The uptake of radiolabelled 14C-histamine into guinea-pig isolated left atria was determined. 2. Mepyramine up to 10(-7) M had no significant effect upon the uptake of total radioactivity. Metiamide (10(-4) M) produced a small but not significant inhibition of uptake. SK & F 91581 (10(-4) M) and amodiaquine (10(-4) M) both significantly inhibited uptake by 48.2 +/- 4.2 and 56.7 +/- 1.2% respectively. 3. The metabolism profiles of radiolabelled histamine after 5 and 30 min incubation were examined by thin-layer chromatography. 4. SK & F 91581 (10(-4) M) and amodiaquine (10(-4) M) reduced the proportion of N tau-methylhistamine and acid metabolites after a 30 min incubation. The levels of unmetabolized histamine were elevated. This may explain their inhibitory action upon histamine uptake. 5. The effects of mepyramine, metiamide, SK & F 91581 and amodiaquine were then examined upon the positive inotropic and chronotropic responses of isolated left and right atria to histamine. 6. Mepyramine (10(-7) M) inhibited the positive inotropic responses only (H1), whereas metiamide (10(-4) M) inhibited the positive chronotropic responses only (H2). SK & F 91581 (10(-4) M) had no effect upon these responses and amodiaquine (10(-5) M) depressed the maxima of the rate response dose-response curves. 7. The relationship between uptake and metabolism of histamine and its pharmacological response is discussed.
摘要
测定了放射性标记的14C-组胺在豚鼠离体左心房中的摄取情况。2. 高达10(-7) M的美吡拉敏对总放射性摄取无显著影响。甲硫咪特(10(-4) M)对摄取产生了轻微但不显著的抑制作用。SK & F 91581(10(-4) M)和阿莫地喹(10(-4) M)分别显著抑制摄取48.2±4.2%和56.7±1.2%。3. 通过薄层色谱法检测了孵育5分钟和30分钟后放射性标记组胺的代谢谱。4. 孵育30分钟后,SK & F 91581(10(-4) M)和阿莫地喹(10(-4) M)降低了Nτ-甲基组胺和酸性代谢产物的比例。未代谢组胺的水平升高。这可能解释了它们对组胺摄取的抑制作用。5. 然后研究了美吡拉敏、甲硫咪特、SK & F 91581和阿莫地喹对离体左、右心房对组胺的正性肌力和变时性反应的影响。6. 美吡拉敏(10(-7) M)仅抑制正性肌力反应(H1),而甲硫咪特(10(-4) M)仅抑制正性变时性反应(H2)。SK & F 91581(10(-4) M)对这些反应无影响,阿莫地喹(10(-5) M)降低了速率反应剂量-反应曲线的最大值。7. 讨论了组胺的摄取、代谢与其药理反应之间的关系。