Kondo K, Misumi J, Okuno T, Nakamura R, Saruta T, Kato E
Prostaglandins Med. 1979 Jan;2(1):67-75. doi: 10.1016/s0161-4630(79)80010-5.
The effects of prostaglandin E2 (PGE2) and indomethacin on the vascular reactivity to norepinephrine were tested in three different isolated rat vascular beds (mesenteric artery, hind limb and splenic artery) perfused with the Krebs bicarbonate solution. In these vascular beds PGE2 (0.1-64 ng/ml) or indomethacin (09.1-96 microgram/ml) in the perfusate did not change the basal pressure. In the mesenteric vascular bed and the hind limb, PGE2 dose-dependently potentiated the vascular response to norephinephrine, whereas PGE2 dose-dependently inhibited the vascular response to norepinephrine in the splenic artery. In these three vascular beds indomethacin in the perfusate dose-dependently attenuated the vascular response to norepinephrine. In the mesenteric artery and the hind limb PGE2 restored the effect of indomethacin, but in the splenic artery PGE2 did not restore the inhibitory effect of indomethacin. These results indicate that the modulating effect of exogenously administrated PGE2 on the vascular action to norepinephrine varies in different vascular beds. It is also suggested that the contribution of endogenous PGE2 synthesized in the vascular wall to the vascular reactivity to norepinephrine is, as well as the effect of exogenous PGE2, different in different vascular beds.
在三种不同的用 Krebs 碳酸氢盐溶液灌注的离体大鼠血管床(肠系膜动脉、后肢和脾动脉)中,测试了前列腺素 E2(PGE2)和吲哚美辛对血管对去甲肾上腺素反应性的影响。在这些血管床中,灌注液中的 PGE2(0.1 - 64 ng/ml)或吲哚美辛(09.1 - 96 μg/ml)不会改变基础压力。在肠系膜血管床和后肢中,PGE2 剂量依赖性地增强血管对去甲肾上腺素的反应,而在脾动脉中,PGE2 剂量依赖性地抑制血管对去甲肾上腺素的反应。在这三种血管床中,灌注液中的吲哚美辛剂量依赖性地减弱血管对去甲肾上腺素的反应。在肠系膜动脉和后肢中,PGE2 恢复了吲哚美辛的作用,但在脾动脉中,PGE2 并未恢复吲哚美辛的抑制作用。这些结果表明,外源性给予的 PGE2 对血管对去甲肾上腺素作用的调节作用在不同血管床中有所不同。还表明,血管壁中合成的内源性 PGE2 对血管对去甲肾上腺素反应性的贡献,与外源性 PGE2 的作用一样,在不同血管床中也不同。