Bell C
Br J Pharmacol. 1974 Sep;52(1):13-7. doi: 10.1111/j.1476-5381.1974.tb09681.x.
1 In the isolated, perfused parametrial artery of the guinea-pig dipyridamole (10-100 ng/ml) potentiated dilator responses to adenosine 5'-triphosphate (ATP), glyceryl trinitrate and non-cholinergic, non-adrenergic inhibitory nerve stimulation to similar extents. In contrast dilator responses to acetylcholine were generally unaffected or reduced.2 These results support previous electro-physiological evidence that in this preparation cholinergic vasodilatation is mediated by a cellular mechanism different from that involved in the response to non-cholinergic dilator nervous activation.3 The results also suggest that potentiation of a neurally-mediated inhibitory response of smooth muscle by dipyridamole does not necessarily implicate ATP as the transmitter involved in this response.
在豚鼠离体灌注的子宫旁动脉中,双嘧达莫(10 - 100纳克/毫升)增强了对5'-三磷酸腺苷(ATP)、硝酸甘油以及非胆碱能、非肾上腺素能抑制神经刺激的舒张反应,增强程度相似。相比之下,对乙酰胆碱的舒张反应通常未受影响或减弱。
这些结果支持了先前的电生理学证据,即在该制剂中,胆碱能血管舒张是由一种不同于对非胆碱能舒张神经激活反应所涉及的细胞机制介导的。
结果还表明,双嘧达莫对平滑肌神经介导的抑制反应的增强并不一定意味着ATP是参与该反应的递质。