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Métodos Terapéuticos y Terapias MTCI
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1.
J Therm Biol ; 93: 102685, 2020 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-33077111

RESUMEN

Thermal trauma can damage organs away from the skin burn site and lead to multiple organ dysfunction. Following thermal injury, all tissues are exposed to ischemia, and as a result, resuscitation and reperfusion occur during the burning shock. Burn damage starts systemic inflammatory reactions that produce toxins and reactive oxygen radicals that lead to peroxidation. This study aimed to investigate, for the first time, the possible antioxidant effects of Myrtus communis ethanol extract on burn-induced oxidative distant organ injury orally. The thermal trauma was generated under ether anesthesia by exposing the dorsum of rats to 90 °C water bath for 10 s. 100 mg/kg/day Mrytus communis ethanol extract was applied orally for two days. Malondialdehyde (MDA) and glutathione (GSH) levels, glutatinone-S-transferase (GST), superoxidedismutase (SOD) and catalase (CAT) activities were determined to detect the possible antioxidant effects of myrtle on small intestine and lung tissues. Burn damage significantly increased MDA levels in lung and small intestine tissues, and significantly decreased GSH levels, CAT and GST activities in the small intestine and lung tissues compared to control group. Mrytus communis ethanol extract decreased MDA level and increased GSH level, SOD, CAT and GST activities significantly in either small intestine or lung tissues. Mrytus communis extract may be an ideal candidate to be used as an antioxidant adjunct to improve oxidative distant organ damage to limit the systemic inflammatory response and decreasing the recovery time after thermal injury.


Asunto(s)
Antioxidantes/uso terapéutico , Quemaduras/tratamiento farmacológico , Intestino Delgado/efectos de los fármacos , Pulmón/efectos de los fármacos , Myrtus/química , Extractos Vegetales/uso terapéutico , Animales , Antioxidantes/farmacología , Catalasa/metabolismo , Glutatión/metabolismo , Intestino Delgado/metabolismo , Pulmón/metabolismo , Malondialdehído/metabolismo , Extractos Vegetales/farmacología , Ratas , Ratas Wistar , Superóxido Dismutasa/metabolismo , Cicatrización de Heridas
2.
Burns ; 45(8): 1856-1863, 2019 12.
Artículo en Inglés | MEDLINE | ID: mdl-31383607

RESUMEN

Thermal skin burns cause local injury as well as triggers acute systemic inflammation response where the imbalance between oxidative and antioxidative system occurs. As an alternative treatment, various medicinal herbs are used to treat burn injuries in many countries. In this study, the possible protective role of oral or topical Myrtle (Myrtus communis L.) treatment against burn-induced damage was investigated. The dorsum of the Wistar Albino rats was shaved and exposed to 90 °C water bath in burn group or 25 °C water bath in control group for 10 s under ether anesthesia. Myrtle extract was applied 100 mg/kg/day for 2 days either orally or topically. In skin samples; malondialdehyde and glutathione levels, catalase, superoxide dismutase, nitric oxide and tissue factor activities were determined. Skin tissues were also examined by light microscopy. Severe thermal skin burn injury caused a significant decrease in glutathione level, superoxide dismutase, catalase and tissue factor activities as well as nitric oxide level, which was accompanied with significant increases in skin malondialdehyde level. Myrtle treatment reversed all these biochemical indices except topical Myrtle treated group's nitric oxide level, as well as histopathological alterations, which were induced by thermal trauma. Both oral and topical Myrtle extract treatment was found to have protective role in the burn induced oxidative injury, which may be attributed to the potential antioxidant effect of Myrtle. As a conclusion, Myrtle significantly diminishes burn-induced damage in skin.


Asunto(s)
Antioxidantes/farmacología , Quemaduras/metabolismo , Myrtus , Estrés Oxidativo/efectos de los fármacos , Extractos Vegetales/farmacología , Piel/efectos de los fármacos , Administración Cutánea , Administración Oral , Animales , Quemaduras/patología , Catalasa/efectos de los fármacos , Catalasa/metabolismo , Glutatión/efectos de los fármacos , Glutatión/metabolismo , Malondialdehído/metabolismo , Óxido Nítrico/metabolismo , Ratas , Ratas Wistar , Piel/lesiones , Piel/metabolismo , Piel/patología , Superóxido Dismutasa/efectos de los fármacos , Superóxido Dismutasa/metabolismo , Tromboplastina/efectos de los fármacos , Tromboplastina/metabolismo
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