Erdö S L, Maksay G
Pharmacological Research Centre, Chemical Works of Gedeon Richter Ltd., Budapest, Hungary.
Eur J Pharmacol. 1988 Mar 1;147(2):279-82. doi: 10.1016/0014-2999(88)90787-x.
The capacity of membranes from the ovaries, oviducts and uteri of rats to bind [35S]t-butylbicyclo-phosphorothionate (TBPS), and the effect of gamma-aminobutyric acid (GABA) and pentobarbital on the specific binding of TBPS were examined. Specific TBPS binding, that could be modulated by GABA and pentobarbital in an allosteric manner, was demonstrated. These findings indicate that the TBPS-labeled chloride ion channels in the female sex organs are regulated by GABA and pentobarbital sites, in a fashion similar to that observed in the brain.
检测了大鼠卵巢、输卵管和子宫的膜结合[35S]叔丁基双环磷硫代酸盐(TBPS)的能力,以及γ-氨基丁酸(GABA)和戊巴比妥对TBPS特异性结合的影响。结果表明,存在可被GABA和戊巴比妥以变构方式调节的TBPS特异性结合。这些发现表明,雌性生殖器官中TBPS标记的氯离子通道受GABA和戊巴比妥位点的调控,其方式与在大脑中观察到的相似。