Evidence map›Paper›PMID 42721182›Full record

ArticlePloS one2026

N-acetylcysteine attenuates oxidative-stress-associated apoptosis and collagen deposition after rat hindlimb ischemia-reperfusion injury.

Hideto Matsunaga, Ryuji Yonemitsu, Katsumasa Ideo, Junnosuke Ide, Masaki Shimada, Makoto Tateyama, Xiao Tian, Shu Takata, Kosei Takata, Shuntaro Tanimura and 18 more

Abstract read
In one paragraph

Article in PloS one, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

28 authors.

Hideto MatsunagaDepartment of Orthopedic Surgery, Faculty of Life Sciences, Kumamoto University, Kumamoto, Japan.ORCID https://orcid.org/0009-0009-7133-7691
Ryuji YonemitsuDepartment of Orthopedic Surgery, Faculty of Life Sciences, Kumamoto University, Kumamoto, Japan.
Katsumasa IdeoDepartment of Orthopedic Surgery, Faculty of Life Sciences, Kumamoto University, Kumamoto, Japan.ORCID https://orcid.org/0000-0003-0460-2087
Junnosuke IdeDepartment of Orthopedic Surgery, Faculty of Life Sciences, Kumamoto University, Kumamoto, Japan.
Masaki ShimadaDepartment of Orthopedic Surgery, Faculty of Life Sciences, Kumamoto University, Kumamoto, Japan.
Makoto TateyamaDepartment of Orthopedic Surgery, Faculty of Life Sciences, Kumamoto University, Kumamoto, Japan.
Xiao TianDepartment of Orthopedic Surgery, Faculty of Life Sciences, Kumamoto University, Kumamoto, Japan.ORCID https://orcid.org/0009-0007-2928-3103
Shu TakataDepartment of Orthopedic Surgery, Faculty of Life Sciences, Kumamoto University, Kumamoto, Japan.
Kosei TakataDepartment of Orthopedic Surgery, Faculty of Life Sciences, Kumamoto University, Kumamoto, Japan.
Shuntaro TanimuraDepartment of Orthopedic Surgery, Faculty of Life Sciences, Kumamoto University, Kumamoto, Japan.
Yuto ShibataDepartment of Orthopedic Surgery, Faculty of Life Sciences, Kumamoto University, Kumamoto, Japan.
Naoto YoshimuraDepartment of Orthopedic Surgery, Faculty of Life Sciences, Kumamoto University, Kumamoto, Japan.
Kazuya MaedaDepartment of Orthopedic Surgery, Faculty of Life Sciences, Kumamoto University, Kumamoto, Japan.
Junki KawakamiDepartment of Orthopedic Surgery, Faculty of Life Sciences, Kumamoto University, Kumamoto, Japan.
Takahiro ArimaDepartment of Orthopedic Surgery, Faculty of Life Sciences, Kumamoto University, Kumamoto, Japan.
Yuki KaiDepartment of Orthopedic Surgery, Faculty of Life Sciences, Kumamoto University, Kumamoto, Japan.
Soichiro KarataDepartment of Orthopedic Surgery, Faculty of Life Sciences, Kumamoto University, Kumamoto, Japan.
Hikaru GoshogawaDepartment of Orthopedic Surgery, Faculty of Life Sciences, Kumamoto University, Kumamoto, Japan.
Satoshi HisanagaDepartment of Orthopedic Surgery, Faculty of Life Sciences, Kumamoto University, Kumamoto, Japan.
Kazuki SugimotoDepartment of Orthopedic Surgery, Faculty of Life Sciences, Kumamoto University, Kumamoto, Japan.
Hironori TanoueDepartment of Orthopedic Surgery, Faculty of Life Sciences, Kumamoto University, Kumamoto, Japan.
Masaki YugamiDepartment of Orthopedic Surgery, Faculty of Life Sciences, Kumamoto University, Kumamoto, Japan.
Takayuki NakamuraDepartment of Orthopedic Surgery, Faculty of Life Sciences, Kumamoto University, Kumamoto, Japan.
Yusuke UeharaDepartment of Orthopedic Surgery, Faculty of Life Sciences, Kumamoto University, Kumamoto, Japan.
Tetsuro MasudaDepartment of Orthopedic Surgery, Faculty of Life Sciences, Kumamoto University, Kumamoto, Japan.
Takuya TokunagaDepartment of Orthopedic Surgery, Faculty of Life Sciences, Kumamoto University, Kumamoto, Japan.
Tatsuki KarasugiDepartment of Orthopedic Surgery, Faculty of Life Sciences, Kumamoto University, Kumamoto, Japan.
Takeshi MiyamotoDepartment of Orthopedic Surgery, Faculty of Life Sciences, Kumamoto University, Kumamoto, Japan.ORCID https://orcid.org/0000-0001-8658-9546

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Proper use of fingers and limbs is crucial for people to carry out normal activities of daily living. Therefore, when fingers or limbs are severed accidentally, replantation is attempted whenever possible. However, even when replantation is successful and fingers or limbs are preserved, functional limitations often arise due to contractures in reattached fingers or limbs, although mechanisms underlying contractures or countermeasures to ameliorate them are not well understood. Here, using a rat femoral artery ischemia-reperfusion (I/R) model, we show that oxidative stress caused by accumulation of oxidative DNA damage occurs in gastrocnemius and soleus muscles after I/R induces muscle cell apoptosis. Moreover, we demonstrate that administration of the antioxidant N-acetyl cysteine (NAC) significantly suppresses oxidative stress accumulation and apoptosis induction in both muscles. We observed that collagen fibers accumulate in the gastrocnemius and soleus muscles after I/R in our model, and that collagen fiber accumulation was significantly suppressed by NAC administration. We demonstrate that adding hydrogen peroxide (H2O2), a reactive oxygen species (ROS), to an in vitro C2C12 myoblast culture system significantly increased expression of the apoptosis-inducing factors Bcl-2-associated X protein (BAX) and Caspase 3, while co-treatment with NAC significantly counteracted this increase and increased expression of the anti-apoptotic factor B-cell lymphoma 2 (Bcl2). Also using the C2C12 myoblast culture system, we show that H2O2 significantly increased expression of Cellular Communication Network Factor 2 (CCN2), which induces fibrosis, while co-addition of NAC with H2O2 significantly suppressed CCN2 induction. Our findings shed light on mechanisms underlying I/R injury in limbs and suggest countermeasures.

Indexed as

AcetylcysteineApoptosisCollagenHindlimbOxidative StressReperfusion InjuryAnimalsAntioxidantsbcl-2-Associated X ProteinCaspase 3Hydrogen PeroxideMaleMuscle, SkeletalRatsRats, Sprague-DawleyReactive Oxygen SpeciesAcetylcysteineAntioxidantsbcl-2-Associated X ProteinCaspase 3CollagenHydrogen PeroxideReactive Oxygen Species

Identifiers

PMID42721182
PMCPMC13561352

What Socratic holds

Textmetadata
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.