Muramatsu I, Kigoshi S
Department of Pharmacology, Fukui Medical School, Japan.
Jpn J Pharmacol. 1992 Aug;59(4):457-9. doi: 10.1254/jjp.59.457.
The selectivity of tizanidine to the imidazoline-receptor and alpha 2-adrenoceptor recognized by 3H-p-aminoclonidine was examined in rat kidney membranes and was compared with those of other imidazoline compounds. Tizanidine bound to the imidazoline-receptors with approximately 20 times higher affinity than the alpha 2-adrenoceptors. The order of relative selectivity to imidazoline receptor was tizanidine greater than oxymetazoline greater than clonidine greater than naphazoline, where clonidine showed an equal affinity to both receptors. Tizanidine may act more potently on the imidazoline-receptors than the alpha 2-adrenoceptors.
在大鼠肾膜中检测了替扎尼定对3H-对氨基可乐定识别的咪唑啉受体和α2-肾上腺素能受体的选择性,并与其他咪唑啉化合物进行了比较。替扎尼定与咪唑啉受体结合的亲和力比α2-肾上腺素能受体高约20倍。对咪唑啉受体的相对选择性顺序为替扎尼定>羟甲唑啉>可乐定>萘甲唑啉,其中可乐定对两种受体表现出同等亲和力。替扎尼定对咪唑啉受体的作用可能比对α2-肾上腺素能受体更强。