Midbrain dopamine receptor availability is inversely associated with novelty-seeking traits in humans.
Midbrain dopamine receptor availability is inversely associated with novelty-seeking traits in humans.
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DOI:
10.1523/jneurosci.2423-08.2008
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发表时间:
2008-12-31
期刊:
影响因子:
--
通讯作者:
Kessler RM
中科院分区:
文献类型:
--
作者:
Zald DH;Cowan RL;Riccardi P;Baldwin RM;Ansari MS;Li R;Shelby ES;Smith CE;McHugo M;Kessler RM
Novelty seeking personality traits are a major risk factor for the development of drug abuse and other unsafe behaviors. Rodent models of temperament indicate that high novelty responding is associated with decreased inhibitory autoreceptor control of midbrain dopamine neurons. It has been speculated that individual differences in dopamine functioning also underlie the personality trait of novelty seeking in humans. However, differences in the dopamine system of rodents and humans, as well as the methods for assessing novelty responding/seeking across species leave unclear to what extent the animal models inform our understanding of human personality. In the present study we examined the correlation between novelty seeking traits in humans and D2-like (D2/D3) receptor availability in the substantia nigra/ventral tegmental area. Based on the rodent literature we predicted that novelty seeking would be characterized by lowered levels of D2-like (auto)receptor availability in the midbrain. 34 healthy adults (18 men, 16 women) completed the Tridimensional Personality Questionnaire-Novelty Seeking Scale and PET scanning with the D2/D3 ligand [18F]fallypride. Novelty seeking personality traits were inversely associated with D2-like receptor availability in the ventral midbrain, an effect that remained significant after controlling for age. We speculate that the lower midbrain (auto)receptor availability seen in high novelty seekers leads to accentuated dopaminergic responses to novelty and other conditions that induce DA release.