Eccentric Exercise Facilitates Mesenchymal Stem Cell Appearance in Skeletal Muscle

Eccentric, or lengthening, contractions result in injury and subsequently stimulate the activation and proliferation of satellite stem cells which are important for skeletal muscle regeneration. The discovery of alternative myogenic progenitors in skeletal muscle raises the question as to whether stem cells other than satellite cells accumulate in muscle in response to exercise and contribute to post-exercise repair and/or growth. In this study, stem cell antigen-1 (Sca-1) positive, non-hematopoetic (CD45-) cells were evaluated in wild type (WT) and α7 integrin transgenic (α7Tg) mouse muscle, which is resistant to injury yet liable to strain, 24 hr following a single bout of eccentric exercise. Sca-1+CD45− stem cells were increased 2-fold in WT muscle post-exercise. The α7 integrin regulated the presence of Sca-1+ cells, with expansion occurring in α7Tg muscle and minimal cells present in muscle lacking the α7 integrin. Sca-1+CD45− cells isolated from α7Tg muscle following exercise were characterized as mesenchymal-like stem cells (mMSCs), predominantly pericytes. In vitro multiaxial strain upregulated mMSC stem cells markers in the presence of laminin, but not gelatin, identifying a potential mechanistic basis for the accumulation of these cells in muscle following exercise. Transplantation of DiI-labeled mMSCs into WT muscle increased Pax7+ cells and facilitated formation of eMHC+DiI− fibers. This study provides the first demonstration that mMSCs rapidly appear in skeletal muscle in an α7 integrin dependent manner post-exercise, revealing an early event that may be necessary for effective repair and/or growth following exercise. The results from this study also support a role for the α7 integrin and/or mMSCs in molecular- and cellular-based therapeutic strategies that can effectively combat disuse muscle atrophy

Suplementação com ácido linoléico conjugado: estabilidade oxidativa dos suplementos e correlações com conteúdo dos lípides totais hepáticos e indicadores da oxidação dos lípides biológicos de ratos Wistar Conjugated linoleic acid supplementation: oxidative stability of supplements and correlations with total hepatic lipid contents and biological lipid oxidation indicators in Wistar rats

OBJETIVO:O objetivo do trabalho foi avaliar a estabilidade oxidativa de misturas comerciais de ácido linoléico conjugado e buscar possível correlação entre a suplementação e o conteúdo total de lípides hepáticos, e também de alguns indicadores da oxidação lipídica em ratos. MÉTODOS:Um ensaio biológico com 30 ratos divididos em três grupos (n=10) caracterizando os grupos controle e suplementados com as misturas comerciais AdvantEdge® e One® foi realizado. A concentração administrada foi de 2% em relação ao consumo de dieta e os animais foram suplementados durante 42 dias. O conteúdo total de lípides do fígado foi determinado e a morfologia do órgão foi examinada por meio de microscopia ótica. Índice de peróxido e malondialdeído foram determinados para avaliar a estabilidade oxidativa dos suplementos in vitro. Índice de peróxido, malondialdeído, 8-iso-PGF2&#945; isoprostana e catalase foram determinados como indicadores da oxidação dos lípides biológicos. RESULTADOS: Os resultados demonstraram baixa estabilidade das misturas comerciais à oxidação in vitro. As associações entre o consumo de ácido linoléico conjugado e malondialdeído (r=-0,7914, p<0,0001) e catalase (r=-0,5991, p=0,008) foram moderadas, negativas e significantes, demonstrando que o ácido linoléico conjugado reduziu a oxidação lipídica in vivo. O conteúdo dos lípides totais hepáticos não aumentou (22,42%, DP=1,40%) e a morfologia do órgão permaneceu íntegra. CONCLUSÃO:Embora esse protocolo de suplementação com ácido linoléico conjugado tenha reduzido a oxidação lipídica, há que considerar a tendência para o aumento de 8-iso-PGF2&#945; isoprostana e de peróxidos como perspectiva de continuidade das pesquisas sobre a reinvestigação do efeito antioxidante do ácido linoléico conjugado.<br>OBJECTIVE:The claimed action of conjugated linoleic acid as an antioxidant is unexpected and unclear, in view of its chemical structure - a conjugated diene, i.e., a fatty acid in its initial stage of autoxidation. Indeed, it can be speculated that it could act as a pro-oxidant, increasing oxidative stress in biological systems, nevertheless it has carbon-carbon bonds in the trans configuration. The objective of the present work was to evaluate the oxidative stability of commercial mixtures, and to investigate a possible correlation between conjugated linoleic acid supplementation and total hepatic lipid content, as well as some lipid oxidation indicators in rats. METHODS:A biological assay was done with thirty rats divided into three groups (n=10) characterized as control and supplemented with the commercial mixtures AdvantEdge® and One®. The mixtures were administered in the concentration of 2% of the total diet consumption, and animals were supplemented for 42 days. The total liver lipid content was determined, and the morphology of the organ was examined by optical microscopy. Peroxide and malondialdehyde indexes were determined in vitro in order to evaluate the oxidative stability of the supplements. Peroxide, malondialdehyde and 8-iso-PGF2&#945; isoprostane and catalase were determined as biological lipid oxidation indicators. RESULTS:Results indicated a low in vitro oxidation stability of commercial mixtures. Associations between conjugated linoleic acid consumption and malondialdehyde (r=-0.7914, p<0.0001), and catalase (r=-0.5991, p=0.008) were moderate, negative and significant, demonstrating that conjugated linoleic acid reduced in vivo lipid oxidation. Total hepatic lipid content did not increase (22.42%, (SD=1.40%), and the organ remained morphologically undamaged. CONCLUSION:However, even though this CLA supplementation protocol did reduce lipid oxidation, a tendency was observed to an increase of 8-iso-PGF2 alpha isoprostane and peroxides induced by conjugated linoleic acid. Further research may be needed to verify its antioxidant effect