The Cognitive Neuroscience of Working Memory: Relevance to CNTRICS and Schizophrenia

doi:10.1016/j.biopsych.2008.03.003

Biol Psychiatry. Author manuscript; available in PMC 2009 July 1.

Published in final edited form as:

Biol Psychiatry. 2008 July 1; 64(1): 11–17.

Published online 2008 April 8. doi: 10.1016/j.biopsych.2008.03.003

PMCID: PMC2483314

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The Cognitive Neuroscience of Working Memory: Relevance to CNTRICS and Schizophrenia

Deanna M. Barch and Ed Smith

Deanna M. Barch, Washington University;

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Corresponding Author: Deanna M. Barch, Ph.D., Washington University, Department of Psychology, Box 1125, One Brookings Drive, St. Louis, MO. 63130, Phone: 314-935-8729, Fax: 314-935-8790, Email: dbarch/at/artsci.wustl.edu

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Abstract

Working memory is one of the central constructs in cognitive science and has received enormous attention in the theoretical and empirical literature. Similarly, working memory deficits have long been thought to be one of the core cognitive deficits in schizophrenia, making it a ripe area for translation. The current article provides a brief overview of the current theories and data on the psychological and neural mechanisms involved in working memory, which is a summary of the presentation and discussion on working memory that occurred at the first CNTRICS meeting in Washington, D.C. At this meeting, the consensus was that the constructs of goal maintenance and interference control were the most ready to be pursued as part of a translational cognitive neuroscience effort in the remaining CNTRICS meetings. The group felt that the constructs of long-term memory reactivation, capacity, and strategic encoding were of great clinical interest, but required more basic research. In addition, the group felt that the constructs of maintenance over time and updating in working memory had growing construct validity at the psychological and neural levels, but required more research in schizophrenia before knowing whether they should be targets for a clinical trials setting.

Working memory is perhaps one of the most frequently studied domains in both cognitive science and cognitive neuroscience, with a wealth of accumulated theoretical and empirical work at both the psychological and neural level [1]. Further, a large body of work has demonstrated that individuals with schizophrenia have deficits on a varied set of working memory tasks [e.g., 2, 3] that are associated with impairments in a range of neural mechanisms [4]. There is some data to suggest that the degree of impairment in certain aspects of working memory predicts later onset of schizophrenia [5, 6]. In addition, the level of working memory impairment predicts the degree of social and occupational impairment in individuals with schizophrenia [e.g., 7, 8]. Further, individuals who share unexpressed genetic components of vulnerability to schizophrenia also experience impairments in working memory function [e.g., 9, 10].

The centrality of working memory deficits in schizophrenia has led this to be one of the most vigorously studied cognitive domains in our attempts to understand the pathophysiology of this disorder. As such, working memory was selected as one of the domains relevant to the Cognitive Neuroscience Treatment Research to Improve Cognition in Schizophrenia (CNTRICS) initiative. This manuscript has two goals. The first is to provide an overview of the summary of the cognitive and neural mechanisms involved in working memory presented at the first CNTRICS meeting in Washington D.C. in February of 2007. The overview talk on working memory was presented by Ed Smith, and the breakout discussion included a range of participants from industry and academia, both from the basic science side (e.g., Randy Engle, Nelson Cowan, John Jonides, Todd Braver, Michael Frank, Trevor Robbins, Patricio O’Donnell) and the clinical science side (e.g., Diane Gooding, Deanna Barch, Jim Gold, Larry Seidman, Angus MacDonald, Dan Ragland). The second goal is to describe which mechanisms involved in working memory were selected as being ripe for translation, and the ways in which these mechanisms met the criteria outlined as part of the CNTRICS initiative. These criteria are described in detail in the overview article by Carter and Barch at the start of this special section. We should note that we do not wish to put forth the results of the discussion about working memory at the first CNTRICs meeting as somehow completely authoritative. There were clearly experts in the field of working memory that were not present at this meeting, and individuals who might disagree with the consensus opinions reached at this meeting, perhaps rightly so. However, there are too many constructs involved in working memory to allow us to pursue measurement of all of them simultaneously as part of the CNTRICS initiative. Thus, we felt that we had to begin to focus on the most promising constructs through some consensus based approach.

Cognitive Neuroscience Theories of Working Memory

Working memory is typically defined as the ability to maintain and manipulate information over short periods of time. There are a number of different influential models of the processes involved in working memory. One such early model is Baddeley’s [11], which distinguishes among four major components; 1) a short-term storage buffer for visual information that is often referred to as the visuo-spatial scratch pad; 2) a short-term storage buffer for verbal information referred to as the phonological loop (which includes both articulatory rehearsal and phonological processing; 3) a central executive component that guides the manipulation and transformation of information held within the storage buffers; and 4) the episodic buffer [12]. Each of these major component processes of working memory can also be further subdivided into subprocesses. A number of studies suggest that articulatory rehearsal is particularly dependent on regions of left ventrolateral prefrontal cortex (VLPFC), including Brodmann’s areas 44 and 45. Functional imaging studies examining rehearsal show activation of this region [13, 14], and lesions to this region impair articulatory rehearsal [15]. In contrast, the processing or storage of phonological representations is thought to be dependent on regions of left posterior parietal cortex [e.g., 13].

One way in which humans may maintain visual spatial information is to use covert shifts of attention to the spatial locations to be remembered, a process that has been referred to as attention based rehearsal [16]. These covert shifts of attention are thought to depend, at least in part, on the same neural systems that support spatial attention processing, including the right posterior parietal cortex [17], part of the dorsal attention system [e.g., 18]. In addition to right posterior parietal cortex, studies of spatial working memory also consistently activate regions such as the frontal eye fields (FEF) and the supplementary eye fields (SEF) [17].

The episodic buffer is a newer addition to Baddeley’s model [12]. Baddeley has suggested that this episodic buffer is able to create or store representations that integrate different types of information, and supports the binding of information into an “episode.” This concept makes contact with other conceptions of binding in working memory, which suggests that multidimensional representations can be maintained in working memory as integrated units rather than sets of independent features [19].

There are a number of different processes that are often referred to as being part of the central executive, including those involved in the manipulation of information being stored in the domain specific buffers, protection from interference due to competing information, temporal coding or sequencing, updating of the contents of working memory, and the maintenance of goal representations in working memory. Importantly, most, if not all, of these processes are unlikely to be specific to working memory. At a general level, dorsolateral regions of prefrontal cortex (DLPFC), typically Brodmann’s areas 46 and 9 bilaterally, have been associated with many of the processes attributed to central executive [20]. However, regions other than DLPFC are also important for the processes ascribed to the central executive and we should not equate DLPFC and executive function. As one example, Jonides and colleagues have shown that a region of left VLPFC is involved in the resolution of proactive interference, a process that many have ascribed to the central executive [21, 22].Further, Wager and Smith (2003) performed a meta-analysis of working-memory tasks that presumably recruit the central executive, and found that the most frequently activated area across studies was in the posterior parietal cortex.

A different, but increasingly influential, model of working memory put forth by Cowan suggests that there are not qualitative or structural differences in the representations used to support working memory as compared to episodic memory, in the sense of there being dedicated storage buffers that only maintain information “contained” in working memory. Instead, Cowan’s model suggests that the information contained in working memory is simply the activated portion of working long-term memory that is currently in the focus of attention. This model is gaining increasing acceptance and provides an excellent fit to much of the extant behavioral and neurobiological data. Further, this model has an interesting, and somewhat different, set of implications for the neural substrates of working memory, as articulated recently by D’Esposito [1]. Specifically, a Cowan type model suggests that the neural systems supporting information that is currently in the focus of attention in working memory should use the same systems used to initially process or store information in long term memory. Work by D’Esposito and colleagues has shown that working memory tasks requiring the maintenance of face information activates the fusiform face area (an area putatively specialized for processing and storing face information), while the maintenance of house representations differentially activated the parahippocampal place area [23] [see also 24, 25].

In a related vein, Engle and colleagues have emphasized the centrality of goal maintenance and interference control in working memory [e.g., 28, 29]. This body of work suggests that a critical aspect of working memory is the ability to maintain goal representations that allow one to select task relevant information from task-irrelevant information, and to protect this information from distraction or interference (i.e., working memory as “controlled attention”). Engle and colleagues have argued that this conceptualization of working memory helps to explain why individual differences in working memory capacity explain performance on tasks such as the antisaccade and the Stroop, which also require goal maintenance [30, 31].

A great deal of work in the cognitive neuroscience of working memory has also focused on understanding the contributions of specific neurotransmitter systems. The dopamine system has received the most attention. Goldman-Rakic and her colleagues [32] have demonstrated that working memory function is impaired in non-human primates following 6-hydroxy-dopamine lesions in prefrontal cortex [33], or administration of dopamine antagonists [34]. Dopamine agents can also modulate working memory function in humans, although the results in this domain vary as a function of facts such as the nature of the task, the ability level of the participants, and even their genetic makeup (for a review, se [4]). A number of researchers have postulated specific computational roles for dopamine in working memory [e.g., 37, 38]. Braver and colleagues have suggested that dopamine may serve as a cue for updating information in working memory, and that phasic dopamine signals help to gate or regulate what information is loaded into working memory, a process that can help to protect from interference due to distracting information [39, 40]. In a similar vein, Frank and O’Reilly have argued that basal ganglia mediated dopamine signals serve to update representations in working memory [41]. Durstewitz has elaborated models in which NMDA activity interacts with dopamine to modulate recurrent activity in neural networks thought to support working memory representations [42].

After a formal presentation on mechanisms involved in working memory given by Ed Smith, the attendees of the CNTRICS meeting engaged in a discussion as to the degree to which various mechanisms involved in working memory met the criteria identified as being important for selecting mechanisms for immediate translation (see Table 1 in the Carter and Barch article). These criteria include the degree of evidence for neural and psychological construct validity, the ability to measure the process in humans (including amenability to use in imaging studies), the evidence for impairment in schizophrenia and links to functional outcome, and the availability of an explicit animal model. This discussion allowed the participants to group mechanisms into three general categories: 1) those recommended for immediate translation; 2) those recommended for more basic and clinical research; and 3) those recommended for more basic research (Table 1).

Table 1

Grouping of Working Memory Constructs in Terms of Their Readiness for Translation

Constructs Ready for Immediate Translation

Goal Maintenance

Clarity of the understanding of the cognitive mechanism

As described above, Engle’s theory of working memory emphasizes the centrality of the ability to maintain goals that delineate the type of information that is currently relevant for the contents of working memory (e.g., the focus of attention) as a means of selecting task-relevant information for inclusion in working memory and as a means of protecting this information from interference from competing information [e.g., 28, 29]. The term “goal” in this context refers to a range of information, including task instructions, representations of target stimuli, and the results of processing prior stimuli. For example, in the type of working memory task used by Luck and colleagues, the goal representation might include information about the task features (color, orientation, etc.) relevant for memory selection [19]. Further, the specific mechanisms by which goals could be actively maintained and bias ongoing information processing in working memory have been delineated in several different computational models that have helped to clarify our understanding of this construct [e.g., 41, 44, 45]. This construct is easily measured in humans through a variety of tasks, such as various versions of complex span tasks [46], task switching tasks, variations on the continuous performance task, etc.

Clarity of the link to a specific neural circuit

Not surprisingly, goal maintenance in working memory has been linked to the function of DLPFC, with both empirical and theoretical work suggesting that dopaminergic inputs to DLPFC are critical (though recent work has specified an important role for both glutamate [42] and norepinephrine [47] as well). Such mechanisms have been explicitly implemented in biologically plausible computational models designed to formalize the interactions between prefrontal and basal ganglia systems in goal maintenance [e.g., 40, 41]. Further, a number of functional imaging studies have shown activation of dorsolateral prefrontal cortex when individuals are required to maintain goals in working memory [e.g., 48, 49].

Strong Evidence of Impairment in Schizophrenia

Numerous studies have provided evidence that individuals with schizophrenia have difficulties maintaining goals in working memory. Such deficits that are present in both medicated and unmedicated individuals and at both acute and chronic stages of the illness [e.g., 50, 51–55]. In addition, such deficits in goal maintenance are found in the first-degree relatives of individuals with schizophrenia [56, 57], as well as in individuals with schizotypal personality disorder [58, 59]. Individuals with schizophrenia also show strong evidence of impairment on other tasks that may tap into goal maintenance, such as the Stroop task [e.g., 60] and the antisaccade task [e.g., 61], as do their first degree relatives [58] Individuals with schizophrenia also show consistent evidence of impaired prefrontal activity, particularly in dorsolateral regions, during tasks that require goal maintenance [e.g., 55, 62, 63]. Again, the first-degree relatives of individuals with schizophrenia also show evidence of impaired prefrontal activation during goal maintenance [57, 64]. Lastly, there is evidence that such deficits in goal maintenance in schizophrenia are specific, and cannot be accounted for by a generalized deficit [e.g., 50, 53–55].

Interference Control

Clarity of the understanding of the cognitive mechanism

The idea that there are mechanisms involved in the protection of information in working memory (as well as long term memory) from interference has a long history and tradition in cognitive science. One of the ways in which this has been more commonly studied is in the domain of proactive interference, in which exposure to or processing of a set of previous stimuli interference with the processing of subsequent stimuli [65]. Proactive interference can lead to slowed responding and impaired performance in a range of domains, and thus is clearly a critical aspect of human information processing [28, 66]. The mechanisms involved in proactive interference and interference control at the psychological level have been well studied [e.g., 67] and formalized in computational models [68]. The majority of the models of the mechanisms involved in interference control suggest that this is accomplished by the maintenance of representations of the relevant task parameters, with the addition of selection mechanisms that may compare incoming information to templates or stored representations. There are numerous paradigms available to study proactive interference in working memory [67], making this a construct easily measured in humans.

Clarity of the link to a specific neural circuit

There is a nice body of research, recently summarized by both Badre and Wagner [65] and Jonides and Nee [67], implicating left ventral lateral prefrontal cortex in interference control in working memory. For example, a number of functional neuroimaging studies have shown activation of left ventral lateral prefrontal cortex on task trials in which individuals have to inhibit the interfering effects of previously presented information on correct responding [e.g., 22, 69]. Further, individuals who are better at preventing proactive interference show greater activity in left ventrolateral prefrontal cortex [70]. In addition, lesions to left ventrolateral prefrontal cortex make individuals more susceptible to proactive interference in working memory [71], as does TMS over left ventrolateral prefrontal cortex [72].

Evidence of Impairment in Schizophrenia

Evidence has existed for deficits in interference control in working memory in schizophrenia as early as the seminal work of Oltmanns and Neale, which demonstrated a differential deficit in working memory span in the face of distraction as compared to no distraction [73]. This finding has been replicated by a number of researchers [e.g., 74, 75]. In more recent work, Brahmbhatt and colleagues have shown heightened sensitivity to proactive interference among individuals with schizophrenia in the context of an n-back working memory task. A number of other researchers have also suggested impaired distractibility in the context of working memory or attention tasks in schizophrenia [e.g., 76]. Interestingly, however, the literature does not suggest strong evidence for enhanced proactive interference among individuals with schizophrenia in the context of long term or episodic memory [e.g., 77], though some studies have found increased proactive interference in episodic memory in schizophrenia [78]. This may reflect the fact that in long-term memory, memory deficits for the stimuli that could cause proactive interference in individuals with schizophrenia may actually reduce the effects of proactive interference. In contrast, interference from concurrent or recently presented stimuli may still be problematic for individuals with schizophrenia.

As described above, the group felt that the constructs of goal maintenance and interference control met the criteria outlined as important for selecting constructs in the CNTRICs survey. Nonetheless, the group still felt that there were some open issues/concerns about these constructs. For example, there is little evidence about the relationship of these constructs to functional impairment in schizophrenia, though this absence reflects a lack of research, rather than negative results in existing research. In addition, there was some concern as to the degree to which goal maintenance and interference control can be considered dissociable constructs, given that successful interference control may depend, at least in part, on intact goal maintenance.

Constructs In Need of More Clinical Research

There were two constructs – rehearsal (active maintenance over time) and updating – that the conference participants felt had reasonable construct validity at the neural and psychological levels, but which they felt needed more research to determine whether these mechanisms were impaired in schizophrenia. Maintenance over time, has been well studied in the basic science literature. As described above, the phonological loop is thought to support rehearsal and maintenance of verbally coded information, while covert shifts of attention may help to support the maintenance of spatial information. Further, at the neural level, many models assume that active maintenance occurs via self-sustained recurrent synaptic activity [e.g., 79, 80]. Alternatively (or in addition), active maintenance may occur via synchronous oscillations between neuronal populations within regions or across regions [79].

The issue in regards to individuals with schizophrenia is whether they show consistent evidence of impaired maintenance over time once initial encoding is equated and when there is no distracting information in the delay interval. Importantly, the seminal studies on spatial working memory in schizophrenia conducted by Park and colleagues used a paradigm in which an interference task occurred during the delay period [e.g., 2]. Thus, these studies cannot be taken as evidence for impaired maintenance in the absence of distraction, as distraction may engage interference control mechanisms. For example, Kim found no impairments in individuals with schizophrenia on maintenance only (without distraction) for either verbal or visual spatial information [81]. However, a study by Tek did equate for initial encoding, and found some evidence for impaired maintenance of spatial information over an unfilled delay of 3 seconds [82]. Similar results were found in a recent study of visual-spatial memory using a 4 second unfilled delay [83].

There is also mixed evidence as to whether the phonological loop is intact in schizophrenia. Though no cognitive task measures a single process, some working memory tasks are more dependent on the phonological loop than others. For example, serial recall tasks with relatively low numbers of items (such as digit span forward, Sternberg or Brown-Petersen paradigms) and no interference are considered by some to be prototypical phonological loop tasks. According to at least some researchers, such tasks require both intact articulatory rehearsal and intact phonological storage/representations to perform successfully. A number of studies have shown that individuals with schizophrenia demonstrate relatively intact performance on digit span forward tasks, particularly when the number of items is at or below working memory span (7+−2) [e.g., 2, 54, 84] and when there is no verbal interference [e.g., 73]. Other work has shown that individuals with schizophrenia do not show disproportionate impairment for recall of lists with phonologically similar versus dissimilar items, suggesting an intact ability to represent phonological information [85]. Further, studies suggest intact serial position curves among individuals with schizophrenia [86], which is indicative of intact articulatory rehearsal mechanisms. However, a recent meta-analysis of the performance of individuals with schizophrenia did find significant impairment on digit span forward, though with a relatively small effect size compared to performance in other memory domains [88]. Thus, more work is needed to establish whether or not there is robust evidence for maintenance deficits in schizophrenia that are not confounded by encoding accuracy or interference control deficits.

The second construct judged to be in need of more clinical research was updating of the contents of working memory. There is a body of cognitive neuroscience research beginning to outline the mechanisms involved in updating. This work suggests that interactions between dorsal frontal and parietal regions may be particularly critical for updating the contents of working memory [e.g., 89]. In addition, there are a number of computational models that now suggest that dopaminergic signals from the basal ganglia serve as “gating” signals that indicate when to update the contents of working memory [40, 90]. Recently work by Galletly using ERPs was interpreted as reflecting deficits in updating [91]. However, the consensus was that there was relatively little evidence as to whether or not individuals with schizophrenia have specific problems with updating the contents of working memory.

Constructs In Need of More Basic Research

There were three constructs that the conference attendees felt were in need of greater basic research to establish psychological and neural construct validity before they were ready for use in a clinical trials context. The first construct was long term memory reactivation, either in terms of the mechanism by which information is moved back into working memory, or in terms of the idea that working memory is simply the activated component of long term memory, as in Cowan’s model [92]. Although there is indirect evidence consistent with the idea that episodic memory mechanisms interact with or contribute to paradigms that we would describe as tapping working memory[27], the specific mechanisms by which this occurs and how it interacts with the other systems involved in working memory awaits further explication.

The construct of capacity in working memory also came under hot debate. In Miller’s original work, human working memory capacities were estimated to be 7 plus or minus 2 [93]. However, more recent work suggests that our capacity really has something more like a mean of 4 for both verbal and non-verbal materials [e.g., 19]. Using a variety of paradigms, there is very good evidence to suggest that individuals with schizophrenia have reduced capacity in working memory [e.g., 94]. However, we do yet have a clear understanding of the mechanisms that drive capacity limitations at either the psychological or neural level. There is exciting work being conducted in computational and neurophysiological modeling that may eventually clarify this question [e.g., 95][96]. Once we have a clearer sense of the basic mechanisms that drive capacity limitations in human working memory, we should be able to use this information to help us determine and measure why individuals with schizophrenia have added capacity limitations.

The last construct felt to be in need of more basic research was the concept of strategic encoding into working memory. By strategic encoding, we mean the ability to spontaneously detect and apply effective encoding strategies that would help maintain information in working memory and protect it from interference. The literature on episodic memory gives us good reason to believe that individuals with schizophrenia have difficulty with the spontaneous generation and application of effective encoding strategies [e.g., 97, 98]. However, we really have very little idea of the mechanisms by which individuals normally spontaneously generate and apply such encoding strategies. Further, we have little idea of the specific neural mechanisms that support the process of generating strategies, other than a general idea that the prefrontal cortex may be important for this process.

Acknowledgments

This work was supported by grants NIMH grants MH60887, MH066031 and MH56584, as well as a Conte Center for Neuroscience of Mental Disorders MH071616 grant.

Footnotes

Disclosures

Dr. Barch reported no biomedical financial interests or potential conflicts of interest

Dr. Smith reported no biomedical financial interests or potential conflicts of interest

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Contributor Information

Deanna M. Barch, Washington University.

Ed Smith, Columbia University.

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