Literature DB >> 6281380

Increasing external K+ blocks phase shifts in a circadian rhythm produced by serotonin or 8-benzylthio-cAMP.

A Eskin.   

Abstract

Serotonin (5-HT) phase shifts the circadian rhythm from the isolated eye of Aplysia. The discovery of the mechanisms involved in phase shifting by 5-HT may help elucidate the nature of the circadian oscillator. We have found that 5-HT appears to phase shift by causing a change in membrane K+ conductance. Solutions containing zero K+(0-K+) phase shift the rhythm and the phase response curve (PRC) for 0-K+ is similar to one previously obtained for 5-HT. The similarity in PRCs for 0-K+ and 5-HT suggested that these treatments may be phase shifting the rhythm through a common mechanism. The nonadditivity of phase shifting by 0-K+ and 5-HT supports this suggestion. A common mechanism of action of 5-HT and 0-K+ might be effects on membrane potentials. The possible involvement of a membrane potential change in mediating the effect of 5-HT and the lack of an effect of large reductions in Na+, Cl-, and Ca2+ ions on phase shifting by 5-HT led us to examine the role of K+ ions in phase shifting by 5-HT. A change in K+ conductance may mediate the effects of 5-HT on the rhythm because HiK (30mM) solutions blocked the phase shift normally produced by 5-HT. The conductance change produced by 5-HT may be an increase in K+ conductance which would produce a hyperpolarization and not a decrease in K+ conductance which would produce a depolarization since depolarizing treatments, HiK (30-110mM), had no effect on the rhythm at the phase where 5-HT produces its largest phase shifts. Since we previously found that the effects of 5-HT appear to be mediated by cAMP, we examined whether HiK solutions could block the effects of 8-benzylthio-cAMP on the rhythm. HiK (40mM) blocked the phase shifts normally produced by 8-benylthio-cAMP. Our working hypothesis for the 5-HT phase-shifting pathway based on these results is 5-HT leads to increased cAMP leads to elevates K+ conductance leads to membrane hyperpolarization leads to phase shifts the rhythm.

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Year:  1982        PMID: 6281380     DOI: 10.1002/neu.480130305

Source DB:  PubMed          Journal:  J Neurobiol        ISSN: 0022-3034


  6 in total

1.  Dopamine D₄ receptor activation controls circadian timing of the adenylyl cyclase 1/cyclic AMP signaling system in mouse retina.

Authors:  Chad R Jackson; Shyam S Chaurasia; Christopher K Hwang; P Michael Iuvone
Journal:  Eur J Neurosci       Date:  2011-06-16       Impact factor: 3.386

2.  The Bulla ocular circadian pacemaker. II. Chronic changes in membrane potential lengthen free running period.

Authors:  D G McMahon; G D Block
Journal:  J Comp Physiol A       Date:  1987-08       Impact factor: 1.836

3.  The Bulla ocular circadian pacemaker. I. Pacemaker neuron membrane potential controls phase through a calcium-dependent mechanism.

Authors:  D G McMahon; G D Block
Journal:  J Comp Physiol A       Date:  1987-08       Impact factor: 1.836

4.  Calcium plays a central role in phase shifting the ocular circadian pacemaker of Aplysia.

Authors:  C S Colwell; D Whitmore; S Michel; G D Block
Journal:  J Comp Physiol A       Date:  1994-10       Impact factor: 1.836

5.  Evidence that potassium channels mediate the effects of serotonin on the ocular circadian pacemaker of Aplysia.

Authors:  C S Colwell; S Michel; G D Block
Journal:  J Comp Physiol A       Date:  1992-12       Impact factor: 1.836

6.  Requirement for protein synthesis in the regulation of a circadian rhythm by serotonin.

Authors:  A Eskin; S J Yeung; M R Klass
Journal:  Proc Natl Acad Sci U S A       Date:  1984-12       Impact factor: 11.205

  6 in total

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