Doxey J C
Eur J Pharmacol. 1979 Feb 15;54(1-2):185-9. doi: 10.1016/0014-2999(79)90423-0.
In the pithed rat electrically induced contractions of the anococcygeus muscle were inhibited by clonidine (0.1--3.0 microgram/kg, i.v.), mecamylamine (1 mg/kg, i.v.) and guanethidine (1 mg/kg, i.v.). Only the inhibition produced by clonidine was antagonised by yohimbine (0.3 mg/kg, i.v.). At higher concentrations (10 microgram/kg, i.v.) clonidine increased the resting tension of the tissue; this effect was antagonised by phentolamine (1 mg/kg, i.v.). The anococcygeus muscle of the pithed rat was used to simultaneously assess pre- and postsynaptic alpha-adrenoceptor agonist activity. Guanfacin was more selective and tiamenidine less selective than clonidine for presynaptic alpha-adrenoceptors. Naphazoline and oxymetazoline were selective postsynaptic alpha-adrenoceptor agonists.
在脊髓横断的大鼠中,可乐定(0.1 - 3.0微克/千克,静脉注射)、美加明(1毫克/千克,静脉注射)和胍乙啶(1毫克/千克,静脉注射)可抑制电刺激引起的肛门尾骨肌收缩。只有可乐定产生的抑制作用可被育亨宾(0.3毫克/千克,静脉注射)拮抗。在较高浓度(10微克/千克,静脉注射)时,可乐定可增加组织的静息张力;此作用可被酚妥拉明(1毫克/千克,静脉注射)拮抗。脊髓横断大鼠的肛门尾骨肌用于同时评估突触前和突触后α-肾上腺素能受体激动剂活性。与可乐定相比,胍法辛对突触前α-肾上腺素能受体更具选择性,而噻美尼定选择性较低。萘甲唑啉和羟甲唑啉是选择性突触后α-肾上腺素能受体激动剂。