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首页> 外文期刊>Journal of biomedical science. >Effect of the effluent released from the canine internal mammary artery after intraluminal and extraluminal perfusion of acetylcholine and adenosine diphosphate
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Effect of the effluent released from the canine internal mammary artery after intraluminal and extraluminal perfusion of acetylcholine and adenosine diphosphate

机译:腔内和腔外灌注乙酰胆碱和二磷酸腺苷对犬乳腺内动脉释放出的影响

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Segments of the canine internal mammary artery (35 mm in length) were suspended in vitro in an organ chamber containing physiological salt solution (95% O2/5% CO2, pH = 7.4, 37°C). Segments were individually cannulated and perfused at 5 ml/minute using a roller pump. Vasorelaxant activity of the effluent from the perfused internal mammary arteries was bioassayed by measuring the decrease in tension induced by the effluent of the coronary artery endothelium-free ring which had been contracted with prostaglandin F2α (2 × 10-6 M). Intraluminal perfusion of adenosine diphosphate (10-5 M) induced significant increase in relaxant activity in the effluent from the perfused blood vessel. However, when adenosine diphosphate (10-5 M) was added extraluminally to the internal mammary artery, no change in relaxant activity in the effluent was noted. In contrast, acetylcholine produced significant increase in the relaxant activity on the effluent of the perfused internal mammary artery with both intraluminal and extraluminal perfusion. The intraluminal and extraluminal release of endothelium-derived relaxing factor (EDRF) by acetylcholine (10-5 M) can be inhibited by site-specific administration of atropine (10-5 M). These experiments indicate that certain agonists can induce the release of EDRF only by binding to intravascular receptors while other agonists can induce endothelium-dependent vasodilatation by acting on neural side receptors.
机译:将犬乳内动脉的各段(长35 mm)在体外悬浮在含有生理盐溶液(95%O2 / 5%CO2,pH = 7.4,37°C)的器官室内。分别对节段进行插管,并使用滚轴泵以5 ml / min的速度灌注。通过测量由前列腺素F2α(2×10-6 M)收缩的无冠状动脉内皮环的流出物引起的张力降低,生物测定了灌注的乳腺内动脉的流出物的血管舒张活性。腔内灌注二磷酸腺苷(10-5 M)导致灌注血管流出液中的松弛剂活性显着增加。但是,当将腺苷二磷酸(10-5 M)腔内外添加至乳内动脉时,流出液中的松弛活性没有变化。相反,在腔内和腔外灌注的情况下,乙酰胆碱对灌注的乳内动脉流出物的松弛活性显着增加。乙酰胆碱(10-5 M)可通过位点特异性阿托品(10-5 M)抑制内皮源性舒张因子(EDRF)在腔内和腔外的释放。这些实验表明,某些激动剂只能通过结合血管内受体来诱导EDRF的释放,而其他激动剂可以通过作用于神经旁受体来诱导内皮依赖性血管舒张。

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