Hostname: page-component-78c5997874-g7gxr Total loading time: 0 Render date: 2024-11-17T18:26:17.228Z Has data issue: false hasContentIssue false

Somatostatin inhibits calcium influx into rat rod bipolar cell axonal terminals

Published online by Cambridge University Press:  10 April 2001

JULIETTE JOHNSON
Affiliation:
Department of Ophthalmology, UCSF, San Francisco
MICHAEL L. CARAVELLI
Affiliation:
Department of Neurobiology, UCLA School of Medicine, Los Angeles
NICHOLAS C. BRECHA
Affiliation:
Department of Neurobiology, UCLA School of Medicine, Los Angeles Department of Medicine, UCLA School of Medicine, Los Angeles Jules Stein Eye Institute, UCLA School of Medicine, Los Angeles CURE: Digestive Diseases Research Center, UCLA School of Medicine, Los Angeles VA Greater Los Angeles Healthcare System, Los Angeles

Abstract

In the retina, somatostatin (SST), an inhibitory peptide that influences neuronal activity, is predominantly expressed by sparsely occurring amacrine cells. The SST subtype 2A receptor is expressed by rod bipolar cells, including their axonal terminals. We used Ca2+-imaging techniques and the ratiometric Ca2+ indicator dye fura-2 AM to investigate Ca2+ dynamics in rod bipolar cell terminals. Depolarization of rod bipolar cells by the addition of high K+ (50 or 100 mM) elicited a sustained increase in [Ca2+]i in rod bipolar terminals that returned to basal levels following K+ removal. The Ca2+ response was dependent on extracellular Ca2+, and was inhibited by the Ca2+ channel blocker Cd2+ and by the selective L-type Ca2+ channel blocker, nimodipine. SST inhibited a K+ depolarization-induced [Ca2+]i response in rod bipolar terminals. This inhibition was observed with 1 nM SST and was maximal with 1 μM SST. These findings indicate that SST may regulate transmitter release from rod bipolar terminals by activating the SST subtype 2A receptor through modulation of intracellular Ca2+.

Type
Research Article
Copyright
2001 Cambridge University Press

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)