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Possible protection by notoginsenoside R1 against glutamate neurotoxicity mediated by N‐methyl‐ D ‐aspartate receptors composed of an NR1/NR2B subunit assembly
Author(s) -
Gu Bin,
Nakamichi Noritaka,
Zhang WenSheng,
Nakamura Yukary,
Kambe Yuki,
Fukumori Ryo,
Takuma Kazuhiro,
Yamada Kiyofumi,
Takarada Takeshi,
Taniura Hideo,
Yoneda Yukio
Publication year - 2009
Publication title -
journal of neuroscience research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.72
H-Index - 160
eISSN - 1097-4547
pISSN - 0360-4012
DOI - 10.1002/jnr.22021
Subject(s) - neurotoxicity , nmda receptor , excitotoxicity , glutamate receptor , propidium iodide , microbiology and biotechnology , intracellular , chemistry , receptor , viability assay , pharmacology , biology , biochemistry , programmed cell death , apoptosis , toxicity , organic chemistry
Notoginsenoside R1 (NTR1) is the main active ingredient in Panax notoginseng , a herbal medicine widely used in Asia for years. The purpose of this study was to investigate pharmacological properties of NTR1 on neurotoxicity of glutamate (Glu) in primary cultured mouse cortical neurons along with its possible mechanism of action. Wefound that NTR1 significantly protected neurons from the loss of cellular viability caused by brief exposure to 10 μM Glu for 1 hr in a dose‐dependent manner at concentrations from 0.1 to 10 μM, without affecting the viability alone. NTR1 significantly inhibited the increased number of cells positive to propidium iodide (PI) staining, increase of intracellular free Ca 2+ ions, overproduction of intracellular reactive oxygen species, and depolarization of mitochondrial membrane potential in cultured neurons exposed to Glu, in addition to blocking decreased Bcl‐2 and increased Bax expression levels. We further evaluated the target site at which NTR1 protects neurons from Glu toxicity by using the acquired expression strategy of N‐methyl‐ D ‐aspartate (NMDA) receptor subunits in human embryonic kidney 293 cells. We found that 10 μM NTR1 protected NR1/NR2B subunit expressing cells from cell death by 100 μM NMDA, but not cells expressing NR1/NR2A subunits, when determined by PI staining. These results suggest that NTR1 may preferentially protect neurons from Glu excitotoxicity mediated by NMDA receptor composed of an NR1/NR2B subunit assembly in the brain. © 2009 Wiley‐Liss, Inc.