Dellouve-Courillon C, Lambolez B, Potier P, Dodd R H
Institut de Chimie des Substances Naturelles, Centre National de la Recherche Scientifique, Gif-sur-Yvette, France.
Eur J Pharmacol. 1989 Aug 3;166(3):557-62. doi: 10.1016/0014-2999(89)90376-2.
Photolabelling of benzodiazepine receptors isolated from rat cortex with a new beta-carboline-type photoaffinity label, ethyl 6-azido-beta-carboline-3-carboxylase, at 254 nm produced a 42% decrease in the maximal number of propyl beta-carboline-3-carboxylate binding sites but practically no decrease in the number of flunitrazepam binding sites. Moreover, the binding affinity of ethyl beta-carboline-3-carboxylase was diminished 11-fold by photolabelling while that of diazepam was diminished less than 2-fold. These results provide additional evidence that beta-carbolines and benzodiazepines bind to discrete sites on the benzodiazepine receptor.
用一种新型β-咔啉类光亲和标记物6-叠氮基-β-咔啉-3-羧酸乙酯在254纳米波长下对从大鼠皮层分离出的苯二氮䓬受体进行光标记,结果显示,羧酸丙酯-β-咔啉-3-羧酸酯结合位点的最大数量减少了42%,而氟硝西泮结合位点的数量几乎没有减少。此外,光标记使β-咔啉-3-羧酸乙酯的结合亲和力降低了11倍,而地西泮的结合亲和力降低不到2倍。这些结果进一步证明了β-咔啉类和苯二氮䓬类药物与苯二氮䓬受体上不同的位点结合。