Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 10 de 10
Filtrar
1.
J Food Prot ; 82(7): 1176-1182, 2019 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-31233360

RESUMEN

HIGHLIGHTS: The aflatoxin M1 content in milk was not related to the enrichment factor. The enrichment factor in 45-day ripened semihard cheese was defined. The enrichment factor in cheese is affected by cheese yield.


Asunto(s)
Aflatoxina M1 , Queso , Microbiología de Alimentos , Leche , Aflatoxina M1/análisis , Animales , Bovinos , Queso/análisis , Queso/microbiología , Queso/normas , Leche/química , Leche/microbiología
2.
Bratisl Lek Listy ; 118(10): 591-597, 2017.
Artículo en Inglés | MEDLINE | ID: mdl-29198125

RESUMEN

BACKGROUND: Due to very sluggish turnover at the molecular and cellular level, the healing of chondral damages has been considered difficult. In the current study, the effects of the Kartogenin, a small heterocyclic molecule on chondrogenic differentiation of stem cells was compared to TGF-ß3. METHODS: Human Adipose-Derived Stem Cells were extracted during an elective surgery. Cell viability was estimated by MTT assay, differentiated cells evaluated by histological and immunohistochemical techniques. Expression of cartilage specific genes (SOX9, Aggrecan, type II and X collagens) assessed by real-time PCR. RESULTS: The real-time PCR assay has revealed the expression of gene marker of chondrogenesis, SOX9, Aggrecan and type II collagen, both in Kartogenin and TGFß3 groups compared to the control group, significantly (p < 0.05). A low expression level of collagen type X as a hypertrophic marker was seen in cartilage produced by using Kartogenin. Meanwhile, the level of type X collagen protein in Kartogenin group was significantly decreased (p > 0.05) compared to TGF-ß3 group. CONCLUSION: Kartogenin was suitable for successful chondrogenic differentiation of human adipose- derived stem cells and a suppressor of the consequent hypertrophy (Tab. 1, Fig. 5, Ref. 31).


Asunto(s)
Anilidas/farmacología , Condrogénesis/efectos de los fármacos , Ácidos Ftálicos/farmacología , Células Madre/efectos de los fármacos , Factor de Crecimiento Transformador beta3/farmacología , Tejido Adiposo/citología , Agrecanos/efectos de los fármacos , Agrecanos/genética , Cartílago , Diferenciación Celular/efectos de los fármacos , Células Cultivadas , Colágeno Tipo II/efectos de los fármacos , Colágeno Tipo II/genética , Colágeno Tipo X/efectos de los fármacos , Colágeno Tipo X/genética , Fibrina , Humanos , Reacción en Cadena en Tiempo Real de la Polimerasa , Factor de Transcripción SOX9/efectos de los fármacos , Factor de Transcripción SOX9/genética , Andamios del Tejido
3.
J Anim Physiol Anim Nutr (Berl) ; 101(5): 893-903, 2017 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-27080058

RESUMEN

The Chianina, one of the oldest and most important cattle breeds of Italy, is now reared all over the world. The Chianina has been known and appreciated since ancient times because, from a nutritional point of view, its meat has no proper rivals. To date, studies have been performed to evaluate the genetic profile of the breed, but knowledge about the chemical profile is generally lacking. Due to the increased interest from farmers regarding breeding of the Chianina, this study proposes a preliminary evaluation of main endogenous urinary corticosteroids (cortisol and cortisone) and most commonly used synthetic one (dexamethasone). Moreover, after recent findings regarding the presence of endogenous prednisolone in the urine of more popular breeds, particular attention was given to analysis of the presence of prednisolone and prednisone, as well. For this aim, the urine samples of 12 young cows and 30 young bulls was collected at the farms and analysed using a fit-for-purpose LC-MS/MS method. The preliminary results of this study show that prednisolone was found only in Chianina females (3 out of 12). Cortisol and cortisone were found at concentrations that showed a high inter-individual variability, and that were higher in female urine compared to that of males.


Asunto(s)
Bovinos/fisiología , Cortisona/orina , Hidrocortisona/orina , Prednisolona/orina , Animales , Bovinos/genética , Bovinos/orina , Cromatografía Liquida , Cortisona/química , Femenino , Hidrocortisona/química , Masculino , Estructura Molecular , Prednisolona/química , Espectrometría de Masas en Tándem
4.
Bratisl Lek Listy ; 117(4): 242-6, 2016.
Artículo en Inglés | MEDLINE | ID: mdl-27075390

RESUMEN

BACKGROUND: Breast cancer cells over-express the adenosine receptor A1 and in most of these cells, P53 gene is a wild type. Because of this finding and relationship between A1 receptor and cell apoptosis and proliferation, this study aimed to determine the effect of agonist and antagonist of A1 receptor on cell apoptosis and proliferation and recognize the relationship between this receptor and P53 expression. METHODS: We used a Real-Time PCR test for measuring expression of p53 gene also flow cytometry assay for apoptotic and survival cell rate after treatment of MCF-7 cells with A1 receptor agonist CPA (N6-Cyclopentyladenosine) and A1 receptor antagonist DPCPX (1,3-dipropyl-8-cyclopentylxanthine) in 24,48 and 72 hours. RESULTS: Our flow cytometry findings indicate that DPCPX significantly induces apoptosis in MCF-7. Also the expression of P53 becomes upregulated with time of DPCPX treatment. CPA treatment increased the survival cell rate and down-regulated this apoptosis-relevant gene P53 (p > 0.05). CONCLUSION: DPCPX can induce P53 expression which consequently promotes the cell apoptosis in MCF-7. Therefore, DPCPX could be used as an anti-cancer agent (Tab. 1, Fig. 3, Ref. 5).


Asunto(s)
Adenosina/análogos & derivados , Neoplasias de la Mama , Receptor de Adenosina A1/metabolismo , Xantinas/farmacología , Adenosina/farmacología , Agonistas del Receptor de Adenosina A1/farmacología , Antagonistas del Receptor de Adenosina A1/farmacología , Apoptosis/efectos de los fármacos , Proliferación Celular/efectos de los fármacos , Supervivencia Celular/efectos de los fármacos , Perfilación de la Expresión Génica , Genes p53/genética , Humanos , Células MCF-7
5.
Adv Biomed Res ; 3: 40, 2014.
Artículo en Inglés | MEDLINE | ID: mdl-24627848

RESUMEN

BACKGROUND: Carbon nanotubes (CNTs) have a large variety of applications in tissue engineering and biomedical devices. The biocompatibility and cytotoxicity of CNTs have been studied widely, however, up until now; there was uncertainty on how nanosized materials behave in the human body and stem cells. The current study describes the functionalized carbon nanotubes on adipose-derived stem cells (ADSCs) for viability and proliferation purposes in vitro. MATERIALS AND METHODS: After chemical modification of the CNTs, the ADSCs were cultured in Dulbecco's Modified Eagle's. Medium (DMEM) having doses of 0.1, 1, 10, 20, 50, and 100 µg/ml of CNTs. On the third and seventh days of the experiment, the cellular viability, proliferation, and stemness were determined, using the MTT, trypan Blue, and flow cytometry assays in variable CNTs dosage. RESULTS: In doses of 0.1 and 1 µg/ml, the expression of the surface markers were similar to the control groups on day three, but decreased in higher dosages on day seven. The viability of both groups was the same on day three, but in comparison to the control groups, was found to decrease in the higher dosages on day seven. CONCLUSION: The effect of CNTs on the viability and proliferation of ADSCs is a function of time and the doses used. Through further investigation by using these particles, we expect that we should be able to increase the viability and proliferation of ADSCs.

SELECCIÓN DE REFERENCIAS
DETALLE DE LA BÚSQUEDA