猫肠系膜血管床中吲哚美辛血管收缩活性的表征

H.L. Lippton, W.M. Armstead, A.L. Hyman, P.J. Kadowitz
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引用次数: 14

摘要

在恒定血流条件下,研究了吲哚美辛对猫肠系膜血管床血管阻力的影响。吲哚美辛产生的肠系膜血管收缩是剂量依赖性的,但活性低于U46619、血栓素模拟物、血管紧张素II、PGF2α和去甲肾上腺素。甲氯芬胺和苯氧苄胺对吲哚美辛的血管收缩反应没有改变。吲哚美辛的剂量阻断了花生四烯酸对全身血管抑制剂的反应,但没有改变肠系膜血管收缩剂对交感神经刺激、去甲肾上腺素、血管紧张素II、U46619和U44609的反应。目前的数据表明,在猫肠道血管床中,吲哚美辛具有明显的血管收缩活性,这种活性不依赖于α -肾上腺素受体的激活和具有加压活性的环加氧酶产物的形成。目前的数据表明,环氧化酶产物不调节血管收缩反应以及交感神经系统在猫的肠道血管床。
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Characterization of the vasoconstrictor activity of indomethacin in the mesenteric vascular bed of the cat

The effects of indomethacin on vascular resistance were investigated in the feline mesenteric vascular bed under conditions of constant blood flow. Indomethacin produced mesenteric vasoconstriction that was dose-dependent but was less active than U46619, the thromboxane mimic, angiotensin II, PGF and norepinephrine. The vasoconstrictor response to indomethacin was not altered by meclofenamate and phenoxybenzamine. Indomethacin, in a dose that blocked the systemic vasodepressor response to arachidonic acid, did not alter mesenteric vasoconstrictor responses to sympathetic nerve stimulation, norepinephrine, angiotensin II, U46619, and U44609. The present data suggest that in the feline intestinal vascular bed indomethacin has marked vasoconstrictor activity that occurs independent of activation of alpha-adrenoceptors and formation of cyclooxygenase products possessing pressor activity. The present data suggest that cyclooxygenase products do not modulate vasoconstrictor responses as well as the sympathetic nervous system in the intestinal vascular bed of the cat.

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