Etchegoyen G S, Del Zotto H
CENEXA-Centro de Endocrinología Experimental y Aplicada (UNLP-CONICET), Facultad de Ciencias Médicas, Universidad Nacional de La Plata, Argentina.
Arch Physiol Biochem. 1995 Aug;103(4):416-21. doi: 10.3109/13813459509047131.
Catecholestrogens (CE), 2-hydroxyestradiol, 2-hydroxyestrone and primary estrogens, estradiol and estrone were tested in their ability to compete for the high affinity uptake of [3H]-GABA into crude synaptosomal fractions. Aliquots of the crude synaptosomal fraction obtained from normal rats were incubated for 10 min at 37 degrees C with [3H]-GABA in the presence, or absence, of estrogens and catecholestrogens. Neither estradiol nor estrone modified the specific [3H]-GABA uptake into crude synaptosomal fractions. On the contrary, CE significantly affected the specific [3H]-GABA uptake in a dose-dependent manner: low concentrations of CE enhanced the uptake; this effect disappeared with high concentrations of the compounds. The stimulatory effect of CE on [3H]-GABA uptake was blocked when samples were coincubated with nipecotic acid, thus suggesting that this effect is specific rather than the result of non-specific interactions of CE with the hypothalamic membrane.
儿茶酚雌激素(CE)、2-羟雌二醇、2-羟雌酮以及主要雌激素雌二醇和雌酮,就它们竞争[3H]-γ-氨基丁酸(GABA)向粗制突触体组分的高亲和力摄取的能力进行了测试。将从正常大鼠获得的粗制突触体组分的等分试样,在有或没有雌激素和儿茶酚雌激素存在的情况下,与[3H]-GABA在37℃孵育10分钟。雌二醇和雌酮均未改变[3H]-GABA向粗制突触体组分的特异性摄取。相反,CE以剂量依赖性方式显著影响[3H]-GABA的特异性摄取:低浓度的CE增强摄取;随着化合物浓度升高,这种作用消失。当样品与尼克酸共同孵育时,CE对[3H]-GABA摄取的刺激作用被阻断,因此表明这种作用是特异性的,而非CE与下丘脑膜非特异性相互作用的结果。