a1 Department of Psychiatry and Biobehavioral Sciences, UCLA, Los Angeles, CA, USA
a2 Veterans Administration Greater Los Angeles Healthcare System, Los Angeles, CA, USA
a3 Department of Physics, UC Irvine, Irvine, CA, USA
a4 Department of Molecular and Medical Pharmacology, UCLA, Los Angeles, CA, USA
a5 Brain Research Institute, UCLA, Los Angeles, CA, USA
Abstract
In previous research, nicotine-dependent men exhibited lower putamen D2/D3 dopamine-receptor availability than non-smokers (Fehr et al. 2008), but parallel assessments were not performed in women. Women and men (19 light smokers, 18 non-smokers) were tested for differences due to sex and smoking in striatal D2/D3 dopamine-receptor availability, using positron emission tomography with [18F]fallypride. Receptor availability was determined using a reference region method, in striatal volumes and in whole-brain, voxel-wise analysis. Significant sex×smoking interactions were observed in the caudate nuclei and putamen. Post-hoc t tests showed that male smokers had significantly lower D2/D3 dopamine-receptor availability than female smokers (−17% caudate, −21% putamen) and male non-smokers (−15% caudate, −16% putamen). Female smokers did not differ from non-smokers. Whole-brain analysis demonstrated no statistically significant voxels or clusters. These results suggest that low receptor availability may confer vulnerability to nicotine dependence or that smoking selectively affects D2/D3 receptor down-regulation in men but not women.
(Received June 07 2011)
(Reviewed July 28 2011)
(Revised November 18 2011)
(Accepted December 12 2011)
(Online publication January 16 2012)
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Correspondence:
c1 Address for correspondence: E. D. London, Ph.D., UCLA Semel Institute of Neuroscience and Biobehavioral Sciences, 760 Westwood Plaza, Rm. C8-831, Los Angeles, CA 90045, USA. Tel.: (310)825-0606 Fax: 310-825-0812 Email: elondon@mednet.ucla.edu