A thalamic reticular networking model of consciousness
© Min; licensee BioMed Central Ltd. 2010
Received: 9 December 2009
Accepted: 30 March 2010
Published: 30 March 2010
It is reasonable to consider the thalamus a primary candidate for the location of consciousness, given that the thalamus has been referred to as the gateway of nearly all sensory inputs to the corresponding cortical areas. Interestingly, in an early stage of brain development, communicative innervations between the dorsal thalamus and telencephalon must pass through the ventral thalamus, the major derivative of which is the thalamic reticular nucleus (TRN). The TRN occupies a striking control position in the brain, sending inhibitory axons back to the thalamus, roughly to the same region where they receive afferents.
The present study hypothesizes that the TRN plays a pivotal role in dynamic attention by controlling thalamocortical synchronization. The TRN is thus viewed as a functional networking filter to regulate conscious perception, which is possibly embedded in thalamocortical networks. Based on the anatomical structures and connections, modality-specific sectors of the TRN and the thalamus appear to be responsible for modality-specific perceptual representation. Furthermore, the coarsely overlapped topographic maps of the TRN appear to be associated with cross-modal or unitary conscious awareness. Throughout the latticework structure of the TRN, conscious perception could be accomplished and elaborated through accumulating intercommunicative processing across the first-order input signal and the higher-order signals from its functionally associated cortices. As the higher-order relay signals run cumulatively through the relevant thalamocortical loops, conscious awareness becomes more refined and sophisticated.
I propose that the thalamocortical integrative communication across first- and higher-order information circuits and repeated feedback looping may account for our conscious awareness. This TRN-modulation hypothesis for conscious awareness provides a comprehensive rationale regarding previously reported psychological phenomena and neurological symptoms such as blindsight, neglect, the priming effect, the threshold/duration problem, and TRN-impairment resembling coma. This hypothesis can be tested by neurosurgical investigations of thalamocortical loops via the TRN, while simultaneously evaluating the degree to which conscious perception depends on the severity of impairment in a TRN-modulated network.
The subjective experience of consciousness is central to our everyday life. However, whether such subjective experiences have neural correlates remains unsolved and open to hypothesis and investigation. For instance, Lamme  supported the notion that feedback connections to the primary visual cortex are necessary for visual awareness, and proposed that a progressive build-up of recurrent interactions results in conscious awareness. Dehaene et al. , in their 'global workspace' model of consciousness, suggested that conscious perception is systematically associated with parieto-frontal activity, causing top-down amplification. On the other hand, Zeki  argued against a single entity of consciousness, claiming that there are multiple hierarchical consciousnesses (the micro-consciousnesses). Therefore, we need a unified theory to integrate these previous theories and provide us with a clearer understanding of all the phenomena of consciousness.
Consciousness: A mental state embodied through TRN-modulated synchronization of thalamocortical networks
As the cortex has gradually evolved to be competent in higher cognition, the thalamus has evolved in parallel . All the thalamocortical pathways may in fact constitute a unified and cyclic oscillatory circuit that is topographically organized . Interestingly, in an early stage of brain development, communicative innervations between the dorsal thalamus and telencephalon must pass through the ventral thalamus , the major component of which is the thalamic reticular nucleus (TRN), a sheer laminar wrapping around the thalamus. It is worth noting that the TRN occupies a striking control position in the brain. The cerebral cortex and thalamus connect in a reciprocal manner, branching onto the TRN as shown in Figure 1. In turn, the TRN sends axons back to the thalamus, roughly to the same region where they receive afferents . The TRN provides a major inhibitory input to thalamic relay nuclei . The inhibitory TRN cells are densely innervated by collaterals from thalamocortical and corticothalamic neurons, both of which generate strong excitatory postsynaptic potentials .
Synchronization within a certain neuronal ensemble is achieved by means of GABAergic inhibitory neurons. For instance, it has been reported that neuronal synchronization is completed via a GABAergic internetwork in some pace-making sources such as the suprachiasmatic nuclei  and hippocampus . In general, confirming synchronization of asynchronous neural activity is a prerequisite for interpreting these signals as physiologically and functionally associated. Synchrony in the interconnected circuitry of the thalamus and cerebral cortex is particularly critical in conscious events . Therefore, there should be a neural controlling system that regulates globally chaotic neural activities into a unitary conscious entity in terms of synchronization. In the conscious state, the experiences of the internal and external milieu merge into a temporally and spatially unitary experience . McCormick  suggested the possibility of a cyclical thalamocortical interaction whose key feature is the strong activation of GABAergic neurons within the thalamus. Taken together, the findings referenced above lead me to hypothesize that the inhibitory TRN cells play a key role in coordinating our conscious perception through the inhibitory feedback network across both the thalamus and the cortex. For instance, it has been suggested that TRN neurons in absence epilepsy may work as a subcortical pacemaker responsible for spike-wave discharges [26, 27]. Intriguingly, the TRN shows axons giving off local branches within the nucleus itself . TRN cells are principally coupled via inhibitory GABAergic synapses , mostly generating gamma activity [30, 31]. Indeed, GABAergic TRN cells demonstrate several frequencies of rhythmic oscillations [32–34]. Some rhythms such as spindle oscillation (7-14 Hz), delta oscillation (3-5 Hz), slow oscillation (0.3-0.5 Hz), and ultraslow rhythm (0.05 Hz) are spontaneously initiated or heavily involved in the TRN [35–38]. It has been suggested that intrinsic pacemaker alpha activity underlies the genesis of spindle waves related to sleep . However, it was found that a large proportion of TRN cells (about 34%) discharged like clocks within a 25-60 Hz frequency bandwidth (i.e., gamma activity) .
When a GABAergic network induces synchronization of neural activity, coherent gamma oscillations are observed . The gamma-range (more than about 30 Hz) synchronization is occasionally considered a key mechanism of information processing in neural networks [41, 42]. Again, the TRN is located in a particularly suitable position for controlling the entire cerebral network. Therefore, TRN-mediated synchronization in the thalamocortical network may result in gamma-band oscillations related to the binding of the stimulus features into a whole [43, 44]. Moreover, cortical gamma activity is concurrent with thalamic gamma activity at discrete conscious events . Most likely, neural synchronization initially driven by the TRN modulates gamma oscillations throughout the thalamocortical loops. Empirically, in an animal study (see Appendix 2), it was proposed that such coherent firing at gamma frequencies reflects a point of equilibrium in the TRN when the leaky K+ conductance is fully suppressed by the metabotropic effects of monoamines or excitatory amino acids .
As for more empirical evidence, we may pay attention to the electrophysiological dynamics of the TRN. For instance, IT (the T-type current underlying prolonged Ca2+-dependent burst firing in GABAergic neurons of rat TRN) of the TRN shows much slower kinetics than do thalamocortical relay cells , where IT is the critical current for controlling the thalamic response mode . More importantly, IT in the TRN needs depolarization for activation. The expression of IT depends on its state of inactivation. At hyperpolarized potentials, as during the early stages of sleep, IT becomes deinactivated and can produce low-threshold spikes during subsequent depolarization. At sufficiently depolarized potentials, as occur more frequently during wakeful activity, inactivation prevents IT conductance . Hence, these different kinetics and specific necessary active conditions between the TRN and thalamic relay cells would critically indicate that interactions between relay cells and the TRN are essential for synchronization . Apparently, if large neural ensembles of the TRN burst rhythmically, their interconnections could facilitate continuance of subsequent synchronous firings. Consistently, bilateral lesion of the rostral pole of the TRN in rats promotes thalamocortical dysrhythmia .
Indeed, TRN cells are called the pacemaker for thalamic oscillation [39, 47, 51–53], and they demonstrate two firing modes: burst-spike and tonic-spike . In relation to the switch mechanism between these two firing modes, Mistry et al.  reported frequency-dependent short-term modulation at glutamatergic synapses in the TRN. They found that TRN neurons exhibited no short-term change in alpha-amino-3-hydroxy-5-methylisoxazole-4-propionic acid (AMPA) receptor-mediated excitatory postsynaptic current amplitudes in response to stimulation at non-gamma frequencies (less than 30 Hz), simulating background activity, but showed short-term depression in such amplitudes at gamma frequencies (more than 30 Hz), simulating sensory transmission . The same study also found that intra-TRN inhibition suppresses TRN tonic-spike selectively at non-gamma stimulus frequencies, which are indicative of background activity. Presumably, in the absence of sensory transmission, the intra-TRN inhibitory network controls the number of spikes fired by TRN cells, consequently regulating the degree of inhibition exerted by the TRN cells onto thalamocortical networks . Therefore, switching between two ranges of stimulus frequencies to TRN cells (gamma and non-gamma range) regulates two physiological modes of TRN cells in the control of TRN output. This switch mechanism, in the TRN-mediated model, may play a gating role in progress to conscious awareness.
As mentioned in the Background section, the thalamus is not a simple relay station in sensory signal processing but is instead involved in many dynamic processes that significantly alter the nature of the information relayed to the cortex . Neurons in the thalamic relay nuclei [57, 58] and the TRN [48, 59] fire in two activity modes (tonic and burst) as mentioned above. From the viewpoint of a gate-keeping state of the thalamus, tonic mode firing in the thalamus may be responsible for a thalamic-gate passive mode (unconscious state), whereas burst firing may account for a thalamic-gate active mode (conscious state) [60–62]. In keeping with such a gate-keeping mechanism, I hypothesize that a conscious state would be established when a TRN-modulated thalamocortical network activates over a certain threshold to initiate overall synchronization. In contrast, in the sub-threshold state, sensory inputs may simply pass through the thalamus without the generation of conscious awareness. In other words, the brain might actually receive such unconscious sensory inputs, but those signals fail to reach the level of conscious awareness. This interpretation is applicable to the case of implicit knowledge, which is revealed in task performance without any corresponding phenomenal awareness .
Furthermore, the main part of the TRN can be divided into functionally distinct 'sectors' on the basis of its afferent connections with groups of thalamic nuclei and cytoarchitectonically definable cortical areas . Therefore, there are relatively accurate topographic maps corresponding to the same modality in the TRN [64, 65]; these cumulative maps of the latticework  appear to indicate a nexus, functionally related to the thalamo-cortico-thalamic pathways . More significantly, the lack of clearly definable borders of the sectors as well as a larger receptive field of the TRN  suggest that the TRN may be associated with integrative information processing and even cross-modal overlapping awareness. The experience of a unitary consciousness is plausible from the viewpoint of the synchronization of crudely overlapped receptive maps on the laminar TRN. Similarly, we can gain a comprehensible sense of the modal-confused symptom in which unconscious priming eliminates the automatic binding of color and alphanumeric form in synaesthesia . Within the framework of a TRN-synchronizing model, a variety of overlapping combinations of neural ensembles for conscious perception are plausible. These types of patterns of neural combinations for conscious awareness may lead to intra-individual variation in conscious perception in terms of 'qualia' and inter-individual 'subjectivity' in experiencing consciousness. I will discuss the topic of conscious awareness in more detail in the following setion for 'awareness'.
Taken together, evidence thus far suggests that the TRN is central in determining the initiation of communicative interactions between the thalamic relay nuclei and the cerebral cortex. Consequently, it likely plays a key role in controlling our unitary conscious perception. Therefore, the feedback synaptic connections from the TRN imply its potentially significant role in modulating the transmission of information in the thalamocortical circuit.
Additionally, to sustain a conscious state, arousal is necessary for the threshold condition of the TRN. Surely there are anatomical connections between the TRN and brainstem cells that control the subject's wakefulness and vigilance . Moreover, an inhibitory influence on the activity of TRN neurons is exerted by threshold stimulation of the mesencephalic reticular formation (MRF), which is the core of the brainstem, while supra-threshold stimulation of the MRF induces the activation of TRN neurons . Those researchers concluded that the synchronizing structure of the brainstem, exerting a blocking impact on the MRF, facilitates the activity of TRN neurons. It is also reported that the brainstem has relatively uniform effects on the response mode of relay cells throughout the thalamus . As mentioned earlier, the response mode of thalamic relay cells is principally under the command of the TRN, so these findings are still comprehensible within the framework of the TRN-mediated conception. Taken together, previous findings indicate that the brainstem exerts substantial control over the activity of TRN neurons, possibly to globally modulate the level of arousal for preparing for consciousness.
Besides, since consciousness is considered a biological phenomenon, gene polymorphism undoubtedly contributes to fine variations in consciousness among individuals. For example, since the TRN-mediated consciousness network principally involves GABAergic synapses, polymorphisms in several GABA-related genes have been associated with differences in the efficiency of mental processing [72–75]. Furthermore, AVPR1a and SLC6A4 gene polymorphisms have been reported in association with creative dance performance, which can be related to altered consciousness states [76–78]. Indeed, consciousness is completed through many neuronal assemblies, so it is substantially subject to diversity in genetic expression. However, the genetic effects on consciousness seem to be relatively modest, since they interact with environment or experience during the development of the network.
Attention: Highlighted thalamocortical synchronous activity coordinated by the TRN and associated cortical areas
As illustrated in Figure 2, the TRN-modulation model is compatible with models of large-scale cortical networks [82, 83] and of parallel distributed processing . Within these frameworks, cognitive functions are widely distributed in cortical networks and processed with basic features such as parallel input-to-output connections and reentry or recurrence, which can occur within and between layers of the cortical hierarchies. It has been suggested that the operation of a large-scale network in cognitive function is principally based on the correlation of the firing of its elements across cortical regions [82, 85, 86], which is the neural manifestation of 'binding' . Therefore, such reentry processes propagating over all of the brain networks are not static but dynamic, which is probably what William James called 'the stream of consciousness' .
Indeed, there is substantial evidence that cortical areas play significant roles in attention and cognition processing. For example, the prefrontal cortex, at the top of the executive hierarchy, is critical in decision-making [88–90]. As it plays a pivotal role in attention and working memory, the prefrontal cortex has occasionally been considered the seat of consciousness . As long as the prefrontal cortex controls cognition, its role in consciousness is obviously important. This is particularly the case in the attentive processes that lead a pattern of behavior, speech, or reasoning to its goal . Among those processes, working memory is the most closely engaged with consciousness in the temporal domain. This is because the prefrontal cortex houses the process of temporal integration, which makes possible the persistence of cognitive content.
Although the prefrontal cortex receives an immense quantity of afferent influences from the rest of the brain, the majority of these influences are, nevertheless, sometimes processed out of consciousness. For example, the prefrontal cortex mediates unconsciously triggered inhibitory control in the Go/No-Go paradigm . Thus, the cortex seems to play a subsidiary role in conscious awareness, either when selecting the information upon which one focuses or when directing the whole neural network involved in information processing. Presumably, the degree and distribution of cortical activity involved in cognition determine the content of consciousness .
However, compared to the functional roles of individually distributed cortices, the TRN seems to play a critical and supervising role in controlling the whole brain network. Attention is eventually accomplished through cooperatively integrating information from attention-related cortical regions (e.g., the dorsolateral prefrontal cortex [92, 93], the parietal cortex [94–97], and the orbitofrontal cortex [98, 99]) and from other sub-cortical regions such as the superior colliculus. In this respect, the inhibitory feedback mechanism of the TRN on the thalamocortical network becomes a potential candidate for controlling and coordinating the orientation of attention. In accordance with this conception, TRN lesions effectively prevented perseverative behavior in rats, while lesions of the orbitofrontal cortex failed to do so .
Several behavioral phenomena regarding attention are comprehensible within the framework of the TRN model. In 'change blindness' experiments, normal observers are thoroughly unaware of an essential part of what is going on in their visual field. One possible mechanism underlying the lack of awareness for events from which attention has been exogenously diverted could be a defective integration of elementary features for these events . This interpretation is understandable from the viewpoint of the integrative and mastery role of the TRN in attention to accomplish complete awareness. Another phenomenon related to exogenous attentional orienting is 'inhibition of return' (IOR) [102, 103]. With reference to the need for responding to novelty while resisting distraction, exogenous orienting processes are good candidates for involvement in drawing attention to novel events  by inhibiting repeated orientations toward the same locations (i.e., IOR). As mentioned earlier, inhibitory control is the crucial feature of the internal dynamics of the TRN model, allowing it to suppress interference effects and promote the exploration of the visual scene. In addition, to successfully cope with a continuously changing environment, efficient mechanisms for 'change-detection' are necessary. A recent study provides experimental evidence that the TRN neurons of the rat respond more strongly to deviant stimuli than standard stimuli, whereas the medial geniculate nucleus showed such deviance detection on a smaller scale . Therefore, the TRN seems to work more dynamically to detect changes than thalamic relay neurons do. Probably, consistent thalamocortical feedforward-feedback processes that act on pre-existing neural representations on the TRN interfere with new incoming signals, eventually competently detecting changes.
From the viewpoint of the TRN model, the Hebbian neural network  can be conceived, for example, in terms of the object-based neural connection for selective attention . Locally and transiently synchronized neural ensembles, possibly evoked by each tentative object (or mental target), could be seen as candidates for a dominant signal that controls the working memory domain (see Appendix 3). Therefore, if one of these object-based neural candidates is selected ('highlighted') as a mental target, we may conventionally refer to this neurophysiological phenomenon as 'paying attention.' Thereby, such multiple activated neural candidates can be analogous to what Zeki called the micro-consciousness . This interpretation is also consistent with Dehaene's conception of pre-conscious processing . Taking into consideration both the TRN-mediated model and the Hebbian cell assembly, substantial synchronization in the TRN would not always be necessary. In other words, if the input information is relatively new to the thalamocortical networks, substantial synchronization in the TRN is explicitly expected. In contrast, for relatively familiar signals, the Hebbian network, already established in the relevant thalamocortical tracks, may facilitate subsequent processes, which would effectively diminish coherent synchronization compared to what is expected for new signals. Therefore, it is probable that TRN-modulated thalamocortical synchronization depends on the familiarity of signals and that the TRN-modulation model is consistent with the Hebbian model. Moreover, it is likely that 'working memory' can be thought of as temporal mental traces of attended conscious awareness during a transient time range around the present. The circulating model explains feasibly how working memory is developed by any related attention. Presumably, working memory is a type of transient active mental tracing network, which is cued by initial looping signals reiterating over their correspondent thalamocortical circuits. Therefore, these neural traces should be critically related to the property of initial signals for the corresponding thalamocortical circuit. Consistently, such an associative property is one of the characteristics of working memory.
Through this TRN-modulation model, the concepts of capacity restriction of attention and the inability of humans to carry on simultaneous multi-attention become understandable. The limited capacity of attention may be caused by mechanical limitations in synchronizing TRN activities as a whole. Finally, such synchronization should yield a dominant single output signal as a unique mental representation related to the attended object. Reasonably, this characteristic of restrictive attention is more severe within the same modality, as the input information of each modality belongs to each corresponding sector in the thalamic relay nuclei as well as in the TRN. Therefore, the finely compartmental configuration of both the thalamus and the TRN is subjected to exclusive competition for the same modal signals. Apparently, this hypothesis is also consistent with bi-stable perception, unilateral neglect, extinction, and simultagnosia, because the TRN in each hemisphere has no direct connection between them. Hence, they are able to exert efficient lateral control over each hemispheric thalamocortical loop. However, ultimately they should communicate indirectly to result in a unitary conscious awareness, which may represent somewhat unclear emotional conscious experiences, such as a melancholy mood. Consistently, there is a connection between the TRN and the limbic system  that is related to emotion. Moreover, the phenomenon of 'attentional blink' appears to be in accord with this TRN-synchronizing model, as the TRN network would need an absolute refractory period in which to switch modes of synchronization in order to shift attention to other upcoming targets. Therefore, such a refractory period in changing attention could account for 'attentional blink'.
In addition, the unilateral characteristic of attention is comprehensible to a certain extent through a number of TRN-lesion studies. For instance, reduced right tecto-pulvinar activity was offset by over-compensatory enhancement in the TRN suppression of left pulvinar activity . Unilateral electrolytic lesions of the TRN elicited metabolic depression in the ipsilateral thalamic centrolateral, mediodorsal, ventromedial, and ventrolateral nuclei, and metabolic activation in the bilateral dorsal tegmental nuclei ; and a selective excitotoxic lesion of the ipsilateral TRN induced changes in the receptive field properties of the contralateral vental posterior medial thalamic nuclei . Furthermore, even in the study of memory impairment, the unilateral inactivation of rats' TRN has been shown to interfere with the acquisition of active avoidance in the contralateral hemisphere . Therefore, the gating role of the TRN in the information flow between thalamus and cortex seems plausible in a unilateral manner, and these anatomical and physiological features may lead to the unilateral characteristic of attention.
Awareness: Conscious perception of an attended mental representation by strengthening relevant neural networks through thalamocortical reiterating
It is important to note that, although attention seems to be a necessary condition for awareness, it appears by no means to be sufficient. For example, exogenous cues presented below a subjective threshold of awareness can capture attention automatically but without awareness . Therefore, we need to identify more complementary mechanisms underlying conscious awareness. Regarding the thalamocortical feedback mechanism, Sherman and Guillery  reported that first-order thalamic relay cells receive their driving afferents from ascending pathways and send these signals to their corresponding cortices for the first time, whereas higher-order thalamic relay cells are held to bring their principal messages from the corresponding cortices. Interestingly, TRN cells send their axons back to the thalamus, particularly two branches of a single axon connected to the first-order and the related higher-order nucleus . Thus, the TRN can be said to act as an integrative junction of different but associated thalamocortical circuits. Sherman and Guillery  suggested that the functional significance of such a gathering venue may be most important for the interactions among first-order and higher-order circuits that belong to the same modality grouping.
Based on such anatomical evidence, the present study hypothesizes that conscious awareness may be embodied in the process of such thalamocortical iterative signal circulation as controlled by the TRN, as depicted in Figure 2. To elaborate the degree of conscious awareness, first-order and higher-order relay cells may interact within the TRN, where the closest relationships between first-order and higher-order relay circuits for any one modality are found . Accordingly, the first-order and higher-order relay circuits controlled by the TRN can yield more refined and thus higher cognitive information, as their circulating feedbacks run over and over again in an integrative reprocessing manner. In this sense, the compact latticework formation of the TRN is advantageous to coordinate the overall conscious experience.
This dynamically circulating model offers one plausible understanding of the typical characteristics of consciousness. For example, although consciousness appears to be continuous, it actually consists of isolated steps [114, 115]. According to the TRN-modulation model, consciousness consists of each mental unit, which is an individual thalamocortical looping mechanism, no matter what cognitive stages it involves. Such individual mental units may behave discordantly, possibly reflected in the discrete characteristic of consciousness. In addition, as we experience everyday life, we require at least a minimal period to become aware of something. Indeed, in the framework of the TRN-mediated thalamocortical looping model, minimal time is necessary for signals to loop the circuit. This model is also in accordance with the recently proposed hypothesis that we are only aware of changes in our underlying cognition ; according to the TRN-modulation model, only dynamically iterating neural signals through thalamocortical loops eventually substantiate our conscious perception.
In line with the plausible account of characteristics of consciousness, the mechanism of dreaming is also explainable within the framework of this circulating model. In spite of nearly complete lack of sensory input from the real world during sleep, the looping circuit of the TRN-centered circulating model could be activated by randomly evoked signals within that loop, which presumably initiates to evoke a dream mechanism. Therefore, during dreaming we can have mental experiences as vivid as those we have in the real world. Similarly, this circulating model is consistent with 'self-consciousness,' because the model allows thalamocortical networks to generate signals for themselves merely by an internally driven cue such as visual imagination (with the eyes closed). This circulating model can explain the priming effect as well. Possibly, a priming signal may boost or initiate the related neural activation of the TRN-mediated thalamocortical network in advance so that a subsequent relevant input signal could advantageously advance this warmed-up activation into more proliferated activation. The priming effect appears therefore to be modality-specific , which is also a particular structural characteristic of the TRN, as mentioned earlier.
Thus far, I have argued that the TRN-modulated thalamocortical network appears to have evolved as the neural correlate for conscious awareness. Presumably, the conscious state is a TRN-modulated synchronized neural state that enables us to facilitate subsequent attention processes. In striking accordance with these hypotheses, if the TRN is somehow impaired, the main symptom resembles coma (akinetic mutism) . The TRN may serve as an action coordinator for controlling our selective attention and subsequently for filtering irrelevant signal processing in conscious perception of a target mental representation. The TRN most likely screens perceptual representation, particularly through its modality-specific sectors. The coarse boundary configuration of representing maps in the TRN likely enables us to experience conscious awareness as a complete entity, which I refer to as unitary conscious awareness. I presume that the framework of conscious awareness is a reiterate circuit looping over the thalamus-TRN-cortex, where the TRN would control a gate-keeping mechanism for attention. Higher cognitive processes are likely to be achieved through such repeated thalamocortical looping. I expect that both top-down and bottom-up signals can communicate in the thalamocortical looping circuits and thus create a finally unified percept by their synchrony, which is mediated substantially by the TRN. To sum up, the TRN may work as a gatekeeper for consciousness and as a communicative screen for conscious awareness. The TRN-modulation hypotheses for consciousness, attention, and awareness can be summarized as follows:
 'Consciousness' is referred to as thalamocortical response modes controlled by the TRN and is embodied in the form of dynamically synchronized thalamocortical networks ready for upcoming attentional processes.
 'Attention' is neurophysiologically substantiated by a highlighted neural ensemble among a number of synchronized thalamocortical candidates, the topographical maps of which are projected onto the TRN.
 Thalamocortical looping via the TRN is necessary for the 'conscious awareness' of an attended object.
We can test these hypotheses experimentally. For example, the degree of conscious awareness could be evaluated along with the severity of the impairment of the TRN. We can also assess the degree of modality-specific conscious perception while investigating the extent of impairment in its functionally relevant thalamocortical loops. The influence of neuroanatomical abnormal connections (whether they are on the first-order track or on higher-order networks) could also tell us more about the significance of iterative thalamocortical loops in accomplishing improved conscious perception. Most likely, the phenomenon of masking  presents compelling evidence for the significance of thalamocortical loops in conscious perception. Masking phenomena can be interpreted as an interruption between the signals circulating through the thalamocortical loops.
The TRN-mediated model could reconcile several major hypotheses for conscious awareness. According to the so-called 'global workspace' model of consciousness , incoming information becomes conscious only if three conditions are met: (1) the existence of represented information by sensory neural networks; (2) the existence of representation long-lasting enough to gain access to a second stage of processing; and (3) the ignition of a combination of bottom-up propagation and top-down amplification to create a state of reverberating, coherent activity. The first condition of the global workspace model is well in accordance with the networking conception of the TRN-mediated model. The second condition of the global workspace model can be understood from the viewpoint of the thalamocortical iterative looping of the TRN-mediated model. Likewise, the third condition of the global workspace model is analogous to the aspect of synchronized neural activation in the TRN-mediated model.
Compared to the global workspace model, the TRN-mediated model seems more plausible in the following respects. The model-specific sectors on the TRN provide us with a deeper understanding of modality-specific conscious awareness. In addition, although the prefrontal cortex is an important center for conscious awareness in the global workspace model generally, the prefrontal cortex is sometimes not necessary to produce a kind of modality-specific awareness in the TRN-mediated model. Based on the TRN-mediated model, the TRN is responsible for controlling thalamocortical networks to be consciously processed, and the prefrontal cortex may work for the conscious evaluation of highlighted thalamocortical networks.
As shown in Figure 2, the concept of locally synchronized loops such as in the occipital, frontal, or parietal region is consistent in all the three models (Dahaene's, Lamme's, and the present TRN model). These locally activating networks indicate either corticocortical regional networks or any subunit of TRN-mediated thalamocortical assemblies. On the other hand, the distributed firing patterns in the global workspace model  are characteristic of the processing stage, when the TRN is initiating to globally control and organize all the locally activating neural networks to bring about the completion of conscious awareness. That is, the TRN invigorates a specific neural ensemble to be consciously processed and simultaneously suppresses other irrelevant neural activations.
In particular, as Lamme  emphasized the importance of feedback connections to the primary visual cortex in terms of visual awareness, the TRN model also highlights the significance of feedback signals from the primary sensory cortex to accomplish conscious awareness. Furthermore, Lamme and Roelfsema  proposed the necessity of recurrent processing in relation to consciousness. This notion is exactly what the TRN-mediated model has highlighted as iterative looping processes for conscious awareness.
As discussed so far, the TRN model does not underestimate the significance of cortical roles in conscious awareness. It simply highlights the physiological significance of the central roles of the TRN, such as controlling, screening, and accumulating neural signals through thalamocortical loops during conscious awareness. Most likely, the cortical layers communicate regularly through their corticocortical connections . In addition, the cortices provide their own substantial contribution to the development of consciousness. That is, they may elaborate not-yet-matured information into highly processed information while managing previous information held in a certain form in the cortical network. For example, the dorsolateral prefrontal cortex is assumed to be the neural correlate for integrating discrete cycles of conscious perception [116, 121]. However, the TRN-modulation model of consciousness can account for more mental experiences while including corticocortical communication within its framework; they are not mutually exclusive. Through the TRN-modulation model, it becomes easier to understand why there are such complicated (seemingly randomized but logically associated) topographic distributions across many cortical areas during conscious awareness. The receptive maps projected on each sector of the TRN are overlapped and may be intercommunicative within the latticework structure of the TRN. Moreover, 'blindsight' phenomena  seem less paradoxical from the viewpoint of the TRN-modulation model; with blindsight, the TRN and the thalamus cannot receive any feedback signals from the V1 (primary visual cortex). Such signals from the primary sensory cortex are necessary to accomplish conscious awareness according to the TRN-modulation model. In other words, visual thalamic nuclei such as the LGN or pulvinar would passively receive continuous input from the retina, but without returning signals from the V1, resulting in unconscious perception.
In addition, the possibility that thalamic relay mixtures such as intralaminar or midline thalamic nuclei play a role in integrating information processes for consciousness cannot be excluded, as expected in the TRN. However, compared to the TRN, they appear to make different contributions, because they are connected principally with the striatum apart from the cerebral cortex . Furthermore, the striatum is connected to the TRN in an unusual manner, such that the external segment of the globus pallidus projects onto the TRN without branching on the motor thalamus . Moreover, there is no innervation to the TRN from the internal segment of the globus pallidus, which projects onto the thalamus . These findings imply that the thalamus and the TRN are regulated differently in terms of motor control. Presumably, the consciousness of voluntary movement and that of sensory processing are different in their neural correlates. Indeed, since the prefrontal cortex receives afferents from thalamus, hypothalamus, limbic structures, and brainstem , presumably conveying information about motivation and intention of movement, and influences movement only indirectly through projections to basal ganglia, secondary motor cortices, and cerebellum , the prefrontal cortex does not seem to be the center of willful motion, but is rather considered as the temporal and executive organization of willful motion . Therefore, we need a more plausible neural controller for initiating and supervising the consciousness of voluntary movement, irrespective of whether it is a whole neural network or a small neural assembly. Given the issue of motion free-will and the remaining questions regarding the functions of thalamic relay mixtures or higher-order relay circuits, further development of the TRN-mediated consciousness model requires further experimental investigation. For example, the interactive relationship between the TRN and higher-order relay cells may be a key feature for screening mental representations to be selected as an attended target and consequently for manifesting conscious awareness of it, as both the TRN and higher-order thalamic relay cells receive feedback signals from the corresponding cortices, where more elaborated information might be uploaded and kept. This crucial relationship requires clarification in further studies. In spite of these remaining challenges, the sophisticated but logically connected thalamocortical circuits passing through the TRN and its inhibitory control function continue to reinforce the significance of the TRN-mediating model of consciousness.
To clarify the descriptions used throughout this paper, I tentatively use the term 'consciousness' as a general mental state of being capable of awareness. In addition, the term 'awareness' is used to represent a specific mental state of being acquainted with something in a conscious manner (conscious perception).
Some empirical evidence regarding the neurophysiology of the TRN used in this paper is based on animal studies; hence, there are limitations regarding the generalization of the TRN-modulation hypothesis of human consciousness. However, as the human TRN might have evolved from the TRN of animals, I believe that such implications concerning our consciousness have considerable value for future studies.
It is another question as to which brain region is responsible for deciding what to attend to. This is perhaps controlled by top-down signals from higher cognitive stages (e.g., the frontal cortex). This issue remains controversial and open to investigation.
I am thankful to Prof. Wolfgang Klimesch (Salzburg University) for his kind permission to reproduce and cite Figure 1.
- Lamme VA: Blindsight: the role of feedforward and feedback corticocortical connections. Acta Psychol (Amst). 2001, 107: 209-228. 10.1016/S0001-6918(01)00020-8.Google Scholar
- Dehaene S, Changeux JP, Naccache L, Sackur J, Sergent C: Conscious, preconscious, and subliminal processing: a testable taxonomy. Trends Cogn Sci. 2006, 10: 204-211. 10.1016/j.tics.2006.03.007.PubMedGoogle Scholar
- Zeki S: The disunity of consciousness. Prog Brain Res. 2008, 168: 11-18. full_text.PubMedGoogle Scholar
- Jones EG: The Thalamus. 1985, New York: Plenum PressGoogle Scholar
- Schmahmann JD, Pandya DN: Disconnection syndromes of basal ganglia, thalamus, and cerebrocerebellar systems. Cortex. 2008, 44: 1037-1066. 10.1016/j.cortex.2008.04.004.PubMed CentralPubMedGoogle Scholar
- Schmahmann JD, Pandya DN: Anatomical investigation of projections from thalamus to posterior parietal cortex in the rhesus monkey: a WGA-HRP and fluorescent tracer study. J Comp Neurol. 1990, 295: 299-326. 10.1002/cne.902950212.PubMedGoogle Scholar
- Jones EG: A description of the human thalamus. Thalamus, Experimental and Clinical Aspects. Edited by: Steriade M, Jones EG, McCormick DA. 1997, New York: Elsevier, 2: 425-499.Google Scholar
- Shatz CJ, Rakic P: The genesis of efferent connections from the visual cortex of the fetal rhesus monkey. J Comp Neurol. 1981, 196: 287-307. 10.1002/cne.901960208.PubMedGoogle Scholar
- Kennedy H, Bullier J: A double-labeling investigation of the afferent connectivity to cortical areas V1 and V2 of the macaque monkey. J Neurosci. 1985, 5: 2815-2830.PubMedGoogle Scholar
- Pandya DN, Rosene DL, Doolittle AM: Corticothalamic connections of auditory-related areas of the temporal lobe in the rhesus monkey. J Comp Neurol. 1994, 345: 447-471. 10.1002/cne.903450311.PubMedGoogle Scholar
- Hackett TA, Stepniewska I, Kaas JH: Thalamocortical connections of the parabelt auditory cortex in macaque monkeys. J Comp Neurol. 1998, 400: 271-286. 10.1002/(SICI)1096-9861(19981019)400:2<271::AID-CNE8>3.0.CO;2-6.PubMedGoogle Scholar
- Mesulam MM, Pandya DN: The projections of the medial geniculate complex within the sylvian fissure of the rhesus monkey. Brain Res. 1973, 60: 315-333. 10.1016/0006-8993(73)90793-2.PubMedGoogle Scholar
- Jones EG, Powell TP: Connexions of the somatic sensory cortex of the rhesus monkey. 3. Thalamic connexions. Brain. 1970, 93: 37-56. 10.1093/brain/93.1.37.PubMedGoogle Scholar
- Jones EG, Powell TP: An anatomical study of converging sensory pathways within the cerebral cortex of the monkey. Brain. 1970, 93: 793-820. 10.1093/brain/93.4.793.PubMedGoogle Scholar
- Ilinsky IA, Kultas-Ilinsky K: Sagittal cytoarchitectonic maps of the Macaca mulatta thalamus with a revised nomenclature of the motor-related nuclei validated by observations on their connectivity. J Comp Neurol. 1987, 262: 331-364. 10.1002/cne.902620303.PubMedGoogle Scholar
- Steriade M: Active neocortical processes during quiescent sleep. Arch Ital Biol. 2001, 139: 37-51.PubMedGoogle Scholar
- Schambra UB, Lauder JM, Silver J: Atlas of the Prenatal Mouse Brain. 1992, San Diego, CA: Academic PressGoogle Scholar
- Wang S, Bickford ME, Van Horn SC, Erisir A, Godwin DW, Sherman SM: Synaptic targets of thalamic reticular nucleus terminals in the visual thalamus of the cat. J Comp Neurol. 2001, 440: 321-341. 10.1002/cne.1389.PubMedGoogle Scholar
- Shu Y, McCormick DA: Inhibitory interactions between ferret thalamic reticular neurons. J Neurophysiol. 2002, 87: 2571-2576.PubMedGoogle Scholar
- Steriade M, Jones EG, McCormick DA: Thalamus. 1997, Amsterdam: Oxford: ElsevierGoogle Scholar
- Lundkvist GB, Kristensson K, Hill RH: The suprachiasmatic nucleus exhibits diurnal variations in spontaneous excitatory postsynaptic activity. J Biol Rhythms. 2002, 17: 40-51. 10.1177/074873002129002320.PubMedGoogle Scholar
- Wang XJ: Pacemaker neurons for the theta rhythm and their synchronization in the septohippocampal reciprocal loop. J Neurophysiol. 2002, 87: 889-900.PubMedGoogle Scholar
- Jones EG: Synchrony in the interconnected circuitry of the thalamus and cerebral cortex. Ann N Y Acad Sci. 2009, 1157: 10-23. 10.1111/j.1749-6632.2009.04534.x.PubMedGoogle Scholar
- Fuster JM: The prefrontal cortex. 2008, Amsterdam; London: Academic, 4Google Scholar
- McCormick DA: Cortical and subcortical generators of normal and abnormal rhythmicity. Int Rev Neurobiol. 2002, 49: 99-114. full_text.PubMedGoogle Scholar
- van Luijtelaar G, Sitnikova E: Global and focal aspects of absence epilepsy: the contribution of genetic models. Neurosci Biobehav Rev. 2006, 30: 983-1003. 10.1016/j.neubiorev.2006.03.002.PubMedGoogle Scholar
- Berdiev RK, Chepurnov SA, Veening JG, Chepurnova NE, van Luijtelaar G: The role of the nucleus basalis of Meynert and reticular thalamic nucleus in pathogenesis of genetically determined absence epilepsy in rats: a lesion study. Brain Res. 2007, 1185: 266-274. 10.1016/j.brainres.2007.09.010.PubMedGoogle Scholar
- Yen CT, Conley M, Hendry SH, Jones EG: The morphology of physiologically identified GABAergic neurons in the somatic sensory part of the thalamic reticular nucleus in the cat. J Neurosci. 1985, 5: 2254-2268.PubMedGoogle Scholar
- Houser CR, Vaughn JE, Barber RP, Roberts E: GABA neurons are the major cell type of the nucleus reticularis thalami. Brain Res. 1980, 200: 341-354. 10.1016/0006-8993(80)90925-7.PubMedGoogle Scholar
- Pinault D, Deschenes M: Control of 40-Hz firing of reticular thalamic cells by neurotransmitters. Neuroscience. 1992, 51: 259-268. 10.1016/0306-4522(92)90313-Q.PubMedGoogle Scholar
- Pinault D, Deschenes M: Voltage-dependent 40-Hz oscillations in rat reticular thalamic neurons in vivo. Neuroscience. 1992, 51: 245-258. 10.1016/0306-4522(92)90312-P.PubMedGoogle Scholar
- Domich L, Oakson G, Steriade M: Thalamic burst patterns in the naturally sleeping cat: a comparison between cortically projecting and reticularis neurones. J Physiol. 1986, 379: 429-449.PubMed CentralPubMedGoogle Scholar
- McCormick DA, Prince DA: Acetylcholine induces burst firing in thalamic reticular neurones by activating a potassium conductance. Nature. 1986, 319: 402-405. 10.1038/319402a0.PubMedGoogle Scholar
- Steriade M, Deschenes M: The thalamus as a neuronal oscillator. Brain Res. 1984, 320: 1-63.PubMedGoogle Scholar
- Avanzini G, de Curtis M, Panzica F, Spreafico R: Intrinsic properties of nucleus reticularis thalami neurones of the rat studied in vitro. J Physiol. 1989, 416: 111-122.PubMed CentralPubMedGoogle Scholar
- Long MA, Landisman CE, Connors BW: Small clusters of electrically coupled neurons generate synchronous rhythms in the thalamic reticular nucleus. J Neurosci. 2004, 24: 341-349. 10.1523/JNEUROSCI.3358-03.2004.PubMedGoogle Scholar
- Xu M, Liu CH, Xiong Y, He J: Corticofugal modulation of the auditory thalamic reticular nucleus of the guinea pig. J Physiol. 2007, 585: 15-28. 10.1113/jphysiol.2007.142240.PubMed CentralPubMedGoogle Scholar
- Mulle C, Madariaga A, Deschenes M: Morphology and electrophysiological properties of reticularis thalami neurons in cat: in vivo study of a thalamic pacemaker. J Neurosci. 1986, 6: 2134-2145.PubMedGoogle Scholar
- Steriade M, Domich L, Oakson G, Deschenes M: The deafferented reticular thalamic nucleus generates spindle rhythmicity. J Neurophysiol. 1987, 57: 260-273.PubMedGoogle Scholar
- Szabadics J, Lorincz A, Tamas G: Beta and gamma frequency synchronization by dendritic gabaergic synapses and gap junctions in a network of cortical interneurons. J Neurosci. 2001, 21: 5824-5831.PubMedGoogle Scholar
- Herrmann CS, Munk MH, Engel AK: Cognitive functions of gamma-band activity: memory match and utilization. Trends Cogn Sci. 2004, 8: 347-355. 10.1016/j.tics.2004.06.006.PubMedGoogle Scholar
- Herrmann CS: Gamma activity as a functional correlate of cognition. special issue. Int J Psychophysiol. 2000, 38: vii-viii. 10.1016/S0167-8760(00)00170-7.PubMedGoogle Scholar
- Engel AK, Singer W: Temporal binding and the neural correlates of sensory awareness. Trends Cogn Sci. 2001, 5: 16-25. 10.1016/S1364-6613(00)01568-0.PubMedGoogle Scholar
- Fries P, Nikolic D, Singer W: The gamma cycle. Trends Neurosci. 2007, 30: 309-316. 10.1016/j.tins.2007.05.005.PubMedGoogle Scholar
- Steriade M: Corticothalamic resonance, states of vigilance and mentation. Neuroscience. 2000, 101: 243-276. 10.1016/S0306-4522(00)00353-5.PubMedGoogle Scholar
- Huguenard JR, Prince DA: A novel T-type current underlies prolonged Ca(2+)-dependent burst firing in GABAergic neurons of rat thalamic reticular nucleus. J Neurosci. 1992, 12: 3804-3817.PubMedGoogle Scholar
- McCormick DA, Bal T: Sleep and arousal: thalamocortical mechanisms. Annu Rev Neurosci. 1997, 20: 185-215. 10.1146/annurev.neuro.20.1.185.PubMedGoogle Scholar
- Hartings JA, Temereanca S, Simons DJ: State-dependent processing of sensory stimuli by thalamic reticular neurons. J Neurosci. 2003, 23: 5264-5271.PubMedGoogle Scholar
- Sherman SM, Guillery RW: On the actions that one nerve cell can have on another: distinguishing "drivers" from "modulators". Proc Natl Acad Sci USA. 1998, 95: 7121-7126. 10.1073/pnas.95.12.7121.PubMed CentralPubMedGoogle Scholar
- Marini G, Ceccarelli P, Mancia M: Thalamocortical dysrhythmia and the thalamic reticular nucleus in behaving rats. Clin Neurophysiol. 2002, 113: 1152-1164. 10.1016/S1388-2457(02)00111-6.PubMedGoogle Scholar
- Bal T, McCormick DA: Mechanisms of oscillatory activity in guinea-pig nucleus reticularis thalami in vitro: a mammalian pacemaker. J Physiol. 1993, 468: 669-691.PubMed CentralPubMedGoogle Scholar
- Steriade M, Contreras D, Curro Dossi R, Nunez A: The slow (< 1 Hz) oscillation in reticular thalamic and thalamocortical neurons: scenario of sleep rhythm generation in interacting thalamic and neocortical networks. J Neurosci. 1993, 13: 3284-3299.PubMedGoogle Scholar
- Steriade M, Dossi RC, Nunez A: Network modulation of a slow intrinsic oscillation of cat thalamocortical neurons implicated in sleep delta waves: cortically induced synchronization and brainstem cholinergic suppression. J Neurosci. 1991, 11: 3200-3217.PubMedGoogle Scholar
- Contreras D, Curro Dossi R, Steriade M: Bursting and tonic discharges in two classes of reticular thalamic neurons. J Neurophysiol. 1992, 68: 973-977.PubMedGoogle Scholar
- Mistry RB, Isaac JT, Crabtree JW: Two differential frequency-dependent mechanisms regulating tonic firing of thalamic reticular neurons. Eur J Neurosci. 2008, 27: 2643-2656. 10.1111/j.1460-9568.2008.06246.x.PubMedGoogle Scholar
- Sherman SM, Guillery RW: Functional organization of thalamocortical relays. J Neurophysiol. 1996, 76: 1367-1395.PubMedGoogle Scholar
- Deschenes M, Paradis M, Roy JP, Steriade M: Electrophysiology of neurons of lateral thalamic nuclei in cat: resting properties and burst discharges. J Neurophysiol. 1984, 51: 1196-1219.PubMedGoogle Scholar
- Lo FS, Lu SM, Sherman SM: Intracellular and extracellular in vivo recording of different response modes for relay cells of the cat's lateral geniculate nucleus. Exp Brain Res. 1991, 83: 317-328. 10.1007/BF00231155.PubMedGoogle Scholar
- Steriade M, Domich L, Oakson G: Reticularis thalami neurons revisited: activity changes during shifts in states of vigilance. J Neurosci. 1986, 6: 68-81.PubMedGoogle Scholar
- Sherman SM: Tonic and burst firing: dual modes of thalamocortical relay. Trends Neurosci. 2001, 24: 122-126. 10.1016/S0166-2236(00)01714-8.PubMedGoogle Scholar
- Ramcharan EJ, Gnadt JW, Sherman SM: Burst and tonic firing in thalamic cells of unanesthetized, behaving monkeys. Vis Neurosci. 2000, 17: 55-62. 10.1017/S0952523800171056.PubMedGoogle Scholar
- Weyand TG, Boudreaux M, Guido W: Burst and tonic response modes in thalamic neurons during sleep and wakefulness. J Neurophysiol. 2001, 85: 1107-1118.PubMedGoogle Scholar
- Schacter DL: Implicit knowledge: new perspectives on unconscious processes. Proc Natl Acad Sci USA. 1992, 89: 11113-11117. 10.1073/pnas.89.23.11113.PubMed CentralPubMedGoogle Scholar
- Conley M, Kupersmith AC, Diamond IT: The Organization of Projections from Subdivisions of the Auditory Cortex and Thalamus to the Auditory Sector of the Thalamic Reticular Nucleus in Galago. Eur J Neurosci. 1991, 3: 1089-1103. 10.1111/j.1460-9568.1991.tb00044.x.PubMedGoogle Scholar
- Crabtree JW, Killackey HP: The Topographic Organization and Axis of Projection within the Visual Sector of the Rabbit's Thalamic Reticular Nucleus. Eur J Neurosci. 1989, 1: 94-109. 10.1111/j.1460-9568.1989.tb00777.x.PubMedGoogle Scholar
- Lozsadi DA: Organization of cortical afferents to the rostral, limbic sector of the rat thalamic reticular nucleus. J Comp Neurol. 1994, 341: 520-533. 10.1002/cne.903410408.PubMedGoogle Scholar
- Sherman SM, Guillery RW: Exploring the thalamus. 2001, San Diego: Academic PressGoogle Scholar
- So YT, Shapley R: Spatial tuning of cells in and around lateral geniculate nucleus of the cat: X and Y relay cells and perigeniculate interneurons. J Neurophysiol. 1981, 45: 107-120.PubMedGoogle Scholar
- Mattingley JB, Rich AN, Yelland G, Bradshaw JL: Unconscious priming eliminates automatic binding of colour and alphanumeric form in synaesthesia. Nature. 2001, 410: 580-582. 10.1038/35069062.PubMedGoogle Scholar
- Nanobashvili ZI, Khizanishvili NA, Bilanishvili IG: [Influence of solitary tract nucleus stimulation on activity of thalamic reticular nucleus and mesencephalic reticular formation of the brain]. Georgian Med News. 2009, 74-78.Google Scholar
- Uhlrich DJ, Cucchiaro JB, Sherman SM: The projection of individual axons from the parabrachial region of the brain stem to the dorsal lateral geniculate nucleus in the cat. J Neurosci. 1988, 8: 4565-4575.PubMedGoogle Scholar
- Henkel V, Baghai TC, Eser D, Zill P, Mergl R, Zwanzger P, Schule C, Bottlender R, Jager M, Rupprecht R: The gamma amino butyric acid (GABA) receptor alpha-3 subunit gene polymorphism in unipolar depressive disorder: a genetic association study. Am J Med Genet B Neuropsychiatr Genet. 2004, 126B: 82-87. 10.1002/ajmg.b.20137.PubMedGoogle Scholar
- Imai K, Harada S, Kawanishi Y, Tachikawa H, Okubo T, Asada T: Association analysis of an (AC)n repeat polymorphism in the GABA(B) receptor gene and schizophrenia. Am J Med Genet. 2002, 114: 605-608. 10.1002/ajmg.10605.PubMedGoogle Scholar
- Winterer G, Smolka M, Samochowiec J, Ziller M, Mahlberg R, Gallinat J, Rommelspacher HP, Herrmann WM, Sander T: Association of EEG coherence and an exonic GABA(B)R1 gene polymorphism. Am J Med Genet B Neuropsychiatr Genet. 2003, 117B: 51-56. 10.1002/ajmg.b.10031.PubMedGoogle Scholar
- Bayazit YA, Yilmaz M, Kokturk O, Erdal ME, Ciftci T, Gokdogan T, Kemaloglu Y, Ileri F: Association of GABA(B)R1 receptor gene polymorphism with obstructive sleep apnea syndrome. ORL J Otorhinolaryngol Relat Spec. 2007, 69: 190-197.PubMedGoogle Scholar
- Nencini P: The shaman and the rave party: social pharmacology of ecstasy. Subst Use Misuse. 2002, 37: 923-939. 10.1081/JA-120004159.PubMedGoogle Scholar
- Bachner-Melman R, Dina C, Zohar AH, Constantini N, Lerer E, Hoch S, Sella S, Nemanov L, Gritsenko I, Lichtenberg P: AVPR1a and SLC6A4 gene polymorphisms are associated with creative dance performance. PLoS Genet. 2005, 1: e42-10.1371/journal.pgen.0010042.PubMed CentralPubMedGoogle Scholar
- Park JR, Yagyu T, Saito N, Kinoshita T, Hirai T: Dynamics of brain electric field during recall of Salpuri dance performance. Percept Mot Skills. 2002, 95: 955-962. 10.2466/PMS.95.7.955-962.PubMedGoogle Scholar
- Desimone R, Duncan J: Neural mechanisms of selective visual attention. Annu Rev Neurosci. 1995, 18: 193-222. 10.1146/annurev.ne.18.030195.001205.PubMedGoogle Scholar
- Stehberg J, Acuna-Goycolea C, Ceric F, Torrealba F: The visceral sector of the thalamic reticular nucleus in the rat. Neuroscience. 2001, 106: 745-755. 10.1016/S0306-4522(01)00316-5.PubMedGoogle Scholar
- Crick F: Function of the thalamic reticular complex: the searchlight hypothesis. Proc Natl Acad Sci USA. 1984, 81: 4586-4590. 10.1073/pnas.81.14.4586.PubMed CentralPubMedGoogle Scholar
- Bressler SL: Large-scale cortical networks and cognition. Brain Res Brain Res Rev. 1995, 20: 288-304. 10.1016/0165-0173(94)00016-I.PubMedGoogle Scholar
- Fuster JM: Cortex and mind: unifying cognition. 2003, New York; Oxford: Oxford University PressGoogle Scholar
- Rumelhart DE, McClelland JL: Parallel distributed processing: explorations in the microstructure of cognition. 1986, Cambridge, Mass.: MIT PressGoogle Scholar
- Gray CM, Singer W: Stimulus-specific neuronal oscillations in orientation columns of cat visual cortex. Proc Natl Acad Sci USA. 1989, 86: 1698-1702. 10.1073/pnas.86.5.1698.PubMed CentralPubMedGoogle Scholar
- Fuster JM: Memory in the cerebral cortex: an empirical approach to neural networks in the human and nonhuman primate. 1995, Cambridge, Mass.: MIT PressGoogle Scholar
- James W: The principles of psychology. 1890, [S.l.]: Macmillan, full_text.Google Scholar
- Fecteau S, Pascual-Leone A, Zald DH, Liguori P, Theoret H, Boggio PS, Fregni F: Activation of prefrontal cortex by transcranial direct current stimulation reduces appetite for risk during ambiguous decision making. J Neurosci. 2007, 27: 6212-6218. 10.1523/JNEUROSCI.0314-07.2007.PubMedGoogle Scholar
- Barraclough DJ, Conroy ML, Lee D: Prefrontal cortex and decision making in a mixed-strategy game. Nat Neurosci. 2004, 7: 404-410. 10.1038/nn1209.PubMedGoogle Scholar
- Manes F, Sahakian B, Clark L, Rogers R, Antoun N, Aitken M, Robbins T: Decision-making processes following damage to the prefrontal cortex. Brain. 2002, 125: 624-639. 10.1093/brain/awf049.PubMedGoogle Scholar
- van Gaal S, Ridderinkhof KR, Fahrenfort JJ, Scholte HS, Lamme VA: Frontal cortex mediates unconsciously triggered inhibitory control. J Neurosci. 2008, 28: 8053-8062. 10.1523/JNEUROSCI.1278-08.2008.PubMedGoogle Scholar
- Johnson JA, Strafella AP, Zatorre RJ: The role of the dorsolateral prefrontal cortex in bimodal divided attention: two transcranial magnetic stimulation studies. J Cogn Neurosci. 2007, 19: 907-920. 10.1162/jocn.2007.19.6.907.PubMedGoogle Scholar
- Vanderhasselt MA, De Raedt R, Baeken C, Leyman L, Clerinx P, D'Haenen H: The influence of rTMS over the right dorsolateral prefrontal cortex on top-down attentional processes. Brain Res. 2007, 1137: 111-116. 10.1016/j.brainres.2006.12.050.PubMedGoogle Scholar
- Buschman TJ, Miller EK: Top-down versus bottom-up control of attention in the prefrontal and posterior parietal cortices. Science. 2007, 315: 1860-1862. 10.1126/science.1138071.PubMedGoogle Scholar
- Grimault S, Robitaille N, Grova C, Lina JM, Dubarry AS, Jolicoeur P: Oscillatory activity in parietal and dorsolateral prefrontal cortex during retention in visual short-term memory: additive effects of spatial attention and memory load. Hum Brain Mapp. 2009, 30: 3378-3392. 10.1002/hbm.20759.PubMedGoogle Scholar
- Malhotra P, Coulthard EJ, Husain M: Role of right posterior parietal cortex in maintaining attention to spatial locations over time. Brain. 2009, 132: 645-660. 10.1093/brain/awn350.PubMed CentralPubMedGoogle Scholar
- Yantis S, Schwarzbach J, Serences JT, Carlson RL, Steinmetz MA, Pekar JJ, Courtney SM: Transient neural activity in human parietal cortex during spatial attention shifts. Nat Neurosci. 2002, 5: 995-1002. 10.1038/nn921.PubMedGoogle Scholar
- Itami S, Uno H: Orbitofrontal cortex dysfunction in attention-deficit hyperactivity disorder revealed by reversal and extinction tasks. Neuroreport. 2002, 13: 2453-2457. 10.1097/00001756-200212200-00016.PubMedGoogle Scholar
- Nobre AC, Coull JT, Frith CD, Mesulam MM: Orbitofrontal cortex is activated during breaches of expectation in tasks of visual attention. Nat Neurosci. 1999, 2: 11-12. 10.1038/4513.PubMedGoogle Scholar
- Andrade P, Fernandez-Guasti A, Carrillo-Ruiz JD, Ulloa RE, Ramirez Y, Reyes R, Jimenez F: Effects of bilateral lesions in thalamic reticular nucleus and orbitofrontal cortex in a T-maze perseverative model produced by 8-OH-DPAT in rats. Behav Brain Res. 2009, 203: 108-112. 10.1016/j.bbr.2009.04.026.PubMedGoogle Scholar
- Bartolomeo P, Chokron S: Orienting of attention in left unilateral neglect. Neurosci Biobehav Rev. 2002, 26: 217-234. 10.1016/S0149-7634(01)00065-3.PubMedGoogle Scholar
- Posner MI, Rafal RD, Choate LS, Vaughan J: Inhibition of return: neural basis and function. Cogn Neuropsychol. 1985, 2: 211-228. 10.1080/02643298508252866.Google Scholar
- Maylor EA, Hockey R: Inhibitory component of externally controlled covert orienting in visual space. J Exp Psychol Hum Percept Perform. 1985, 11: 777-787. 10.1037/0096-1518.104.22.1687.PubMedGoogle Scholar
- Yantis S, Jonides J: Abrupt visual onsets and selective attention: voluntary versus automatic allocation. J Exp Psychol Hum Percept Perform. 1990, 16: 121-134. 10.1037/0096-1522.214.171.124.PubMedGoogle Scholar
- Yu XJ, Xu XX, He S, He J: Change detection by thalamic reticular neurons. Nat Neurosci. 2009, 12: 1165-1170. 10.1038/nn.2373.PubMedGoogle Scholar
- Hebb DO: The organization of behaviour: a neuropsychological theory. 1949, [S.l.]: Chapman and HallGoogle Scholar
- Duncan J: Selective attention and the organization of visual information. J Exp Psychol Gen. 1984, 113: 501-517. 10.1037/0096-34126.96.36.1991.PubMedGoogle Scholar
- Weddell RA: Subcortical modulation of spatial attention including evidence that the Sprague effect extends to man. Brain Cogn. 2004, 55: 497-506. 10.1016/j.bandc.2004.02.075.PubMedGoogle Scholar
- Raos VC, Savaki HE: Functional anatomy of the thalamic reticular nucleus as revealed with the [14C]deoxyglucose method following electrical stimulation and electrolytic lesion. Neuroscience. 1995, 68: 287-297. 10.1016/0306-4522(95)00113-W.PubMedGoogle Scholar
- Lee SM, Friedberg MH, Ebner FF: The role of GABA-mediated inhibition in the rat ventral posterior medial thalamus. I. Assessment of receptive field changes following thalamic reticular nucleus lesions. J Neurophysiol. 1994, 71: 1702-1715.PubMedGoogle Scholar
- Bucherelli C, Tassoni G, Bures J: Differential effect of functional ablation of thalamic reticular nucleus on the acquisition of passive and active avoidance. Int J Neurosci. 1993, 73: 77-84. 10.3109/00207459308987213.PubMedGoogle Scholar
- McCormick PA: Orienting attention without awareness. J Exp Psychol Hum Percept Perform. 1997, 23: 168-180. 10.1037/0096-15188.8.131.52.PubMedGoogle Scholar
- Pinault D, Bourassa J, Deschenes M: Thalamic reticular input to the rat visual thalamus: a single fiber study using biocytin as an anterograde tracer. Brain Res. 1995, 670: 147-152. 10.1016/0006-8993(94)01303-Y.PubMedGoogle Scholar
- Koch C: The quest for consciousness: a neurobiological approach. 2004, Reading, Pa.: Roberts; Bloxham: ScionGoogle Scholar
- Libet B: Mind time: the temporal factor in consciousness. 2004, Boston, Mass.; London: Harvard University PressGoogle Scholar
- Bodovitz S: The neural correlate of consciousness. J Theor Biol. 2008, 254: 594-598. 10.1016/j.jtbi.2008.04.019.PubMedGoogle Scholar
- Roediger HL, Blaxton TA: Effects of varying modality, surface features, and retention interval on priming in word-fragment completion. Mem Cognit. 1987, 15: 379-388.PubMedGoogle Scholar
- Watson RT, Valenstein E, Heilman KM: Thalamic neglect. Possible role of the medial thalamus and nucleus reticularis in behavior. Arch Neurol. 1981, 38: 501-506.PubMedGoogle Scholar
- Lamme VA, Roelfsema PR: The distinct modes of vision offered by feedforward and recurrent processing. Trends Neurosci. 2000, 23: 571-579. 10.1016/S0166-2236(00)01657-X.PubMedGoogle Scholar
- Zeki S, Shipp S: The functional logic of cortical connections. Nature. 1988, 335: 311-317. 10.1038/335311a0.PubMedGoogle Scholar
- Lau HC, Passingham RE: Relative blindsight in normal observers and the neural correlate of visual consciousness. Proc Natl Acad Sci USA. 2006, 103: 18763-18768. 10.1073/pnas.0607716103.PubMed CentralPubMedGoogle Scholar
- Weiskrantz L, Barbur JL, Sahraie A: Parameters affecting conscious versus unconscious visual discrimination with damage to the visual cortex (V1). Proc Natl Acad Sci USA. 1995, 92: 6122-6126. 10.1073/pnas.92.13.6122.PubMed CentralPubMedGoogle Scholar
- McFarland NR, Haber SN: Organization of thalamostriatal terminals from the ventral motor nuclei in the macaque. J Comp Neurol. 2001, 429: 321-336. 10.1002/1096-9861(20000108)429:2<321::AID-CNE11>3.0.CO;2-A.PubMedGoogle Scholar
- Asanuma C: GABAergic and pallidal terminals in the thalamic reticular nucleus of squirrel monkeys. Exp Brain Res. 1994, 101: 439-451. 10.1007/BF00227337.PubMedGoogle Scholar
- Sidibe M, Bevan MD, Bolam JP, Smith Y: Efferent connections of the internal globus pallidus in the squirrel monkey: I. Topography and synaptic organization of the pallidothalamic projection. J Comp Neurol. 1997, 382: 323-347. 10.1002/(SICI)1096-9861(19970609)382:3<323::AID-CNE3>3.0.CO;2-5.PubMedGoogle Scholar
- Fuster JM: Prefrontal cortex in motor control. Handbook of Physiology: Motor control. Edited by: Brooks VB. 1981, Bethesda, MD: American Physiological Society, 1149-1178.Google Scholar
- Cheney PD: Role of cerebral cortex in voluntary movements. A review. Phys Ther. 1985, 65: 624-635.PubMedGoogle Scholar
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.