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1.
Cell Biol Toxicol ; 23(4): 267-78, 2007 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-17180447

RESUMEN

Cadmium represents a major environmental pollutant that may induce severe damage, especially in the kidney where cadmium accumulates. While cadmium is known to severely impair renal tubular functions, glomerular structures are also potential targets. Owing to their contractile properties, glomerular mesangial cells play a major role in the control of glomerular hemodynamics and influence the ultrafiltration coefficient. Cell cultures provide alternative and fruitful models for study of in vitro toxicology. However, the use of primary human mesangial cell cultures is hampered by their limited survival span and their rapid dedifferentiation during passages. This study presents a human stable immortalized mesangial cell line, designated IP15. Cell characteristics were investigated by the detection of known mesangial markers, as well as their ability to contract in response to angiotensin II. IP15 cells were used to investigate cadmium uptake and morphological changes such as cell contraction and cytoskeleton protein expression. The IC(50) cytotoxicity index was obtained with 3.55 micromol/L using neutral red assay for 24 h. After cadmium exposure (1 micromol/L, determined as nonlethal concentration), 0.38 microg Cd/mg protein was internalized by the cells as evaluated by inductively coupled plasma optical emission spectrometry (ICP/OES). Cadmium induced a significant cell surface reduction that correlated with smooth-muscle alpha-actin disorganization. Thus, the IP15 cell line is a suitable model for study of in vitro cadmium cytotoxicity in mesangial cells and allows sufficient material to be obtained for future studies of the intracellular effects of cadmium exposure.


Asunto(s)
Alternativas a las Pruebas en Animales , Cloruro de Cadmio/toxicidad , Contaminantes Ambientales/toxicidad , Mesangio Glomerular/efectos de los fármacos , Modelos Biológicos , Biomarcadores/metabolismo , Cloruro de Cadmio/metabolismo , Línea Celular Transformada , Membrana Celular/efectos de los fármacos , Supervivencia Celular/efectos de los fármacos , Proteínas del Citoesqueleto/metabolismo , Relación Dosis-Respuesta a Droga , Contaminantes Ambientales/metabolismo , Mesangio Glomerular/metabolismo , Mesangio Glomerular/patología , Humanos , Procesamiento de Imagen Asistido por Computador , Concentración 50 Inhibidora
2.
Toxicol In Vitro ; 15(4-5): 525-9, 2001.
Artículo en Inglés | MEDLINE | ID: mdl-11566587

RESUMEN

The main objective of the present work was to assess the potentiality of in vitro models to improve our understanding of cadmium-induced toxicity, especially on epithelial renal cells. Indeed cadmium, a potent toxic metal, poses a serious environmental threat and the mechanisms of its renal toxicity need to be clarified. Cytotoxicity studies presented here were performed in a tubular proximal original established porcine kidney cell line (LLC-PK(1)). We have compared cytotoxicity induced by different chemical cadmium forms in LLC-PK(1) cells as a function of media cell culture pH and protein content. Cadmium stock solutions were prepared either by dissolving cadmium chloride or cadmium sulphate with increasing protein concentrations in the media cell culture. Its pH was monitored during experiments. Cytotoxicity was measured by neutral red uptake after 24 h of exposure. Dose-dependent cytotoxicity curves, calculated with REGTOX, were systematically correlated with pH and protein content. Experiments in vitro revealed that cadmium was dose-dependently toxic for LLC-PK(1) for concentrations ranging from 10(-4) to 10(-6) M. We have noticed a lack of influence of the media cell culture pH on the cadmium cytotoxicity. REGTOX determines closely the EC(50) values but EC(50)CdCl(2)>EC(50)CdSO(4) and cadmium have been assayed with an inductively coupled atomic emission spectrometer (ICP/AES) directly in the media cell culture and the cellular pellet.


Asunto(s)
Cadmio/toxicidad , Túbulos Renales Proximales/efectos de los fármacos , Pruebas de Toxicidad/métodos , Alternativas a las Pruebas en Animales , Animales , Cadmio/clasificación , Cadmio/metabolismo , Supervivencia Celular/efectos de los fármacos , Células Cultivadas , Medios de Cultivo/química , Relación Dosis-Respuesta a Droga , Concentración de Iones de Hidrógeno , Túbulos Renales Proximales/metabolismo , Rojo Neutro/metabolismo , Proteínas/análisis , Espectrofotometría Atómica , Porcinos
3.
Rev Laryngol Otol Rhinol (Bord) ; 120(2): 133-5, 1999.
Artículo en Francés | MEDLINE | ID: mdl-10444989

RESUMEN

The authors present the story of Physiomer. It began in 1988 in Goemar's 'Laboratory of the Sea', with an original idea of making a product manufactured from sea water and transforming it into an isotonic solution, while preserving all the elements of natural sea water, specially the trace elements and the alkaline PH. Scientific analysis has shown that the chemical composition of the product is true to the original, and that it has a positive action on cellular growth in respiratory tract mucosa in experimental culture, and it is very well tolerated. Clinical tests using nasal washings have confirmed beneficial action on the nasal and sinus mucosa in medical disease and after surgery. Tests have been carried out on 410 cases, 344 of which were treated with Physiomer, and on 199 cases after surgery on the nose or sinuses. Physiomer nasal washings have proved their value. It now remains for all the potential qualities of sea water to be demonstrated, using other preparations or other combinations.


Asunto(s)
Mucosa Nasal , Agua de Mar , Irrigación Terapéutica , Adulto , Preescolar , Ensayos Clínicos como Asunto , Humanos , Lactante , Soluciones Isotónicas , Estudios Multicéntricos como Asunto , Nariz/cirugía , Senos Paranasales/cirugía , Cuidados Posoperatorios , Estudios Retrospectivos
4.
Biomaterials ; 20(6): 523-7, 1999 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-10213355

RESUMEN

Ureteral endoprostheses are urinary catheters made of polymeric biomaterials made radio-opaque through the addition of X-ray absorbing additives such as barium, bismuth, tantale or tungsten. The aim of this work was to study the in vitro toxicity of solutions of these radio-opacifiers using two cell culture models. Primary-cultures of human urothelial cells (HUC) arising from normal adult urinary tract and permanent urothelial cell line were used. Solutions at different dilutions were placed into the wells containing monolayers of confluent cells. After 24 h incubation period, the solutions were removed and cell viability and cell metabolic activity tests were performed (Neutral Red assay and MTT assay). At a concentration lower than 1 mg l(-1) the different radio-opacifiers used showed no toxicity. From 1 to 3 mg l(-1) one can note a significant dose-dependent decrease of cell metabolic activity of solely HUC for barium chloride. At 3 mg l(-1) one can note a significant deleterious effect on HUC metabolic activity, with bismuth and tantale. For tungsten, there is no deleterious effect, but on the contrary a significant increase in HUC metabolic activity at a 0.5 mg l(-1) concentration. None of the solutions did provoke alterations in HUC viability for concentrations less than 3 mg l(-1). Interestingly, for permanent cell line one can note a solely significant decrease of cell viability at 3 mg l(-1) for tantale. All the other tested salts on permanent cell line were not significantly different from controls for cell viability as well as cell metabolic activity. HUC culture model may be of relevance for the screening of radio-opacifiers intended for ureteral endoprostheses.


Asunto(s)
Bario/toxicidad , Materiales Biocompatibles/toxicidad , Bismuto/toxicidad , Stents , Tungsteno/toxicidad , Cateterismo Urinario/instrumentación , Urotelio/efectos de los fármacos , Adulto , Línea Celular , Supervivencia Celular/efectos de los fármacos , Células Cultivadas , Humanos , Obstrucción Ureteral/terapia , Urotelio/citología , Urotelio/patología , Rayos X
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