Dopamine is generally accepted as a major neurotransmitter associated with
light-adaptive processes in the retina. However, little is known about its
precise release pattern in vivo, largely due to the lack of an unambiguous
method for the determination of dopamine release. We have found that vitrea
l levels of dihydroxyphenylacetic acid (DOPAC) reflect the rate of dopamine
release in chickens. Blocking re-uptake with nomifensine significantly low
ered vitreal DOPAC and retinal dopamine, confirming the retinal origin and
reliance of vitreal DOPAC on intact re-uptake mechanisms. Further, inhibiti
on of monoamine oxidase with pargyline reduced vitreal as well as retinal D
OPAC levels, confirming that the DOPAC detected is generated by monoamine o
xidase. Finally, we found that DOPAC diffused freely into and out of isolat
ed vitreous bodies and we found the vitreous to be metabolically inert with
respect to DOPAC, supporting the idea that vitreal levels of DOPAC are con
sequential to the retinal metabolism of dopamine. Exposure to light, which
is known to increase retinal dopamine release, readily increased vitreal DO
PAC levels. The accumulation of DOPAC in the vitreous over 6 h light fitted
a mathematical model of DOPAC accumulation based on zero-order influx (pro
portional to dopamine release rates) and diffusion driven, first-order effl
ux.