, 2009). When taken together, these considerations have supported the conceptualisation of ascending systems as exerting powerful modulatory, but primarily nonspecific, functions such as ‘arousal’, ‘activation’, ‘information gating’, or ‘increasing the signal-to-noise ratio’. The intuitive allure of these traditional views persists in the contemporary

literature (e.g. Hornung, 2003; Eggermann & Feldmeyer, 2009; Lee & Dan, 2012; Sara & Bouret, 2012; Moran et al., 2013; Varela, 2013). The usefulness of such poorly-defined functional concepts for guiding research on the functions of ascending systems has been questioned selleck compound (Robbins & Everitt, 1995). Moreover, newer evidence concerning the basal forebrain system indicates a highly structured and topographic organisation of efferent projections and the presence of clusters of cholinergic terminals in the cortical innervation space (e.g., Zaborszky, 2002; Zaborszky et al., 2008, 2013). The presence of phasic actions of ascending neurotransmitter systems (Dayan & Yu, 2006; Parikh et al., 2007; Howells et al., 2012) further challenges the classification of the neurotransmitters of

ascending projection systems as strictly neuromodulators (Parikh & Sarter, 2008; Dayan, 2012; Marder, 2012; Picciotto et al., 2012; Sun et al., 2013). Below we review Dabrafenib supplier the available evidence in support of the hypothesis that basal forebrain cholinergic Protein kinase N1 projections to the cortex form an integral part of cortical circuitry, capable of mediating, as opposed to modulating, discrete cognitive and behavioral functions. In other words, cortical and subcortical projections employ cholinergic

inputs to contribute to cortical information processing (Fig. 1). Furthermore, these cholinergic inputs themselves are subject to neuromodulation by cortical and subcortical input (Fig. 1; below). This review does not cover the basic organisation of the cholinergic system and evidence indicating neuromodulatory functions (Wenk, 1997; Deco & Thiele, 2008; Schliebs & Arendt, 2011; Picciotto et al., 2012). Rather, we will focus specifically on the evidence in support of the idea that cortical circuitry integrates a component of the ascending systems to support cortical information processing and therefore has deterministic functions. By reviewing the evidence in support of this hypothesis we are not rejecting the importance or presence of a neuromodulatory component of ascending systems, including a component of the cortically-projecting basal forebrain cholinergic system (St Peters et al., 2011; see also further below for a conceptualisation of cholinergic neuromodulation). Rather, we propose that separate from and in addition to their role as a neuromodulator, these ascending projections take part in highly specialised cortical information processing (Aston-Jones & Cohen, 2005; Zaborszky et al.