Lycium barbarum Polysaccharides Protect against Trimethyltin Chloride‐Induced Apoptosis via Sonic Hedgehog and PI3K/Akt Signaling Pathways in Mouse Neuro‐2a Cells

• DOI: 10.1155/2016/9826726
• Publication Date: 2016-04-08T11:33:15Z
• Authors: Wanyun Zhao; Xiaoqi Pan; Tao Li; Changchun Zhang; Nian Shi
• Keywords: 0301 basic medicine; Glycogen Synthase Kinase 3 beta; Caspase 3; Pyridines; Morpholines; Apoptosis; Cell Line; 3. Good health; Mice; Oxidative Stress; Phosphatidylinositol 3-Kinases; 03 medical and health sciences; Microscopy, Fluorescence; Proto-Oncogene Proteins c-bcl-2; Chromones; Animals; Anilides; Hedgehog Proteins; Lipid Peroxidation; Phosphorylation; Proto-Oncogene Proteins c-akt; Research Article; Drugs, Chinese Herbal; Phosphoinositide-3 Kinase Inhibitors

Trimethyltin chloride (TMT) is a classic neurotoxicant that can cause severe neurodegenerative diseases. Some signaling pathways involving cell death play pivotal roles in the central nervous system. In this study, the role of Sonic Hedgehog (Shh) and PI3K/Akt pathways in TMT‐induced apoptosis and protective effect of Lycium barbarum polysaccharides (LBP) on mouse neuro‐2a (N2a) cells were investigated. Results showed that TMT treatment significantly enhanced apoptosis, upregulated proapoptotic Bax, downregulated antiapoptotic Bcl‐2 expression, and increased caspase‐3 activity in a dose‐dependent manner in N2a cells. TMT induced oxidative stress in cells, performing reactive oxygen species (ROS) and malondialdehyde (MDA) excessive generation, and superoxide dismutase (SOD) activity reduction. TMT significantly decreased phosphorylated glycogen synthase kinase‐3β (GSK‐3β) and inhibited Shh and PI3K/Akt pathways. However, the addition of LBP upregulated GSK‐3β phosphorylation, activated Shh and PI3K/Akt pathways, and eventually reduced apoptosis and oxidative stress caused by TMT. The interaction between Shh and PI3K/Akt pathways was clarified by specific PI3K inhibitor LY294002 or Shh inhibitor GDC‐0449. Moreover, LY294002 and GDC‐0449 pretreatment both induced phosphorylated GSK‐3β downregulation and significantly promoted apoptosis induced by TMT. These results suggest that LBP could reduce TMT‐induced N2a cells apoptosis by regulating GSK‐3β phosphorylation, Shh, and PI3K/Akt signaling pathways.