A comparison of D2 receptor specific binding in obese and normal‐weight individuals using PET with (N‐[11C]methyl)benperidol. Issue 11 (30th May 2013)
- Record Type:
- Journal Article
- Title:
- A comparison of D2 receptor specific binding in obese and normal‐weight individuals using PET with (N‐[11C]methyl)benperidol. Issue 11 (30th May 2013)
- Main Title:
- A comparison of D2 receptor specific binding in obese and normal‐weight individuals using PET with (N‐[11C]methyl)benperidol
- Authors:
- Eisenstein, Sarah A.
Antenor‐Dorsey, Jo Ann V.
Gredysa, Danuta M.
Koller, Jonathan M.
Bihun, Emily C.
Ranck, Samantha A.
ArbelÁez, Ana Maria
Klein, Samuel
Perlmutter, Joel S.
Moerlein, Stephen M.
Black, Kevin J.
Hershey, Tamara - Abstract:
- <abstract abstract-type="main"> <title>ABSTRACT</title> <p>Previous PET imaging studies have demonstrated mixed findings regarding dopamine D2/D3 receptor availability in obese relative to nonobese humans. Nonspecific D2/D3 radioligands do not allow for separate estimation of D2 receptor (D2R) and D3 receptor (D3R) subtypes of the D2 receptor family, which may play different roles in behavior and are distributed differently throughout the brain. These radioligands are also displaceable by endogenous dopamine, confounding interpretation of differences in receptor availability with differing levels of dopamine release. The present study used PET imaging with the D2R‐selective radioligand (<italic>N</italic>‐[<sup>11</sup>C] methyl)benperidol ([<sup>11</sup>C]NMB), which is nondisplaceable by endogenous dopamine, to estimate D2R specific binding (BP<sub>ND</sub>) and its relationship to body mass index (BMI) and age in 15 normal‐weight (mean BMI = 22.6 kg/m<sup>2</sup>) and 15 obese (mean BMI = 40.3 kg/m<sup>2</sup>) men and women. Subjects with illnesses or taking medications that interfere with dopamine signaling were excluded. Striatal D2R BP<sub>ND</sub> was calculated using the Logan graphical method with cerebellum as a reference region. D2R BP<sub>ND</sub> estimates were higher in putamen and caudate relative to nucleus accumbens, but did not differ between normal‐weight and obese groups. BMI values did not correlate with D2R BP<sub>ND</sub>. Age was negatively<abstract abstract-type="main"> <title>ABSTRACT</title> <p>Previous PET imaging studies have demonstrated mixed findings regarding dopamine D2/D3 receptor availability in obese relative to nonobese humans. Nonspecific D2/D3 radioligands do not allow for separate estimation of D2 receptor (D2R) and D3 receptor (D3R) subtypes of the D2 receptor family, which may play different roles in behavior and are distributed differently throughout the brain. These radioligands are also displaceable by endogenous dopamine, confounding interpretation of differences in receptor availability with differing levels of dopamine release. The present study used PET imaging with the D2R‐selective radioligand (<italic>N</italic>‐[<sup>11</sup>C] methyl)benperidol ([<sup>11</sup>C]NMB), which is nondisplaceable by endogenous dopamine, to estimate D2R specific binding (BP<sub>ND</sub>) and its relationship to body mass index (BMI) and age in 15 normal‐weight (mean BMI = 22.6 kg/m<sup>2</sup>) and 15 obese (mean BMI = 40.3 kg/m<sup>2</sup>) men and women. Subjects with illnesses or taking medications that interfere with dopamine signaling were excluded. Striatal D2R BP<sub>ND</sub> was calculated using the Logan graphical method with cerebellum as a reference region. D2R BP<sub>ND</sub> estimates were higher in putamen and caudate relative to nucleus accumbens, but did not differ between normal‐weight and obese groups. BMI values did not correlate with D2R BP<sub>ND</sub>. Age was negatively correlated with putamen D2R BP<sub>ND</sub> in both groups. These results suggest that altered D2R specific binding is not involved in the pathogenesis of obesity per se and underscore the need for additional studies evaluating the relationship between D3R, dopamine reuptake, or endogenous dopamine release and human obesity. Synapse <bold>67:748–756, 2013.</bold>. © 2013 Wiley Periodicals, Inc.</p> </abstract> … (more)
- Is Part Of:
- Synapse. Volume 67:Issue 11(2013:Nov.)
- Journal:
- Synapse
- Issue:
- Volume 67:Issue 11(2013:Nov.)
- Issue Display:
- Volume 67, Issue 11 (2013)
- Year:
- 2013
- Volume:
- 67
- Issue:
- 11
- Issue Sort Value:
- 2013-0067-0011-0000
- Page Start:
- 748
- Page End:
- 756
- Publication Date:
- 2013-05-30
- Subjects:
- Synapses -- Periodicals
612 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1098-2396 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/syn.21680 ↗
- Languages:
- English
- ISSNs:
- 0887-4476
- Deposit Type:
- Legaldeposit
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- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 8585.880200
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- 4059.xml