CONANTOKIN-G - A NOVEL PEPTIDE ANTAGONIST TO THE N-METHYL-D-ASPARTIC ACID (NMDA) RECEPTOR

被引:89
作者
MENA, EE
GULLAK, MF
PAGNOZZI, MJ
RICHTER, KE
RIVIER, J
CRUZ, LJ
OLIVERA, BM
机构
[1] SALK INST BIOL STUDIES,CLAYTON LABS PEPTIDE BIOL,LA JOLLA,CA 92138
[2] UNIV UTAH,DEPT BIOL,SALT LAKE CITY,UT 84112
关键词
Conantokin; Excitatory amino acid antagonist; NMDA antagonist; Peptide venom; Sleeper peptide; Snail venom;
D O I
10.1016/0304-3940(90)90637-O
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Conantokin-G is a 17 amino acid peptide isolated from the venom of the fish-eating snail Conus geographus which produces hyperactivity when injected into the brains of adult mice. We show that this peptide is a selective N-methyl-d-aspartate (NMDA) antagonist based on its ability to block NMDA-induced elevation of cGMP in rat cerebellar slices in vitro (IC50 = 171 nM), but not kainic acid-induced elevations. This inhibition could not be overcome by increasing the NMDA concentration, indicating non-competitive inhibition. Conantokin-G displayed no affinity for binding sites for thienylcyclohexylpiperidine, various glutamate subclasses or those for several other neurotransmitters/neuromodulators. This peptide, however, enhanced [3H]glycine binding to rat forebrain membranes but not to spinal cord membranes. The activity profile of the peptide in various assays indicates that it is a novel type of non-competitive NMDA antagonist. © 1990.
引用
收藏
页码:241 / 244
页数:4
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