Allen J M, Burke E P, Johnston M G, McHale N G
Br J Pharmacol. 1984 Jun;82(2):509-14. doi: 10.1111/j.1476-5381.1984.tb10787.x.
Spontaneous contractions and those elicited by two different methods of electrical stimulation were studied in isolated segments of bovine mesenteric lymphatic vessels. The effect of aspirin (a cyclo-oxygenase inhibitor) on spontaneous and evoked contractions of isolated lymphatic vessels was investigated. Aspirin at doses of 10(-6) M or greater depressed both spontaneous and action potential-dependent evoked contractions, but failed to inhibit contractions evoked by high current field stimulation. These latter contractions were rapidly depressed by the application of D600. When aspirin was applied for five minute periods, inhibition never occurred within the period of drug administration but was delayed, with maximum inhibition occurring approximately 10 min after washout of the drug. It is concluded that the inhibitory action of aspirin is unlikely to be a non-specific depression of the contractile mechanism, but rather a reduction in excitability probably as a result of cyclo-oxygenase inhibition.
在牛肠系膜淋巴管的离体节段中研究了自发收缩以及由两种不同电刺激方法引发的收缩。研究了阿司匹林(一种环氧化酶抑制剂)对离体淋巴管自发收缩和诱发收缩的影响。剂量为10^(-6) M或更高的阿司匹林可抑制自发收缩和依赖动作电位的诱发收缩,但不能抑制高电流场刺激诱发的收缩。后一种收缩可被D600迅速抑制。当应用阿司匹林5分钟时,在给药期间从未发生抑制作用,而是延迟出现,最大抑制作用大约在药物洗脱后10分钟出现。结论是,阿司匹林的抑制作用不太可能是对收缩机制的非特异性抑制,而更可能是由于环氧化酶抑制导致的兴奋性降低。