Evidence map›Paper›PMID 40908362›Full record

ArticleMolecular psychiatry2026

Rapid and long-lasting antidepressant-like effects of the pituitary adenylate cyclase-activating polypeptide receptor antagonist PA-915 in chronic stress mouse models.

Yusuke Shintani, Atsuko Hayata-Takano, Ichiro Takasaki, Takashi Kurihara, Atsuro Miyata, Yui Yamano, Manato Ikuta, Rei Takeshita, Kenichiro Murata, Taisei Oguri and 10 more

Abstract read
In one paragraph

Article in Molecular psychiatry, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

3 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
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

20 authors.

Yusuke Shintani *Laboratory of Molecular Neuropharmacology, Graduate School of Pharmaceutical Sciences, The University of Osaka, 1-6 Yamadaoka, Suita, Osaka, 565-0871, Japan.
Atsuko Hayata-Takano *Laboratory of Molecular Neuropharmacology, Graduate School of Pharmaceutical Sciences, The University of Osaka, 1-6 Yamadaoka, Suita, Osaka, 565-0871, Japan. hayata.atsuko.dent@osaka-u.ac.jp.ORCID http://orcid.org/0000-0002-4992-2845
Ichiro TakasakiGraduate School of Innovative Life Science, University of Toyama, Toyama, 930-0194, Japan.
Takashi KuriharaDepartment of Pharmacology, Graduate School of Medical and Dental Sciences, Kagoshima University, Sakuragaoka 8-35-1, Kagoshima, 890-8544, Japan.ORCID http://orcid.org/0000-0003-4001-6771
Atsuro MiyataDepartment of Drug Discovery for DDS, Graduate School of Medical and Dental Sciences, Kagoshima University, Sakuragaoka 8-35-1, Kagoshima, 890-8544, Japan.
Yui YamanoLaboratory of Molecular Neuropharmacology, Graduate School of Pharmaceutical Sciences, The University of Osaka, 1-6 Yamadaoka, Suita, Osaka, 565-0871, Japan.
Manato IkutaLaboratory of Molecular Neuropharmacology, Graduate School of Pharmaceutical Sciences, The University of Osaka, 1-6 Yamadaoka, Suita, Osaka, 565-0871, Japan.
Rei TakeshitaLaboratory of Molecular Neuropharmacology, Graduate School of Pharmaceutical Sciences, The University of Osaka, 1-6 Yamadaoka, Suita, Osaka, 565-0871, Japan.
Kenichiro MurataLaboratory of Molecular Neuropharmacology, Graduate School of Pharmaceutical Sciences, The University of Osaka, 1-6 Yamadaoka, Suita, Osaka, 565-0871, Japan.
Taisei OguriLaboratory of Molecular Neuropharmacology, Graduate School of Pharmaceutical Sciences, The University of Osaka, 1-6 Yamadaoka, Suita, Osaka, 565-0871, Japan.
Chiaki AsakaLaboratory of Molecular Neuropharmacology, Graduate School of Pharmaceutical Sciences, The University of Osaka, 1-6 Yamadaoka, Suita, Osaka, 565-0871, Japan.
Kazuto NunomuraCenter for Supporting Drug Discovery and Life Science Research, Graduate School of Pharmaceutical Science, The University of Osaka, 1‑6 Yamadaoka, Suita, Osaka, 565‑0871, Japan.
Bangzhong LinCenter for Supporting Drug Discovery and Life Science Research, Graduate School of Pharmaceutical Science, The University of Osaka, 1‑6 Yamadaoka, Suita, Osaka, 565‑0871, Japan.
Shinsaku NakagawaCenter for Supporting Drug Discovery and Life Science Research, Graduate School of Pharmaceutical Science, The University of Osaka, 1‑6 Yamadaoka, Suita, Osaka, 565‑0871, Japan.
Takuya OkadaGraduate School of Innovative Life Science, University of Toyama, Toyama, 930-0194, Japan.
Naoki ToyookaGraduate School of Innovative Life Science, University of Toyama, Toyama, 930-0194, Japan.
Toru TakumiDepartment of Physiology and Cell Biology, Kobe University School of Medicine, Chuo, Kobe, 650-0017, Japan.ORCID http://orcid.org/0000-0001-7153-266X
Yukio AgoLaboratory of Biopharmaceutics, Graduate School of Pharmaceutical Sciences, The University of Osaka, 1‑6 Yamadaoka, Suita, Osaka, 565-0871, Japan.ORCID http://orcid.org/0000-0001-7562-4000
Kazuhiro TakumaMolecular Research Center for Children's Mental Development, United Graduate School of Child Development, The University of Osaka, Kanazawa University, Hamamatsu University School of Medicine, Chiba University, and University of Fukui, 2-2 Yamadaoka, Suita, Osaka, 565-0871, Japan.
Hitoshi HashimotoLaboratory of Molecular Neuropharmacology, Graduate School of Pharmaceutical Sciences, The University of Osaka, 1-6 Yamadaoka, Suita, Osaka, 565-0871, Japan. hasimoto@phs.osaka-u.ac.jp.ORCID http://orcid.org/0000-0001-6548-4016

Funding

Japan Agency for Medical Research and Development (AMED) JP21dm0207117Japan Agency for Medical Research and Development (AMED) JP24ama121052Japan Agency for Medical Research and Development (AMED) JP24ama121052, JP24ama121054MEXT | Japan Society for the Promotion of Science (JSPS) JP19K07121, JP20H03429, JP23K06162MEXT | Japan Society for the Promotion of Science (JSPS) JP20H00492, JP23H00395, JP24K22022, JP18H05416MEXT | Japan Society for the Promotion of Science (JSPS) JP20H03429MEXT | Japan Society for the Promotion of Science (JSPS) JP20H03429,MEXT | Japan Society for the Promotion of Science (JSPS) JP24K02185
6 · The paper itself

Abstract

Stress-related disorders, such as depression and anxiety, have been one of the most important medical issues. Accumulating evidence suggests that the activation of the pituitary adenylate cyclase-activating polypeptide and its receptor PAC1 are involved in the stress axis and the development of stress-related disorders. We recently developed PA-915, a small-molecule, non-peptide, high-affinity PAC1 antagonist, and demonstrated that it significantly suppresses anxiety-like behavior in acute stress-induced mice. In this study, we aimed to investigate the behavioral effects of PA-915 in chronic stress-induced mouse models of depression, which included repeated social defeat stress, repeated corticosterone administration, and social isolation rearing. PA-915 ameliorated the increased immobility time in the forced swim test in these stress-induced mice. In repeated social defeat stress mice, PA-915 improved anxiety-like and depression-like behaviors and cognitive dysfunction, as assessed by the light-dark, open field, elevated plus maze, sucrose preference, forced swim, Y-maze, and novel object recognition tests. In addition, we evaluated the usefulness of PA-915 as an antidepressant and compared it with ketamine and fluoxetine. In the sucrose preference test, an antidepressant-like effect was observed for 8 weeks in mice that received a single dose of PA-915, which was a similar effect observed with ketamine. In non-stressed control mice, PA-915 did not induce behavioral abnormalities, such as hyperlocomotion, cognitive dysfunction, or dependency. The present results show that PA-915 improves anxiety-like behaviors and cognitive impairment and exerts rapid and long-lasting antidepressant effects in chronic stress-induced mouse models of anxiety and depression, proposing a promising treatment option for stress-related disorders.

Indexed as

Antidepressive AgentsReceptors, Pituitary Adenylate Cyclase-Activating Polypeptide, Type IStress, PsychologicalAnimalsAnxietyBehavior, AnimalCorticosteroneDepressionDisease Models, AnimalKetamineMaleMaze LearningMiceMice, Inbred C57BLPituitary Adenylate Cyclase-Activating PolypeptideSocial DefeatAntidepressive AgentsCorticosteroneKetaminePituitary Adenylate Cyclase-Activating PolypeptideReceptors, Pituitary Adenylate Cyclase-Activating Polypeptide, Type I

Identifiers

PMID40908362
PMCPMC12815653

What Socratic holds

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LicenceCC BY
Read underepoch 390

Registered trials

None linked

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 Socratic graph.