Darmani N A, Broadley K J
Eur J Pharmacol. 1986 Jun 24;125(3):353-62. doi: 10.1016/0014-2999(86)90791-0.
Adenosine, theophylline and enprofylline induced concentration-dependent relaxations of guinea-pig isolated tracheal spirals whether they had intrinsic tone or were precontracted with carbachol or histamine. The potency order was enprofylline greater than theophylline greater than adenosine and the maximum relaxation in absolute terms was generally less for adenosine. The maximum relaxation (measured in absolute terms of change in tension) induced by the three spasmolytics in preparations with intrinsic tone was generally less than in precontracted tissues. This was attributed to the higher resting tone of precontracted tissues than the intrinsic tone. The adenosine transport inhibitor dipyridamole potentiated adenosine but not theophylline or enprofylline so that the potency order became adenosine greater than enprofylline greater than theophylline. Without dipyridamole, theophylline in a concentration producing 10-30% relaxation of the trachea, failed to antagonize adenosine. However, in the presence of dipyridamole, adenosine was antagonized, indicating that the relaxation by adenosine was mediated via an extracellular P1 receptor. Enprofylline, in a concentration producing equivalent direct effects, failed to antagonize adenosine. It is concluded that the tracheal relaxation by xanthines is independent of adenosine antagonism.
腺苷、茶碱和恩丙茶碱可引起豚鼠离体气管螺旋条浓度依赖性舒张,无论其有无内在张力,或已用卡巴胆碱或组胺预收缩。效价顺序为恩丙茶碱大于茶碱大于腺苷,腺苷的绝对最大舒张通常较小。三种解痉剂在有内在张力的制剂中引起的最大舒张(以张力变化的绝对值衡量)通常小于在预收缩组织中的舒张。这归因于预收缩组织的静息张力高于内在张力。腺苷转运抑制剂双嘧达莫增强腺苷的作用,但不增强茶碱或恩丙茶碱的作用,因此效价顺序变为腺苷大于恩丙茶碱大于茶碱。在没有双嘧达莫的情况下,产生气管10 - 30%舒张的浓度的茶碱不能拮抗腺苷。然而,在双嘧达莫存在的情况下,腺苷被拮抗,这表明腺苷的舒张作用是通过细胞外P1受体介导的。产生等效直接作用浓度的恩丙茶碱不能拮抗腺苷。结论是黄嘌呤类药物引起的气管舒张与腺苷拮抗无关。