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Decreased Beta 2 *‐nicotinic acetylcholine receptor availability after chronic ethanol exposure in nonhuman primates
Author(s) -
Cosgrove Kelly P.,
Kloczynski Tracy,
Bois Frederic,
Pittman Brian,
Tamagnan Gilles,
Seibyl John P.,
Krystal John H.,
Staley Julie K.
Publication year - 2010
Publication title -
synapse
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.809
H-Index - 106
eISSN - 1098-2396
pISSN - 0887-4476
DOI - 10.1002/syn.20795
Subject(s) - ethanol , nicotinic acetylcholine receptor , medicine , beta (programming language) , endocrinology , self administration , cortex (anatomy) , nicotinic agonist , acetylcholine receptor , alcohol , chemistry , thalamus , anesthesia , pharmacology , receptor , psychology , neuroscience , biochemistry , computer science , programming language
Ethanol associated behaviors have been linked to the β 2 ‐subunit containing nicotinic acetylcholine receptors (β 2 *‐nAChR); however, there is conflicting evidence on ethanol‐induced changes in nAChR expression during and after chronic ethanol consumption. In this study, five male animals orally self‐administered ethanol for 18 ± 1 weeks. Animals were scanned with [ 123 I]5‐IA‐85380 and SPECT prior to ethanol self‐administration, and at 24 h and 5‐13 wks withdrawal. β 2 *‐nAChR availability was not significantly different from baseline at 24 h withdrawal, but was significantly decreased compared to baseline at 5‐13 wks withdrawal throughout the cortex and in the thalamus, but not the midbrain. The percent decrease in β 2 *‐nAChR availability from baseline to 5‐13 wks withdrawal in the parietal cortex was negatively correlated with total grams of ethanol consumed in lifetime and in the midbrain was negatively correlated with average daily ethanol consumption (g/kg). Prolonged withdrawal from chronic ethanol consumption is associated with a decrease in β 2 *‐nAChR availability. The decrease in β 2 *‐nAChR availability is influenced by alcohol consumption, suggesting the chronicity and severity of alcohol consumption may underlie persistent changes in β 2 *‐nAChR availability. Synapse 64:729–732, 2010. © 2010 Wiley‐Liss, Inc.