Pulges Oliver, Rinken Ago
Institute of Organic and Bioorganic Chemistry, University of Tartu, Jakobi Str. 2, 51014 Tartu, Estonia.
Neurochem Res. 2008 Mar;33(3):477-82. doi: 10.1007/s11064-007-9457-z. Epub 2007 Aug 31.
Functional activation of alpha 2A adrenergic receptors in the crude membranes from rat frontal cortex was studied by a [35S]-guanosine 5'-O-(gamma-thiotriphosphate) ([35S]GTP gamma S) binding assay. alpha 2A agonists UK14304 and guanfacine decreased the ability of GDP to compete with [35S]GTP gamma S binding to the membranes and 0.1 mM GDP was found to be optimal for the following functional experiments. However, even after careful optimization of experimental conditions the specificity of ligands for rat alpha 2 adrenoceptors were not sufficient, as agonists as well as antagonists became activators of other signal transduction systems before achieving their maximal effect in the alpha 2A-adrenergic system. Only using compromising concentration of agonist (up to 1 microM UK14304) and antagonist (up to 1 microM RS79948) to inhibit agonist's effect, allowed us to filtrate out alpha 2A specific effect for characterization of signal transduction in rat frontal cortex membranes for the comparison efficacies of this system for different animals from behavioral experiments.
通过[35S] - 鸟苷5'-O -(γ-硫代三磷酸)([35S] GTPγS)结合试验研究了大鼠额叶皮质粗制膜中α2A肾上腺素能受体的功能激活。α2A激动剂UK14304和胍法辛降低了GDP与[35S] GTPγS竞争结合膜的能力,并且发现0.1 mM GDP对于以下功能实验是最佳的。然而,即使在仔细优化实验条件之后,配体对大鼠α2肾上腺素能受体的特异性仍不足,因为激动剂和拮抗剂在α2A - 肾上腺素能系统中达到最大效应之前就成为其他信号转导系统的激活剂。仅使用折中的激动剂浓度(高达1μM UK14304)和拮抗剂浓度(高达1μM RS79948)来抑制激动剂的作用,使我们能够滤出α2A特异性效应,以表征大鼠额叶皮质膜中的信号转导,用于比较该系统在行为实验中对不同动物的功效。