Evidence map›Paper›PMID 41511173›Full record

ArticleFASEB journal : official publication of the Federation of American Societies for Experimental Biology2026

Orexin Receptor Antagonism Improves Sleep Quality and Mitigates Lipopolysaccharide-Induced Inflammatory Responses in a Mouse Model.

Dai Horiuchi, Yoko Irukayama-Tomobe, Jun-Dal Kim, Yoshitoshi Kasuya, Tsuyoshi Nemoto, Takuji Suzuki, Yoshimi Nakagawa, Koichiro Tatsumi

Abstract read
In one paragraph

Article in FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Orexin Receptor Antagonism Improves Sleep Quality and Mitigates Lipopolysaccharide-Induced Inflammatory Responses in a Mouse Model.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2026
    Article
  2. 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

8 authors.

Dai HoriuchiDepartment of Respirology, Graduate School of Medicine, Chiba University, Chiba, Japan.
Yoko Irukayama-TomobeDepartment of Respirology, Graduate School of Medicine, Chiba University, Chiba, Japan.
Jun-Dal KimDivision of Complex Biosystem Research, Department of Research and Development, Institute of National Medicine, University of Toyama, Toyama, Japan.ORCID 0000-0002-7361-0999
Yoshitoshi KasuyaDepartment of Respirology, Graduate School of Medicine, Chiba University, Chiba, Japan.
Tsuyoshi NemotoChiba University Hospital, Chiba, Japan.
Takuji SuzukiDepartment of Respirology, Graduate School of Medicine, Chiba University, Chiba, Japan.
Yoshimi NakagawaDivision of Complex Biosystem Research, Department of Research and Development, Institute of National Medicine, University of Toyama, Toyama, Japan.ORCID 0000-0001-8710-5232
Koichiro TatsumiDepartment of Respirology, Graduate School of Medicine, Chiba University, Chiba, Japan.

Funding

Japan Agency for Medical Research and Development (AMED) JP21gm1410010MEXT | JSPS | Japan Society for the Promotion of Science London (JSPS) 24K08827MEXT | JSPS | Japan Society for the Promotion of Science London (JSPS) 24K11336Ministry of Health
6 · The paper itself

Abstract

Alterations in the immune system, stemming from sleep/wakefulness disorders, increase the risk of inflammatory pathologies. Orexin, a hypothalamic neuropeptide, regulates sleep and wakefulness. However, the role of orexin in inflammatory responses-whether it is protective or pathological-is still unclear. In this study, our aim was to elucidate the role of orexin in sleep and inflammatory states through the examination of a lipopolysaccharide (LPS)-induced systemic inflammatory model and the effects of daridorexant, a dual orexin receptor antagonist. Intraperitoneal LPS administration significantly decreased rapid eye-movement (REM) sleep and wakefulness while increasing non-REM sleep. Pretreatment with daridorexant enhanced REM sleep recovery in LPS-induced systemic inflammation, evidenced by extended duration and increased episode frequency. Transcriptomic profiling demonstrated a rise in the expression of pro-inflammatory cytokines (Cxcl1, Ccl2, Ccl7, and Tnf) within the hypothalamus of LPS-challenged mice, which was mitigated by daridorexant administration. In addition, daridorexant mitigated LPS-induced acute lung inflammation. These findings suggest that by reducing pro-inflammatory cytokine expression, the inhibition of orexin activity mitigates the lethargy associated with systemic inflammation, while also improving sleep quality. This study explores the potential of orexin receptor antagonists as strategic options for inflammatory pathologies and their associated sleep disorders.

Indexed as

InflammationLipopolysaccharidesOrexin Receptor AntagonistsOrexin ReceptorsSleepAnimalsCytokinesDisease Models, AnimalHypothalamusMaleMiceMice, Inbred C57BLSleep, REMWakefulnessCytokinesLipopolysaccharidesOrexin Receptor AntagonistsOrexin Receptorscytokinesdaridorexantinflammationlipopolysaccharidesleep/wakefulness disorders

Identifiers

PMID41511173
PMCPMC12785484

What Socratic holds

Textmetadata
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.