Hadházy P, Nagy L, Juhász F, Malomvölgyi B, Magyar K
Eur J Pharmacol. 1983 Aug 5;91(4):477-84. doi: 10.1016/0014-2999(83)90173-5.
The actions of indomethacin (IND), PGE2 and PGI2 were studied on the tone of isolated mesenteric arteries obtained from operated patients. The cyclooxygenase inhibitors IND (3 mumol/l) and suprofen (0.58 mumol/l) increased the resting tone and potentiated the contractile responses to electrical stimulation and noradrenaline. Low concentrations of PGE2 (0.7-5.6 X 10(-9) mol/l) decreased the baseline tone and reduced the stimulation-evoked contractions whereas higher concentrations (from 5.7 X 10(-8) mol/l) increased the tone of vessels. PGI2 (0.7-10.8 X 10(-9) mol/l) also relaxed IND-treated arteries but, in contrast to PGE2, it did not produce contraction even at a concentration of 10(-6) mol/l. Prostacyclin reduced the tone evoked and sustained by a high concentration of PGE2 or PGF2 alpha, the IC50 values being 46.2 or 7.9 X 10(-9) mol/l, respectively. The contractile responses to electrical stimulation and to noradrenaline were also inhibited by PGI2 (IC50 5.6 and 6.8 X 10(-9) mol/l, respectively). These results suggest that the smooth muscle cells of human mesenteric arteries are just as sensitive to IND, PGE2 and PGI2 as are those from laboratory animals. Our observations may be of clinical importance.
研究了吲哚美辛(IND)、前列腺素E2(PGE2)和前列环素(PGI2)对手术患者离体肠系膜动脉张力的作用。环氧合酶抑制剂IND(3 μmol/l)和舒洛芬(0.58 μmol/l)可增加静息张力,并增强对电刺激和去甲肾上腺素的收缩反应。低浓度的PGE2(0.7 - 5.6×10⁻⁹ mol/l)可降低基线张力并减少刺激诱发的收缩,而较高浓度(从5.7×10⁻⁸ mol/l起)则增加血管张力。PGI2(0.7 - 10.8×10⁻⁹ mol/l)也可使经IND处理的动脉舒张,但与PGE2不同的是,即使在10⁻⁶ mol/l的浓度下它也不会引起收缩。前列环素可降低高浓度PGE2或前列腺素F2α(PGF2α)诱发并维持的张力,其半数抑制浓度(IC50)值分别为46.2或7.9×10⁻⁹ mol/l。PGI2还可抑制对电刺激和去甲肾上腺素的收缩反应(IC50分别为5.6和6.8×10⁻⁹ mol/l)。这些结果表明,人肠系膜动脉的平滑肌细胞对IND、PGE2和PGI2的敏感性与实验动物的平滑肌细胞相同。我们的观察结果可能具有临床意义。