Abstract
The uptake of labeled L-glutamate by the isolated rat retina was measured over a large range of external concentrations (1 .mu.M-1mM). The results obtained from measurements of the initial velocity of L-glutamate uptake at different concentrations did not follow simple hyperbolic kinetics. The error structure of replicate velocity measurements was examined and found to be normally distributed and heteroscedastic. Descriptive models were fitted directly to data, weighted by the invariance, using non-linear regression analysis. The most suitable descriptive model consisted of a saturable hyperbola (Vm = 285 nmol/g wet wt per min, Km = 252 .mu.M) and a linear term (b = 0.45 min-1).