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1.
J Wound Care ; 31(10): 872-881, 2022 Oct 02.
Artículo en Inglés | MEDLINE | ID: mdl-36240793

RESUMEN

OBJECTIVE: Alcohol consumption combined with ageing alters the healing process of the skin. We evaluated whether ageing decreases the healing of incisional wounds in the skin of Wistar rats of Universidade de Chile of variety B (UChB). METHOD: A total of 20 adult rats and 20 older UChB rats, divided into two groups which underwent surgical aggression in the anterior region of the abdomen, were used: G1, adult rats (100 days old, control) with water and 10% ethanol; G2, aged rats (540 days old, experimental) with water and 10% ethanol; evaluated at 4, 7, 14 and 21 days after surgery. RESULTS: Ageing did not alter the rupture force and collagen elasticity and resistance. There were increases in telomerase with the implementation of cellular senescence, in interleukin 1-alpha (IL-1α) at 14 days of healing, in epidermal growth factor (EGF) at 14 and 21 days of healing with delayed growth and development of keratinocytes, also an increase of IL-ß at 4 days, and decrease in tumour necrosis factor (TNFα) at 7 days, associated with chronic scarring. There was an increase in vascular endothelial growth factor (VEGF) at 4 and 7 days, responsible for the early vessels re-establishment. There was a decrease in transforming growth factor 2-beta (TGFß2) and ß3 at 4 and 7 days of healing respectively, and estradiol at 4 days. CONCLUSION: Ageing decreases the skin healing in incisional wounds in alcohol-preferring rats.


Asunto(s)
Telomerasa , Factor A de Crecimiento Endotelial Vascular , Envejecimiento , Animales , Colágeno/metabolismo , Factor de Crecimiento Epidérmico , Estradiol/metabolismo , Etanol/metabolismo , Interleucina-1/metabolismo , Ratas , Ratas Wistar , Piel/lesiones , Telomerasa/metabolismo , Factor de Crecimiento Transformador beta , Factores de Crecimiento Transformadores/metabolismo , Factor de Necrosis Tumoral alfa/metabolismo , Factores de Crecimiento Endotelial Vascular/metabolismo , Agua/metabolismo
2.
Injury ; 51(4): 840-849, 2020 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-32081392

RESUMEN

Poincianella pluviosa has already been described as capable of healing skin wounds. In an attempt to prolong contact of the drug with the wound, it was proposed in this study to evaluate wound healing using a crude extract (CE) of P. pluviosa incorporated in carboxymethylcellulose polymer films. The chromatographic profile of the semipurified fraction of P. pluviosa was evaluated by ultra-high performance liquid chromatography (UHPLC), confirming the compounds gallic acid, geraniin, and ellagic acid. The films were evaluated for their physical and mechanical properties, water vapor permeability, moisture absorption capacity, and FTIR spectroscopy. For in vivo experiments, wounds were made on the back of rats and treated daily for 4, 7, 10, or 14 days with film containing CE or control film. At the end of each period, skin permeation analysis and histological analysis were made using re-epithelialisation, cell proliferation, and collagen formation. Statistical significance was determined by GraphPad Prism using t test and Mann-Whitney test. Anti-staphylococcal activity was evaluated with standard strains of Staphylococcus aureus, methicillin-resistant, and coagulase negative. It was demonstrated that the presence of CE in the films increased the capacity to absorb water and decreased resistance and permeability. The CE of the film permeated the skin, reaching the dermis and was able to influence re-epithelisation, cell proliferation, and collagen formation. Satisfactory results were observed against S. aureus strains, particularly coagulase negative. Films with CE of P. pluviosa can be an alternative in the wound healing, protecting against opportunistic infections and giving comfort to the patient.


Asunto(s)
Antibacterianos/farmacología , Fabaceae/química , Extractos Vegetales/farmacología , Staphylococcus aureus/efectos de los fármacos , Cicatrización de Heridas/efectos de los fármacos , Animales , Cromatografía Líquida de Alta Presión , Masculino , Corteza de la Planta/química , Polímeros , Ratas , Piel/efectos de los fármacos , Piel/lesiones , Staphylococcus aureus/crecimiento & desarrollo
3.
Appl Physiol Nutr Metab ; 44(11): 1199-1208, 2019 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-30901524

RESUMEN

The pressure injury environment is characterized by overproduction of reactive oxygen species and exacerbated inflammation, which impair the healing of these lesions. Mediterranean-like diet may be a good intervention to improve the healing of pressure injury owing to its anti-inflammatory and antioxidant components. Thus, this study evaluated the hypothesis that olive oil, as a main source of lipid in Mediterranean diet, could improve cutaneous wound healing of pressure injury in mice. Male Swiss mice were randomly divided into standard, olive oil, or soybean oil plus olive oil groups and fat represented 10% of total calories in all groups. Four weeks after the beginning of diet administration, 2 cycles of ischemia-reperfusion (IR) by external application of 2 magnets disks were performed in the dorsal skin to induce pressure injury formation. Fourteen days after the end of the second IR cycle, olive oil-based diet reduced neutrophils cells and cyclooxygenase-2 protein expression and increased nitric oxide synthase-2 and protein and lipid oxidation. Olive oil based-diet also increased nuclear factor erythroid 2-related factor 2 protein expression and collagen type I precursor protein expression. In addition, administration of olive oil-based diet promoted wound closure at 7, 10, and 14 days after the end of the second IR cycle. These findings support the hypothesis that olive oil-based diet improves cutaneous wound healing of pressure injury in mice through the reduction of inflammation and stimulation of redox equilibrium.


Asunto(s)
Lesiones por Aplastamiento , Dieta , Factor 2 Relacionado con NF-E2 , Óxido Nítrico Sintasa de Tipo II , Aceite de Oliva , Úlcera por Presión , Piel , Cicatrización de Heridas , Animales , Masculino , Ratones , Colágeno Tipo I/metabolismo , Lesiones por Aplastamiento/terapia , Ciclooxigenasa 2/metabolismo , Factor 2 Relacionado con NF-E2/metabolismo , Óxido Nítrico Sintasa de Tipo II/metabolismo , Aceite de Oliva/farmacología , Distribución Aleatoria , Especies Reactivas de Oxígeno/metabolismo , Piel/lesiones , Úlcera por Presión/terapia
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