Abstract
Serotonin has a major role in neural circuits of mood regulation, substance abuse, and neurodevelopment (Azmitia, Neuropsychopharmacology 21:1S–45S, 1999). Although they differ in cellular and anatomical location, the two brain proteins most strongly implicated in influencing serotonin levels are monoamine oxidase A and the serotonin transporter (Blier and De Montigny, J Neurosci 3:1270–1278, 1983; Bel and Artigas, Eur J Pharmacol 229:101–103, 1992; Synapse 15:243–245, 1993; Naunyn Schmiedebergs Arch Pharmacol 351:475–482, 1995; Dreshfield et al., Neurochem Res 21:557–562, 1996; Moret and Briley, Eur J Pharmacol 295:189–197, 1996; Mathews et al., Soc Neurosci 30:624, 2000; Youdim et al., Nat Rev Neurosci 7:295–309, 2006). Coincidentally, there have been major advances in positron emission tomography (PET) radioligand development for these two targets over the past decade, and the application of these advances has greatly increased our knowledge about fundamental processes in many important, impactful conditions including major depressive disorder, early postpartum, cigarette smoking, aggressive behavior, antidepressant development, ecstasy abuse, obsessive-compulsive disorder, and seasonal affective disorder as reviewed in this chapter.
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Meyer, J.H. (2014). Monoamine Oxidase A and Serotonin Transporter Imaging with Positron Emission Tomography. In: Dierckx, R., Otte, A., de Vries, E., van Waarde, A., Luiten, P. (eds) PET and SPECT of Neurobiological Systems. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-42014-6_25
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