Withaferin A-Caused Production of Intracellular Reactive Oxygen Species Modulates Apoptosis via PI3K/Akt and JNKinase in Rabbit Articular Chondrocytes.
10.3346/jkms.2014.29.8.1042
- Author:
Seon Mi YU
1
;
Song Ja KIM
Author Information
1. Department of Biological Sciences, Kongju National University, Gongju, Korea. ksj85@kongju.ac.kr
- Publication Type:Original Article ; Research Support, Non-U.S. Gov't
- Keywords:
Apoptosis;
Chondrocytes;
Reactive Oxygen Species
- MeSH:
Animals;
Anti-Inflammatory Agents/administration & dosage;
Apoptosis/drug effects/physiology;
Cartilage, Articular/cytology/drug effects/*metabolism;
Cells, Cultured;
Chondrocytes/drug effects/*metabolism;
Dose-Response Relationship, Drug;
MAP Kinase Kinase 4/*metabolism;
Phosphatidylinositol 3-Kinases/*metabolism;
Proto-Oncogene Proteins c-akt/metabolism;
Rabbits;
Reactive Oxygen Species/*metabolism;
Withanolides/*administration & dosage
- From:Journal of Korean Medical Science
2014;29(8):1042-1053
- CountryRepublic of Korea
- Language:English
-
Abstract:
Withaferin A (WFA) is known as a constituent of Ayurvedic medicinal plant, Withania somnifera, and has been used for thousands of years. Although WFA has been used for the treatment of osteoarthritis (OA) and has a wide range of biochemical and pharmacologic activities, there are no findings suggesting its properties on chondrocytes or cartilage. The aim of the present study is to investigate the effects of WFA on apoptosis with focus on generation of intracellular reactive oxygen species (ROS). Here we showed that WFA significantly increased the generation of intracellular ROS in a dose-dependent manner. We also determined that WFA markedly leads to apoptosis as evidenced by accumulation of p53 by Western blot analysis. N-Acetyl-L-Cystein (NAC), an antioxidant, prevented WFA-caused expression of p53 and inhibited apoptosis of chondrocytes. We also found that WFA causes the activation of PI3K/Akt and JNKinase. Inhibition of PI3K/Akt and JNKinase with LY294002 (LY)/triciribine (TB) or SP600125 (SP) in WFA-treated cells reduced accumulation of p53 and inhibited fragmented DNA. Our findings suggested that apoptosis caused by WFA-induced intracellular ROS generation is regulated through PI3K/Akt and JNKinase in rabbit articular chondrocytes.
