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Norepinephrine Uptake Sites in the Locus Coeruleus of Rat Lines Selectively Bred for High and Low Alcohol Preference: A Quantitative Autoradiographic Binding Study Using [ 3 H]‐Tomoxetine
Author(s) -
Hwang Bang H.,
Wang GuoMing,
Wong David T.,
Lumeng Lawrence,
Li T.K.
Publication year - 2000
Publication title -
alcoholism: clinical and experimental research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.267
H-Index - 153
eISSN - 1530-0277
pISSN - 0145-6008
DOI - 10.1111/j.1530-0277.2000.tb02029.x
Subject(s) - locus coeruleus , norepinephrine , alcohol , galanin , chemistry , medicine , endocrinology , desipramine , central nervous system , biochemistry , neuropeptide , dopamine , biology , receptor , hippocampus , antidepressant
Background: The locus coeruleus (LC) is the largest norepinephrinergic cell group in the central nervous system and contains a high density of norepinephrine (NE) uptake sites. Alcohol‐preferring (AP) rats and high–alcohol‐drinking (HAD) rats are selectively bred for high alcohol preference, whereas alcohol‐nonpreferring (NP) rats and low–alcohol‐drinking (LAD) rats are bred for low alcohol preference. However, it is unknown whether NE uptake sites in the LC are associated with alcohol preference in AP and HAD rats when compared with their respective control rats, NP and LAD rats. This study was designed to examine this question. Methods: Animals were decapitated and brains were removed, frozen with dry ice powder, and stored in a deep freezer. The LC tissue blocks were cut into 14 μ cryostat sections, collected on glass slides, and incubated with 0.6 nM [ 3 H]‐tomoxetine in 50 mM Tris‐HCl buffer system. For nonspecific binding, 1 μM desipramine was added to the radioactive ligand. Sections were rinsed, quickly dried, and processed for quantitative autoradiography. In addition, galanin content in the LC was also studied. Results: The LC possessed a high density of [ 3 H]‐tomoxetine binding sites. There were fewer tomoxetine binding sites (fmol/mg protein) in the AP rats (433.0 ± 8.1) than in the NP rats (495.6 ± 3.7). HAD rats (386.5 ± 13.2) also possessed fewer tomoxetine binding sites than LAD rats (458.7 ± 10.1). Galanin content in the LC was similar between AP and NP rats and between HAD and LAD rats. Conclusions: Because both AP rats and HAD rats were selectively bred for alcohol preference, the finding of consistently low levels of [ 3 H]‐tomoxetine binding in the LC of these two lines of rats with high alcohol preference suggests that down‐regulation of NE transporters in the LC of AP and HAD rats may be associated with alcohol‐seeking behavior. A possible involvement of the coerulear NE uptake sites in depression is also discussed. Galanin in the LC may not relate to alcohol preference.