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Pharmacol Rep ; 71(6): 1228-1234, 2019 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-31670059

RESUMEN

BACKGROUND: Sepsis causes organ dysfunctions via elevation of oxidative stress and inflammation. Lipopolysaccharide (LPS) is the major surface molecule of most gram-negative bacteria and routinely used as a sepsis model in investigation studies. Crocin is an active compound of saffron which has different pharmacological properties such as anti-oxidant and anti-inflammatory. In this research, the protective effect of crocin was evaluated against LPS-induced toxicity in the embryonic cardiomyocyte cell line (H9c2). METHODS: The cells were pre-treated with different concentration of crocin (10, 20 and 40 µM) for 24 h, and then LPS was added (10 µg/ml) for another 24 h. Afterward, the percentage of cell viability and the levels of inflammatory cytokines (TNF-α, PGE2, IL-1ß, and IL-6), gene expression levels (TNF-α, COX-2, IL-1ß, IL-6, and iNOS), and the level of nitric oxide (NO) and thiol were measured. RESULTS: Our results showed that LPS reduced cell viability, increased the levels of cytokines, gene-expression, nitric oxide, and thiol. Crocin attenuated the LPS-induced toxicity in H9c2 cells via reducing the levels of inflammatory factors (TNF-α, PGE2, IL-1ß, and IL-6, p < 0.001), gene expression (TNF-α, COX-2, IL-1ß, IL-6, and iNOS, p < 0.001), and NO (p < 0.001), whereas increased the level of thiol content (p < 0.001). CONCLUSION: The observed results revealed that crocin has preventive effects on the LPS induced sepsis and its cardiac toxicity in-vitro model. Probably, these findings are related to anti-inflammatory and anti-oxidant properties of crocin. However, performing further animal studies are necessary to support the therapeutic effects of crocin in septic shock cardiac dysfunction.


Asunto(s)
Carotenoides/farmacología , Inflamación/inducido químicamente , Inflamación/tratamiento farmacológico , Lipopolisacáridos/farmacología , Miocitos Cardíacos/efectos de los fármacos , Sustancias Protectoras/farmacología , Animales , Antiinflamatorios/farmacología , Antioxidantes/farmacología , Línea Celular , Supervivencia Celular/efectos de los fármacos , Citocinas/metabolismo , Inflamación/metabolismo , Mediadores de Inflamación/metabolismo , Miocitos Cardíacos/metabolismo , Óxido Nítrico/metabolismo , Ratas , Transducción de Señal/efectos de los fármacos
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