Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 8 de 8
Filtrar
Mais filtros











Base de dados
Intervalo de ano de publicação
1.
Vox Sang ; 115(8): 647-654, 2020 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-32350880

RESUMO

BACKGROUND AND OBJECTIVES: Red-blood-cells (RBCs) undergo structural and metabolic changes with prolonged storage, which ultimately may decrease their survival after transfusion. Although the storage-induced damage to RBCs has been rather well described biochemically, little is known about the mechanisms underlying the recognition and rapid clearance of the damaged cells by macrophages. MATERIALS AND METHODS: We, here, used a murine model for cold (+4°C) RBC storage and transfusion. Phagocytosis of human or murine RBCs, liquid stored for 6-8 weeks or 10-14 days, respectively, was investigated in murine peritoneal macrophages. RESULTS: The effects of storage on murine RBCs resembled that described for stored human RBCs with regard to decreased adenosine triphosphate (ATP) levels, accumulation of microparticles (MPs) during storage, and RBC recovery kinetics after transfusion. Under serum-free conditions, phagocytosis of stored human or murine RBCs in vitro was reduced by 70-75%, as compared with that in the presence of heat-inactivated fetal calf serum (FCS). Human serum promoted phagocytosis of stored human RBCs similar to that seen with FCS. By adding fucoidan or dextran sulphate (blockers of scavenger receptors class A (SR-A)), phagocytosis of human or murine RBCs was reduced by more than 90%. Phagocytosis of stored human RBCs was also sensitive to inhibition by the phosphatidylinositol 3 kinase-inhibitor LY294002, the ERK1/2-inhibitor PD98059, or the p38 MAPK-inhibitor SB203580. CONCLUSION: RBCs damaged during liquid storage may be recognized by macrophage SR-A and serum-dependent mechanisms. This species-independent recognition mechanism may help to further understand the rapid clearance of stored RBCs shortly after transfusion.


Assuntos
Preservação de Sangue , Sulfato de Dextrana/farmacologia , Eritrócitos/imunologia , Fagocitose/efeitos dos fármacos , Polissacarídeos/farmacologia , Trifosfato de Adenosina , Animais , Micropartículas Derivadas de Células , Feminino , Humanos , Macrófagos , Masculino , Camundongos
2.
J Sports Med Phys Fitness ; 60(7): 1040-1048, 2020 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-32343079

RESUMO

BACKGROUND: We have previously evaluated muscle functions and morphology in power athletes of long term (5 to15 years) abuse of anabolic androgen steroids (AAS; Doped) and in clean power athletes (Clean), and observed significant improvements in both muscle morphology and muscle functions in Doped. To our knowledge, the effects of long term AAS abuse on human muscle protein profile have never been studied. METHODS: The study examined further the muscle biopsies using a two-dimensional difference gel electrophoresis (2D DIGE) for proteomic screening and protein expression. Cellular localization/distribution of specific proteins identified by proteomic analysis was examined using immunohistochemistry (IHC). RESULTS: Different protein profiles were observed between Doped and Clean, and a valid orthogonal projection of latent structure discriminant analysis model was built (N.=16, x=5, R2=0.88/Q2=0.84, P=0.0005), which separated Doped from Clean. Liquid chromatography followed by tandem spectrometry identified 14 protein spots (representing nine different proteins) of significant difference in relative quantity (P<0.05), of which nine spots were down-regulated in Doped compared with Clean. IHC revealed no significant alteration in cellular localization in phosphoglucomutase-1 and heat shock protein beta-1, but indeed in two reference proteins desmin and F-actin in Doped. CONCLUSIONS: Long term abuse of AAS in combination with training is potentially associated with alterations in skeletal muscle protein profile and protein expression, and structural proteins rather than non-structural proteins are preferentially affected in cellular localization/distribution.


Assuntos
Anabolizantes/efeitos adversos , Dopagem Esportivo , Proteínas Musculares/efeitos dos fármacos , Músculo Esquelético/efeitos dos fármacos , Actinas/análise , Adulto , Anabolizantes/farmacologia , Biópsia , Desmina/análise , Proteínas de Choque Térmico HSP27/análise , Humanos , Imuno-Histoquímica , Proteínas Musculares/biossíntese , Músculo Esquelético/anatomia & histologia , Músculo Esquelético/metabolismo , Fosfoglucomutase/análise , Proteômica
3.
Sports (Basel) ; 7(5)2019 May 23.
Artigo em Inglês | MEDLINE | ID: mdl-31126126

RESUMO

Positive effects from sports are achieved primarily through physical activity, but secondary effects bring health benefits such as psychosocial and personal development and less alcohol consumption. Negative effects, such as the risk of failure, injuries, eating disorders, and burnout, are also apparent. Because physical activity is increasingly conducted in an organized manner, sport's role in society has become increasingly important over the years, not only for the individual but also for public health. In this paper, we intend to describe sport's physiological and psychosocial health benefits, stemming both from physical activity and from sport participation per se. This narrative review summarizes research and presents health-related data from Swedish authorities. It is discussed that our daily lives are becoming less physically active, while organized exercise and training increases. Average energy intake is increasing, creating an energy surplus, and thus, we are seeing an increasing number of people who are overweight, which is a strong contributor to health problems. Physical activity and exercise have significant positive effects in preventing or alleviating mental illness, including depressive symptoms and anxiety- or stress-related disease. In conclusion, sports can be evolving, if personal capacities, social situation, and biological and psychological maturation are taken into account. Evidence suggests a dose-response relationship such that being active, even to a modest level, is superior to being inactive or sedentary. Recommendations for healthy sports are summarized.

4.
Transfusion ; 53(1): 28-33, 2013 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-22612879

RESUMO

BACKGROUND: Transfusion of stored red blood cells (RBCs) can be associated with adverse side effects. Recent studies in mice transfused with stored RBCs showed that a strong proinflammatory cytokine storm was induced due to extravascular hemolysis already at 2 hours after transfusion. Therefore, we here investigated if transfusion of 2 units of cryopreserved autologous RBCs induced a proinflammatory response in healthy human volunteers. STUDY DESIGN AND METHODS: Two units of autologous RBCs, cryopreserved for 16 weeks, were transfused into 10 healthy human volunteers. Serum and blood samples taken at 2 hours before and at 2 and 48 hours after transfusion were analyzed for signs of extravascular hemolysis and the presence of proinflammatory cytokines. RESULTS: At 2 hours after transfusion, transferin-bound serum iron, as well as transferin saturation and total bilirubin, were already significantly increased. These measures all returned back toward that in pretransfusion samples at 48 hours after transfusion. No increases in the production of the proinflammatory cytokines interleukin (IL)-1ß, IL-6, IL-8, monocyte chemotactic protein-1, macrophage inflammatory protein-1ß, or tumor necrosis factor-α were detected at any time point after transfusion. CONCLUSION: Although a significant level of extravascular hemolysis already occurred at 2 hours after transfusion of cryopreserved RBCs, there were no signs of proinflammatory cytokine production up to 48 hours after transfusion.


Assuntos
Criopreservação , Citocinas/metabolismo , Transfusão de Eritrócitos/efeitos adversos , Eritrócitos/citologia , Eritrócitos/metabolismo , Hemólise/fisiologia , Adulto , Quimiocina CCL2 , Humanos , Interleucina-10/metabolismo , Interleucina-1beta/metabolismo , Interleucina-6/metabolismo , Interleucina-8/metabolismo , Masculino , Fator de Necrose Tumoral alfa/metabolismo , Adulto Jovem
5.
Histochem Cell Biol ; 138(1): 89-99, 2012 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-22487949

RESUMO

Using proteomics combined with immunohistochemistry (IHC), we re-evaluated our previous hypothesis that voluntary eccentric exercise does not result in inflammation or necrosis while it does lead to muscular adaptation/remodeling through Z-band related proteins. Muscle biopsies from m. vastus lateralis were taken from five control and five exercised subjects 48 h after 45 min of downhill running. General muscle morphology was examined using histology and histochemistry. Proteomics was used to reveal protein profiles and novel proteins. IHC with specific antibody against three Z-band related proteins identified by proteomics was also performed. General morphology showed no muscle degeneration or inflammation in any exercised biopsy. Proteomics revealed that out of 612 individual protein spots, the exercised biopsy presented three proteins with significant (p < 0.05) higher expression ratio and four proteins of lower ratio compared to controls. Four of the proteins desmin, actin, Rab-35 and LDB3 are Z-band related; the former two have long been the focus of interest and were found to be up-regulated in the study; the latter two are Z-band assembly/stabilization protein and were for the first time observed to be down-regulated in exercised muscles. The other three proteins are related with either cellular metabolism or calcium homeostasis and none is related with muscle necrosis or inflammation. IHC observations that both desmin and actin were increased whereas LDB3 was completely absent in some focal areas are consistent with proteomic results and with our previous observations. The results of the study confirmed our previous findings and therefore strengthened the hypothesis that voluntary eccentric exercise does not cause human muscle necrosis or inflammation; instead, muscular remodeling occurs specifically through Z-band related proteins.


Assuntos
Exercício Físico/fisiologia , Inflamação/metabolismo , Músculo Esquelético/patologia , Adulto , Feminino , Humanos , Imuno-Histoquímica , Masculino , Pessoa de Meia-Idade , Contração Muscular , Proteômica
6.
Histochem Cell Biol ; 124(2): 167-75, 2005 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-16059740

RESUMO

The morphological appearance of the vastus lateralis (VL) muscle from high-level power-lifters on long-term anabolic steroid supplementation (PAS) and power-lifters never taking anabolic steroids (P) was compared. The effects of long- and short-term supplementation were compared. Enzyme-immunohistochemical investigations were performed to assess muscle fiber type composition, fiber area, number of myonuclei per fiber, internal myonuclei, myonuclear domains and proportion of satellite cells. The PAS group had larger type I, IIA, IIAB and IIC fiber areas (p<0.05). The number of myonuclei/fiber and the proportion of central nuclei were significantly higher in the PAS group (p<0.05). Similar results were seen in the trapezius muscle (T) but additionally, in T the proportion of fibers expressing developmental myosin isoforms was higher in the PAS group compared to the P group. Further, in VL, the PAS group had significantly larger nuclear domains in fibers containing > or = 5 myonuclei. The results of AS on VL morphology in this study were similar to previously reported short-term effects of AS on VL. The initial effects from AS appear to be maintained for several years.


Assuntos
Anabolizantes/farmacologia , Fibras Musculares de Contração Rápida/efeitos dos fármacos , Fibras Musculares de Contração Lenta/efeitos dos fármacos , Músculo Esquelético/efeitos dos fármacos , Levantamento de Peso , Adulto , Núcleo Celular/efeitos dos fármacos , Núcleo Celular/patologia , Humanos , Masculino , Fibras Musculares de Contração Rápida/metabolismo , Fibras Musculares de Contração Rápida/patologia , Fibras Musculares Esqueléticas/efeitos dos fármacos , Fibras Musculares Esqueléticas/metabolismo , Fibras Musculares de Contração Lenta/metabolismo , Fibras Musculares de Contração Lenta/patologia , Músculo Esquelético/metabolismo , Músculo Esquelético/patologia , Miosinas/metabolismo , Isoformas de Proteínas/metabolismo
7.
J Physiol ; 556(Pt 3): 983-1000, 2004 May 01.
Artigo em Inglês | MEDLINE | ID: mdl-14766942

RESUMO

Muscular adaptation to physical exercise has previously been described as a repair process following tissue damage. Recently, evidence has been published to question this hypothesis. The purpose of this study was to investigate inflammatory processes in human skeletal muscle and epimysium after acute physical exercise with large eccentric components. Three groups of subjects (n= 19) performed 45 min treadmill running at either 4 deg (n= 5) or 8 deg (n= 9) downhill or 4 deg uphill (n= 5) and one group served as control (n= 9). One biopsy was taken from each subject 48 h post exercise. Blood samples were taken up to 7 days post exercise. Compared to the control group, none of the markers of inflammation in muscle and epimysium samples was different in any exercised group. Only subjects in the Downhill groups experienced delayed onset of muscle soreness (DOMS) and increased serum creatine kinase activity (CK). The detected levels of immunohistochemical markers for T cells (CD3), granulocytes (CD11b), leukaemia inhibitory factor (LIF) and hypoxia-inducible factor 1beta (HIF-1beta) were greater in epimysium from exercised subjects with DOMS ratings >3 (0-10 scale) compared to exercised subjects without DOMS but not higher than controls. Eccentric physical exercise (downhill running) did not result in skeletal muscle inflammation 48 h post exercise, despite DOMS and increased CK. It is suggested that exercise can induce DOMS by activating inflammatory factors present in the epimysium before exercise. Repeated physical training may alter the content of inflammatory factors in the epimysium and thus reduce DOMS.


Assuntos
Citocinas/metabolismo , Substâncias de Crescimento/metabolismo , Hormônios/metabolismo , Leucócitos/metabolismo , Músculo Esquelético/fisiologia , Corrida/fisiologia , Adolescente , Adulto , Antígenos CD/análise , Antígenos CD/metabolismo , Antígenos de Diferenciação Mielomonocítica/análise , Antígenos de Diferenciação Mielomonocítica/metabolismo , Translocador Nuclear Receptor Aril Hidrocarboneto , Proteína C-Reativa/análise , Proteína C-Reativa/metabolismo , Antígeno CD11b/análise , Antígeno CD11b/metabolismo , Complexo CD3/análise , Complexo CD3/metabolismo , Antígeno CD56/análise , Antígeno CD56/metabolismo , Creatina Quinase/sangue , Creatina Quinase/metabolismo , Citocinas/análise , Citocinas/sangue , Proteínas de Ligação a DNA/análise , Proteínas de Ligação a DNA/metabolismo , Teste de Esforço/métodos , Fáscia/química , Fáscia/metabolismo , Feminino , Citometria de Fluxo , Granulócitos/citologia , Frequência Cardíaca/fisiologia , Hormônios/sangue , Humanos , Imuno-Histoquímica , Fator de Crescimento Insulin-Like I/análise , Fator de Crescimento Insulin-Like I/metabolismo , Interleucina-6/análise , Interleucina-6/sangue , Interleucina-6/metabolismo , Contração Isométrica/fisiologia , Antígeno Ki-67/análise , Antígeno Ki-67/metabolismo , Fator Inibidor de Leucemia , Subunidade alfa de Receptor de Fator Inibidor de Leucemia , Contagem de Leucócitos , Leucócitos/química , Leucócitos/citologia , Linfócitos/citologia , Linfócitos/metabolismo , Masculino , Pessoa de Meia-Idade , Monócitos/citologia , Monócitos/metabolismo
8.
Exerc Immunol Rev ; 8: 116-67, 2002.
Artigo em Inglês | MEDLINE | ID: mdl-12690940

RESUMO

When exploring the possible mechanisms by which adaptation to physical exercise can occur, the immune system appears to be a likely candidate of importance, because physical exercise will exert both systemic and local effects on the immune system. This review will focus on the immune system in the perspective of skeletal muscle tissue adaptation to physical exercise. The involvement of circulating and tissue bound leukocytes, cytokines, hormones and growth factors will be discussed. A few new hypotheses are presented: 1) The primary mechanism governing skeletal muscle adaptation to physical exercise is suggested to be of non-inflammatory origin; 2) it is suggested that IL-10 may function as one of the signals transmitted by skeletal muscle cells when substrate levels are low; 3) creatine kinase could have immuno-modulatory actions, thereby serving as a messenger molecule between skeletal muscles and the immune system. Based on the intricate and complex array of events governing life and death in other cells types, a simple explanation of the issues of skeletal muscle development, regeneration and adaptation is unlikely. There are large individual differences in the immune response to the same relative or absolute exercise intensity, suggesting that interpreting the average effect of exercise on a group of individuals may not reveal the cause and effect of any given immunological variable. More sophisticated analyses of collected data is suggested in future studies and perhaps some re-evaluation of existing data is also needed. If we can understand the mechanisms behind muscle adaptation, we can also optimize training programs and athletic performance.


Assuntos
Exercício Físico/fisiologia , Músculo Esquelético/imunologia , Adaptação Fisiológica , Adesão Celular , Creatina Quinase/imunologia , Citocinas/metabolismo , Humanos , Tolerância Imunológica , Inflamação/etiologia , Inflamação/imunologia , Linfócitos/imunologia , Macrófagos/imunologia , Monócitos/imunologia , Músculo Esquelético/lesões , Músculo Esquelético/fisiologia , Neutrófilos/imunologia , Transdução de Sinais , Estresse Fisiológico/imunologia
SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA