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Silymarin Inhibits Cytokine-Stimulated Pancreatic Beta Cells by Blocking the ERK1/2 Pathway.
Kim, Eun Jeong; Kim, Jeeho; Lee, Min Young; Sudhanva, Muddenahalli Srinivasa; Devakumar, Sundaravinayagam; Jeon, Young Jin.
Afiliação
  • Kim EJ; Department of Pharmacology, School of Medicine, Chosun University, Gwangju 501-759, Republic of Korea.
  • Kim J; Department of Pharmacology, School of Medicine, Chosun University, Gwangju 501-759, Republic of Korea.
  • Lee MY; Department of Pharmacology, School of Medicine, Chosun University, Gwangju 501-759, Republic of Korea.
  • Sudhanva MS; Department of Pharmacology, School of Medicine, Chosun University, Gwangju 501-759, Republic of Korea.
  • Devakumar S; Department of Pharmacology, School of Medicine, Chosun University, Gwangju 501-759, Republic of Korea.
  • Jeon YJ; Department of Pharmacology, School of Medicine, Chosun University, Gwangju 501-759, Republic of Korea.
Biomol Ther (Seoul) ; 22(4): 282-7, 2014 Jul.
Article em En | MEDLINE | ID: mdl-25143805
We show that silymarin, a polyphenolic flavonoid isolated from milk thistle (Silybum marianum), inhibits cytokine mixture (CM: TNF-α, IFN-γ, and IL-1ß)-induced production of nitric oxide (NO) in the pancreatic beta cell line MIN6N8a. Immunostaining and Western blot analysis showed that silymarin inhibits iNOS gene expression. RT-PCR showed that silymarin inhibits iNOS gene expression in a dose-dependent manner. We also showed that silymarin inhibits extracellular signal-regulated protein kinase-1 and 2 (ERK1/2) phosphorylation. A MEK1 inhibitor abrogated CM-induced nitrite production, similar to silymarin. Treatment of MIN6N8a cells with silymarin also inhibited CM-stimulated activation of NF-κB, which is important for iNOS transcription. Collectively, we demonstrate that silymarin inhibits NO production in pancreatic beta cells, and silymarin may represent a useful anti-diabetic agent.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2014 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2014 Tipo de documento: Article