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Hum Exp Toxicol ; 40(12_suppl): S460-S474, 2021 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-34610774

RESUMO

BACKGROUND: Diabetes is a serious global health concern which severely affected public health as well as socio-economic growth worldwide. Scutellarin (SCU), a bioactive flavonoid, is known for its efficacious action against a range of ailments including cardiovascular problems. The present study was conducted to find out possible protective effect and its associated mechanisms of SCU on experimental type 2 diabetes-induced cardiac injury. METHODS: Type 2 diabetes was induced by treating animals with high fat diet for 4 weeks and a single intraperitoneal dose (35 mg/kg body weight) of streptozotocin and diabetic animals received SCU (10 or 20 mg/kg/day) for 6 weeks. RESULTS: Scutellarin attenuated type 2 diabetes-induced hyperglycemia, bodyweight loss, hyperlipidaemia, cardiac functional damage with histopathological alterations and fibrosis. Scutellarin treatment to type 2 diabetic mice ameliorated oxidative stress, inflammatory status and apoptosis in heart. Furthermore, the underlying mechanisms for such mitigation of oxidative stress, inflammation and apoptosis in heart involved modulation of Nrf2/Keap1 pathway, TLR4/MyD88/NF-κB mediated inflammatory pathway and intrinsic (mitochondrial) apoptosis pathway, respectively. CONCLUSIONS: The current findings suggest that SCU is effective in protecting type 2 diabetes-induced cardiac injury by attenuating oxidative stress and inflammatory responses and apoptosis, and it is also worth considering the efficacious potential of SCU to treat diabetic cardiomyopathy patients.


Assuntos
Apigenina/uso terapêutico , Diabetes Mellitus Tipo 2/induzido quimicamente , Glucuronatos/uso terapêutico , Cardiopatias/tratamento farmacológico , Cardiopatias/etiologia , Inflamação/tratamento farmacológico , Estresse Oxidativo/efeitos dos fármacos , Animais , Apoptose/efeitos dos fármacos , Biomarcadores/metabolismo , Glicemia/efeitos dos fármacos , Peso Corporal/efeitos dos fármacos , Fármacos Cardiovasculares/uso terapêutico , Diabetes Mellitus Experimental , Dieta Hiperlipídica , Relação Dose-Resposta a Droga , Regulação da Expressão Gênica/efeitos dos fármacos , Lipídeos/sangue , Masculino , Camundongos , RNA Mensageiro/genética , RNA Mensageiro/metabolismo
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