Evidence map›Paper›PMID 40977516›Full record

ArticleJournal of cellular and molecular medicine2025

Therapeutic Efficacy of HPβ-CD-Angiotensin-(1-7) Oral Formulation in Muscle Injury Recovery in Rat.

Nádia Lúcia Totou, Ana Maria Sampaio Rocha, Samara Silva de Moura, César Henrique Pereira, Fabricio Sampaio Coelho, Douglas Daniel Dophine, Daniel Barbosa Coelho, Emerson Cruz de Oliveira, Robson Augusto Souza Dos Santos, Lenice Kappes Becker and 1 more

Abstract read
In one paragraph

Article in Journal of cellular and molecular medicine, 2025. 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

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

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

11 authors.

Nádia Lúcia TotouBiological Sciences Research Center-Postgraduate Program in Biological Sciences, Federal University of Ouro Preto, Ouro Preto, Brazil.
Ana Maria Sampaio RochaBiological Sciences Research Center-Postgraduate Program in Biological Sciences, Federal University of Ouro Preto, Ouro Preto, Brazil.
Samara Silva de MouraSchool of Physical Education, Federal University of Ouro Preto, Ouro Preto, Brazil.
César Henrique PereiraBiological Sciences Research Center-Postgraduate Program in Biological Sciences, Federal University of Ouro Preto, Ouro Preto, Brazil.
Fabricio Sampaio CoelhoBiological Sciences Research Center-Postgraduate Program in Biological Sciences, Federal University of Ouro Preto, Ouro Preto, Brazil.
Douglas Daniel DophineBiological Sciences Research Center-Postgraduate Program in Biological Sciences, Federal University of Ouro Preto, Ouro Preto, Brazil.
Daniel Barbosa CoelhoSchool of Physical Education, Federal University of Ouro Preto, Ouro Preto, Brazil.
Emerson Cruz de OliveiraSchool of Physical Education, Federal University of Ouro Preto, Ouro Preto, Brazil.ORCID 0000-0002-8982-4705
Robson Augusto Souza Dos SantosDepartment of Physiology and Biophysics, Institute of Biological Sciences, Federal University of Minas Gerais, Belo Horizonte, Brazil.
Lenice Kappes BeckerSchool of Physical Education, Federal University of Ouro Preto, Ouro Preto, Brazil.
Wanderson Geraldo de LimaBiological Sciences Research Center-Postgraduate Program in Biological Sciences, Federal University of Ouro Preto, Ouro Preto, Brazil.

Funding

Federal University of Ouro Preto using resources from the Pro-Rectorate of Research, Graduate Studies and Innovation (PROPPI)Higher Education Personnel Improvement Coordination (CAPES)Minas Gerais State Research Foudation (FAPEMIG) APQ-02511-22Minas Gerais State Research Foundation (FAPEMIG) APQ-00662-22Minas Gerais State Research Foundation (FAPEMIG) APQ-02511-22Minas Gerais State Research Foundation (FAPEMIG) APQ-04983-22National Council for Scientific and Technological Development (CNPq)National Nanobiofar Technology Institute (INCT-Nanobiofar)Personal resources of the researchers
6 · The paper itself

Abstract

To evaluate the therapeutic effect of oral treatment with HPβ-CD-angiotensin-(1-7) (Ang-(1-7)) on muscle recovery after laceration injury. Wistar rats were divided into four groups: Control (n = 10); HPβ-CD-Ang-(1-7) (n = 10); muscle injury + HPβ-CD (MI + Placebo) (n = 24); and muscle injury + HPβ-CD-Ang-(1-7) (MI + Ang-(1-7)) (n = 24). After 7-21 days of treatment, physical performance, histological features and the expression of pro- and anti-fibrotic genes were evaluated. The MI + Ang-(1-7) group showed improved control of the inflammatory phase and reduced deposition of collagen types I and III compared to MI + Placebo. CTGF gene expression analysis revealed lower levels of pro-fibrotic markers and higher expression of proteins involved in blocking fibrotic pathways. In treadmill tests, MI + Ang-(1-7) animals also showed superior physical performance at all evaluated time points. Oral treatment with Ang-(1-7) is effective in promoting recovery from muscle injuries, particularly fibrotic lesions, while preserving muscle function and enhancing physical performance.

Indexed as

Angiotensin IMuscle, SkeletalPeptide Fragments2-Hydroxypropyl-beta-cyclodextrinAdministration, OralAnimalsBody Mass IndexCollagenFibrosisGene Expression RegulationMalePhysical Conditioning, AnimalRatsRats, WistarTranscription, GeneticWound Healing2-Hydroxypropyl-beta-cyclodextrinAngiotensin Iangiotensin I (1-7)CollagenPeptide Fragmentsangiotensinconnective tissue growth factorfibrosisinflammationmuscle injury

Identifiers

PMID40977516
PMCPMC12451399

What OpenQuestion holds

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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.