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1.
Comp Immunol Microbiol Infect Dis ; 72: 101519, 2020 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-32717528

RESUMO

Antimicrobial resistance (AMR) is one of the most important threats of the 21 st century. Wild birds have been described as reservoirs of AMR in different bacterial species, such as Salmonella spp. Privation of food, climate change and overpopulation have forced many wild species to modify their feeding habits, attending urban areas. In this context, the aim of this study was to study Salmonella presence, as well as related AMR in urban birds that inhabit the city and its surroundings. A total of 300 urban birds were sampled for Salmonella detection according to the ISO 6579-1:2017 (Annex D) recommendations, and serotyping was carried out according to the White-Kauffman-Le Minor scheme. Antimicrobial susceptibility was tested following 2013/652/EU Decision guides. Wild birds analysed were positive for Salmonella in 12.3 % of cases, with white storks fed in landfills as the most Salmonella prevalent species (p < 0.05). The most common serovars isolated were zoonotic (S. Enteritidis, S. Typhimurium and S. Typhimurium monophasic variant). From Salmonella isolated strains, 40.5 % were resistant to the most prevalent AMRs found in urban birds were ciprofloxacin (36.4 %), nalidixic acid (36.4 %) and colistin (27.3 %). The scientific community, public administration and population in general should work together to control antimicrobial administration and drug waste management in order to decrease the development and spread of AMR.


Assuntos
Doenças das Aves , Aves/microbiologia , Farmacorresistência Bacteriana Múltipla , Salmonelose Animal , Salmonella/classificação , Animais , Antibacterianos/farmacologia , Doenças das Aves/epidemiologia , Doenças das Aves/microbiologia , Farmacorresistência Bacteriana , Testes de Sensibilidade Microbiana/veterinária , Salmonella/efeitos dos fármacos , Salmonelose Animal/epidemiologia , Sorotipagem/veterinária , Espanha/epidemiologia
2.
Reproduction ; 151(1): 1-7, 2016 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-26475708

RESUMO

Offspring telomere length (TL) has been correlated with paternal TL, but the mechanism for this parent of origin-specific inheritance remains unclear. The objective of this study has been to determine the role of spermatozoa TL in embryonic telomere lengthening by using two mouse models showing dimorphism in their spermatozoa TL: Mus musculus vs Mus spretus and old vs young Mus musculus. Mus spretus spermatozoa displayed a shorter TL than Mus musculus. Hybrid offspring exhibited lower TL compared with Mus musculus starting at the two-cell stage, before the onset of telomerase expression. To analyze the role of spermatozoa telomeres in early telomere lengthening, we compared the TL in oocytes, zygotes, two-cell embryos and blastocysts produced by parthenogenesis or by fertilization with Mus musculus or Mus spretus spermatozoa. TL was significantly higher in spermatozoa compared with oocytes, and it increased significantly from the oocyte to the zygote stage in those embryos fertilized with Mus musculus spermatozoa, but not in those fertilized with Mus spretus spermatozoa or produced by parthenogenesis. A further increase was noted from the zygote to the two-cell stage in fertilized Mus musculus embryos, whereas hybrid embryos maintained the oocyte TL. Spermatozoa TL shortened with age in Mus musculus and the offspring from young males showed a significantly higher TL compared with that fathered by old males. These significant differences were already noticeable at the two-cell stage. These results suggest that spermatozoa telomeres act as a guide for telomerase-independent telomere lengthening resulting in differences in TL that persist after birth.


Assuntos
Embrião de Mamíferos/ultraestrutura , Espermatozoides/ultraestrutura , Telômero/ultraestrutura , Envelhecimento , Animais , Sequência de Bases , Blastocisto/ultraestrutura , Feminino , Fertilização in vitro , Masculino , Camundongos , Dados de Sequência Molecular , Oócitos/ultraestrutura , Partenogênese , Telomerase/metabolismo , Telômero/química , Homeostase do Telômero , Zigoto/ultraestrutura
3.
Allergol Immunopathol (Madr) ; 43(6): 593-600, 2015.
Artigo em Inglês | MEDLINE | ID: mdl-25982580

RESUMO

BACKGROUND: Diamine oxidase (DAO) is a polyamine-degrading enzyme also implicated in histamine metabolism. Chronic urticaria (CU) has a wide spectrum of clinical presentations and causes. Anisakis sensitisation associated chronic urticaria (CU+) has been characterised as a phenotype with different clinical and immunological characteristics and possibly associated with previous acute parasitism. We aimed to analyse serum DAO levels in different CU phenotypes. We further analysed the possible association of DAO with fish eating habits. METHODS: We studied 35 CU+ patients and 39 non-sensitised CU patients (CU-) as well as 19 controls. We analysed fish-eating frequency as well as fish intake associated exacerbation of CU (FIAE) or gastro-intestinal complaints (GI). DAO levels were further analysed with respect to lymphoproliferative responses, cytokine and specific IgE production. RESULTS: DAO levels were not different between CU and controls, but were significantly higher in CU+ than in CU-. CU+ patients with FIAE had lower DAO levels, but no differences were detected in patients with GI. DAO levels correlated positively with oily and canned fish consumption in CU-. In CU+, DAO levels correlated positively with specific Anisakis IgE, percentages of proliferation in Anisakis stimulated peripheral blood lymphocytes, serum IL-2 and IL-6, but correlated negatively with mitogen stimulated TGF-ß in supernatants. CONCLUSIONS: DAO levels in CU depend on fish-eating habits and in CU+ on the amount of specific IgE production. In the CU+ phenotype, lower levels of DAO predispose to urticaria exacerbation after fish intake, probably due to a relative insufficient enteric availability of this enzyme.


Assuntos
Anisaquíase/diagnóstico , Anisakis/imunologia , Ingestão de Alimentos/imunologia , Gastroenteropatias/diagnóstico , Urticária/diagnóstico , Adulto , Alérgenos/imunologia , Animais , Anisaquíase/classificação , Antígenos de Helmintos/imunologia , Proliferação de Células , Doença Crônica , Citocinas/metabolismo , Dieta , Feminino , Produtos Pesqueiros , Gastroenteropatias/classificação , Humanos , Imunoglobulina E/sangue , Ativação Linfocitária , Masculino , Pessoa de Meia-Idade , Urticária/classificação
4.
J Helminthol ; 89(6): 707-13, 2015 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-24991841

RESUMO

Toxoplasma gondii is a food-borne and orofecal microorganism which produces chronic infection, and attempts have been made to prove its negative association with atopy in the context of the hygiene hypothesis. Anisakis simplex is a fish parasite associated with chronic urticaria (CU) in endemic regions. We analysed the relationship between both infectious agents in CU. We included 42 patients with chronic urticaria (18 patients with CU associated with A. simplex sensitization and 24 not sensitized CU patients). Patients were assessed for atopy by a skin prick test (SPT) against common aeroallergens and for respiratory symptoms. Anisakis simplex sensitization was assessed by SPT and specific IgE by CAP fluoro-enzyme immunoassay (CAP-FEIA). Anti-T. gondii IgG levels were measured by enzyme-linked immunosorbent assay (ELISA). CU patients were analysed with respect to T. gondii seropositivity, A. simplex sensitization, atopy and immigrant status. The seroprevalence of T. gondii was 40.5% in CU patients and 42.1% in the control group. Immigrants were more frequently infected by T. gondii (41.2% versus 12%; P =0.036). Anti-T. gondii IgG antibodies were associated with past A. simplex parasitism (odds ratio 6.73; P =0.03) and independently with atopic sensitization (odds ratio 5.85; P =0.04). In CU patients, T. gondii has no protective effect on atopic sensitization or A. simplex sensitization.


Assuntos
Anisaquíase/imunologia , Anisakis/imunologia , Toxoplasma/imunologia , Urticária/imunologia , Adulto , Animais , Anisaquíase/parasitologia , Anticorpos Anti-Helmínticos/imunologia , Anticorpos Antiprotozoários/imunologia , Doença Crônica , Ensaio de Imunoadsorção Enzimática , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Estudos Soroepidemiológicos , Testes Cutâneos , Urticária/parasitologia , Adulto Jovem
5.
Scand J Immunol ; 79(2): 120-6, 2014 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-24219647

RESUMO

IgG4 and IgE are immunoglobulin isotypes which are mediated by the same Th2-mediated mechanism. The postulated pathogenic and protective function of IgE or IgG4, respectively, in allergic disease is opposite in parasitic infection. The possible role of IgG4 against recombinant major allergens on the appearance of different forms of Anisakis simplex-associated allergic disease was studied. Gastro-allergic anisakiasis (GAA) and Anisakis-sensitization-associated chronic urticaria (CU+) were compared for specific IgE, IgG4 and the respective recognition of Ani s 1 and Ani s 7. Gastro-allergic anisakiasis showed higher IgE and IgG4 levels against crude extract and both recombinant allergens. Whereas IgE recognition of Ani s 7 did not differ and supports both clinical entities to be associated with previous acute parasitism, the IgE recognition rates of Ani s 1 and IgG4 recognition of both Ani s 1 and Ani s 7 were higher in GAA. IgG4 levels were associated with IgE, but also with age, time to last parasitic episode and frequency of fish intake. Logistic regression analysis showed that the presence of specific IgG4 against Ani s 7 was an independent marker associated with GAA. In the diagnosis of Anisakis-associated allergic disease phenotypes (GAA versus CU+), measurement of specific IgG4 against recombinant allergens could be useful. Further, evaluation of specific IgE and IgG4 facilitates more insight into the protective versus pathogenic potential of IgE and IgG4.


Assuntos
Anisakis/imunologia , Hipersensibilidade/etiologia , Imunoglobulina G/fisiologia , Adulto , Idoso , Animais , Feminino , Humanos , Hipersensibilidade/diagnóstico , Imunoglobulina E/sangue , Imunoglobulina G/sangue , Modelos Logísticos , Masculino , Pessoa de Meia-Idade
6.
Reprod Fertil Dev ; 26(3): 367-74, 2014 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-23458081

RESUMO

This study examined the effect of a single administration of human chorionic gonadotrophin (hCG) on Day 1 to 4 after oestrus on corpus luteum (CL) development and circulating progesterone (P4). Oestrus-synchronized heifers (n=43) were administered a single intramuscular injection of saline on Day 1 (control) or 3000IU hCG on Day 1, 2, 3 or 4 after oestrus. Administration of hCG on Day 1 had no effect on CL area, on Day 2 increased CL area from Day 6 to 12 (P<0.05), on Day 3 increased CL area from Day 9 to 11, while on Day 4 increased CL size on Days 9 and 10 (P<0.05). Administration of hCG on Day 4 induced the formation of an accessory CL in 89% of heifers, resulting in a significant increase in total luteal tissue area on the ovaries compared with all other groups. Consistent with the effects on the CL, hCG on Day 1 did not affect P4 concentrations, on Day 2 significantly increased P4 compared with the control from Day 6 to 11 (P<0.05), on Day 3 resulted in a non-significant increase in P4 while hCG on Day 4 increased P4 from Day 8 to 13 compared with the control (P<0.05). In conclusion, administration of hCG as early as Day 2 after oestrus results in increased P4 in circulation from Day 6, which should have beneficial downstream effects in terms of uterine receptivity and conceptus elongation.


Assuntos
Gonadotropina Coriônica/farmacologia , Corpo Lúteo/crescimento & desenvolvimento , Luteinização/fisiologia , Progesterona/sangue , Animais , Cruzamento/métodos , Bovinos , Corpo Lúteo/diagnóstico por imagem , Corpo Lúteo/efeitos dos fármacos , Sincronização do Estro , Feminino , Humanos , Luteinização/efeitos dos fármacos , Modelos Estatísticos , Ultrassonografia
7.
Rev. psiquiatr. infanto-juv ; 31(4): 16-28, 2014. tab
Artigo em Espanhol | IBECS | ID: ibc-185787

RESUMO

La obesidad representa un importante problema de salud pública en el mundo de características epidémicas. Existe una relación entre el sobrepeso-obesidad en la población infanto-juvenil y la presencia de psicopatología en la que interviene la personalidad. Este estudio descriptivo intenta caracterizar y encontrar relaciones entre dimensiones y perfiles psicopatológicos de personalidad y sobrepeso-obesidad en niños de 9-14 años atendidos en Pediatría. Se utiliza el Inventario Infanto Juvenil de Temperamento y Carácter de Cloninger (JTCI), basado en el inventario original de Cloninger, para estudiar la personalidad, junto con la recogida de información sociodemográfica, clínica, antropométrica y académica. Se emplean técnicas estadísticas descriptivas y análisis multivariante de regresión logística. Las dimensiones dependencia de la recompensa, fantasía y evitación del daño presentan los valores más extremos, no mostrando perfiles psicopatológicos el 93% de la muestra. El perfil psicopatológico relacionado con los trastornos por déficit de atención con/sin hiperactividad y bipolar (TDAH/BP) es el más frecuente. El perfil TDAH/BP presenta un Índice de Masa Corporal (IMC) significativamente superior al resto. Ser hombre y repetir curso incrementan el riesgo de padecer sobrepeso-obesidad, mientras el aumento de edad y la dimensión persistencia se comportan como factores protectores en el análisis multivariante. Es necesario comprender mejor la relación entre personalidad y sobrepeso-obesidad en la infancia y adolescencia para identificar terapias más efectivas


Obesity is a major public health problem in the world of epidemic proportions. There is a relationship between overweight-obesity in the pediatric population and the presence of psychopathology where personality is involved. This descriptive study attempts to characterize and find relationships between dimensions and psychopathological personality profiles and overweight-obesity in children 9-14 years treated in Pediatrics. Junior Temperament and Character Inventory of Cloninger (JTCI), instrument based on the original inventory of Cloninger, is used to study personality along with sociodemographic, clinical, anthropometric and academic information collection. Descriptive statistics and multivariate logistic regression analysis techniques are used. The dimensions reward dependence, fantasy and harm avoidance have the most extreme values, showing no psychopathological profiles 93% of the sample. Psychopathological profile associated with Attention deficit hyperactivity disorder and Bipolar disorder (ADHD/BP) is the most common. ADHD/BP profile has a Body Mass Index (BMI) significantly higher than the rest. Being male and repeat course increases the risk of overweight-obesity, while increasing age and persistence dimension behave as protective factors in the multivariate analysis. A better understanding of the relationship between personality and overweight-obesity in children and adolescents to identify more effective therapies is needed


Assuntos
Humanos , Masculino , Feminino , Criança , Adolescente , Sobrepeso/psicologia , Obesidade/psicologia , Personalidade , Psicopatologia , Obesidade Infantil/psicologia , Fatores Socioeconômicos
8.
Reprod Fertil Dev ; 25(1): 38-47, 2012.
Artigo em Inglês | MEDLINE | ID: mdl-23244827

RESUMO

Preimplantation developmental plasticity has evolved in order to offer the best chances of survival under changing environments. Conversely, environmental conditions experienced in early life can dramatically influence neonatal and adult biology, which may result in detrimental long-term effects. Several studies have shown that small size at birth, which is associated with a greater risk of metabolic syndrome, is largely determined before the formation of the blastocysts because 70%-80% of variation in bodyweight at birth has neither a genetic nor environmental component. In addition, it has been reported that adult bodyweight is programmed by energy-dependent process during the pronuclear stage in the mouse. Although the early embryo has a high developmental plasticity and adapts and survives to adverse environmental conditions, this adaptation may have adverse consequences and there is strong evidence that in vitro culture can be a risk factor for abnormal fetal outcomes in animals systems, with growing data suggesting that a similar link may be apparent for humans. In this context, male and female preimplantation embryos display sex-specific transcriptional and epigenetic regulation, which, in the case of bovine blastocysts, expands to one-third of the transcripts detected through microarray analysis. This sex-specific bias may convert the otherwise buffered stochastic variability in developmental networks in a sex-determined response to the environmental hazard. It has been widely reported that environment can affect preimplantation development in a sex-specific manner, resulting in either a short-term sex ratio adjustment or in long-term sex-specific effects on adult health. The present article reviews current knowledge about the natural phenotypic variation caused by epigenetic mechanisms and the mechanisms modulating sex-specific changes in phenotype during early embryo development resulting in sex ratio adjustments or detrimental sex-specific consequences for adult health. Understanding the natural embryo sexual dimorphism for programming trajectories will help understand the early mechanisms of response to environmental insults.


Assuntos
Desenvolvimento Embrionário , Epigênese Genética , Crescimento , Animais , Peso ao Nascer , Exposição Ambiental/efeitos adversos , Feminino , Desenvolvimento Fetal , Retardo do Crescimento Fetal/etiologia , Retardo do Crescimento Fetal/patologia , Humanos , Masculino , Caracteres Sexuais , Aumento de Peso
9.
Arch Dermatol Res ; 304(4): 283-8, 2012 May.
Artigo em Inglês | MEDLINE | ID: mdl-22249742

RESUMO

Diagnosis in gastro-allergic anisakiasis (GAA) is straightforward, when clinical history is combined with further allergological evaluation of specific IgE by means of skin prick test and serum specific IgE. In Anisakis simplex sensitisation associated chronic urticaria (CU+), clinical evaluation of possible previous parasitism is difficult, and positive serum specific IgE could be due to cross-reactivity or other unknown factors. In this study, we evaluated the association between IgE seropositivity to the recombinant allergens Ani s 1 and Ani s 7 and several A. simplex-associated allergic disorders. Twenty-eight patients with GAA and 40 patients with CU+ were studied and their IgE responses were compared with a control group composed of patients with chronic urticaria not sensitized to A. simplex (CU-) according to the skin prick test, as well as a group of 15 healthy subjects not referring urticaria or currently A. simplex associated symptoms. 82.1% of GAA patients and 42.5% of CU+ patients were positive for Ani s 1 (P < 0.001), while the Ani s 7 allergen was recognized by 92.9 and 92.5% of sera from patients with GAA and CU+, respectively. The combined positivity obtained for both allergens reached 100% in GAA, and 95% in CU+. IgE determinations to Ani s 1 and Ani s 7 allergens are useful to diagnose the Anisakis infections and to differentiate among several A. simplex-associated allergic disorders. The IgE responses to Ani s 1 are mainly associated with GAA, while this molecule cannot be considered a major allergen in CU+ patients.


Assuntos
Alérgenos/imunologia , Anisaquíase/diagnóstico , Anisaquíase/imunologia , Anisakis/imunologia , Antígenos de Helmintos/imunologia , Proteínas de Ligação ao Cálcio/imunologia , Proteínas de Helminto/imunologia , Animais , Feminino , Humanos , Hipersensibilidade , Imunoglobulina E/sangue , Imunoglobulina E/imunologia , Masculino , Pessoa de Meia-Idade , Proteínas Recombinantes/imunologia , Urticária/imunologia
10.
Reprod Domest Anim ; 46 Suppl 3: 2-10, 2011 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-21854456

RESUMO

In the last years, enormous progress has been made in the analysis of gene transcription at the blastocyst stage. The study of gene expression at this early stage of development is challenging because of the very small amount of starting material, which limits the use of traditional mRNA analysis approaches such as Northern blot. Another problem is the difficulty for data normalization, particularly the identification of the best housekeeping gene with the lowest fluctuation under different developmental conditions. Moreover, the transcriptional analysis of embryo biopsies or individual embryos needs to take into consideration that the blastocyst is a transitional stage of development, which is composed of three different types of cells (trophoblast, epiblast and primitive ectoderm) with different patterns of gene expression, and that there are large differences between male and female blastocysts. In this review, we analyse the different specific and sensitive tools available to compare mRNA expression levels of specific genes at the blastocyst stage, and how the protocol and the analytical method used can influence the results dramatically. Finally, we describe future research challenges to identify candidate genes related to developmental competence of bovine blastocysts, not only in terms of pregnancy rates but also in relation to adverse long-term consequences in the adult animal.


Assuntos
Blastocisto/fisiologia , Regulação da Expressão Gênica no Desenvolvimento/fisiologia , Transcrição Gênica , Animais , Bovinos , Feminino , Masculino , Gravidez , RNA Mensageiro/genética , RNA Mensageiro/metabolismo
11.
Parasite Immunol ; 33(6): 357-62, 2011 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-21554330

RESUMO

The knowledge on immune mechanisms of chronic urticaria (CU) at the cytokine level is widely scarce. We compared pro- and anti-inflammatory as well as Th1- and Th2-associated serum cytokine levels in two phenotypes of CU: associated with (CU+) and without (CU⁻) sensitization against Anisakis simplex, a ubiquitous fish parasite, that has been associated with acute urticaria in gastro-allergic anisakiasis (GAA) and with CU+. Thirteen CU+ and 19 CU⁻ patients were compared with 13 GAA patients and 15 control subjects for cytokines, measured by cytometric bead array. Urticaria activity score was positively correlated with IL-6 in CU⁻. Serum levels of IL-10 were lower in CU+ and CU⁻ with respect to the control group. Median IFN-γ was lower in all urticaria groups. Patients with previous parasitism by A. simplex displayed higher TGF-ß levels than subjects without previous parasitism. The main finding was lower levels of IL-17 in CU+ with respect to GAA or controls, with a further tendency to even lower levels in CU⁻. Different urticaria phenotypes are associated with distinct serum cytokine levels.


Assuntos
Anisaquíase/complicações , Anisaquíase/imunologia , Anisakis/imunologia , Citocinas/sangue , Urticária/imunologia , Adulto , Animais , Doença Crônica , Feminino , Citometria de Fluxo , Humanos , Masculino , Pessoa de Meia-Idade , Soro/química
12.
Am J Med Genet A ; 155A(1): 197-202, 2011 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-21204232

RESUMO

Thanatophoric dysplasia (TD) is a lethal form of short-limb skeletal dysplasia that is associated with macrocephaly, and variably cloverleaf skull. Two types of TD are clinically recognized, TD1 and TD2, mainly distinguished by their radiographic characteristics. The differences between the two are principally observed in the femur, which appears curved in TD1, while it remains straight but with a proximal medial spike in TD2, and are a less severe overall affectation in TD2. Both types of TD are caused by mutations in different functional domains of the FGFR3 gene. However, whereas several mutations in the different domains of FGFR3 cause TD1, the K650E mutation involving the change of a lysine to glutamic acid ("Lys650Glu") has been found in all TD2 cases to date. Here we describe a newborn infant with TD2 associated with brain defects that have either been infrequently observed (encephalocele) or not hitherto described (holoprosencephaly). Based on recent studies, we consider encephaloceles described in TD to be pseudoencephaloceles, since they are secondary to the intracranial pressure generated by severe hydrocephaly and to severe cranial structural anomalies. Finally, to analyze the mechanisms of holoprosencephaly observed in the case described here, we include a concise review on the current understanding of how FGFs and their receptors are expressed in the rostral signaling center (particularly Fgf8). In addition, we evaluated recent observations that FGF ligands and receptors (including FGFR3) act in concert to organize the whole telencephalon activity, rather than independently patterning different areas.


Assuntos
Encefalocele/genética , Holoprosencefalia/genética , Holoprosencefalia/fisiopatologia , Fenótipo , Receptor Tipo 3 de Fator de Crescimento de Fibroblastos/genética , Encefalocele/patologia , Evolução Fatal , Feminino , Holoprosencefalia/patologia , Humanos , Recém-Nascido , Mutação de Sentido Incorreto/genética , Crânio/anormalidades , Crânio/patologia , Displasia Tanatofórica/genética , Displasia Tanatofórica/patologia
16.
Theriogenology ; 71(6): 1005-10, 2009 Apr 01.
Artigo em Inglês | MEDLINE | ID: mdl-19157529

RESUMO

Neurotrophins and basic fibroblast growth factor are ligands of tyrosine kinase receptors, though they bind to different tyrosine kinase receptor classes. Neurotrophins bind to receptor tyrosine kinase class VII, Trk receptor family, while basic fibroblast growth factor binds to receptor tyrosine kinase class IV, FGF receptor family. The mammalian uterine tract immunolocalizes neurotrophins and bFGF; therefore their cognate receptors might exert a role during embryonic development. Using RT-PCR, we found mRNA for p75(NTR) TrkA, TrkC and FGFr2 throughout the early bovine embryonic development in vitro. Immunofluorescent staining, assessed by confocal microscopy, showed the expression of TrkA and TrkC proteins in oocytes and all embryonic stages analyzed. We have provided a novel description of TrkA and TrkC proteins, and TrkA, TrkC, p75(NTR) and FGFr2 mRNA expression throughout mammalian embryonic development. This work may help to design future research with neurotrophins in bovine embryo culture and embryonic stem cells.


Assuntos
Bovinos/embriologia , Técnicas de Cultura Embrionária/veterinária , Receptor Tipo 2 de Fator de Crescimento de Fibroblastos/análise , Receptor trkA/análise , Receptor trkC/análise , Animais , Blastocisto/química , Western Blotting , Desenvolvimento Embrionário , Imunofluorescência , Imuno-Histoquímica , Microscopia Confocal , Mórula/química , Oócitos/química , RNA Mensageiro/análise , Receptor Tipo 2 de Fator de Crescimento de Fibroblastos/genética , Receptor trkA/genética , Receptor trkC/genética , Reação em Cadeia da Polimerase Via Transcriptase Reversa , Zigoto/química
17.
Rev. esp. enferm. dig ; 100(10): 648-651, oct. 2008. ilus, tab
Artigo em Es | IBECS | ID: ibc-71055

RESUMO

Introducción: la pancreatitis autoinmune es un tipo de pancreatitiscrónica caracterizado por un infiltrado linfoplasmocitarioy una elevación de IgG e IgG4, que se ha descrito asociada a diversasmanifestaciones extrapancreáticas y enfermedades autoinmunes,lo cual apoya la teoría de un mecanismo autoinmune fisiopatólogicode base.Caso clínico: presentamos el caso de un varón que debutó simultáneamentecon una pancreatitis autoinmune asociada a fibrosisretroperitoneal y lesión de la vía biliar extrapancreática, conrespuesta total tras tratamiento con corticoides durante 4 meses yausencia de recurrencia tras 24 meses de seguimiento.Discusión: la pancreatitis autoinmune es un tipo de pancreatitiscrónica que probablemente forme parte de un proceso sistémicoautoinmune, cuyas manifestaciones extrapancreáticas másfrecuentes son la fibrosis retroperitoneal y las lesiones de la vía biliarextrapancreática. Su correcto diagnóstico e inicio precoz deltratamiento puede favorecer la resolución completa de las lesiones,principalmente en los casos de bajo grado de actividad, conmenor probabilidad de recurrencia


Introduction: autoimmune pancreatitis is a kind of chronicpancreatitis characterized by the presence of lymphoplasmacyticinfiltration and severely elevated serum IgG and IgG4, which hasbeen associated to many extrapancreatic lesions and other autoimmunedisorders, leading to the theory of an autoimmunemechanism involved in the pathogenesis of this disease.Case report: we report the case of a man who simultaneouslypresented with autoimmune pancreatitis associated withretroperitonal fibrosis, and a lesion of the extrapancreatic bileduct, with total response to corticosteroid treatment for 4 mothsand absence of recurrence after 24 months of follow-up.Discussion: autoimmune pancreatitis is a kind of chronicpancreatitis that is probably a part of a systemic autoinmune disease,with retroperitoneal fibrosis and extrapancreatic bile duct lesionbeing the most commonly associated extrapancreatic lesions.A correct diagnosis and early treatment of this disease may aid inthe total resolution of lesions, especially in cases with a low activity grade (AU)


Assuntos
Humanos , Masculino , Pessoa de Meia-Idade , Doenças Autoimunes/complicações , Pancreatite/complicações , Fibrose Retroperitoneal/complicações , Anti-Inflamatórios/uso terapêutico , Doenças Autoimunes/diagnóstico , Seguimentos , Glucocorticoides/uso terapêutico , Metilprednisolona/uso terapêutico , Pancreatite/diagnóstico , Radiografia Abdominal , Fibrose Retroperitoneal/diagnóstico , Fatores de Tempo , Tomografia Computadorizada por Raios X , Resultado do Tratamento
18.
Theriogenology ; 69(9): 1159-64, 2008 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-18420262

RESUMO

Bovine embryonic stem cells are of potentially big value in transgenic research and studies of lineage commitment and development. Nevertheless, key aspects of the establishment of bovine embryonic stem cells such as the identification of specific pluripotency markers need to be clarified to achieve successful results. Bovine blastocysts were produced in vitro and cultured for 8 days up to the expanded or hatched stage. The trophectoderm, the inner cell mass and its embryonic stem cell-derived lines, all showed a common positive immunocytochemical staining for stage-specific embryonic antigen-4, tumour-rejection antigen gp96 and NANOG proteins. The antigenic profile obtained partially agrees with previous data from bovine and other species. Until a validated pluripotent bovine stem cell marker can be identified, it might be advisable to combine the use of epiblast and trophoblast-specific markers to rule out the presence of early committed trophectoderm cells in bovine embryonic stem cell cultures.


Assuntos
Biomarcadores/metabolismo , Blastocisto/citologia , Bovinos/embriologia , Células-Tronco Pluripotentes/fisiologia , Animais , Blastocisto/metabolismo , Técnicas de Cultura de Células , Linhagem Celular , Fibroblastos/citologia , Fibroblastos/fisiologia , Regulação da Expressão Gênica
20.
Rev Esp Enferm Dig ; 100(10): 648-51, 2008 Oct.
Artigo em Espanhol | MEDLINE | ID: mdl-19119793

RESUMO

INTRODUCTION: Autoimmune pancreatitis is a kind of chronic pancreatitis characterized by the presence of lymphoplasmacytic infiltration and severely elevated serum IgG and IgG4, which has been associated to many extrapancreatic lesions and other autoimmune disorders, leading to the theory of an autoimmune mechanism involved in the pathogenesis of this disease. CASE REPORT: We report the case of a man who simultaneously presented with autoimmune pancreatitis associated with retroperitonal fibrosis, and a lesion of the extrapancreatic bile duct, with total response to corticosteroid treatment for 4 months and absence of recurrence after 24 months of follow-up. DISCUSSION: Autoimmune pancreatitis is a kind of chronic pancreatitis that is probably a part of a systemic autoimmune disease, with retroperitoneal fibrosis and extrapancreatic bile duct lesion being the most commonly associated extrapancreatic lesions. A correct diagnosis and early treatment of this disease may aid in the total resolution of lesions, especially in cases with a low activity grade.


Assuntos
Doenças Autoimunes/complicações , Pancreatite/complicações , Fibrose Retroperitoneal/complicações , Anti-Inflamatórios/administração & dosagem , Anti-Inflamatórios/uso terapêutico , Doenças Autoimunes/diagnóstico , Doenças Autoimunes/diagnóstico por imagem , Doenças Autoimunes/tratamento farmacológico , Seguimentos , Glucocorticoides/administração & dosagem , Glucocorticoides/uso terapêutico , Humanos , Masculino , Metilprednisolona/administração & dosagem , Metilprednisolona/uso terapêutico , Pessoa de Meia-Idade , Pancreatite/diagnóstico , Pancreatite/diagnóstico por imagem , Pancreatite/tratamento farmacológico , Radiografia Abdominal , Fibrose Retroperitoneal/diagnóstico , Fibrose Retroperitoneal/diagnóstico por imagem , Fatores de Tempo , Tomografia Computadorizada por Raios X , Resultado do Tratamento
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