Evidence map›Paper›PMID 25852565›Full record

ArticleFrontiers in physiology2015

Leucine minimizes denervation-induced skeletal muscle atrophy of rats through akt/mtor signaling pathways.

Carolina B Ribeiro, Daiane C Christofoletti, Vitor A Pezolato, Rita de Cássia Marqueti Durigan, Jonato Prestes, Ramires A Tibana, Elaine C L Pereira, Ivo V de Sousa Neto, João L Q Durigan, Carlos A da Silva

Open access · goldAbstract read
In one paragraph

Article in Frontiers in physiology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.7field-weighted citation impact, top 17% of its field
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

13 citing papers in PubMed, 23 citations in OpenAlex.

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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

10 authors at 3 institutions in 1 country.

Carolina B RibeiroPrograma de Pós-graduação em Ciências do Movimento Humano, Methodist University of Piracicaba, UNIMEP Piracicaba, Brazil.
Daiane C ChristofolettiPrograma de Pós-graduação em Ciências do Movimento Humano, Methodist University of Piracicaba, UNIMEP Piracicaba, Brazil.
Vitor A PezolatoPrograma de Pós-graduação em Ciências do Movimento Humano, Methodist University of Piracicaba, UNIMEP Piracicaba, Brazil.
Rita de Cássia Marqueti DuriganGraduate Program of Science and Technology of Health, University of Brasília Brasilia, Brazil.
Jonato PrestesGraduate Program of Physical Education, Catholic University of Brasília Brasilia, Brazil.
Ramires A TibanaGraduate Program of Physical Education, Catholic University of Brasília Brasilia, Brazil.
Elaine C L PereiraGraduate Program of Science and Technology of Health, University of Brasília Brasilia, Brazil.
Ivo V de Sousa NetoGraduate Program of Physical Education, Catholic University of Brasília Brasilia, Brazil.
João L Q DuriganGraduate Program of Science and Technology of Health, University of Brasília Brasilia, Brazil ; Graduate Program of Physical Education, University of Brasília Brasilia, Brazil.
Carlos A da SilvaPrograma de Pós-graduação em Ciências do Movimento Humano, Methodist University of Piracicaba, UNIMEP Piracicaba, Brazil.
Methodist University of Piracicaba · BRUniversidade Católica de Brasília · BRUniversidade de Brasília · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The aim of the present study was to evaluate the effect of leucine treatment (0.30 mM) on muscle weight and signaling of myoproteins related to synthesis and degradation pathways of soleus muscle following seven days of complete sciatic nerve lesion. Wistar rats (n = 24) of 3-4 months of age (192 ± 23 g) were used. The animals were randomly distributed into four experimental groups (n = 6/group): control, treated with leucine (L), denervated (D) and denervated treated with leucine (DL). Dependent measures were proteins levels of AKT, AMPK, mTOR, and ACC performed by Western blot. Leucine induced a reduction in the phosphorylation of AMPK (p < 0.05) by 16% in the L and by 68% in the DL groups as compared with control group. Denervation increased AMPK by 24% in the D group as compared with the control group (p < 0.05). AKT was also modulated by denervation and leucine treatment, highlighted by the elevation of AKT phosphorylation in the D (65%), L (98%) and DL (146%) groups as compared with the control group (p < 0.05). AKT phosphorylation was 49% higher in the D group as compared with the DL group. Furthermore, denervation decreased mTOR phosphorylation by 29% in the D group as compared with the control group. However, leucine treatment induced an increase of 49% in the phosphorylation of mTOR in the L group as compared with the control group, and an increase of 154% in the DL as compared with the D group (p < 0.05). ACC phosphorylation was 20% greater in the D group than the control group. Furthermore, ACC in the soleus was 22% lower in the in the L group and 50% lower in the DL group than the respective control group (p < 0.05). In conclusion, leucine treatment minimized the deleterious effects of denervation on rat soleus muscle by increasing anabolic (AKT and mTOR) and decreasing catabolic (AMPK) pathways. These results may be interesting for muscle recovery following acute denervation, which may contribute to musculoskeletal rehabilitation after denervation.

Indexed as

degradation pathwaysdenervationleucinemuscle atrophyrehabilitationsynthesis pathways

Identifiers

PMID25852565
PMCPMC4364154
OpenAlexW1968884865

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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.