Takayanagi I, Konno F, Ishii C, Takemasa T, Yanagida Y, Shimizu M, Mori H, Sugane H
Gen Pharmacol. 1984;15(3):239-41. doi: 10.1016/0306-3623(84)90166-6.
Tizanidine behaved as the partial agonist on the alpha 1-adrenoceptor in high doses (10(-6) -10(-4)M) and as the alpha 2-adrenoceptor agonist in low doses (3 X 10(-9) - 10(-6)M). Tizanidine is about one-third as potent as clonidine in alpha 2-agonistic effect
替扎尼定在高剂量(10⁻⁶ - 10⁻⁴M)时对α1 - 肾上腺素能受体表现为部分激动剂,在低剂量(3×10⁻⁹ - 10⁻⁶M)时为α2 - 肾上腺素能受体激动剂。替扎尼定的α2激动效应约为可乐定的三分之一。