Cognitive Function and Monoamine Neurotransmission in Schizophrenia: Evidence From Positron Emission Tomography Studies.

Positron emission tomography (PET) is a non-invasive imaging technique used to assess various brain functions, including cerebral blood flow, glucose metabolism, and neurotransmission, in the living human brain. In particular, neurotransmission mediated by the monoamine neurotransmitters dopamine, serotonin, and norepinephrine, has been extensively examined using PET probes, which specifically bind to the monoamine receptors and transporters. This useful tool has revealed the pathophysiology of various psychiatric disorders, including schizophrenia, and the mechanisms of action of psychotropic drugs. Because monoamines are implicated in various cognitive processes such as memory and executive functions, some PET studies have directly investigated the associations between monoamine neurotransmission and cognitive functions in healthy individuals and patients with psychiatric disorders. In this mini review, I discuss the findings of PET studies that investigated monoamine neurotransmission under resting conditions, specifically focusing on cognitive functions in patients with schizophrenia. With regard to the dopaminergic system, some studies have examined the association of dopamine D1 and D2/D3 receptors, dopamine transporters, and dopamine synthesis capacity with various cognitive functions in schizophrenia. With regard to the serotonergic system, 5-HT1A and 5-HT2A receptors have been studied in the context of cognitive functions in schizophrenia. Although relatively few PET studies have examined cognitive functions in patients with psychiatric disorders, these approaches can provide useful information on enhancing cognitive functions by administering drugs that modulate monoamine transmission. Moreover, another paradigm of techniques such as those exploring the release of neurotransmitters and further development of radiotracers for novel targets are warranted.

Introduction

Positron emission tomography (PET) is a non-invasive imaging technique used to assess various brain functions, including cerebral blood flow, glucose metabolism, and neurotransmission, in the living human brain. In particular, neurotransmission via the monoamine neurotransmitters dopamine, serotonin, and norepinephrine, has been extensively examined using PET probes, which specifically bind to the receptors, transporters, and other target molecules of these monoamines. PET provides various aspects of neurotransmission such as presynaptic and postsynaptic functions, along with anatomical information. This useful tool has revealed aspects of the pathophysiology of various psychiatric disorders, including schizophrenia, and the mechanisms of action of psychotropic drugs since monoamines are the primary targets for antipsychotic and antidepressant drugs (1). Specifically, the differences between patients and healthy controls, associations with symptomatology and psychopathology in patients, and receptor/transporter occupancy by psychotropic drugs have been reported, albeit the results have been inconsistent among studies. Since previous animal studies and human pharmacological studies have implicated monoamines in various cognitive functions, some PET studies have directly explored the associations between monoamine neurotransmission and cognitive functions in healthy individuals and patients with psychiatric disorders.

Schizophrenia, one of the most severe and complex psychiatric disorders, with a lifetime prevalence of approximately 1% worldwide, is characterized by psychosis (positive symptoms), negative symptoms, and cognitive dysfunction (2). In recent years, cognitive impairment has been considered a core feature of this disorder (3, 4), with the largest effect sizes reported in both verbal memory and executive function (5, 6). A number of functional neuroimaging studies that measured cerebral blood flow using functional magnetic resonance imaging (fMRI) and PET have revealed a relationship between cognitive deficit and altered regional brain functions (5–9). However, not many studies have used PET to explore the relationship between monoamine neurotransmission and cognitive dysfunction in schizophrenia. In this mini review, I discuss the findings of monoamine PET studies, specifically focusing on neurocognitive functions in individuals with schizophrenia.

PET techniques for evaluation of monoamine transmission

Most of the radiotracers used for neuroimaging-based quantification of receptors and transporters are pharmacologically antagonists that reversibly and specifically bind to these targets. The main outcome measure is the binding potential relative to the concentration of non-displaceable radiotracer in the brain (BPND), corresponding to the ratio of the density of receptors or transporters available to bind radiotracer in vivo (Bavail) to the dissociation constant of the radiotracer (KD) (10, 11). The gold standard of kinetic analysis of brain PET measurements is a compartment analysis with arterial input function, which requires arterial blood sampling and metabolite analysis of the parent compound. However, simplified methods can be applied if a reference region that is devoid of the receptor/transporter, such as the cerebellum, is present. These simplified methods are less invasive and more suitable for clinical use. For this review, I have selected PET studies performed under resting conditions (mainly for unmedicated individuals), which evaluate receptor/transporter availability and neurotransmitter synthesis capacity. Single photon emission computed tomography (SPECT) studies were not included because PET has a much higher sensitivity and spatial resolution than does SPECT, and more tracers have been developed for PET than for SPECT. The main PET tracers used for the measurement of central monoaminergic transmission are listed in Table 1. Some PET tracers have been reported to measure dopamine release, however, I did not include these challenge studies because my primary interest was to provide an overview of various monoamine transmissions in basic and simple conditions. A summary of studies that investigated both monoamine PET and cognitive functions in patients with schizophrenia and/or healthy subjects is listed in Table 2.

Table 1

PET probes used for the measurement of central monoaminergic transmission.

Monoamine	Target	Name of PET probes
Dopamine	D1	[11C]SCH23390, [11C]NNC112
	D2/D3	[11C]raclopride*, [11C]FLB457*, [18F]fallypride*
	Transporter	[11C]CFT
	Synthesis	[18F]DOPA, [11C]DOPA
Serotonin	1A	[11C]WAY100635
	2A	[18F]altanserin
	Transporter	[11C]DASB
Norepinephrine	Transporter	[18F]FMeNER-D2

These probes can be used to measure dopamine release.

Table 2

Summary of studies that investigated both monoamine PET and cognitive functions in patients with schizophrenia and/or healthy subjects.

Study	Year	Subjects	Cognitive tasks	PET probe	Findings
Okubo et al. (20)	1997	17 with Sch and 18 HV	WCST	[11C]SCH23390	Reduced prefrontal D1RA was associated with poor WCST performance
Abi-Dargham et al. (21)	2002	16 with Sch and 16 HV	N-back	[11C]NNC112	Increased prefrontal D1RA was associated with poor working memory
Takahashi et al. (22)	2008	23 HV	WCST, ROCFT, RAVLT	[11C]SCH23390	An inverted U-shaped relationship between prefrontal D1RA and WCST performance
Hirvonen et al. (27)	2005	11 unaffected co-twins with Sch and 7 twin HV	WMS-R, CVLT	[11C]raclopride	Higher D2RA in the caudate was associated with a poor performance on tasks related to schizophrenia vulnerability
Cervenka et al. (29)	2008	16 HV	Pair associative learning, delayed pattern recognition memory, word recognition, WAIS-R, category fluency	[11C]raclopride	D2RA in the limbic striatum was related to episodic memory, D2RA in the associative and sensorimotor striatum showed associations with non-episodic tasks
Vyas et al. (35)	2017	25 with Sch and 19 HV	WCST, CVLT	[18F]fallypride	In individuals with Sch, D2RA was negatively correlated with WCST and CVLT performance whereas positive correlation was observed in HV
Takahashi et al. (36)	2007	25 HV	RAVLT, ROCFT, WCST	[11C]FLB457	Hippocampal D2RA was positively correlated with memory and also associated with frontal lobe functions
Yoder et al. (38)	2004	10 with Sch (most were medicated)	PANSS	[11C]CFT	Striatal DAT availability was inversely correlated with scores on the cognitive subscale of PANSS
Velnaleken et al. (48)	2007	11 HV	CPT, Stroop, TMT, WCST	[18F]DOPA	Positive correlations between DA synthesis capacity in the caudate nucleus, putamen, and midbrain with performance on TMT-B, CPT, and Stroop test
Meyer-Lindenberg et al. (41)	2002	6 with Sch and 6 HV	WCST	[18F]DOPA	Decreased PFC activation measured with fMRI predicted exaggerated striatal DA synthesis capacity
McGowan et al. (49)	2004	16 medicated individuals with Sch and 12 HV	Stroop, VF, SDMT	[18F]DOPA	Negative correlations between Stroop interference scores and DA synthesis capacity in the ACC in both individuals with Sch and HV
Howes et al. (43)	2009	24 prodromal individuals with Sch, 6 with Sch, and 12 HV	VF	[18F]DOPA	Within the prodromal Sch group, performance on the semantic VF task was negatively correlated with striatal DA synthesis capacity
Yasuno et al. (58)	2003	16 HV	WMS-R	[11C]WAY100635	Negative correlation between explicit memory function and 5-HT1ARA in hippocampus
Borg et al. (59)	2006	24 HV	Claeson–Dahl Learning and Memory Test, CPT, spatial working memory test, ROCFT, controlled oral assessment, WCST	[11C]WAY100635	No correlation between performance on any of the cognitive tests and 5-HT1ARA in the raphe, hippocampus, and neocortex
Penttila et al. (60)	2016	24 HV	WCST, WMS-R	[11C]WAY100635	Global 5-HT1ARA was positively correlated with verbal memory
Rasmussen et al. (61)	2010	30 with Sch and 30 HV	Spatial working memory, Stockings of Cambridge, Intra-Extradimensional set-shifting, rapid visual information processing	[18F]altanserin	No correlation between neurocognitive measures and 5-HT2ARA in any region
Madsen et al. (63)	2011	32 HV	Stroop, TMT, RAVLT, ROCFT, Intelligenz-Struktur-Test 2000 R	[11C]DASB	Positive associations between 5-HTT availability and Stroop test performance and logical reasoning. No association between 5-HTT availability and memory

Sch, schizophrenia; HV, healthy volunteer; RA, receptor availability; WCST, Wisconsin Card Sorting Test; ROCFT, Rey-Osterrieth's Complex Figure Test; RAVLT, Rey's Auditory Verbal Learning Test; WMS-R, Wechsler Memory Scale-Revised; CVLT, California Verbal Learning Test; WAIS-R, Wechsler Adult Intelligent Scale-Revised; DLPFC, dorsolateral prefrontal cortex; PANSS, Positive and Negative Syndrome Scale; DAT, dopamine transporter; CPT, Continuous Performance Test; TMT, Trail Making Test; fMRI, functional magnetic resonance imaging; VF, verbal fluency; SDMT, Symbol-Digit Modality Test; ACC, anterior cingulate cortex; 5-HT1A, 5-hydroxytryptamine 1A; 5-HT2A, 5-hydroxytryptamine 2A; 5-HTT, 5-hydroxytryptamine transporter.

Dopamine

Dopamine is the main neurotransmitter involved in the pathophysiology and treatment of schizophrenia (12). Dopamine pathways have been well illustrated by PET with different radiotracers (13) and these PET tracers have been used to elucidate various aspects of aberrant dopaminergic transmission in schizophrenia for review see (14–16).

D1 receptors

D1 receptors are densely localized in the striatum, and uniformly distributed in the neocortical regions (13). Evidence from animal and clinical research has suggested the presence of prefrontal dysfunctions in schizophrenia, and the D1 receptors in this brain region are considered to play crucial roles in various frontal lobe functions such as working memory (17–19).

Using the tracer [11C]SCH23390, Okubo et al. showed that patients with schizophrenia had lower D1 availability in the prefrontal cortex (20). They examined 17 male patients with schizophrenia (10 antipsychotic-naïve and 7 antipsychotic-free) and 18 healthy male controls. Availability of the D1 receptor in the prefrontal cortex was negatively correlated with the severity of negative symptoms, and was also associated with poor performance on the Wisconsin Card Sorting Test (WCST), which assesses executive function and prefrontal function. In contrast, using the tracer [11C]NNC112, Abi-Dargham et al. reported increased availability of the D1 receptor in the dorsolateral prefrontal cortex of 16 untreated patients with schizophrenia (7 antipsychotic-naïve and 9 antipsychotic-free) compared to that in 16 healthy subjects (21). The increased availability was related to n-back task performance, which represents working memory. The discrepancy in these results could arise owing to difference in the background of patients (age, sex, and prior exposure to antipsychotics) and the different tracers used. Additionally, the results of a study by Takahashi et al. provide a potential explanation for this discrepancy. Using [11C]SCH23390 PET in healthy subjects, they found a U-shaped relationship between prefrontal D1 receptor availability and the performance on the WCST, indicating that too little or too much D1 receptor stimulation hampers working memory or set shifting (22, 23), which was also hypothesized from the results of animal studies (18, 19).

D2/D3 receptors

The striatum, which has dense dopamine innervation, is usually imaged using a moderate-affinity PET probe such as [11C]raclopride, and extrastriatal regions with very low levels of D2/D3 receptors, including the cortex, limbic regions, and thalamus, are imaged by high-affinity PET probes such as [11C]FLB457 and [18F]fallypride (Table 1). All these tracers are benzamide derivatives and antagonistically bind to both D2 and D3 receptors.

Dopamine D2 receptors are the primary target of currently available antipsychotic drugs owing to their potential to block these receptors (1, 2). Accordingly, several PET studies have investigated dopamine D2 receptors in schizophrenia beginning from the 1980's. However, previous reviews and meta-analyses PET and SPECT studies showed no difference or a small elevation in striatal D2/D3 receptor availability in unmedicated patients with schizophrenia compared to that in healthy controls under resting conditions (15, 24–26); however, the elevation was not evident in drug-naïve patients (26). Among these studies, a few evaluated cognitive functions because most studies focused on the psychopathology, particularly positive symptoms; therefore, less attention was given to cognitive impairment involving striatal dopamine D2 receptors in schizophrenia. Using PET and [11C]raclopride, Hirvonen and colleagues (27) examined 6 monozygotic and 5 dizygotic unaffected co-twins of patients with schizophrenia and 4 monozygotic and 3 dizygotic healthy control twins. They found that dopamine D2 receptor availability in the caudate was upregulated in unaffected monozygotic co-twins, and this upregulation was associated with poor performance on cognitive tasks such as a part of the Wechsler Memory Scale-Revised and the California Verbal Learning Test (CVLT).

The striatum can be divided into three functional subdivisions: the limbic, associative, and sensorimotor striatum (28). In healthy subject, using [11C]raclopride PET, Cervenka et al. found a distinct pattern of correlations among the striatal subregions; D2 receptor availability in the limbic striatum was related to performance on episodic memory, while that in the associative and sensorimotor striatum showed associations to non-episodic tasks (29).

With regard to extrastriatal D2/D3 receptors, significant differences in their availability between schizophrenia and healthy controls have been reported particularly in the thalamus (30–33); a meta-analysis found the summary effect size for thalamic D2/D3 availability was d = −0.32, however, did not reach significance (34). In a very recent comprehensive study, Vyas et al. used [18F]fallypride to evaluate executive dysfunction and memory impairment in patients with schizophrenia (35). Twenty medication-naïve and 5 drug-free patients with schizophrenia underwent the WCST and CVLT. Patients with schizophrenia showed negative or low correlations between D2/D3 receptor availability and WCST performance, while healthy subjects showed positive correlations, suggesting better performance with higher D2/D3 receptor availability; the difference was marked in the thalamus. Similarly, patients showed negative or very low correlations between D2/D3 receptor availability in the fronto-striatal-thalamic regions and performance on the CVLT, while healthy subjects showed a positive correlation. In another study in healthy subjects, Takahashi et al. reported a relationship between hippocampal dopamine D2 receptors and not only memory but also frontal functions such as executive functions and verbal fluency (36).

Dopamine transporter (DAT)

The majority of molecular imaging studies investigating striatal DAT availability failed to find any significant differences between healthy controls and untreated patients with schizophrenia (15), and this finding was supported by the results of recent meta-analyses that included PET and SPECT studies (26, 37). One study showed that schizophrenia patients with tardive dyskinesia had lower DAT availability than schizophrenia patients without tardive dyskinesia, and that striatal DAT availability was correlated with the severity of negative symptoms, and cognitive and depression/anxiety scores on the positive and negative syndrome scale (38). However, most of the subjects in the study were medicated and the medication effect needs to be considered. In addition, no MRI scans were available for all patients, and positive and negative syndrome scale scores were not assessed for some patients. To the best of my knowledge, measures of cognitive functions were not evaluated in any other PET studies on DAT in schizophrenia.

L-DOPA uptake (dopamine synthesis capacity)

The endogenous dopamine synthesis rate is commonly measured using 6-[18F]fluoro-L-DOPA or L-[β-11C]DOPA, two radioactive analogs of the dopamine precursor L-DOPA, which are indicative of dopamine synthesis capacity in presynaptic terminals (13, 16). In schizophrenia compared to healthy controls, increased dopamine synthesis capacity has been consistently shown in the majority of previous studies (39–46) (for review see (15, 16)) and recent meta-analyses confirmed the findings with large effect sizes (26, 47).

In a study investigating the association between human cognitive function and dopamine synthesis capacity, Velnaleken et al. (48) found significant positive correlations in healthy subjects between the dopamine synthesis capacity in the striatum and performance on the trail-making test-B, continuous performance test, and Stroop test. In one study with unmedicated schizophrenia patients (41), PET with [18F]DOPA and [15O]H2O (which measures cerebral blood flow) revealed that patients with schizophrenia had higher dopamine synthesis capacity in the striatum than healthy controls did, indicating exaggerated presynaptic dopamine function. In patients with schizophrenia, the increase in cerebral blood flow in the dorsolateral prefrontal cortex during the WCST task was tightly coupled with striatal dopamine synthesis capacity; this relationship was not found in healthy controls. In another study, [18F]DOPA PET in patients with schizophrenia on antipsychotic medication revealed that the dopamine synthesis capacity in the dorsal anterior cingulate was correlated with performance on the Stroop Color-Word Test (49).

During the manifestation of prodromal symptoms of schizophrenia before the onset of psychosis, patients showed elevated striatal dopamine synthesis capacity in the associative striatum (43). In that study, the at-risk mental state group showed a negative correlation between the dopamine synthesis capacity in the associative striatum and the performance on the semantic verbal fluency task, i.e., greater elevation in synthesis was associated with fewer correct responses and a similar negative correlation was observed for phonologic verbal fluency.

Serotonin (5-hydroxytryptamine, 5-HT)

In the human brain, the serotonergic system has 14 diverse receptor subtypes and transporters (50). Because of the availability of suitable radiotracers, extensive PET studies have been performed to investigate the availability of 5-HT1A and 5-HT2A receptors and the 5-HT transporter in various neuropsychiatric disorders. These receptors and transporters are of interest because they are main targets of pharmacotherapy via psychotropic drugs (51, 52). However, the number of imaging studies investigating the central serotonergic system in schizophrenia is limited (53).

5-HT1A receptors

5-HT1A receptors are widely distributed in the hippocampal regions, insula, neocortical regions, and dorsal raphe nucleus (54). In addition, because the 5-HT1A receptor modulates the entire serotonin system, it is one of the most important 5-HT receptor subtypes (55). Several lines of evidence from animal studies and pharmacological studies indicate that the 5-HT1A receptor plays an important role in cognitive function and is a promising target for the treatment of cognitive and affective symptoms in neuropsychiatric disorders, including schizophrenia (51, 52, 55).

Thus far, four studies have examined 5-HT1A availability in schizophrenia, using the same PET tracer [11C]WAY100635. One study reported an increase in 5-HT1A availability in the medial temporal cortex of schizophrenia patients (56), whereas another reported a decrease in the amygdala (57); the remaining two reported no difference in 5-HT1A availability between schizophrenia patients and healthy controls, although a meta-analysis of postmortem studies found an elevation in prefrontal 5-HT1A in schizophrenia (53).

With regard to cognitive function in healthy subjects, Yasuno et al. found a negative correlation between explicit memory function and 5-HT1A receptor availability in the hippocampus (58), while Borg et al., who performed [11C]WAY100635 PET and used the same simplified reference model, found no correlation between regional 5-HT1A receptor availability in the raphe nuclei, hippocampus, and neocortex and various domains of cognitive performance (55, 59). However, a recent study by Penttila et al. found that global 5-HT1A receptor binding, measured with the gold standard method based on kinetic modeling using arterial blood samples, was positively correlated with measures of verbal memory in healthy subjects (60). To date, no 5-HT1A PET data have been reported for patients with schizophrenia in relation to cognitive function.

5-HT2A receptor

A large body of evidence from postmortem and pharmacological studies suggests that 5-HT2A receptors play an important role in schizophrenia and cognition (51, 52). A meta-analysis of postmortem studies found a reduction in prefrontal 5-HT2A receptors in patients with schizophrenia (53). However, only a few PET studies have been performed on first-episode antipsychotic-naïve patients with schizophrenia, and their results are inconsistent (53). In a recent study with the largest sample size to date, a total of 30 patients with schizophrenia and matched healthy controls underwent [18F]altanserin PET scans, which are highly selective for 5-HT2A receptors (61). Patients with schizophrenia showed lower 5-HT2A availability in the frontal cortex than healthy controls did. However, no correlations were found between 5-HT2A availability and cognitive functions such as working memory, attention, and executive functions, suggesting that 5-HT2A receptors are not involved in cognitive dysfunction, at least in the early stage of schizophrenia.

Serotonin transporter (5-HTT)

A previous PET study with the 5-HTT-selective tracer [11C]DASB found no significant difference in 5-HTT availability between patients with schizophrenia and healthy control subjects, and no correlation between 5-HTT availability and schizophrenia symptoms (62). In contrast, another [11C]DASB PET study with healthy subjects found that 5-HTT availability in the fronto-striatal regions was associated with better performance on executive function and logical reasoning (63). To date, however, no PET studies have investigated the association between 5-HTT availability and cognitive function in patients with schizophrenia.

Other serotonergic system

PET probes for 5-HT1B, 5HT4, 5-HT6, and 5-HT synthesis have been successfully used for human brain imaging (50); however, to date, no clinical studies have used these probes for imaging of the brains of patients with schizophrenia.

Norepinephrine

The central norepinephrine system plays crucial roles in arousal and concentration, and the norepinephrine transporter is a target in pharmacotherapy for depression and attention-deficit hyperactivity disorder. Despite this, few PET probes have been developed for norepinephrine transporter (NET) imaging (64). To date, there have been no reports of PET imaging of the NET in patients with schizophrenia.

Discussion and future directions

PET provides a direct way of investigating the neurotransmission and neurobiology of schizophrenia. Numerous PET studies have revealed differences between the brains of patients with schizophrenia and those of healthy controls, and the association of these brain changes with symptom scales, suggesting the underpinnings of the pathophysiology of this disorder. As reviewed above, however, only a limited number of PET studies have directly investigated the relationship between cognitive dysfunctions, assessed using neuropsychological tests, and monoamine transmission in vivo, and found significant associations between them. Consequently, dysregulated striatal dopamine synthesis capacity, and prefrontal D1 receptor and extrastriatal D2/D3 receptor availability might be at least partly indicative of cognitive impairment in schizophrenia. However, studies are scarce and not systematic: differences in radiotracers used, methods of quantification, neurocognitive tests employed, and patient characteristics (such as phase of the illness, prior exposure to antipsychotics, age, and sex) could be confounders. This scarcity and lack of systematic approaches occurs largely because it is difficult to recruit many patients with unmedicated schizophrenia; therefore, multi-site studies with common protocols are needed. Moreover, different approaches such as measuring endogenous release of transmitters rather than focusing only on baseline receptor availability, could be useful for precise evaluation of neurotransmission (65, 66). In summary, pharmacological challenge techniques such as that with amphetamine and dopamine depletion using [11C]raclopride, which reflect presynaptic dopamine function, have been well replicated to detect dysregulated dopamine neurotransmission as a pathophysiology of schizophrenia (14, 67). Another approach is to measure changes in receptor binding of a radiotracer while performing a cognitive task as it accurately reflects the amount of neurotransmitter released during the task (68–70). Furthermore using agonist tracers such as [11C]-(+)-PHNO and [11C]MNPA, that can be more sensitive to endogenous transmitters, might help detect high affinity states of dopamine D2 receptors that could be more responsible for the pathophysiology based on a hypothesis from in vitro studies (71). Although studies on 5-HT1A receptors and 5-HT2A receptors have not demonstrated their involvement in cognition in schizophrenia, newer serotonergic targets, such as 5-HT4, might potentially be associated with cognitive functions (50). Regarding the norepinephrine system, one study reported a relationship between attention function and NET availability in patients with depression (72), which might be applicable to some patients with schizophrenia. Moreover, other neurotransmitter systems such as glutaminergic or cholinergic systems might also be involved in cognitive impairment in schizophrenia. Further development of optimal PET tracers and new techniques to measure more precise neurotransmission in human PET imaging will also provide new insights to the neurobiology of cognitive dysfunction in schizophrenia.

Author contributions

The author confirms being the sole contributor of this work and approved it for publication.

Conflict of interest statement

The author declares that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.