Literature DB >> 16687300

Daily torpor alters multiple gene expression in the suprachiasmatic nucleus and pineal gland of the Djungarian hamster (Phodopus sungorus).

Annika Herwig1, Florent Revel, Michel Saboureau, Paul Pévet, Stephan Steinlechner.   

Abstract

Circadian rhythms are still expressed in animals that display daily torpor, implying a temperature compensation of the pacemaker. Nevertheless, it remains unclear how the clock works in hypothermic states and whether torpor itself, as a temperature pulse, affects the circadian system. To reveal changes in the clockwork during torpor, we compared clock gene and neuropeptide expression by in situ hybridization in the suprachiasmatic nucleus (SCN) and pineal gland of normothermic and torpid Djungarian hamsters (Phodopus sungorus). Animals from light-dark (LD) 8ratio16 were sacrificed at 8 time points throughout 24 h. To investigate the effect of a previous torpor episode on the clock, we sacrificed a group of normothermic hamsters 1 day after torpor. In normothermic animals, Per1 peaked at zeitgeber time (ZT)4; whereas, Bmal1 reached maximal expression between ZT16 and ZT19. AVP mRNA in the SCN showed highest levels at ZT7. On the day of torpor, the levels of all mRNAs investigated, except for AVP mRNA, were increased during the torpor bout. Moreover, the Bmal1 rhythm was advanced. On the day after the hypothermia, Bmal1 and AVP rhythms showed severely depressed amplitude. Those distinct amplitude changes of Bmal1 and AVP on the day after a torpor episode expression suggests that torpor affects the circadian system, probably by altered translational processes that might lead to a modified protein feedback on gene expression. In the pineal gland, an important clock output, Aanat expression, peaked between ZT16 and ZT22 in normothermic animals. Aanat levels were significantly advanced on the day of hypothermia, an effect which was still visible 1 day afterward. In summary, this study showed that daily torpor affects the phase and amplitude of rhythmic clock gene and clock-controlled gene expression in the SCN. Furthermore, the rhythmic gene expression in a peripheral oscillator, the pineal gland, is also affected.

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Year:  2006        PMID: 16687300     DOI: 10.1080/07420520500522424

Source DB:  PubMed          Journal:  Chronobiol Int        ISSN: 0742-0528            Impact factor:   2.877


  4 in total

1.  The circadian clock stops ticking during deep hibernation in the European hamster.

Authors:  Florent G Revel; Annika Herwig; Marie-Laure Garidou; Hugues Dardente; Jérôme S Menet; Mireille Masson-Pévet; Valérie Simonneaux; Michel Saboureau; Paul Pévet
Journal:  Proc Natl Acad Sci U S A       Date:  2007-08-21       Impact factor: 11.205

2.  Seasonal loss and resumption of circadian rhythms in hibernating arctic ground squirrels.

Authors:  Cory T Williams; Maya Radonich; Brian M Barnes; C Loren Buck
Journal:  J Comp Physiol B       Date:  2017-03-22       Impact factor: 2.200

Review 3.  Is Adenosine Action Common Ground for NREM Sleep, Torpor, and Other Hypometabolic States?

Authors:  Alessandro Silvani; Matteo Cerri; Giovanna Zoccoli; Steven J Swoap
Journal:  Physiology (Bethesda)       Date:  2018-05-01

4.  Hypothalamic control systems show differential gene expression during spontaneous daily torpor and fasting-induced torpor in the Djungarian hamster (Phodopus sungorus).

Authors:  Ceyda Cubuk; Hanna Markowsky; Annika Herwig
Journal:  PLoS One       Date:  2017-10-12       Impact factor: 3.240

  4 in total

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