Weder H G
Arzneimittelforschung. 1978;28(5):752-5.
The neuroleptics chlorpromazine, fluphenazine, triflupromazine and thioridazine seem to effect the aggregation of glutamate dehydrogenase by binding to one single site of the polypeptide chain, possibly the GTP site. This interaction could biologically be of importance for the degree of activity at high enzyme concentrations found in vivo. Amitriptyline and fluorazepam also bind to a specific single site of the polypeptide chain without effecting the aggregation of the oligomers. Because of the rather low affinity of these sites the binding of these drugs in vivo does not seem to cause a concentrating effect in the mitochondria.
神经安定药氯丙嗪、氟奋乃静、三氟丙嗪和硫利达嗪似乎通过与多肽链的一个单一部位(可能是GTP部位)结合来影响谷氨酸脱氢酶的聚集。这种相互作用在生物学上可能对体内发现的高酶浓度下的活性程度很重要。阿米替林和氟西泮也与多肽链的一个特定单一部位结合,但不影响寡聚体的聚集。由于这些部位的亲和力相当低,这些药物在体内的结合似乎不会在线粒体中产生浓缩效应。