Evidence map›Paper›PMID 42752818›Full record

ArticleThe international journal of neuropsychopharmacology2026

Disruption of ultrasonic vocalizations with systemic administration of the non-competitive N-methyl-D-aspartate receptor antagonist MK-801 in adult male mice.

Ryuto Tamura, Mizuki Yamamoto, Yusuke Ujihara, Haruki Kasahara, Shuntaro Matsushima, Daiki Nasukawa, Kazuko Hayashi, Kota Yamada, Masashi Tanaka, Koji Toda

Abstract read
In one paragraph

Article in The international journal of neuropsychopharmacology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Ryuto TamuraDepartment of Psychology, Keio University, Minato-ku, Tokyo, Japan.
Mizuki YamamotoDepartment of Psychology, Keio University, Minato-ku, Tokyo, Japan.ORCID 0009-0002-9064-6384
Yusuke UjiharaDepartment of Anatomy and Neurobiology, University of Tennessee Health Science Center, Memphis, TN, United States.ORCID 0009-0000-6939-9871
Haruki KasaharaDepartment of Psychology, Keio University, Minato-ku, Tokyo, Japan.
Shuntaro MatsushimaDepartment of Psychology, Keio University, Minato-ku, Tokyo, Japan.
Daiki NasukawaDepartment of Psychology, Keio University, Minato-ku, Tokyo, Japan.
Kazuko HayashiDepartment of Psychology, Keio University, Minato-ku, Tokyo, Japan.ORCID 0000-0002-8560-4430
Kota YamadaJapan Society for the Promotion of Science, Chiyoda-ku, Tokyo, Japan.ORCID 0000-0002-6249-5489
Masashi TanakaFaculty of Letters, Arts, and Sciences, Shinjuku-ku, Tokyo, Waseda University, Japan.ORCID 0000-0002-3076-8606
Koji TodaDepartment of Psychology, Keio University, Minato-ku, Tokyo, Japan.ORCID 0000-0002-2194-8998

Funding

HOKUTO Foundation for the Promotion of Biological ScienceJSPS KAKENHI 18KK0070JSPS KAKENHI 19H01769JSPS KAKENHI 19H05316JSPS KAKENHI 19K03385JSPS KAKENHI 20J21568JSPS KAKENHI 22H01105JSPS KAKENHI 23H02787JSPS KAKENHI 23K22376JSPS KAKENHI 23K27478JSPS KAKENHI 24H00729JSPS KAKENHI 24K06626JSPS KAKENHI 24K16869JSPS KAKENHI 24KJ0069JSPS KAKENHI 25KJ0306JSPS KAKENHI 26K00589JSPS KAKENHI 26K22216Keio Academic Development FundKeio Gijuku Fukuzawa Memorial Fund for the Advancement of Education and ResearchSmoking Research Foundation
6 · The paper itself

Abstract

objectiveSocial behavior and communication, including ultrasonic vocalizations (USVs), are important for survival and reproductive success across species. N-methyl-D-aspartate (NMDA) receptors contribute to the neural mechanisms underlying social behavior, and pharmacological modulation of these receptors can alter both social behavior and USVs in rodents. However, the effects of NMDA receptor blockade on dyadic USVs and social approach during male-female interactions in mice remain incompletely understood. We therefore investigated the effects of systemic administration of MK-801, a non-competitive NMDA receptor antagonist, on dyadic vocal activity, social approach, locomotor behavior, and excretory outcomes in adult male mice.

methodsSexually experienced male mice were tested in male-female interaction and same-sex social-preference tasks. Using VocalMat, a machine-learning-based tool, we classified the USVs recorded during male-female interactions into 11 call categories and examined their temporal relationship to the proximity of the male subject to the female stimulus.

resultsAdministration of MK-801 to the male dose-dependently reduced the total number of USVs recorded from the male-female dyad, with a marked reduction at the highest dose, while leaving the treated male's proximity to the female stimulus unchanged. In the same-sex social-preference task, MK-801 reduced the time spent near the social stimulus at the highest dose, although preference for the social stimulus over the non-social object remained significant under all treatment conditions. MK-801 also increased locomotor activity and reduced fecal output and estimated urine output in the open-field task. These findings demonstrate that systemic NMDA receptor blockade differentially affects dyadic vocal communication, social approach, locomotor activity, and excretory outcomes.

conclusionSystemic MK-801 administration to the male reduced the number of USVs recorded during male-female interactions and produced distinct effects on social approach, locomotor activity, and excretory outcomes. These findings indicate that NMDA receptor blockade differentially affects multiple behavioral domains, although the mechanisms underlying the reduction in USVs remain to be determined.

Indexed as

Dizocilpine MaleateExcitatory Amino Acid AntagonistsReceptors, N-Methyl-D-AspartateSocial BehaviorVocalization, AnimalAnimalsFemaleMaleMiceDizocilpine MaleateExcitatory Amino Acid AntagonistsReceptors, N-Methyl-D-Aspartateautomated vocalization analysisbehavioral pharmacologyglutamatergic signalingNMDA receptor hypofunctionsocial communication

Identifiers

PMID42752818
PMCPMC13647287

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.