Table 1.
GluN1–1a | rise time (ms) | τfast (ms) | τslow (ms) | % fast | τw (ms) | n |
---|---|---|---|---|---|---|
A/A | 3.9 ± 0.3 | 87 ± 7 | - | 100a | 87 ± 7#,$ | 7 |
AC1/AC2 | 4.2 ± 0.9 | 78 ± 13 | - | 100a | 78 ± 13*,#,$ | 7 |
AC1/BC2 | 10.9 ± 6.2 | 93 ± 27 | 180 ± 62 | 63 ± 19 | 140 ± 10*,#,$ | 5 |
B/B | 14.9 ± 1.2 | 240 ± 23 | 1020 ± 72 | 59 ± 5 | 548 ± 45*,$ | 12 |
BC1/BC2 | 15.1 ± 2.7 | 205 ± 35 | 1045 ± 129 | 58 ± 8 | 533 ± 58*,$ | 8 |
BC1/DC2 | 10.9 ± 2.5 | 516 ± 42 | 3521 ± 446 | 54 ± 6 | 1767 ± 117*,#,$ | 6 |
D/D | 6.2 ± 0.7 | 832 ± 146 | 7436 ± 890 | 24 ± 3 | 5714 ± 458*,# | 7 |
DC1/DC2 | 8.6 ± 4.8 | 527 ± 225 | 6912 ± 848 | 17 ± 7 | 5700 ± 561*,# | 4 |
A/A | 4.8 ± 0.3 | 56 ± 6 | - | 100a | 56 ± 6#,$ | 6 |
AC1/AC2 | 6.3 ± 2.8 | 53 ± 7 | - | 100a | 53 ± 7#,$ | 5 |
AC1/BC2 | 3.7 ± 0.5 | 47 ± 4 | 160 ± 25 | 69 ± 12 | 74 ± 5*,#,$ | 5 |
B/B | 10.3 ± 1.5 | 81 ± 8 | 208 ± 49 | 58 ± 12 | 155 ± 19*,$ | 6 |
BC1/BC2 | 8.3 ± 1.6 | 101 ± 15 | 360 ± 89 | 84 ± 6 | 138 ± 13*,$ | 7 |
BC1/DC2 | 9.2 ± 1.3 | 127 ± 31 | 634 ± 132 | 50 ± 15 | 288 ± 22*,#,$ | 8 |
D/D | 3.5 ± 0.4 | 245 ± 32 | 1609 ± 148 | 40 ± 7 | 992 ± 68*,# | 10 |
DC1/DC2 | 4.5 ± 0.7 | 256 ± 92 | 1399 ± 141 | 14 ± 4 | 1230 ± 86*,# | 5 |
Responses from NMDA receptors expressed in Xenopus oocytes were measured using outside-out patch-clamp recordings. Naming of subtypes is such that e.g. A/A indicates diheteromeric GluN1/2A/2A receptors and AC1/AC2 indicates diheteromeric GluN1/2AC1/2AC2 receptors that contain the C1 and the C2 tags. Responses were activated by a brief application (3–5 ms) of 1 mM glutamate in the continuous presence of 100 μM glycine. Rise times are for 10–90% of the response amplitude, deactivation time constants were determined using two-exponential fits to obtain τfast, τslow, and % fast is the fitted percentage of the fast component.
indicates that only a single-exponential was fitted to the deactivation time course. Weighted time constants (τw) were calculated as τw = τfast · Ifast/(Ifast + Islow) + τslow · Islow/(Ifast + Islow). Data are mean ± SEM, and n is the number of patches used to generate the data. Deactivation rates (i.e. 1/τw) were used for statistical comparisons using one-way ANOVA with Tukey’s post hoc test.
indicates significantly different from A/A,
indicates significantly different from B/B, and §indicates significantly different from D/D.