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. 2003 Mar 1;23(5):1688–1696. doi: 10.1523/JNEUROSCI.23-05-01688.2003

Fig. 5.

Fig. 5.

Saturation isotherms for the high-affinity Na+-dependent transport of glutamate in cortical (a), hippocampal (b), and striatal (c) synaptosomes prepared from end-stage G93A transgenic rats and age-matched controls. Glutamate uptake into P2 synaptosomal fractions was measured as described in Materials and Methods for the estimation of the kinetic parametersKm and Vmax. Initial rates of Na+-dependent glutamate uptake were expressed as picomoles per minute per milligram of synaptosomal protein after subtraction of the uptake observed in the absence of extracellular Na+ (equimolar replacement of NaCl with choline chloride). Kinetic constants Kmand Vmax were estimated from the saturation isotherm using the Michaelis-Menten equation and are presented in Table3. Data represent mean ± SEM values from three independent experiments.