Timmermans P B, Van Zwieten P A
Eur J Pharmacol. 1977 Oct 1;45(3):229-36. doi: 10.1016/0014-2999(77)90003-6.
The central hypotensive activity of clonidine and of 12 structurally related analogues was determined following intravenous administration to pentobarbital-anaesthetized, normotensive rats. This sympathoinhibitory action was characterized by means of a pC30, calculated from dose-response curves. The centrally mediated depressor activity (pC30) was correlated with the peripherally induced pressor activity of the compounds (pC100) reported on previously and which had been established after intravenous application to pithed rats. In these correlations, the quantitative ability of the substances to penetrate into the central nervous system had been taken into account. The octanol/buffer (pH = 7.4) partition coefficients were used as a measure of lipophilic behaviour. A positive correlation was found between the central hypotensive activity and the linear combination of peripheral alpha-sympathomimetic activity and lipophilicity.
在戊巴比妥麻醉的正常血压大鼠静脉注射后,测定可乐定及12种结构相关类似物的中枢性降压活性。这种交感神经抑制作用通过从剂量反应曲线计算得出的pC30来表征。中枢介导的降压活性(pC30)与先前报道的化合物外周诱导的升压活性(pC100)相关,后者是在向脊髓切断大鼠静脉给药后确定的。在这些相关性研究中,已考虑到物质渗透到中枢神经系统的定量能力。用辛醇/缓冲液(pH = 7.4)分配系数作为亲脂行为的量度。发现中枢降压活性与外周α-拟交感神经活性和亲脂性的线性组合之间存在正相关。