Evidence map›Paper›PMID 40939142›Full record

ArticlePhysiological reports2025

Myostatin antisense administration prevents sepsis-induced muscle atrophy and weakness in male mice.

Nobuto Nakanishi, Kazuhiro Maeta, Yuko Ono, Takumi Hirabayashi, Daisuke Tatebayashi, Kensuke Nakamura, Shigeaki Inoue, Masafumi Matsuo, Joji Kotani

Abstract read
In one paragraph

Article in Physiological reports, 2025. 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. Article
  2. 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

9 authors.

Nobuto NakanishiDivision of Disaster and Emergency Medicine, Department of Surgery Related, Kobe University Graduate School of Medicine, Kobe, Hyogo, Japan.ORCID 0000-0002-2394-2688
Kazuhiro MaetaQuality Assurance Section, Pharmaceutical Quality Assurance Dept., KNC Laboratories Co., Ltd., Izumo, Shimane, Japan.
Yuko OnoDivision of Disaster and Emergency Medicine, Department of Surgery Related, Kobe University Graduate School of Medicine, Kobe, Hyogo, Japan.
Takumi HirabayashiDivision of Rehabilitation Medicine, Kobe University Hospital, Kobe, Hyogo, Japan.
Daisuke TatebayashiDivision of Rehabilitation, Sapporo Medical University Hospital, Sapporo, Hokkaido, Japan.
Kensuke NakamuraDivision of Disaster and Emergency Medicine, Department of Surgery Related, Kobe University Graduate School of Medicine, Kobe, Hyogo, Japan.
Shigeaki InoueDepartment of Emergency and Critical Care Medicine, Wakayama Medical University, Wakayama, Japan.
Masafumi MatsuoGraduate School of Science, Technology and Innovation, Kobe University, Kobe, Hyogo, Japan.
Joji KotaniDivision of Disaster and Emergency Medicine, Department of Surgery Related, Kobe University Graduate School of Medicine, Kobe, Hyogo, Japan.

Funding

Japan Society for the Promotion of Science London (JSPS) 24K19491
6 · The paper itself

Abstract

Muscle atrophy and weakness are serious problems associated with sepsis. However, only a few pharmacological interventions are available to date. In this study, myostatin antisense was used to prevent sepsis-induced muscle atrophy and weakness. Sepsis was induced in 8-week-old male C57BL/6J mice via intraperitoneal injection of 1 mg/g cecal slurry (CS). Myostatin antisense was injected into the right tibialis anterior muscle. Myostatin mRNA was measured in the tibialis anterior and quadriceps femoris muscles on Day 1. The body weight, grip strength, and cross-sectional area of the tibialis anterior muscle were measured on Day 6. The administration of myostatin antisense decreased myostatin expression on Day 1 in the injected side (0.023 ± 0.010 in CS vs. 0.008 ± 0.002 in CS + antisense) as well as in the noninjected muscles. It also decreased the myostatin protein level (2.0 ± 0.3 in CS vs. 1.2 ± 0.5 in CS + antisense, p = 0.04). Body weight reduction (94.9% ± 2.0% vs. 98.2% ± 1.8%, p < 0.01) and grip strength reduction (77.0% ± 12.3%vs. 89.8% ± 8.3%, p = 0.04) were suppressed by the injection. The cross-sectional area of the right tibialis anterior muscle increased after the treatment (1116 ± 530 μm

Indexed as

Muscle WeaknessMuscular AtrophyMyostatinOligonucleotides, AntisenseSepsisAnimalsMaleMiceMice, Inbred C57BLMuscle, SkeletalMstn protein, mouseMyostatinOligonucleotides, Antisenseantisenseatrophymusclemyostatinsepsis

Identifiers

PMID40939142
PMCPMC12431578

What OpenQuestion 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 OpenQuestion graph.