Literature DB >> 2341986

Circadian and light-induced conductance changes in putative pacemaker cells of Bulla gouldiana.

M R Ralph1, G D Block.   

Abstract

The ocular circadian rhythm of compound action potential frequency in Bulla gouldiana is driven by rhythmic changes in the membrane potential of putative circadian pacemaker cells. Changes in the membrane potential of these neurons is required for light-induced phase shifts of the rhythm. We have tested the proposition that these changes in membrane potential reflect underlying changes in ionic conductances. We have found that: 1. Membrane conductance in the dark is highest during the subjective night when the cells are hyperpolarized, decreases as the cells depolarize spontaneously near projected dawn and is lowest during the subjective day. The changes in membrane potential and conductance follow a similar time course. 2. Long pulses of light delivered to eyes during their subjective night produce a characteristic response: There is initially a large, phasic depolarization accompanied by a burst of CAPs; this is followed by a repolarizing phase during which CAP activity is reduced to zero; and finally a tonic depolarization develops that is accompanied by a resumption of CAP activity at a steady rate. 3. During the subjective night, the tonic depolarization is accompanied by a decrease in conductance compared to the previous dark value. However, light pulses of similar duration delivered to eyes during their subjective day causes tonic depolarizations and increased CAP activity, but no measurable change in conductance. 4. Membrane responses to light are sensitive to agents that reduce Ca2+ flux. Light pulses during the subjective night produce a phasic depolarization, but the repolarization phase is eliminated in low Ca2+/EGTA seawater and is reduced in 5 mM Ni2+.(ABSTRACT TRUNCATED AT 250 WORDS)

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Year:  1990        PMID: 2341986     DOI: 10.1007/bf00240008

Source DB:  PubMed          Journal:  J Comp Physiol A            Impact factor:   1.836


  11 in total

1.  Dye marking neurons in the eye of Aplysia.

Authors:  J W Jacklet
Journal:  Comp Biochem Physiol A Comp Physiol       Date:  1976

2.  Localization of a circadian pacemaker in the eye of a mollusc, bulla.

Authors:  G D Block; S F Wallace
Journal:  Science       Date:  1982-07-09       Impact factor: 47.728

3.  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

4.  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

5.  Spontaneous and light-induced compound action potentials in the isolated eye of Aplysia: initiation and synchronization.

Authors:  G Audesirk
Journal:  Brain Res       Date:  1973-09-14       Impact factor: 3.252

Review 6.  Calcium channel.

Authors:  S Hagiwara; L Byerly
Journal:  Annu Rev Neurosci       Date:  1981       Impact factor: 12.449

7.  Adenylate cyclase activation shifts the phase of a circadian pacemaker.

Authors:  A Eskin; J S Takahashi
Journal:  Science       Date:  1983-04-01       Impact factor: 47.728

8.  Calcium channels mediate phase shifts of the Bulla circadian pacemaker.

Authors:  S B Khalsa; G D Block
Journal:  J Comp Physiol A       Date:  1988-12       Impact factor: 1.836

9.  Mechanism of calcium-dependent inactivation of a potassium current in Aplysia neuron R15: interaction between calcium and cyclic AMP.

Authors:  R H Kramer; E S Levitan; M P Wilson; I B Levitan
Journal:  J Neurosci       Date:  1988-05       Impact factor: 6.167

10.  The calcium current of Helix neuron.

Authors:  N Akaike; K S Lee; A M Brown
Journal:  J Gen Physiol       Date:  1978-05       Impact factor: 4.086

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  1 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

  1 in total

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