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1.
Drug Deliv ; 25(1): 91-101, 2018 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-29250977

RESUMO

Epithelial to mesenchymal transition (EMT) has emerged as a key process in the development of renal fibrosis. In fact, EMT-derived fibroblasts contribute to the progression of chronic renal disease. In addition, anti-inflammatory M2 macrophages have exhibited a great influence on renal fibrosis. However, because of the high impact that the inputs of different environmental cytokines have on their phenotype, macrophages can easily lose this property. We aim to known if microencapsulated macrophages on M2-inducing alginate matrices could preserve macrophage phenotype and thus release factors able to act on epithelial cells to prevent the epithelial differentiation towards mesenchymal cells. We reproduced an in vitro model of EMT by treating adipose-derived stem cells with all-trans retinoic acid (ATRA) and induced their transformation toward epithelia. Dedifferentiation of epithelial cells into a mesenchymal phenotype occurred when ATRA was retired, thus simulating EMT. Results indicate that induction of M2 phenotype by IL-10 addition in the alginate matrix produces anti-inflammatory cytokines and increases the metabolic activity and the viability of the encapsulated macrophages. The released conditioned medium modulates EMT and maintains healthy epithelial phenotype. This could be used for in vivo cell transplantation, or alternatively as an external releaser able to prevent epithelial to mesenchymal transformation for future anti-fibrotic therapies.


Assuntos
Meios de Cultivo Condicionados/metabolismo , Transição Epitelial-Mesenquimal/fisiologia , Macrófagos/fisiologia , Animais , Diferenciação Celular/fisiologia , Linhagem Celular , Células Epiteliais/metabolismo , Células Epiteliais/fisiologia , Fibroblastos/metabolismo , Fibroblastos/fisiologia , Interleucina-10/metabolismo , Macrófagos/metabolismo , Masculino , Camundongos , Fenótipo , Células RAW 264.7
2.
Pain Res Treat ; 2015: 512673, 2015.
Artigo em Inglês | MEDLINE | ID: mdl-26240758

RESUMO

Objective. To evaluate the usefulness of the pain tracking technique in acute mechanical low back pain. Method. We performed an experimental prospective (longitudinal) explanatory study between January 2011 and September 2012. The sample was randomly divided into two groups. Patients were assessed at the start and end of the treatment using the visual analogue scale and the Waddell test. Treatment consisted in applying the pain tracking technique to the study group and interferential current therapy to the control group. At the end of treatment, cryotherapy was applied for 10 minutes. The Wilcoxon signed-rank test and the Mann Whitney test were used. They were performed with a predetermined significance level of p ≤ 0.05. Results. Pain was triggered by prolonged static posture and intense physical labor and intensified through trunk movements and when sitting and standing. The greatest relief was reported in lateral decubitus position and in William's position. The majority of the patients had contracture. Pain and disability were modified with the rehabilitation treatment in both groups. Conclusions. Both the pain tracking and interferential current techniques combined with cryotherapy are useful treatments for acute mechanical low back pain. The onset of analgesia is faster when using the pain tracking technique.

3.
4.
In. Martín Cordero, Jorge Enrique. Agentes físicos terapéuticos. LA Habana, Ecimed, 2008. .
Monografia em Espanhol | CUMED | ID: cum-42560
6.
In. Martín Cordero, Jorge Enrique. Agentes físicos terapéuticos. LA Habana, Ecimed, 2008. , ilus.
Monografia em Espanhol | CUMED | ID: cum-42558
7.
In. Martín Cordero, Jorge Enrique. Agentes físicos terapéuticos. LA Habana, Ecimed, 2008. , ilus.
Monografia em Espanhol | CUMED | ID: cum-42557
8.
In. Martín Cordero, Jorge Enrique. Agentes físicos terapéuticos. LA Habana, Ecimed, 2008. , ilus.
Monografia em Espanhol | CUMED | ID: cum-42556
9.
In. Martín Cordero, Jorge Enrique. Agentes físicos terapéuticos. LA Habana, Ecimed, 2008. , ilus.
Monografia em Espanhol | CUMED | ID: cum-42555
12.
In. Martín Cordero, Jorge Enrique. Agentes físicos terapéuticos. LA Habana, Ecimed, 2008. , ilus.
Monografia em Espanhol | CUMED | ID: cum-42552
13.
In. Martín Cordero, Jorge Enrique. Agentes físicos terapéuticos. LA Habana, Ecimed, 2008. , ilus.
Monografia em Espanhol | CUMED | ID: cum-42551
14.
In. Martín Cordero, Jorge Enrique. Agentes físicos terapéuticos. LA Habana, Ecimed, 2008. , ilus.
Monografia em Espanhol | CUMED | ID: cum-42550
15.
In. Martín Cordero, Jorge Enrique. Agentes físicos terapéuticos. LA Habana, Ecimed, 2008. , ilus.
Monografia em Espanhol | CUMED | ID: cum-42549
16.
In. Martín Cordero, Jorge Enrique. Agentes físicos terapéuticos. LA Habana, Ecimed, 2008. , ilus.
Monografia em Espanhol | CUMED | ID: cum-42548
17.
In. Martín Cordero, Jorge Enrique. Agentes físicos terapéuticos. LA Habana, Ecimed, 2008. , ilus.
Monografia em Espanhol | CUMED | ID: cum-42547
18.
In. Martín Cordero, Jorge Enrique. Agentes físicos terapéuticos. LA Habana, Ecimed, 2008. , ilus.
Monografia em Espanhol | CUMED | ID: cum-42546
19.
In. Martín Cordero, Jorge Enrique. Agentes físicos terapéuticos. LA Habana, Ecimed, 2008. , ilus.
Monografia em Espanhol | CUMED | ID: cum-42545
20.
In. Martín Cordero, Jorge Enrique. Agentes físicos terapéuticos. LA Habana, Ecimed, 2008. .
Monografia em Espanhol | CUMED | ID: cum-42544
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