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Neuropsychopharmacology Reports

ISSN 2574-173X

10 papers in the library · 65 citations · publishing 2021-2025

Papers

Functional connectivity between the amygdala and subgenual cingulate gyrus predicts the antidepressant effects of ketamine in patients with treatment‐resistant depression

Neuropsychopharmacology Reports February 21, 2021 Tomoyuki Nakamura, Masaru Tomita, N. Horikawa et al. 29 citations

About one-third of patients with major depressive disorder have treatment-resistant depression. Of those, one-third do not respond to ketamine, a newer antidepressant. Resting-state functional MRI was tested for its ability to predict which patients with treatment-resistant depression would respond to ketamine treatment.

MDMA-assisted psychotherapy for the treatment of PTSD: A systematic review and meta-analysis of randomized controlled trials (RCTs).

Neuropsychopharmacology Reports December 1, 2024 Ghada Shahrour, Kainat Sohail, Safa Elrais et al. 21 citations

MDMA-assisted psychotherapy (MDMA-AT) significantly reduces PTSD symptoms and improves response and remission rates in people with chronic, treatment-resistant PTSD, according to a meta-analysis of nine randomized controlled trials involving 297 participants. The treatment led to a large reduction in clinician-rated PTSD severity scores compared to control conditions (inactive MDMA doses or placebo). Patients receiving MDMA-AT were about 1.6 times more likely to show a meaningful response and over twice as likely to achieve remission. No significant differences were found between groups in rates of treatment-emergent adverse events, severe adverse events, or suicidal ideation, indicating a favorable safety profile.

Development of the Japanese version of the 30‐item Mystical Experience Questionnaire

Neuropsychopharmacology Reports March 13, 2024 Kengo Yonezawa, Hideaki Tani, Shinichiro Nakajima et al. 5 citations

A Japanese version of the Mystical Experiences Questionnaire (MEQ30) has been developed to assess mystical experiences induced by psychedelics, which are being studied as potential treatments for mental illness. Two Japanese psychiatrists independently translated the original English questionnaire into Japanese, then reconciled the translations into a unified version. This version was back-translated into English and reviewed by the original authors through an iterative process until they approved the final back-translated version. The authorized Japanese MEQ30 is now available for use in psychedelic-assisted therapy research with Japanese speakers, though further studies are needed to evaluate its reliability and validity.

Nonresponse to Ketamine in Treatment‐Resistant Bipolar Depression

Neuropsychopharmacology Reports July 20, 2025 Zofia Kachlik, Wiesław Jerzy Cubała, Michał Walaszek et al. 3 citations

Ketamine is a fast-acting antidepressant for treatment-resistant bipolar depression, but about 40% of patients do not respond. Among 35 patients receiving a four-week ketamine regimen, nonresponders had more psychiatric comorbidities (median 2 vs. 1) and were more likely to have any psychiatric comorbidity (78.6% vs. 33.3%) and prior benzodiazepine use (64.3% vs. 23.8%). Individual comorbidities and baseline suicidality were not linked to response. Ketamine remains safe and well-tolerated for short-term use, but a heavier comorbidity burden and benzodiazepine use may predict nonresponse.

Dual actions of 5‐MeO‐DIPT at the serotonin transporter and serotonin 5‐HT1A receptor in the mouse striatum and prefrontal cortex

Neuropsychopharmacology Reports February 6, 2021 Yoko Hagino, F. Scott Hall, George R. Uhl et al. 3 citations

The hallucinogenic tryptamine analogue 5-MeO-DIPT decreases extracellular serotonin in the striatum but not in the prefrontal cortex of mice. In mice lacking the serotonin transporter, 5-MeO-DIPT does not affect serotonin levels, indicating its action depends on that transporter. When a 5-HT1A receptor antagonist is present, 5-MeO-DIPT substantially increases serotonin, suggesting the drug's serotonin reuptake inhibition is masked by its concurrent activation of 5-HT1A receptors. 5-MeO-DIPT also dose-dependently increases extracellular dopamine in the prefrontal cortex regardless of serotonin transporter presence, an effect not blocked by the 5-HT1A antagonist. Thus, 5-MeO-DIPT dually acts on the serotonin transporter and 5-HT1A receptors, limiting serotonin elevation while independently raising dopamine in the prefrontal cortex.

Development of the Japanese version of the Ego‐Dissolution Inventory (EDI)

Neuropsychopharmacology Reports March 13, 2024 Keisuke Kusudo, Hideaki Tani, Kengo Yonezawa et al. 2 citations

A Japanese version of the Ego-Dissolution Inventory (EDI) was developed through a translation and back-translation process following international guidelines. Two Japanese psychiatrists independently translated the original English EDI, reconciled differences, and had the resulting version back-translated into English. The original authors reviewed and approved the back-translated version after iterative revisions. The final Japanese EDI is intended to help assess ego-dissolution experiences during psychedelic-assisted therapy in Japanese-speaking populations. Further research is needed to test the reliability and validity of this new instrument.

Possible Involvement of Hallucinogenic Effects in the Aversive Effects Induced by Kappa‐Opioid and 5‐ HT 2A / 2C Receptor Agonists in Mice

Neuropsychopharmacology Reports November 23, 2025 Hideaki Kato, Yoshimi Ichimaru, Masaaki Kurihara et al. 1 citation

A simple behavioral test in mice may help regulators quickly identify new hallucinogenic drugs. Mice given the hallucinogen-like compound DOI showed aversive effects in a conditioned place aversion test and abnormal behavior in a marble-burying test. These responses likely stem from the drug's hallucinogenic properties. The findings suggest that such rodent tests could serve as a rapid, accurate screening method for designating new psychoactive substances as controlled drugs, aiding prevention of drug abuse.

Development of the Japanese version of the Challenging Experience Questionnaire

Neuropsychopharmacology Reports November 8, 2024 Hideaki Tani, Kengo Yonezawa, Keisuke Kusudo et al. 1 citation

A Japanese version of the Challenging Experience Questionnaire (CEQ) was developed to assess difficult aspects of psychedelic experiences in Japanese speakers. Following international guidelines for translation and cultural adaptation, two psychiatrists independently translated the original English CEQ into Japanese, reconciled the versions, and had them back-translated into English. The original authors reviewed the back-translation and approved the final version after revisions. The resulting questionnaire enables evaluation of challenging experiences during psychedelic-assisted therapy for Japanese-speaking populations, though further studies are needed to confirm its reliability and validity.

Effects of 3,4-methylenedioxymethamphetamine on neural activity in the nucleus accumbens of male mice engaged in social behavior.

Neuropsychopharmacology Reports March 1, 2025 Naoya Nishitani, Yuki Sasaki, Katsuyuki Kaneda

MDMA, a recreational drug known for prosocial effects, was studied in mice to examine how it affects neural activity in the nucleus accumbens (NAc) during social behaviors. Using fiber photometry, researchers measured NAc activity while mice interacted with novel mice. NAc activity transiently increased at the onset of turning toward and sniffing novel mice, though turning was infrequent. MDMA reduced the duration of sniffing per bout but did not alter the transient NAc activity at the onset of these social behaviors, suggesting the drug does not affect this specific neural response.

Risk factors for cannabis use disorders and cannabis psychosis in Japan: Second report of a survey on cannabis-related health problems among community cannabis users using social networking services.

Neuropsychopharmacology Reports March 1, 2023 Yuji Masataka, Takeshi Sugiyama, Yoshiyuki Akahoshi et al.

Among 3142 Japanese cannabis users surveyed online in 2021, those who started using cannabis at a younger age, had a family history of mental health problems, had psychiatric disorders before using cannabis, or used cannabis products other than dry flower were more likely to develop cannabis use disorders. Cannabis psychosis was linked to younger age at first use and family history of mental health problems. The causal direction of these associations remains unclear.