Timmermans P B, Van Zwieten P A
Pharmacology. 1978;16(2):106-14. doi: 10.1159/000136754.
2-(2,6-Dichlorophenylimino)piperimidine with HNO3 (St-404), 2-(2,6-dichlorophenyl)-5,6-dihydroimidazo[2,1-b]thiazole fumarate (compound 44-549) and 1,2,3,5-tetrahydroimidazo[2,1-b]quinazoline with HCl (TIQ) were studied with respect to their effects on blood pressure and heart rate in the anaesthetized, normotensive rat following intravenous administration and in the chloralose-anaesthetized cat by means of infusions via the left vertebral artery. St-404 and compound 44-549 possess central hypotensive and bradycardic activities and display modes of action similar to that of clonidine. Central alpha-adrenergic receptors are presumably involved. In the anaesthetized, normotensive rat St-404 is about 3,400 times less active than clonidine, whereas compound 44-549 is 5 times more effective in lowering arterial pressure. The hypotensive effect of TIQ is brought about by a mechanism of action which is different from that of clonidine. The alpha-sympatholytic properties of TIQ suggested previously by others are not confirmed by the experiments presented in this paper.
研究了2-(2,6-二氯苯基亚氨基)哌啶与硝酸(St-404)、2-(2,6-二氯苯基)-5,6-二氢咪唑并[2,1-b]噻唑富马酸盐(化合物44-549)以及1,2,3,5-四氢咪唑并[2,1-b]喹唑啉与盐酸(TIQ)在静脉给药后对麻醉的正常血压大鼠的血压和心率的影响,以及通过左椎动脉输注对水合氯醛麻醉猫的影响。St-404和化合物44-549具有中枢性降压和心动过缓活性,其作用方式与可乐定相似。推测涉及中枢α-肾上腺素能受体。在麻醉的正常血压大鼠中,St-404的活性比可乐定低约3400倍,而化合物44-549在降低动脉血压方面的效果则比可乐定高5倍。TIQ的降压作用是通过一种与可乐定不同的作用机制实现的。本文所做的实验未证实其他人先前提出的TIQ的α-交感神经阻滞特性。