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BACKGROUND: Fibromyalgia (FM) is a complex syndrome to diagnose and treat because of its unknown etiology. However, previous studies reported that patients with FM experience oxidative stress. OBJECTIVES: In this study, we investigated single-nucleotide polymorphisms (SNPs) in genes encoding enzymes involved in oxidative stress (superoxide dismutase 1 [SOD1], catalase, and NADPH oxidase [CYBA]) in patients with FM and in healthy subjects, as well as the possible relation with demographic and clinical manifestations of FM. METHODS: A total of 141 patients with FM and 73 healthy subjects participated in this case-control study. For DNA extraction, buccal swabs were collected from patients with FM, and a peripheral blood sample was extracted from controls. We analyzed SNPs in genes related to oxidative stress (rs10432782 in SOD1, rs1001179 in catalase, and rs4673 in CYBA) using TaqMan probes. In patients with FM, severity of FM, fatigue, and pain were assessed by Fibromyalgia Impact Questionnaire, Multidimensional Fatigue Inventory, and Visual Analogue Scale (VAS), respectively. Physical (PCS-12) and mental (MCS-12) health statuses were evaluated by the 12-Item Short-Form Health Survey. RESULTS: The selected SNPs did not show significant differences between patients with FM and controls. The rs10432782 (SOD1) was associated with Fibromyalgia Impact Questionnaire scores in patients with FM, whereas the rs4673 (CYBA) was associated with the Multidimensional Fatigue Inventory score, MCS-12 score, and duration of the disease. DISCUSSION: We have identified significant correlations between SOD1 and CYBA variants with clinical manifestations of FM. These results provide new insights into the pathogenesis of FM that could be useful for guiding future studies along the way to find the cause(s) of this syndrome.
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Fibromialgia/genética , Fibromialgia/fisiopatologia , Predisposição Genética para Doença , Voluntários Saudáveis/estatística & dados numéricos , Estresse Oxidativo/genética , Polimorfismo de Nucleotídeo Único , Adulto , Idoso , Idoso de 80 Anos ou mais , Estudos de Casos e Controles , Catalase/genética , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , NADPH Oxidases/genética , Superóxido Dismutase/genética , Inquéritos e QuestionáriosRESUMO
Lipids are a heterogeneous group of substances characterized by their solubility in organic solvents and insolubility in water. Lipids can be found as normal components of different tissues and organs, and they can be affected by several pathological conditions. The histochemical identification of lipids plays an important role in the histopathological diagnosis and research, but successful staining depends on adequate fixation and processing of the tissue. Here we describe methods to fix, cryoprotect, and process tissue samples for the histochemical identification of lipids in frozen or paraffin-embedded tissues.
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Lipídeos , Água , Formaldeído , Inclusão em Parafina/métodos , Solventes , Fixação de Tecidos/métodosRESUMO
Wharton's jelly stem cells (WJSC) from the human umbilical cord (UC) are one of the most promising mesenchymal stem cells (MSC) in tissue engineering (TE) and advanced therapies. The cell niche is a key element for both, MSC and fully differentiated tissues, to preserve their unique features. The basement membrane (BM) is an essential structure during embryonic development and in adult tissues. Epithelial BMs are well-known, but similar structures are present in other histological structures, such as in peripheral nerve fibers, myocytes or chondrocytes. Previous studies suggest the expression of some BM molecules within the Wharton's Jelly (WJ) of UC, but the distribution pattern and full expression profile of these molecules have not been yet elucidated. In this sense, the aim of this histological study was to evaluate the expression of main BM molecules within the WJ, cultured WJSC and during WJSC microtissue (WJSC-MT) formation process. Results confirmed the presence of a pericellular matrix composed by the main BM molecules-collagens (IV, VII), HSPG2, agrin, laminin and nidogen-around the WJSC within UC. Additionally, ex vivo studies demonstrated the synthesis of these BM molecules, except agrin, especially during WJSC-MT formation process. The WJSC capability to synthesize main BM molecules could offer new alternatives for the generation of biomimetic-engineered substitutes where these molecules are particularly needed.
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Células-Tronco Mesenquimais , Geleia de Wharton , Adulto , Feminino , Gravidez , Humanos , Agrina/metabolismo , Cordão Umbilical , Células-Tronco Mesenquimais/metabolismo , Técnicas de Cultura de Células , Membrana BasalRESUMO
Purpose: We carried out a histological characterization analysis of the stromal layer of human heterotypic cornea substitutes generated with extra-corneal cells to determine their putative usefulness in tissue engineering. Methods: Human bioartificial corneas were generated using nanostructured fibrin-agarose biomaterials with corneal stromal cells immersed within. To generate heterotypical corneas, umbilical cord Wharton's jelly stem cells (HWJSC) were cultured on the surface of the stromal substitutes to obtain an epithelial-like layer. These bioartificial corneas were compared with control native human corneas and with orthotypical corneas generated with human corneal epithelial cells on top of the stromal substitute. Both the corneal stroma and the basement membrane were analyzed using histological, histochemical and immunohistochemical methods in samples kept in culture and grafted in vivo for 12 months in the rabbit cornea. Results: Our results showed that the stroma of the bioartificial corneas kept ex vivo showed very low levels of fibrillar and non-fibrillar components of the tissue extracellular matrix. However, in vivo implantation resulted in a significant increase of the contents of collagen, proteoglycans, decorin, keratocan and lumican in the corneal stroma, showing higher levels of maturation and spatial organization of these components. Heterotypical corneas grafted in vivo for 12 months showed significantly higher contents of collagen fibers, proteoglycans and keratocan. When the basement membrane was analyzed, we found that all corneas grafted in vivo showed intense PAS signal and higher contents of nidogen-1, although the levels found in human native corneas was not reached, and a rudimentary basement membrane was observed using transmission electron microscopy. At the epithelial level, HWJSC used to generate an epithelial-like layer in ex vivo corneas were mostly negative for p63, whereas orthotypical corneas and heterotypical corneas grafted in vivo were positive. Conclusion: These results support the possibility of generating bioengineered artificial corneas using non-corneal HWJSC. Although heterotypical corneas were not completely biomimetic to the native human corneas, especially ex vivo, in vivo grafted corneas demonstrated to be highly biocompatible, and the animal cornea became properly differentiated at the stroma and basement membrane compartments. These findings open the door to the future clinical use of these bioartificial corneas.
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Because cartilage has limited regenerative capability, a fully efficient advanced therapy medicinal product is needed to treat severe cartilage damage. We evaluated a novel biomaterial obtained by decellularizing sturgeon chondral endoskeleton tissue for use in cartilage tissue engineering. In silico analysis suggested high homology between human and sturgeon collagen proteins, and ultra-performance liquid chromatography confirmed that both types of cartilage consisted mainly of the same amino acids. Decellularized sturgeon cartilage was recellularized with human chondrocytes and four types of human mesenchymal stem cells (MSC) and their suitability for generating a cartilage substitute was assessed ex vivo and in vivo. The results supported the biocompatibility of the novel scaffold, as well as its ability to sustain cell adhesion, proliferation and differentiation. In vivo assays showed that the MSC cells in grafted cartilage disks were biosynthetically active and able to remodel the extracellular matrix of cartilage substitutes, with the production of type II collagen and other relevant components, especially when adipose tissue MSC were used. In addition, these cartilage substitutes triggered a pro-regenerative reaction mediated by CD206-positive M2 macrophages. These preliminary results warrant further research to characterize in greater detail the potential clinical translation of these novel cartilage substitutes.
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Novel artificial tissues with potential usefulness in local-based therapies have been generated by tissue engineering using magnetic-responsive nanoparticles (MNPs). In this study, we performed a comprehensive in vivo characterization of bioengineered magnetic fibrin-agarose tissue-like biomaterials. First, in vitro analyses were performed and the cytocompatibility of MNPs was demonstrated. Then, bioartificial tissues were generated and subcutaneously implanted in Wistar rats and their biodistribution, biocompatibility and functionality were analysed at the morphological, histological, haematological and biochemical levels as compared to injected MNPs. Magnetic Resonance Image (MRI), histology and magnetometry confirmed the presence of MNPs restricted to the grafting area after 12 weeks. Histologically, we found a local initial inflammatory response that decreased with time. Structural, ultrastructural, haematological and biochemical analyses of vital organs showed absence of damage or failure. This study demonstrated that the novel magnetic tissue-like biomaterials with improved biomechanical properties fulfil the biosafety and biocompatibility requirements for future clinical use and support the use of these biomaterials as an alternative delivery route for magnetic nanoparticles.
Assuntos
Nanopartículas de Magnetita , Nanopartículas , Animais , Materiais Biocompatíveis/farmacologia , Ratos , Ratos Wistar , Distribuição Tecidual , Engenharia TecidualRESUMO
We have recently reported that patients with fibromyalgia (FM) may be at increased risk for cardiovascular disease. Olive oil reportedly has cardioprotective effects. We examined the influence of olive oil consumption on cardiovascular risk factors in FM. This preliminary study was performed on blood samples of women with FM who consumed 50 mL of organic olive oil daily for 3 weeks. Patients were randomized into two groups: 15 women ingested extra virgin olive oil (EVOO) and 15 refined olive oil (ROO). Cardiovascular risk markers were measured at baseline (pre measure) and after consumption of olive oil (post measure). Red blood cell count and erythrocyte sedimentation rate (ESR; both p < 0.05) declined significantly post-treatment in the EVOO group. Consumption of ROO increased mean platelet volume and reduced platelet distribution width (PDW), neutrophil-to-lymphocyte ratio, ESR and fibrinogen (all p < 0.05). Significant differences were found in pre-post change between the EVOO and ROO groups for cortisol and PDW (both p < 0.05). Our results have shown that consumption of olive oil may have antithrombotic and antiinflammatory properties in patients with FM, thereby improving a number of cardiovascular risk markers. Both EVOO and ROO may be useful as adjuvants for the prevention and/or treatment of cardiovascular disorders in these patients.
Assuntos
Doenças Cardiovasculares/epidemiologia , Fibromialgia/epidemiologia , Fatores de Risco de Doenças Cardíacas , Azeite de Oliva/farmacologia , Sedimentação Sanguínea , Citocinas/sangue , Método Duplo-Cego , Feminino , Fibrinogênio/análise , Humanos , Hidrocortisona/sangue , Lipídeos/sangue , Pessoa de Meia-IdadeRESUMO
Generation of biocompatible and biomimetic tissue-like biomaterials is crucial to ensure the success of engineered substitutes in tissue repair. Natural biomaterials able to mimic the structure and composition of native extracellular matrices typically show better results than synthetic biomaterials. The aim of this study was to perform an in vivo time-course biocompatibility analysis of fibrin-agarose tissue-like hydrogels at the histological, imagenological, hematological, and biochemical levels. Tissue-like hydrogels were produced by a controlled biofabrication process allowing the generation of biomechanically and structurally stable hydrogels. The hydrogels were implanted subcutaneously in 25 male Wistar rats and evaluated after 1, 5, 9, and 12 weeks of in vivo follow-up. At each period of time, animals were analyzed using magnetic resonance imaging (MRI), hematological analyses, and histology of the local area in which the biomaterials were implanted, along with major vital organs (liver, kidney, spleen, and regional lymph nodes). MRI results showed no local or distal alterations during the whole study period. Hematology and biochemistry showed some fluctuation in blood cells values and in some biochemical markers over the time. However, these parameters were progressively normalized in the framework of the homeostasis process. Histological, histochemical, and ultrastructural analyses showed that implantation of fibrin-agarose scaffolds was followed by a progressive process of cell invasion, synthesis of components of the extracellular matrix (mainly, collagen) and neovascularization. Implanted biomaterials were successfully biodegraded and biointegrated at 12 weeks without any associated histopathological alteration in the implanted zone or distal vital organs. In summary, our in vivo study suggests that fibrin-agarose tissue-like hydrogels could have potential clinical usefulness in engineering applications in terms of biosafety and biocompatibility.
RESUMO
OBJECTIVES: The aim of this study was to investigate thrombosis-related parameters (blood coagulation parameters, platelet indices, red blood cell [RBC] count, and inflammatory markers) in patients with fibromyalgia (FM). METHOD: We carried out a case-control study with 35 women with FM and 12 age-matched healthy volunteers to analyze fibrinogen levels, prothrombin time, cephaline time, platelet count, platelet distribution width (PDW), mean platelet volume (MPV), RBC count, neutrophil-to-lymphocyte ratio, and platelet-to-lymphocyte ratio (PLR). RESULTS: The results showed significantly increased fibrinogen levels ( p < .05), platelet count ( p < .05), PDW ( p = .059), RBC count ( p < .05), and PLR ( p < .05) in women with FM versus the healthy volunteers. Prothrombin time ( p < .05) and MPV ( p < .05) were significantly lower in patients with FM than in the controls. CONCLUSIONS: Elevated platelet and RBC counts, PDW values, and fibrinogen levels as well as decreased prothrombin time are all indicative of a prothrombotic state in FM patients, which may be enhanced by an increased inflammatory tone. This prothrombotic state may increase the risk of thrombosis-related cardiovascular disease in patients with FM.
Assuntos
Fibromialgia/sangue , Fibromialgia/patologia , Inflamação/sangue , Protrombina/análise , Trombose/diagnóstico , Trombose/patologia , Adulto , Biomarcadores/sangue , Estudos de Casos e Controles , Feminino , Humanos , Inflamação/patologia , Linfócitos/patologia , Volume Plaquetário Médio , Pessoa de Meia-Idade , Neutrófilos/patologia , Contagem de PlaquetasRESUMO
Lipoxygenase activity in olive fruits increases considerably when the enzyme is extracted using extraction buffer with ethylenediaminetetraacetate, Triton X-100, dithiothreitol, sodium meta-bisulfite, and hydrated polyvinylpolypyrrolidone. In the absence of these compounds the activity measured of the crude extract is almost negligible, and further effects of the enzymatic reaction, such as bleaching activity on chloroplast pigments, do not appear. Moreover, when the oxidizing level of the medium is increased by the addition of linoleic acid or soybean lipoxygenase with linoleic acid, the crude enzymatic extracts of olives reduce the destructive capacity of soybean lipoxygenase on chlorophylls to one-sixth. These results suggest a double pigment protection against lipoxygenase in the olive crude extract, one inhibiting the enzyme and the other interrupting the chain of oxidative reactions beginning with hydroperoxide formation.
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Cloroplastos/metabolismo , Frutas/metabolismo , Lipoxigenase/metabolismo , Pigmentos Biológicos/metabolismo , Frutas/enzimologiaRESUMO
Perinatal stem cells such as human umbilical cord Wharton's jelly stem cells (HWJSCs) are excellent candidates for tissue engineering because of their proliferation and differentiation capabilities. However, their differentiation potential into epithelial cells at in vitro and in vivo levels has not yet been reported. In this work we have studied the capability of HWJSCs to differentiate in vitro and in vivo to oral mucosa and skin epithelial cells using a bioactive three-dimensional model that mimics the native epithelial-mesenchymal interaction. To achieve this, primary cell cultures of HWJSCs, oral mucosa, and skin fibroblasts were obtained in order to generate a three-dimensional heterotypical model of artificial oral mucosa and skin based on fibrin-agarose biomaterials. Our results showed that the cells were unable to fully differentiate to epithelial cells in vitro. Nevertheless, in vivo grafting of the bioactive three-dimensional models demonstrated that HWJSCs were able to stratify and to express typical markers of epithelial differentiation, such as cytokeratins 1, 4, 8, and 13, plakoglobin, filaggrin, and involucrin, showing specific surface patterns. Electron microscopy analysis confirmed the presence of epithelial cell-like layers and well-formed cell-cell junctions. These results suggest that HWJSCs have the potential to differentiate to oral mucosa and skin epithelial cells in vivo and could be an appropriate novel cell source for the development of human oral mucosa and skin in tissue engineering protocols.
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Epitélio/fisiologia , Células-Tronco Mesenquimais/citologia , Mucosa Bucal/citologia , Regeneração/fisiologia , Pele/citologia , Pele/crescimento & desenvolvimento , Geleia de Wharton/citologia , Animais , Diferenciação Celular , Células Epiteliais/citologia , Células Epiteliais/metabolismo , Proteínas Filagrinas , Citometria de Fluxo , Imunofluorescência , Humanos , Proteínas de Filamentos Intermediários/metabolismo , Queratinas/metabolismo , Antígenos Comuns de Leucócito/metabolismo , Camundongos , Camundongos Nus , Modelos Biológicos , Mucosa Bucal/fisiologia , Mucosa Bucal/ultraestrutura , Precursores de Proteínas/metabolismo , Pele/ultraestrutura , Antígenos Thy-1/metabolismo , gama Catenina/metabolismoRESUMO
Ampullary organs of Acipenser naccarii sturgeons were examined by optical and electronic microscopy (transmission electron microscopy and scanning electron microscopy) from hatching until 1 month later when the juvenile phase is completely established. It was observed that, when A. naccarii begins to feed actively, the ultrastructural characteristics of ampullary organs already correspond to those of adult animals. These organs may, therefore, be functional and, together with taste buds, facilitate food search after exhaustion of yolk sac food reserves. Mature ampullary organs of A. naccarii are formed by an ampulla that communicates with the exterior by means of a short channel. These ampullae correspond to the sensory portion of these receptors and are formed by two cell types: receptor cells and support cells. Receptor cells present a kinocilium on their free surface and establish ribbon synapses with axon nerve endings that arise from the underlying conjunctive tissue. Support cells enclose receptor cells, bear stereocilia and occasional cilia, and are of a secretory nature. The mucus associated with ampullary organs mainly comprises neutral mucopolysaccharides, whereas mucopolysaccharides are usually acid in other fish groups.
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Peixes/anatomia & histologia , Órgãos dos Sentidos/ultraestrutura , Células Receptoras Sensoriais/ultraestrutura , Animais , Cílios/ultraestrutura , Peixes/embriologia , Peixes/crescimento & desenvolvimento , Glicosaminoglicanos/análise , Microscopia Eletrônica de Varredura , Microscopia Eletrônica de Transmissão , Muco/química , Organogênese , Órgãos dos Sentidos/química , Órgãos dos Sentidos/embriologia , Órgãos dos Sentidos/crescimento & desenvolvimento , Células Receptoras Sensoriais/embriologia , Células Receptoras Sensoriais/crescimento & desenvolvimentoRESUMO
Variations of Na(+)/K(+)-ATPase activity and fatty-acid composition in the gills of the sturgeon Acipenser naccarii subjected to progressive acclimation to full seawater (35 ppt) were determined in relation to the hypo-osmoregulatory capacity of this species in the hyperosmotic medium. Blood samples were taken and gills arches were removed at intermediate salinity levels between 0 and 35 ppt and after 20 days at constant salinity (35 ppt). Plasma osmolality and Na(+)/K(+)-ATPase activity increased significantly with growing environmental salinity. Total saturated fatty acids (SFAs) decreased, while total polyunsaturated fatty acids (PUFAs) increased significantly with increasing salinity due mainly to changes in n-3 PUFAs (20:5n-3 and 22:6n-3). The n-3/n-6 ratio increased significantly during the acclimation process. The results show a direct relationship between salinity, increased gill Na(+)/K(+)-ATPase activity and ultrastructural changes of the gill chloride cells. Changes in the fatty-acid composition in gills of A. naccarii during progressive acclimation to full seawater suggest that variations of gill fatty acids may also have a role in osmoregulatory mechanisms.
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Aclimatação/fisiologia , Peixes/fisiologia , Brânquias/fisiologia , Água do Mar , ATPase Trocadora de Sódio-Potássio/fisiologia , Equilíbrio Hidroeletrolítico/fisiologia , Animais , Ácidos Graxos/metabolismo , Peixes/sangue , Água Doce , Brânquias/ultraestrutura , Microscopia Eletrônica de Transmissão , Concentração OsmolarRESUMO
Se presentó un paciente adolescente portador de espolones calcáneos bilateral, rara patología a esta edad en nuestro país. Se expuso el cuadro clínico y la terapéutica adecuada. Se revisó la literatura.
An adolescent patient presented with bilateral calcareal spurs, which is very rare pathology at this age in our country. The clinical chart was exponed and the therapy was carried out. The literatura was consulted.
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Objetivo: Conocer los resultados en el tratamiento de la colangitis infecciosa aguda (CIA) e identificar factores de riesgo relacionados con el desarrollo de complicaciones muerte. Material y métodos: Se revisaron los expedientes de pacientes con CIA atendidos en un período de 7 años. Se analizaron el cuadro clínico, enfermedades asociadas, métodos diagnósticos y tratamientos aplicados. Resultados: Se incluyeron 85 pacientes (61 por ciento mujeres y 39 por ciento hombres). Los datos clínicos más frecuentes fueron dolor abdominal, fiebre e ictericia. La causa de obstrucción fue coledocolitiasis en 75 por ciento, neoplasia en 12 por ciento y otras causas en 13 por ciento. Todos los pacientes recibieron antibióticos, además de alguna forma de drenaje de la vía biliar en 74 por ciento. Se observaron complicaciones en 32 por ciento de los casos y 14 por ciento murieron. La presencia de neoplasia como causante de obstrucción biliar se asoció a un riesgo significativo de muerte (RM 11.1). Conclusiones: La CIA es un padecimiento potencialmente fatal, principalmente en grupos de alto riesgo, como los pacientes con obstrucción biliar de origen maligno.
Assuntos
Humanos , Masculino , Feminino , Adolescente , Adulto , Pessoa de Meia-Idade , Colangite/diagnóstico , Colangite/fisiopatologia , Colangite/terapia , Técnicas de Laboratório Clínico , Indicadores de Morbimortalidade , Sinais e Sintomas , Síndrome de Resposta Inflamatória SistêmicaRESUMO
Objetivo. Informar de dos pacientes femeninas con quiste de colédoco. Sede. Servicio de Cirugía del Hospital General de Zona "Aragón" 29 IMSS. Descripción de los casos: Caso 1. Mujer de 29 años, con antecedente de colecistectomía 10 años antes de su ingreso, acude al hospital por dolor abdominal, náusea, vómito, fiebre e ictericia. Con leucocitosis de 16,700 y 93 por ciento de neutrófilos, con pruebas de funcionamiento hepático con patrón obstructivo tipo extrahepático. Se efectuó ultrasonido abdominal y colangiografía retrógrada endoscópica que confirmó el diagnóstico de quiste de colédoco tipo 1; interviniéndose quirúrgicamente con resección completa del quiste y reconstrucción tipo hepático yeyuno anastomosis. Fue dada de alta en buenas condicioens y actualmente en control en consulta externa. Caso II. Mujer de 20 años, con embarazo de 22 semanas, con antecedente de dolor abdominal desde la edad de 6 años, ingresó por exacerbación del cuadro doloroso, náusea, vómito y fiebre; se le efectuó ultrasonografía abdominal y colangiografía retrógrada endoscópica que demostraron quistes de colédoco tipo I. Presentó evolución clínica tórpida, por lo que fue intervenida quirúrgicamente, efectuándose colecistostomía; evolucionó satisfactoriamente, fue dada de alta en buenas condiciones. Cuatro semanas posteriores a la resolución del embarazo, se intervino quirúrgicamente, se hizo resección completa del quiste y hepatoyeyuno anastomosis. La evolución fue satisfactoria, actualmente bajo control y vigilancia en consulta externa