Abstract: |
The μ opioid receptor (MOR-1) mRNA was quantified in rat CNS by a sensitive solution hybridization (SH) technique, employing a 32P-labeled riboprobe derived from the coding region of MOR-1cDNA. In a Northern blot analysis this riboprobe hybridized to a 14 kb form of rat MOR-1 mRNA. The linear range of SH assay extends from 1 to 250 pg of MOR-1 sense transcript (equivalent to 9.3- 2325 pg of MOR-1 mRNA). A microdissection technique for reproducible sampling of selected CNS regions,followed by the SH assay, allowed for a quantitative study of MOR-1 mRNA distribution. The highest levels of MOR-1 mRNA were present in medial thalamus (17.8 ± 0.3 pg/μg RNA), and the lowest in the cerebellum (0.4 ± 0.1 pg/μg RNA). Hypothalamus, dorsal spinal horn, nucleus raphe, periaqueductal gray, and sensorimotor cortex contained intermediate levels. This distribution closely parallels the pattern of μ receptor binding, suggesting that both the mRNA and the receptor protein are colocalized within most of the regions studied. © Rapid Communications of Oxford Ltd. |
Keywords: |
controlled study; nonhuman; sensitivity and specificity; linear models; reproducibility of results; animal; animal tissue; central nervous system; amino acid sequence; molecular sequence data; messenger rna; rna, messenger; spinal cord; rat; reference values; rats; rats, sprague-dawley; mu opiate receptor; brain region; receptors, opioid, mu; northern blotting; rna probes; male; priority journal; article; brain regions; support, non-u.s. gov't; support, u.s. gov't, p.h.s.; adult rat; rna quantitation; solution hybridization; μ opioid receptor mrna
|