Peltonen J M, Pihlavisto M, Scheinin M
Department of Pharmacology and Clinical Pharmacology, University of Turku, Finland.
Eur J Pharmacol. 1998 Aug 21;355(2-3):275-9. doi: 10.1016/s0014-2999(98)00518-4.
We measured agonist-stimulated binding of the stable GTP-analog guanosine-5'-O-(3-[35S]thiotriphosphate) ([35S]GTPgammaS) as a functional assay to monitor G-protein activation by recombinant human alpha2-adrenoceptor subtypes alpha2A, alpha2B and alpha2C. (-)-Noradrenaline was a full agonist in all receptors. Dexmedetomidine, UK14,304, clonidine and oxymetazoline showed subtype-selectivity in efficacy. Dexmedetomidine was a full agonist at alpha2B and a partial agonist at alpha2A; UK14,304 was a full agonist at alpha2A and a partial agonist at alpha2B. Clonidine and oxymetazoline were weak partial agonists at the alpha2B-subtype, but appeared inactive at alpha2A and alpha2C. The [35S]GTPgammaS binding assay provides functional information on pertussis toxin-sensitive G-protein activation, complementing radioligand binding assays and conventional second messenger assays.
我们测定了稳定的GTP类似物鸟苷-5'-O-(3-[35S]硫代三磷酸)([35S]GTPγS)的激动剂刺激结合,以此作为一种功能测定方法,来监测重组人α2-肾上腺素能受体亚型α2A、α2B和α2C对G蛋白的激活作用。(-)-去甲肾上腺素在所有受体中均为完全激动剂。右美托咪定、UK14,304、可乐定和羟甲唑啉在效能上表现出亚型选择性。右美托咪定在α2B受体上是完全激动剂,在α2A受体上是部分激动剂;UK14,304在α2A受体上是完全激动剂,在α2B受体上是部分激动剂。可乐定和羟甲唑啉在α2B亚型上是弱部分激动剂,但在α2A和α2C亚型上似乎无活性。[35S]GTPγS结合测定提供了关于百日咳毒素敏感的G蛋白激活的功能信息,补充了放射性配体结合测定和传统的第二信使测定。