加巴能
海马体
神经肽
安定
肽
内生
化学
大脑皮层
神经科学
药理学
内科学
生物
内分泌学
生物化学
抑制性突触后电位
医学
受体
作者
Hannu Alho,E. Costa,P. Ferrero,Meiko Fujimoto,Dano Cosenza-Murphy,Alessandro Guidotti
出处
期刊:Science
[American Association for the Advancement of Science]
日期:1985-07-12
卷期号:229 (4709): 179-182
被引量:232
标识
DOI:10.1126/science.3892688
摘要
An endogenous polypeptide of rat brain has been identified that is capable of displacing 1,4-benzodiazepines and the esters of the 3-carboxylic acid derivatives of β-carbolines from their specific synaptic binding sites. This polypeptide was termed diazepam-binding inhibitor (DBI). Previous studies have shown that DBI injected intraventricularly in rodents elicits "proconflict" responses and antagonizes the "anticonflict" action of benzodiazepines. An antiserum to this peptide, directed toward an immunodeterminant near its amino terminus, makes it possible to detect, measure, and study the neuronal location of this peptide in rat brain. In the rat cerebral cortex, DBI immunoreactivity is located in neurons that are not GABAergic (GABA, γ-aminobutyric acid); in the cerebellum and hippocampus, however, it might be present also in GABAergic neurons.
科研通智能强力驱动
Strongly Powered by AbleSci AI