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2019, NeuroscienceCitation Excerpt :Another, more recently identified clearance mechanism, called Uptake-2, involves at least two additional transporters: organic cation transporter 3 (OCT3; SLC22A3) and plasma membrane monoamine transporter (PMAT, SLC29A4; Eisenhofer, 2001; Engel et al., 2004; Koepsell et al., 2007; Wang, 2016). These two low-affinity/high-capacity, Na+-independent, polyspecific cation transporters are widely expressed in the central nervous system, including the dopaminergic (DAergic) nigro-striatal pathway (Stamford et al., 1986; Amphoux et al., 2006; Dahlin et al., 2007; Vialou et al., 2008; Cui et al., 2009; Duan and Wang, 2010; Miura et al., 2017) where they likely support DAT in regulating extracellular DA (Sader-Mazbar et al., 2013; Nishijima and Tomiyama, 2016). Although Uptake-2 has traditionally been described as ‘extraneuronal’ (mainly expressed in glia cells; Russ et al., 1996b; Inazu et al., 1999), more recent studies have demonstrated OCT3 and/or PMAT expression also in neurons, including the DAergic and non-DAergic neurons in ventral midbrain (Vialou et al., 2004; Dahlin et al., 2007; Vialou et al., 2007; Cui et al., 2009; Mayer et al., 2018).
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2006, Journal of Neuroscience MethodsWireless transmission of fast-scan cyclic voltammetry at a carbon-fiber microelectrode: Proof of principle
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