JN Fuel your research with LabChart
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


J Neurophysiol 72: 2864-2874, 1994;
0022-3077/94 $5.00
This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Baines, R. A.
Right arrow Articles by Bacon, J. P.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Baines, R. A.
Right arrow Articles by Bacon, J. P.

Journal of Neurophysiology, Vol 72, Issue 6 2864-2874, Copyright © 1994 by APS


ARTICLES

Pharmacological analysis of the cholinergic input to the locust VPLI neuron from an extraocular photoreceptor system

R. A. Baines and J. P. Bacon
Sussex Centre for Neuroscience, University of Sussex, Brighton, United Kingdom.

1. The brain of the locust contains an extraocular photoreceptor (EOP), which provides the major synaptic excitation to the vasopressin-like immunoreactive (VPLI) interneuron of the suboesophageal ganglion. Although the precise location of the EOP remains unknown, its activity can be determined indirectly by intracellular recording from the VPLI neuron. The excitatory drive to the VPLI neuron occurs only in darkness and is absent in the light. 2. The EOP is preferentially sensitive to light of wavelength 494 +/- 7 (SD) nm (blue-green) and has an absorption spectrum characteristic of a rhodopsin-like photopigment. 3. In the presence of high divalent saline (20 mM Ca2+ and Mg2+), the VPLI neuron receives excitatory input in the light. This indicates that the excitatory input to the VPLI neuron is from a tonically active descending input, which normally is inhibited by the light-induced activation of the presynaptic EOP. 4. Stimulation of the connectives while recording the resultant excitatory postsynaptic potential (EPSP) evoked in VPLI shows that the descending input projects beyond the suboesophageal ganglion, extending as far as the metathoracic ganglion. 5. Pharmacological analysis shows that the descending input to the VPLI neuron is cholinergic: acetylcholine (ACh) strongly depolarizes the neuron and eserine, an ACh esterase inhibitor, markedly potentiates the synaptic excitation of the VPLI neuron. 6. Nicotinic and muscarinic receptor antagonists show that the excitation of VPLI consists of two pharmacologically discrete components. Nicotinic ACh receptors mediate a fast depolarization, whereas muscarinic ACh receptors evoke a more sustained depolarization. Accordingly, both a fast and slow depolarization can be evoked selectively in VPLI by direct application of either nicotine or muscarine. 7. Voltage-clamp analysis shows that the fast EPSP evoked current is similar to that produced by nicotine in that it decreases linearly with membrane depolarization. The current associated with the sustained depolarization is similar to that evoked by muscarine, increasing nonlinearly with membrane depolarization. 8. Activity of the descending input, or application of muscarine, lowers the spike-initiation threshold of the VPLI neuron, thereby increasing its excitability. 9. It is concluded that the presence of two ACh receptor subtypes act synergistically to allow continuous activity of the VPLI neuron for sustained periods (i.e., throughout the hours of darkness).


This article has been cited by other articles:


Home page
J. Neurophysiol.Home page
C. Wegener, Y. Hamasaka, and D. R. Nassel
Acetylcholine Increases Intracellular Ca2+ Via Nicotinic Receptors in Cultured PDF-Containing Clock Neurons of Drosophila
J Neurophysiol, February 1, 2004; 91(2): 912 - 923.
[Abstract] [Full Text] [PDF]


Home page
J. Exp. Biol.Home page
B Wenzel and B Hedwig
Neurochemical control of cricket stridulation revealed by pharmacological microinjections into the brain
J. Exp. Biol., January 8, 1999; 202(16): 2203 - 2216.
[Abstract] [PDF]


Home page
J. Neurosci.Home page
R. A. Baines and M. Bate
Electrophysiological Development of Central Neurons in the Drosophila Embryo
J. Neurosci., June 15, 1998; 18(12): 4673 - 4683.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Visit Other APS Journals Online