Enero M A
Acta Physiol Lat Am. 1979;29(2-3):101-6.
A study was made on the force of spontaneous mechanical activity in the rat portal vein. Prostaglandin inhibitor, sodium meclofenamate, phosphodiesterase inhibitors, aminophylline and dipyridamole, adenosine and blockade of calcium entry by isoptin all reduced the force of spontaneous activity in a concentration-dependent manner, while imidazole enhanced it. Low concentration of aminophylline (10 microM), dipyridamole (6 microM) and meclofenamate (10 microM) depressed the spontaneous contraction of the vein by about 50% without modifying the response to noradrenaline. At higher concentration of these drugs, spontaneous mechanical contraction was reduced further and the response to noradrenaline antagonized. Low concentration of isoptin also reduced the mechanical activity without affecting maximum response to noradrenaline. A common mechanism of action for the drugs tested, namely the limiting of Ca2+ availability for muscular contraction, is discussed. Adenosine markedly reduced the spontaneous mechanical activity of the rat portal vein. Its relaxation effect could be due to the activation of a specific adenosine receptor.
对大鼠门静脉的自发机械活动力进行了一项研究。前列腺素抑制剂甲氯芬那酸钠、磷酸二酯酶抑制剂氨茶碱和双嘧达莫、腺苷以及异搏定对钙内流的阻断均以浓度依赖的方式降低了自发活动力,而咪唑则增强了自发活动力。低浓度的氨茶碱(10微摩尔)、双嘧达莫(6微摩尔)和甲氯芬那酸钠(10微摩尔)使静脉的自发收缩降低约50%,而不改变对去甲肾上腺素的反应。在这些药物的较高浓度下,自发机械收缩进一步降低,且对去甲肾上腺素的反应受到拮抗。低浓度的异搏定也降低了机械活动,而不影响对去甲肾上腺素的最大反应。讨论了所测试药物的共同作用机制,即限制Ca2+用于肌肉收缩的可用性。腺苷显著降低了大鼠门静脉的自发机械活动。其舒张作用可能归因于特定腺苷受体的激活。