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1.
Pediatr Dermatol ; 38(1): 226-228, 2021 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-33155718

RESUMEN

Intrathoracic infantile hemangiomas (IHs) are extremely rare. They may be located in the pericardium, trachea, bronchia, diaphragm, mediastinum, or the lungs and may be associated with cutaneous IHs. We present a newborn with multiple pulmonary IHs in the absence of skin lesions that showed a dramatic response to oral propranolol.


Asunto(s)
Hemangioma Capilar , Hemangioma , Neoplasias Cutáneas , Administración Oral , Antagonistas Adrenérgicos beta/uso terapéutico , Hemangioma/tratamiento farmacológico , Hemangioma Capilar/diagnóstico , Hemangioma Capilar/tratamiento farmacológico , Humanos , Lactante , Recién Nacido , Pulmón , Propranolol/uso terapéutico , Neoplasias Cutáneas/tratamiento farmacológico , Resultado del Tratamiento
2.
Fitoterapia ; 82(3): 414-21, 2011 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-21129455

RESUMEN

In the present study, we evaluated the effects of extracts and purified compounds from fresh leaves of Rosmarinus officinalis L. Pretreatment with the major anti-inflammatory compounds, carnosic acid (CA) and carnosol (CS), inhibited phorbol 12-myristate 13-acetate (PMA)-induced ear inflammation in mice with an EC(50) of 10.20 µg/cm(2) and 10.70 µg/cm(2), respectively. To further understand the anti-inflammatory mechanism of these compounds, we analyzed the in vivo expression of several inflammation-associated genes in mouse skin by reverse transcriptase-polymerase chain reaction (RT-PCR). Our data showed that CA and CS reduced the expression of IL-1ß and TNF-α but had less effect on fibronectin and ICAM-1 expression. Interestingly, both compounds selectively inhibited COX-2 but not COX-1. Histopathological analysis of hematoxylin and eosin (H&E)-stained tissue revealed a marked reduction in leukocyte infiltration and epidermal ulceration of PMA-treated ears when ears were pretreated with ethanolic extracts or pure CA. In vitro, we showed that ethanolic extract, carnosic acid and carnosol significantly inhibited the overproduction of nitric oxide (NO) in a dose-dependent manner in the RAW 264.7 murine macrophage cell line. For the first time in vivo, we showed that CA and CS differentially regulate the expression of inflammation-associated genes, thus demonstrating the pharmacological basis for the anti-inflammatory properties reported for CA and CS.


Asunto(s)
Abietanos/uso terapéutico , Inflamación/tratamiento farmacológico , Fitoterapia , Extractos Vegetales/uso terapéutico , Rosmarinus/química , Piel/efectos de los fármacos , Abietanos/farmacología , Animales , Inhibidores de la Ciclooxigenasa 2/farmacología , Inhibidores de la Ciclooxigenasa 2/uso terapéutico , Relación Dosis-Respuesta a Droga , Fibronectinas/genética , Fibronectinas/metabolismo , Expresión Génica , Inflamación/inducido químicamente , Inflamación/metabolismo , Molécula 1 de Adhesión Intercelular/genética , Molécula 1 de Adhesión Intercelular/metabolismo , Interleucina-1beta/genética , Interleucina-1beta/metabolismo , Macrófagos/efectos de los fármacos , Macrófagos/metabolismo , Masculino , Ratones , Ratones Endogámicos BALB C , Infiltración Neutrófila/efectos de los fármacos , Óxido Nítrico/biosíntesis , Extractos Vegetales/farmacología , Reacción en Cadena de la Polimerasa de Transcriptasa Inversa , Piel/metabolismo , Piel/patología , Acetato de Tetradecanoilforbol , Factor de Necrosis Tumoral alfa/genética , Factor de Necrosis Tumoral alfa/metabolismo
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