Combretum lanceolatum flowers extract shows antidiabetic activity through activation of AMPK by quercetin

• Autor(a) principal: Dechandt,Carlos Roberto Porto
• Data de Publicação: 2013
• Outros Autores: Siqueira,Juliany Torres, Souza,Damiana Luiza Pereira de, Araujo,Lais Cobianchi Junqueira, Silva,Virginia Claudia da, Sousa Junior,Paulo Teixeira de, Andrade,Claudia Marlise Balbinotti, Kawashita,Nair Honda, Baviera,Amanda Martins
• Tipo de documento: Artigo
• Idioma: eng
• Título da fonte: Revista Brasileira de Farmacognosia (Online)
• Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0102-695X2013000200014
• topic: AMPK; antidiabetic activity; Combretum lanceolatum; metformin; quercetin; streptozotocin-diabetic rats

The present study evaluated the antidiabetic activity of the Combretum lanceolatum Pohl ex Eichler, Combretaceae, flowers extract (ClEtOH) in diabetic rats. Streptozotocin-diabetic rats were divided into four groups: diabetic control, diabetic treated with 500 mg/kg of metformin and diabetic treated with 250 or 500 mg/kg of ClEtOH for 21 days. The treatment of diabetic rats with 500 mg/kg of ClEtOH promoted an increase in the weight of liver, white adipose tissues and skeletal muscles, improving body weight gain. Diabetic rats treated with 500 mg/kg of ClEtOH also presented reduction in glycemia, glycosuria and urinary urea levels, and increase in liver glycogen content. HPLC chromatogram showed that quercetin is the major compound in the extract. The phosphorylation levels of adenosine monophosphate-activated protein kinase were increased in liver slices incubated in vitro with 50 µg/mL of ClEtOH, similarly to the incubation with metformin (50 µg/mL) or quercetin (10 µg/mL). The antihyperglycemic effect of ClEtOH was similar to that of metformin and appears to be through inhibition of gluconeogenesis, since urinary urea was reduced and skeletal muscle mass was increased. These data indicate that the antidiabetic activity of the Combretum lanceolatum extract could be mediated, at least in part, through activation of adenosine monophosphateactivated protein kinase by quercetin.