With regard to modification of GLUT1 transport rate, it is known from studies on red blood cells that GLUT1 can be substantially inhibited by binding of ATP, an effect that is inhibited by AMP. When ATP hydrolysis is stimulated, ATP concentrations decrease and AMP concentrations increase, both of these events acting to release inhibition of GLUT1 [322, 524]. This effect can be large, a four to tenfold increase in glucose transport. Because increased AMP can increase both recruitment and activity of GLUT1 at the cell surface, it is easily imagined that small changes in AMP levels in endothelial cells could increase glucose transport sufficiently to support increased nervous activity.