The core features of schizophrenia (SCZ) include cognitive deficits and impaired sensory gating represented by P50 inhibition deficits, which appear to be related to the α7 nicotinic acetylcholine receptor (nAChR). An agonist of nAChR receptor may improve these defects. This study aimed to investigate how administering multiple doses of tropisetron, a partial agonist of nAChR, for 1 day would affect cognitive deficits and P50 inhibition deficits in SCZ patients. We randomized 40 SCZ non-smokers into a double-blind clinical trial with four groups: placebo, 5 mg/d, 10 mg/d, and 20 mg/d of oral tropisetron. Their P50 ratios were all more than 0.5 and they took risperidone at 3–6 mg/day for at least a month before participating in the experiment. We measured the Repeatable Battery for the Assessment of Neuropsychological Status (RBANS) and P50 inhibition before and one day after treatment. After one day of treatment, the total RBANS scores of the 20 mg and 5 mg tropisetron groups, and the immediate memory of the 10 mg group were significantly higher than placebo group. The P50 ratio was smaller in the 5 mg and 10 mg groups than in the placebo group (both p < 0.05) after treatment. Furthermore, the improvement in RBANS total score was correlated with increased S1 latency (p < 0.05), and the increase in immediate memory score was correlated with decreased S2 amplitude. One day of treatment with tropisetron improved both cognitive and P50 inhibition deficits, suggesting that longer term treatment with α7 nAChR agonists for these deficits in SCZ may be promising.
Impaired neurocognitive function is a core feature of schizophrenia (SCZ)  affecting memory [2, 3], executive function [4, 5], and attention . Cognitive impairment of SCZ begins before the onset and persists for many years [7,8,9], leading to social dysfunction and a decline in overall quality of life [10, 11]. Cognitive impairment therefore has become a treatment target for SCZ research . However, the pathophysiological mechanisms of cognitive deficits in SCZ patients remain unclear. Sensory gating is a mechanism that filters stimuli, suppresses irrelevant stimuli and protects the integrity of cognitive function [13, 14]. Sensory gating deficits appear to be sensitive biomarkers of cognitive impairment in SCZ patients [15,16,17]. Abnormalities in the P50 component of the electroencephalogram (EEG) recorded during repeated auditory stimuli can assess this inhibition deficit [17,18,19]. The neurochemical mechanism for this deficit appears to be through a genetic polymorphism in the 15q14 locus of the gene coding for the α7 nicotinic acetylcholine receptor (nAChR), and agonists for this receptor are considered potential therapies to improve the sensory gating and cognitive deficits of SCZ patients [20,21,22].
Tropisetron, a commonly used medicine against nausea and vomiting caused by chemotherapy and surgical anesthesia, is both a potent serotonin-3 receptor antagonist and a high-affinity partial agonist of the nAChR [23,24,25]. Due to its nAChR activity, tropisetron has improved auditory inhibition and cognitive deficits in mice [26,27,28]. In patients with SCZ, 10 mg per day of tropisetron significantly enhanced P50 deficiencies and cognitive deficits [23,24,25, 29]. In our previous study, we demonstrated that daily doses of tropisetron at 5, 10, and 20 mg significantly improved overall cognitive deficits and P50 inhibition defects after 10 days of treatment .
The primary goal of this study was to compare the immediate effects of either 5, 10, or 20 mg of tropisetron on cognitive and sensory gating deficits in patients with chronic SCZ after 1 day of treatment. Since a number of previous studies demonstrated the effectiveness of the 10 mg/day dose [23, 30], we also considered 5 and 20 mg/day to examine the dose-response effects. Since risperidone does not have significant nAChR agonism or 5-HT3 receptor antagonism , we used it as an antipsychotic in this study. At the same time, we sought to examine the relationship between changes in sensory gating and cognitive improvement to verify the hypothesis that sensory gating acts on cognition by activating nAChRs.
We recruited 40 non-smoking hospitalized patients with SCZ from the Shantou University Mental Health Center. Trained psychiatrists used DSM-IV for structured clinical interviews for diagnosis (SCID) to make a diagnosis. All participants were Han Chinese, aged between 20 and 55 years old. Prior to participation in this study, participants continued to receive a steady dose of oral risperidone (3–6 mg/day) for more than 1 month without taking any other antipsychotic medications. All participants had sensory gating defects with P50 ratios > 0.5. We excluded participants with cardiovascular or neurological disorders, a history of head trauma with a loss of consciousness, physical abnormalities, a DSM-IV dependent substance disorder, or a current mood or anxiety disorder. All participants had normal hearing acuity (subjective hearing threshold of 40 dB).
All subjects went through a complete examination of their medical history, physical and laboratory indicators, and electrocardiogram. No one had alcohol or other substance dependence problems. A power analysis with the parameters of 0.85 (P < 0.05), and a medium effect size showed that our sample of 40 participants was adequate. All participants signed an informed consent form after fully understanding the procedure. The institutional review board of the Mental Health Center of Shantou University approved this study.
The experiment started with a 2-week placebo lead-in introduction. We performed sensory gating screening on 62 patients, yielding 40 patients with a P50 ratio >0.5. Patients with sensory gating defects compared with patients without sensory gating defects did not have any differences in demographic characteristics or disease duration (all p > 0.05). The 40 participants were randomized into four groups of ten each, receiving either placebo, 5 mg, 10 mg, or 20 mg per day of tropisetron (Navoban, Novartis Pharmaceuticals, Ltd., Beijing). All capsules looked the same, and participants took them once a day. Participants also took a steady dose of 3–6 mg of risperidone per day during the experiment and did not take other antipsychotic drugs.
We recorded the P50 auditory evoked potentials at baseline and one hour after taking tropisetron or placebo. The electrophysiology test used a signal generator and a digital 40-channel EBNeuro Sirius EEG system (EBNeuro, Florence, Italy) data acquisition system. According to previous studies , participants sat in a chair and focused on a fixed point. A 90-dB pulse stimulation signal lasting 0.1 ms generated an event-related potential waveform. A meta-analysis previously reported that the best sound intensity for stimulation was between 85 and 90 dB , consistent with the recommendation to use a standard stimulus of 50 dB above the hearing threshold. Each trial showed a pair of stimuli with an inter-stimulus interval of 500 ms and an inter-pair interval of 10 s [30, 32, 34, 35]. The number of trials was 32. Each epoch lasted 1000 ms, including 100 ms before the first stimulation, 500 ms between stimuli, and 400 ms after the second stimulation. The event-related potential response was amplified and band-pass filtered by a 0.1–300 Hz analog filter and a 50 Hz notch filter. The sample rate was 512 Hz. The data were analyzed offline, with 10–50 Hz, 12 dB/ octave roll-off bandpass filtering. We excluded from the analysis any value greater than ±50 μV at any electrode. We recorded eye movements via two electro-oculography (EOG) with Ag/AgCl disc electrodes placed at the outer canthus and below the right eye. We corrected the ocular artifact using a regression method provided by EBNeuro digital EEG analysis and processing system. We referenced recordings to the left temporal apophysis and reduced the impedance to <5 kΩ. Throughout the process, we continued to provide 70 dB(A) broadband white noise to avoid interference by background noise.
We calculated the P50 at the electrode sites of the vertex (CZ site) as the ratio of the S2 amplitude to the S1 amplitude [30, 32]. The S1 was the maximum amplitude within 30–90 ms after the first stimulus occurred. The S2 was the maximum amplitude closest to the S1 latency after the second stimulus.
Two independent neurophysiologists analyzed the P50 test results, unaware of the participants’ status. If the results they reported were inconsistent, the two examiners reanalyzed the results together to reach a consensus.
We used the Repeatable Battery for the Assessment of Neuropsychological Status (RBANS)  to assess cognitive function. The RBANS includes 12 sub-tests for calculating a total score and five age-adjusted index scores, including immediate memory, visuospatial/constructional, language, attention, and delayed memory. Our team translated this tool into Chinese and established its clinical validity and test-retest reliability in healthy subjects and SCZ patients [37, 38]. We performed the RBANS and P50 tests on the same day.
We performed repeated measures (RM) multivariate analysis of variance (MANOVA) on RBANS total score and subscale scores, including a between-group medicine factor (placebo, 5, 10, 20 mg) and a within-group time factor (baseline and 1-day). The normal distribution was evaluated by the Kolmogorov Smirnov specimen test (p > 0.05). Levene’s test was used to assess variance homogeneity (p > 0.05), and Mauchly’s test for the assumption of sphericity (p > 0.05). We used age, education, gender, duration of disease, and risperidone dose as covariates if the interactive effect of medicine Χ time in RM MANOVA was significant. When the overall treatment effect was significant, we used the covariance analysis (ANCOVA) with the baseline score as the covariate, and then performed the Dunnett test to compare the differences between the dose groups. If the overall treatment effect was significant, we compared the RBANS total and subscale scores for each dose group with the placebo group by covariance analysis (ANCOVA). We used a similar RM ANOVA to analyze the P50 data. We performed Pearson correlations between the changes in RBANS and P50 gating ratios. Other statistical analyses included analysis of variance (ANOVA) for continuous variables, and chi-square test for categorical variables. To correct for multiple tests, we used the Bonferroni test, because it allows for tight control of multiple tests and reduces the probability of false positives type I errors. Since we performed six comparisons in the four groups, the adjusted level of significance with the Bonferroni test was set to p = 0.05/6 = 0.0083. We used R version 3.5.2 (http://cran.r-project.org)  to do all the statistical analyses with a two-tailed significance level of ≤0.05 and expressed data as mean ± standard deviation.
Demographic characteristics and duration of illness showed no significant differences between the four treatment groups (see Table 1). Risperidone doses differed between groups at baseline (p < 0.01). Therefore, subsequent analysis included risperidone dose as a covariate.
Effects of tropisetron treatment on cognitive performance
The RBANS total and index scores (Table 2) were not different between the treatment groups at baseline (all p > 0.05). The RBANS total score (F = 3.19, df = 3, 34, p < 0.05) and the immediate memory score (F = 3.55, df = 3, 34, p < 0.05) showed significant tropisetron dose-by-time effects. When the effects were examined by adding age, education, sex, duration of disease, and risperidone dose as covariates to the RM MANOVA, the immediate memory (F = 3.52, df = 3, 29, p < 0.05) was still significant, while the total score (F = 2.33, df = 3, 29, P < 0.1) was not.
Using the baseline value as covariate, the ANCOVA analysis showed a main effect of doses on the total RBANS score (F = 3.81, df = 3, 29, p < 0.05). Dunnett post hoc testing showed that the total RBANS score of the 20 mg (p = 0.02, Cohen’s d = 1.36) and 5 mg (p = 0.018, Cohen’s d = 1.30) tropisetron groups was significantly higher than that of the placebo group after one day of treatment. Further, dose had a main effect on immediate memory (F = 3.92, df = 3, 29, p < 0.05), showing that the immediate memory score was significantly higher for the 10 mg than the placebo group (p = 0.008, Cohen’s d = 1.44), which remained significant after a Bonferroni correction. However, the three tropisetron dose groups did not differ in the RBANS total score and index scores (all p > 0.05).
Effects of tropisetron treatment on P50 Inhibition
The four groups showed no significant differences in the P50 components at baseline (all p > 0.05), and the P50 components showed no significant effect of the dose-by-time (p > 0.05) (see Table 3).
Using the baseline P50 ratio as a covariate, we showed a main effect of tropisetron doses on the P50 ratio (F = 3.39, df = 3, 29, p < 0.05). Dunnett post hoc testing showed that the P50 ratio was smaller in the 5 mg group (p = 0.02, Cohen’s d = −1.28) and the 10 mg group (p = 0.035, Cohen’s d = −1.17) than that in the placebo group. However, none of these differences passed the Bonferroni correction (Bonferroni corrected p = 0.0083), and the three tropisetron dose groups were not different in P50 components (all p > 0.05).
Relationship between changes in P50 inhibition and cognitive performance
After treatment, the increase in the latency of S1 (Day one score minus baseline) was associated with the improvement in RBANS total score (r = 0.32, p < 0.05, Fig. 1), but the decrease in S2 amplitude was not, although S2 amplitude change had a trend toward significant correlation with the increase in immediate memory score (r = 0.32, p = 0.053). Additionally, the 10 and 20 mg doses of tropisetron showed no difference in effects on the P50 gating ratio, which is characteristic of partial agonists at high doses (Fig. 2).
This study found that one dose of 5, 10, and 20 mg tropisetron treatment significantly improved immediate memory. The improvement in immediate memory in the 10 mg group was more significant and passed the Bonferroni correction. A previous study found that after ten days of treatment, taking 10 mg of tropisetron per day was associated with increased immediate memory, while taking 20 mg per day was associated with increased delayed memory . Another study showed that after 2 weeks of treatment, 10 mg of tropisetron per day improved sustained visual attention . Consistent with previous studies, we found that only one-dose of tropisetron treatment improved cognitive performance, especially immediate memory in patients with chronic SCZ.
The study also found improved P50 inhibition deficits in the active treatment group, showing a reduction in both the P50 ratio and the S2 amplitude. However, the three-tropisetron dose groups did not differ in improving P50 inhibition. This is consistent with previous studies, which reported that tropisetron improved P50 deficiency in patients with SCZ within a limited dose range [23,24,25, 30]. In addition, our current study also demonstrated that only one-day of treatment with tropisetron may improve neurological function.
Interestingly, we found that there was a significant association between cognitive improvement and improvement in P50 inhibition defects in SCZ patients. Specifically, the increase in the total RBANS score was associated with the change in S1 latency. Our findings are consistent with two previous studies, which found that the increase in the total of RBANS score was associated with a change in the P50 ratio in SCZ patients treated by low-dose DMXB-A (a nicotinic agonist) or by 10 days of tropisetron [30, 40]. However, another small sample-size study did not find a correlation between cognitive improvement and P50 composition in SCZ patients treated with tropisetron .
Tropisetron appears to improve P50 inhibition and cognitive deficits in patients with SCZ through its excitatory effects on α7 nAChRs [23, 30, 41, 42]. Mouse studies found that tropisetron improved inhibition processing defects [26,27,28]. Similarly, other studies found that the nAChR agonist DMXB-A improved P50 inhibition defects and cognitive deficits in patients with SCZ [23,24,25, 43]. However, tropisetron may improve cognitive performance due to its potent antagonism of the 5-HT3 receptor. However, in a mouse model of phencyclidine-induced SCZ, tropisetron and the nAChR agonist SSR180711 improved cognitive deficits, whereas the 5-HT3 receptor antagonist ondansetron did not [44, 45]. Moreover, when taking the α7 nAChRs antagonist methyllycaconitine, the effects of the agonists tropisetron and SSR180711 were blocked [44, 45]. A previous PET study also demonstrated that oral administration of tropisetron at 5, 10, or 20 mg acted on α7 nAChRs in a dose-dependent manner .
More than 80% of patients with chronic SCZ depend on nicotine, which is two to four times that of the general population or other patients with severe mental disorders [45,46,47,48,49]. The problem of nicotine abuse usually exists before the onset of SCZ . Studies have shown that the appropriate amount of nicotine can improve the cognitive process of healthy people, as well as the attention and memory of SCZ [51,52,53,54,55]. The abnormal P50 ratio in SCZ is related to the increased incidence of ChRNA7 allele variation in the α7 nicotine acetylcholine receptor (NAChR) subunit gene . The increase in smoking rate in patients with SCZ is related to ChRNA7 . Smoking can temporarily improve the P50 inhibition deficits in SCZ patients . Nicotine can also normalize cholinergic nerve conduction defects in patients with SCZ . Smoking in SCZ patients has also been explained as an attempt to self-treat underlying pathophysiological gating mechanisms [59,60,61]. In this study, smokers were not required to quit from nicotine before the test. Therefore, the results were statistically significant and robust.
Risperidone is a commonly used drug in SCZ patients and contains benzoxazole and piperidine, which are antagonists of the D1 (D1, D5) and D2 (D2, D3, D4) receptor families, acting on the central nervous system, especially on the mesolimbic, prefrontal corticolimbic, and tuberoinfundibular pathways . Also, risperidone affects the alpha 2 adrenergic receptors, which affect positive symptoms, negative symptoms, mood and cognition . Although most second-generation antipsychotic drugs may have cognitive improvement effects , risperidone has been shown to be ineffective against P50 inhibition defects in patients with chronic SCZ [65,66,67,68]. Before participating in this study, participants were required to continue to receive a stable dose of oral risperidone (3–6 mg/day) for more than a month without taking any other antipsychotic drugs. The study also set up a placebo group. Therefore, the drug has little effect on the results of this study. However, we still need to explore the effects of risperidone on cognition and P50 ratio in first-episode, drug-naive SCZ patients.
Alzheimer’s disease (AD) is the most common age-related neurodegenerative disease . There is accumulating evidence that the interaction between amyloid-β peptides (Aβ) and α7 nAChRs is indispensable in the pathological process of AD [27, 70]. The interaction between Aβ peptides and α7 nAChRs may cause Aβ deposition and inflammation in the brain, leading to the loss of cholinergic neurons and α7 nAChRs . These neurotoxic events may promote cognitive decline, which in turn leads to mild cognitive impairment (MCI) and ultimately AD . Tropisetron binds to α7 nAChRs as an agonist, to serotonin 5-HT3 receptor as an antagonist, and to APP with sub-micromolar affinity . The interaction of tropisetron with 5-HT3 receptors also plays a role in the anti-inflammatory and neuroprotective effects against Aβ-induced neurotoxicity . Taken together, tropisetron may be a potential drug for the treatment of AD if it is used during MCI or early stages of AD. It may reduce cognitive impairment and P50 inhibition defects in AD patients, but the specific effect still needs to be further studied.
While these rapid results are exciting, this study has some limitations. First, the sample size was relatively small, and the findings in our current study should be confirmed in larger sample size of studies. Second, the P50 component represents only the neural activity that occurs at the surface of the brain. Cognitive deficits in schizophrenia may involve activity in deeper brain regions. Third, cholinergic regulation may affect cognitive performance and P50 testing. However, we did not collect data on smoking status in this study, which should be remedied in future studies. Therefore, future research should use a larger sample size, including data on smoking status and other techniques, such as functional magnetic resonance imaging.
In summary, our results indicate that one dose of tropisetron treatment can improve cognitive deficits and P50 inhibition deficits in patients with SCZ. Interestingly, improvements of these two deficits showed a significant correlation, likely due to tropisetron’s effect on α7 nAChRs. Future studies can extend these findings using a large sample of patients with first-episode of SCZ, including a variety of data such as smoking status, and a combination of techniques such as ERP and functional MRI to investigate the effects of tropisetron on cognitive and sensory gating deficits.
Funding and disclosure
Funding for this study was provided by the National Natural Science Foundation of China (81371477) and the CAS Pioneer Hundred Talents Program. No conflict of interest was disclosed for each author.
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Xia, L., Liu, L., Hong, X. et al. One-day tropisetron treatment improves cognitive deficits and P50 inhibition deficits in schizophrenia. Neuropsychopharmacol. 45, 1362–1368 (2020). https://doi.org/10.1038/s41386-020-0685-0