylation of ERK1/2 and Elk-1 in the suprachiasmatic nuclei of the Syrian hamster.

Authors:  Andrew N Coogan; Hugh D Piggins
Journal:  J Neurosci       Date:  2003-04-01       Impact factor: 6.167

3.  Photic regulation of map kinase phosphatases MKP1/2 and MKP3 in the hamster suprachiasmatic nuclei.

Authors:  Gastón A Pizzio; Diego A Golombek
Journal:  J Mol Neurosci       Date:  2007-12-05       Impact factor: 3.444

Review 4.  Physiological responses of the circadian clock to acute light exposure at night.

Authors:  Michael C Antle; Victoria M Smith; Roxanne Sterniczuk; Glenn R Yamakawa; Brooke D Rakai
Journal:  Rev Endocr Metab Disord       Date:  2009-12       Impact factor: 6.514

Review 5.  Linking neural activity and molecular oscillations in the SCN.

Authors:  Christopher S Colwell
Journal:  Nat Rev Neurosci       Date:  2011-09-02       Impact factor: 34.870

6.  Circadian regulation of a viral gene promoter in live transgenic mice expressing firefly luciferase.

Authors:  Anne M Collaco; Sima Rahman; Edward J Dougherty; Brett B Williams; Michael E Geusz
Journal:  Mol Imaging Biol       Date:  2005 Sep-Oct       Impact factor: 3.488

Review 7.  Intracellular and intercellular processes determine robustness of the circadian clock.

Authors:  John B Hogenesch; Erik D Herzog
Journal:  FEBS Lett       Date:  2011-04-28       Impact factor: 4.124

8.  Na(V)1.1 channels are critical for intercellular communication in the suprachiasmatic nucleus and for normal circadian rhythms.

Authors:  Sung Han; Frank H Yu; Michael D Schwartz; Jonathan D Linton; Martha M Bosma; James B Hurley; William A Catterall; Horacio O de la Iglesia
Journal:  Proc Natl Acad Sci U S A       Date:  2012-01-05       Impact factor: 11.205

9.  Circadian expression and functional characterization of PEA-15 within the mouse suprachiasmatic nucleus.

Authors:  Kelin Wheaton; Sydney Aten; Lucas Sales Queiroz; Kyle Sullivan; John Oberdick; Kari R Hoyt; Karl Obrietan
Journal:  Eur J Neurosci       Date:  2018-02-19       Impact factor: 3.386

10.  Voluntary wheel running during adolescence distinctly alters running output in adulthood in male and female rats.

Authors:  Dvijen C Purohit; Atulya D Mandyam; Michael J Terranova; Chitra D Mandyam
Journal:  Behav Brain Res       Date:  2019-09-12       Impact factor: 3.332

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.