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Ficus carica leaves extract inhibited pancreatic ß-cell apoptosis by inhibiting AMPK/JNK/caspase-3 signaling pathway and antioxidation.
Zhang, Yin; Li, Yingying; Ma, Ping; Chen, Jincheng; Xie, Weiping.
Afiliación
  • Zhang Y; Department of Pharmacy, The Second Affiliated Hospital of Fujian Medical University, Quanzhou, 362000, People's Republic of China. Electronic address: zyin1973@163.com.
  • Li Y; Department of Pharmacy, The Second Affiliated Hospital of Fujian Medical University, Quanzhou, 362000, People's Republic of China. Electronic address: 734215150@qq.com.
  • Ma P; Department of Pharmacy, The Second Affiliated Hospital of Fujian Medical University, Quanzhou, 362000, People's Republic of China. Electronic address: 1078693909@qq.com.
  • Chen J; Department of Pharmacy, The Second Affiliated Hospital of Fujian Medical University, Quanzhou, 362000, People's Republic of China. Electronic address: 453886460@qq.com.
  • Xie W; Department of Physical and Chemical Analysis, Quanzhou Center for Disease Control and Prevention, Quanzhou, 362000, People's Republic of China. Electronic address: xweiping2000@163.com.
Biomed Pharmacother ; 122: 109689, 2020 Feb.
Article en En | MEDLINE | ID: mdl-31786467
The aim of this study was to explore the inhibitory effects of Ficus carica leaves (FCL) extract on AMPK/JNK/caspase3 signaling pathway and antioxidation in pancreatic ß-cells. H&E staining, insulin immunohistochemistry, and TUNEL methods were used to investigate the effects of FCL on pancreatic histopathology in type 1 diabetic mice. The expression levels of caspase-3, AMPK, and JNK protein in the pancreatic tissue and MIN6 cells [induced by palmitic acid (PA) and hydrogen peroxide] were determined. Flow cytometry was used to detect the effects of FCL on apoptosis and ROS production of MIN6 cells. FCL (2 g/kg, continuous gavage for 6 weeks) significantly improved the pancreatic tissue injury in type 1 diabetic mice and reduced the expression levels of apoptosis-related proteins such as FasL, caspase8, Bax/Bcl-2, Cyt-C, caspase-3, p-AMPK, and p-JNK. FCL inhibited cell apoptosis induced by PA and the protein expression levels of caspase-3, p-AMPK, and p-JNK. The AMPK agonist AICAR could reverse the protective effects of FCL on MIN6 cells. The AMPK inhibitor compound C had a similar effect on MIN6 cells as that of FCL. FCL could inhibit cell apoptosis induced by hydrogen peroxide and reduced the production of ROS. In conclusion, FCL could inhibit pancreatic ß-cell apoptosis by inhibiting the AMPK/JNK/caspase-3 signaling pathway and by antioxidation properties.
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Proteínas Quinasas / Extractos Vegetales / Apoptosis / Ficus / MAP Quinasa Quinasa 4 / Células Secretoras de Insulina Tipo de estudio: Prognostic_studies Idioma: En Revista: Biomed Pharmacother Año: 2020 Tipo del documento: Article

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Proteínas Quinasas / Extractos Vegetales / Apoptosis / Ficus / MAP Quinasa Quinasa 4 / Células Secretoras de Insulina Tipo de estudio: Prognostic_studies Idioma: En Revista: Biomed Pharmacother Año: 2020 Tipo del documento: Article