J Physiol Wellcome Trust-funded researchers
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH
 QUICK SEARCH:   [advanced]


     


Physiology in Press

First published online on September 1, 2005.
Copyright © 2005 by The Physiological Society
This Article
Right arrow Full Text (Rapid PDF)
Right arrow All Versions of this Article:
569/2/575    most recent
jphysiol.2005.092239v1
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 Xu, J.
Right arrow Articles by Slaughter, M. M.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Xu, J.
Right arrow Articles by Slaughter, M. M.

Received June 7, 2005
Revised July 7, 2005
Accepted after revision September 1, 2005

Photoreceptor encoding of supersaturating light stimuli in salamander retina

Jianwei Xu1, Mingli Hou2, and Malcolm M. Slaughter2*

1 University of Pennsylvania
2 University at Buffalo

* To whom correspondence should be addressed. E-mail: mslaught{at}buffalo.edu.

In the dark adapted salamander retina, spikes could be elicited from rods under normal physiological conditions. Spike activity was observed in rods during the recovery phase of the response to saturating light. These action potentials were calcium spikes, blocked by cadmium and L-type calcium channel blockers. In response to light stimuli that saturate the rod peak response, calcium action potentials occurred with a delay that depended on light intensity, with stronger light increasing spike latency. Therefore, these spikes encode rod visual information at light intensities beyond rod saturation. Postsynaptic currents of similar time course were observed in second and third order neurons. Since rods exposed to brighter light stimuli produced more delayed spike activity, these signals might contribute to negative afterimages.


Key words: Calcium action potential • Photoreceptor • Retinal rod




This article has been cited by other articles:


Home page
IOVSHome page
A. S. Pawar, N. M. Qtaishat, D. M. Little, and D. R. Pepperberg
Recovery of Rod Photoresponses in ABCR-Deficient Mice
Invest. Ophthalmol. Vis. Sci., June 1, 2008; 49(6): 2743 - 2755.
[Abstract] [Full Text] [PDF]


Home page
IOVSHome page
B. Wissinger, S. Dangel, H. Jagle, L. Hansen, B. Baumann, G. Rudolph, C. Wolf, M. Bonin, K. Koeppen, T. Ladewig, et al.
Cone Dystrophy with Supernormal Rod Response Is Strictly Associated with Mutations in KCNV2
Invest. Ophthalmol. Vis. Sci., February 1, 2008; 49(2): 751 - 757.
[Abstract] [Full Text] [PDF]


Home page
J. Physiol.Home page
R. Heidelberger
Mechanisms of tonic, graded release: lessons from the vertebrate photoreceptor
J. Physiol., December 15, 2007; 585(3): 663 - 667.
[Abstract] [Full Text] [PDF]


Home page
J. Physiol.Home page
M. J. Palmer
Modulation of Ca2+-activated K+ currents and Ca2+-dependent action potentials by exocytosis in goldfish bipolar cell terminals
J. Physiol., May 1, 2006; 572(3): 747 - 762.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH
Copyright © 2005 The Physiological Society.