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Author (up) Mori, K.; Obara, Y.; Hirota, M.; Azumi, Y.; Kinugasa, S.; Inatomi, S.; Nakahata, N. url  openurl
  Title Nerve growth factor-inducing activity of Hericium erinaceus in 1321N1 human astrocytoma cells Type Journal Article
  Year 2008 Publication Biological & Pharmaceutical Bulletin Abbreviated Journal Biol Pharm Bull  
  Volume 31 Issue 9 Pages 1727-1732  
  Keywords Agaricales/*chemistry; Animals; Astrocytoma/*metabolism; Brain Chemistry/drug effects; Brain Neoplasms/*metabolism; Cell Line, Tumor; Gene Expression/drug effects; Hippocampus/drug effects/metabolism; Humans; Immunoblotting; Immunoenzyme Techniques; JNK Mitogen-Activated Protein Kinases/metabolism; Mice; Mice, Inbred ICR; Nerve Growth Factor/*biosynthesis; PC12 Cells; Phenols/*pharmacology; Powders; RNA, Messenger/biosynthesis/genetics; Rats; Reverse Transcriptase Polymerase Chain Reaction  
  Abstract Neurotrophic factors are essential to maintain and organize neurons functionally; thereby neurotrophic factor-like substances or their inducers are expected to be applied to the treatment of neurodegenerative diseases such as Alzheimer's disease. In the present study, we firstly examined the effects of ethanol extracts of four edible mushrooms, Hericium erinaceus (Yamabushitake), Pleurotus eryngii (Eringi), Grifola frondosa (Maitake), and Agaricus blazei (Himematsutake), on nerve growth factor (NGF) gene expression in 1321N1 human astrocytoma cells. Among the four mushroom extracts, only H. erinaceus extract promoted NGF mRNA expression in a concentration-dependent manner. In addition, secretion of NGF protein from 1321N1 cells was enhanced by H. erinaceus extracts, and the conditioned medium of 1321N1 cells incubated with H. erinaceus extract enhanced the neurite outgrowth of PC12 cells. However, hericenones C, D and E, constituents of H. erinaceus, failed to promote NGF gene expression in 1321N1 cells. The enhancement of NGF gene expression by H. erinaceus extracts was inhibited by the c-jun N-terminal kinase (JNK) inhibitor SP600125. In addition, H. erinaceus extracts induced phosphorylation of JNK and its downstream substrate c-Jun, and increased c-fos expression, suggesting that H. erinaceus promotes NGF gene expression via JNK signaling. Furthermore we examined the efficacy of H. erinaceus in vivo. ddY mice given feed containing 5% H. erinaceus dry powder for 7 d showed an increase in the level of NGF mRNA expression in the hippocampus. In conclusion, H. erinaceus contains active compounds that stimulate NGF synthesis via activation of the JNK pathway; these compounds are not hericenones.  
  Address Department of Cellular Signaling, Graduate School of Pharmaceutical Sciences, Tohoku University, Aramaki, Aoba-ku, Sendai, Japan  
  Corporate Author Thesis  
  Publisher Place of Publication Editor  
  Language English Summary Language Original Title  
  Series Editor Series Title Abbreviated Series Title  
  Series Volume Series Issue Edition  
  ISSN 0918-6158 ISBN Medium  
  Area Expedition Conference  
  Notes PMID:18758067 Approved no  
  Call Number refbase @ user @ Serial 24  
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