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. 2002 Nov 1;22(21):9210–9220. doi: 10.1523/JNEUROSCI.22-21-09210.2002

Table 5.

Quantitative autoradiography of ORL1 receptor binding in wild-type (+/+) and homozygous (−/−) A2A mutant mice

Region Segments from rat atlas [3H]nociceptin-specific binding (fmol/mg) % Change in binding
Wild-type (+/+) Homozygous (−/−) (−/−)
Cervical C1 and C6
 Superficial layers (laminas I and II) 52.9  ± 3.6 55.8  ± 6.3 5.5
 Laminas III–VII 36.9  ± 1.7 36.5  ± 1.9 −1.1
 Lamina X 46.8  ± 3.7 50.5  ± 2.8 7.9
 Laminas VIII and IX 20.4  ± 1.4 19.0  ± 2.1 −6.9
 Dorsal horn (laminas I–VI) 40.8  ± 2.1 42.0  ± 2.7 2.9
Thoracic T3 and T6
 Superficial layers (laminas I and II) 54.6  ± 3.6 67.8  ± 8.5 24.2
 Laminas III–VII 45.9  ± 2.5 48.8  ± 2.6 6.3
 Lamina X 54.0  ± 2.8 57.7  ± 2.6 6.9
 Laminas VIII and IX 23.7  ± 1.0 23.1  ± 1 −2.5
 Dorsal horn (laminas I–VI) 48.3  ± 3.3 54.4  ± 4.6 12.6
Sacral S4
 Superficial layers (laminas I and II) 66.3  ± 3.6 75.6  ± 11.2 14.0
 Laminas III–VII 50.5  ± 1.8 51.4  ± 2.6 1.8
 Lamina X 73.6  ± 6.6 82.1  ± 7.2 11.5
 Laminas VIII and IX 24.0  ± 1.7 22.4  ± 1.3 −6.7
 Dorsal horn (laminas I–VI) 56.2  ± 2.3 59.2  ± 5.6 5.3

The mean specific binding (n = 4) of [3H]nociceptin (femtomoles per milligram) ± SEM in spinal cord regions of wild-type (+/+) and homozygous (−/−) A2A receptor knock-out mice. Measurements in the regions were performed at the bregma coordinates taken from the rat atlas ofPaxinos and Watson (1986). Regional determinates were made from both left and right sides of the sections, which were cut 300 μm apart. The labeling was performed on sections from +/+ and −/− mice in a completely paired protocol. Specific binding was >90% in all regions. Comparison of genotypes was not statistically significant (p > 0.05; ANOVA). The percentage (%) change in binding represents the change in binding levels in −/− spinal cords compared with +/+. A minus sign indicates a percentage decrease in binding levels. The overall mean and median percentage changes across regions were 5.3 and 5.3%, respectively.