Hostname: page-component-78c5997874-lj6df Total loading time: 0 Render date: 2024-11-11T08:36:56.533Z Has data issue: false hasContentIssue false

A dissection of the electroretinogram from the isolated rat retina with microelectrodes and drugs

Published online by Cambridge University Press:  01 July 1999

DANIEL G. GREEN
Affiliation:
Department of Ophthalmology, University of Michigan, Ann Arbor Department of Biomedical Engineering, University of Michigan, Ann Arbor
NATALIA V. KAPOUSTA-BRUNEAU
Affiliation:
Department of Ophthalmology, University of Michigan, Ann Arbor

Abstract

The origins of the a- and b-wave of the ERG were studied using simultaneous recordings made across the receptor layer and the full thickness of a piece of isolated albino rat retina. An inwardly directed current flowing across the rod outer segments was eliminated from the recording when postsynaptic activity was blocked with cobalt or when current source density measurements were made along the length of the outer segments. Rod photovoltages were inferred by removing extraneous field potentials from the recordings made across the photoreceptor layer. The spatial properties of the photovoltage indicates the responses came from an area about 100 μm in diameter. The glutamate analog, APB, which blocks depolarizing bipolar cells, eliminated the b-wave but left the a-wave unaffected. The ERG component due to depolarizing bipolar cells was inferred by subtracting recordings obtained before and after APB. After treatment with APB a slow component remained. This component was completely blocked by barium (200 μM), which blocks potassium channels on Müller cells. Barium had virtually no effect on low-intensity photovoltages but did affect the amplitude and shape of the saturated responses. Barium increased the amplitude of the component of the ERG which underlies the b-wave. It was concluded that the depolarizing bipolar cells directly generate the b-wave of the ERG.

Type
Research Article
Copyright
1999 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.)