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1 Department of Ophthalmology, The University of Chicago Chicago, Ill.
Histochemical and chemical evidence has suggested the existence of dopaminergic neurons at the junction of the retinal inner nuclear and inner plexiform layers. In order that dopamine be identified as the chemical transmitter of these neurons, its uptake into the retina and release as a result of retinal stimulation must be shown. The present study revealed that uptake of H3-dopamine into the retina after carotid infusion was not inhibited by superior cervical ganglionectomy. In addition, exogenous dopamine was degraded to expected metabolites after uptake, and these were identified chromatographically. Subsequently, an experimental preparation in cats called preretinal perfusion was developed, and retinal uptake and light-stimulated release of tritiated dopamine was measured in vivo. The material released was chromatographically identified as dopamine. In dark-adapted animals, the rate of release and the amount of dopamine released per light flash increased nonlinearly with increasing flash frequency. In light-adapted animals, high rates of dopamine release were found regardless of flash frequency. On the basis of this and other evidence reviewed and to be presented in subsequent papers, it is suggested that dopamine acts as an inhibitory retinal neurotransmitter which may mediate a neural component of retinal sensitivity control.
Note:
Presented in part at the Spring National Meeting of the Association for Research in Vision and Ophthalmology, April, 1971. Submitted in partial fulfillment of the requirements for the Ph.D. degree at the University of Chicago.
Reprint requests: Dr. Steven G. Kramer, Department of Ophthalmology, 950 E. 59th St., Chicago, Ill. 60637.
Key Words: dopamine catecholamines neurotransmission chemical transmission dopaminergic retina amacrine cell adrenergic junctional cell chromatography radiochromatography
Submitted on April 12, 1971
Accepted on April 16, 1971
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