Table 2

Effects of glutamate agonists on APP release from cortical and hippocampal slices

Glutamate agonistAPP release
Cortical slicesHippocampal slices
% of first 10-min period
l-Glutamic acid (μM)
 093  ± 4  (12)93  ± 3  (11)
 5100  ± 6  (4)116  ± 10  (6)
 50102  ± 8  (7)114  ± 6  (6)
 500139  ± 9  (13)2-a 124  ± 7  (11)2-a
trans-(1S,3R)-ACPD (μM)
 088  ± 6  (9)93  ± 6  (9)
 1152  ± 17  (6)2-a 128  ± 20  (8)
 10188  ± 13  (8)2-a 137  ± 18  (9)2-a
 100163  ± 16  (7)2-a 159  ± 17  (9)2-a
Quisqualic acid (μM)
 083  ± 4  (11)91  ± 5  (9)
 1108  ± 5  (11)2-a 127  ± 7  (9)2-a
 10114  ± 5  (11)2-a 125  ± 6  (9)2-a
 100118  ± 6  (11)2-a 114  ± 9  (9)
Kainic acid (μM)
 092  ± 6  (9)89  ± 4  (8)
 597  ± 7  (9)114  ± 6  (8)
 5095  ± 8  (9)97  ± 8  (8)
 500109  ± 8  (9)100  ± 8  (8)
AMPA (μM)
 086  ± 9  (9)92  ± 4  (8)
 196  ± 7  (9)109  ± 7  (8)
 1089  ± 6  (9)100  ± 6  (8)
 10092  ± 7  (9)107  ± 7  (8)
NMDA (μM)
 099  ± 6  (8)97  ± 7  (8)
 10115  ± 15  (9)94  ± 7  (8)
 100100  ± 12  (9)98  ± 9  (8)
 320111  ± 14  (8)102  ± 6  (8)

Cortical and hippocampal slices were perfused for 60 min (0.8 ml/min) and incubated for 20 min with Krebs’ medium. After an 80-min equilibration period, slices were incubated in 1 ml of Krebs’ medium for two consecutive 10-min periods. During the second 10-min incubation period, the incubation medium contained the concentrations of glutamate agonist indicated. Incubation media were removed at the end of each 10-min incubation period, and the slices were rinsed with 0.5 ml of Krebs’ medium and assayed as described in table 1. Data are mean ± S.E.M. The number of measurements is given in parentheses.

  • 2-a Significantly higher than the corresponding control (0) value.