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. 2012 Jul 25;32(30):10226–10237. doi: 10.1523/JNEUROSCI.0007-12.2012

Table 1.

Expression levels of α6* nAChRs in α6-GFP mice determined by radioligand binding assays

[125I]-Epibatidine binding Control α6-GFP
CX MII-res 63.3 ± 8.2 55.0 ± 9.5
CX MII-sens 2.0 ± 2.2 0.2 ± 0.9
TH MII-res 101.4 ± 15.6 99.9 ± 4.1
TH MII-sens 5.3 ± 2.7 9.8 ± 1.1
ST MII-res 45.6 ± 4.9 42.5 ± 2.4
ST MII-sens 7.1 ± 0.9 10.5 ± 0.8
OT MII-res 30.3 ± 1.9 28.6 ± 2.3
OT MII-sens 7.1 ± 1.1 6.5 ± 0.7
SC MII-res 73.2 ± 13.0 81.7 ± 6.1
SC MII-sens 15.1 ± 1.8 12.7 ± 7.3
vMB MII-res 81.7 ± 6.8 87.1 ± 7.6
vMB MII-sens 6.0 ± 1.7 5.8 ± 2.1
CX cyt-res −0.6 ± 0.7 −0.2 ± 0.5
CX cyt-sens 65.9 ± 1.0 55.4 ± 0.8
TH cyt-res 4.3 ± 1.8 5.0 ± 1.4
TH cyt-sens 102.4 ± 2.6 104.6 ± 2.1
ST cyt-res 2.1 ± 0.0 2.1 ± 0.2
ST cyt-sens 47.5 ± 0.3 52.3 ± 0.0
OT cyt-res 3.8 ± 0.6 4.3 ± 0.5
OT cyt-sens 34.4 ± 0.9 29.6 ± 0.7
SC cyt-res 4.9 ± 1.2 4.8 ± 0.2
SC cyt-sens 79.0 ± 2.0 86.9 ± 0.8
vMB cyt-res 3.9 ± 0.8 3.9 ± 0.8
vMB cyt-sens 84.0 ± 2.0 89.0 ± 0.8

Each indicated brain region was dissected and the tissue was prepared for binding experiments as described in Materials and Methods. Samples were labeled with [125I]-epibatidine with or without competition with excess, unlabeled αCtxMII or cytisine. αCtxMII and cytisine-sensitive and -resistant components are shown. For all experiments, data from groups of α6-GFP and control (nontransgenic) littermate mice were compared. CX, cortex; OT, olfactory tubercle; SC, superior colliculus; ST, dorsal striatum; TH, thalamus; vMB, ventral midbrain. Data (in fmol/mg protein) are mean ± SEM (n = 5 mice).