Shikada K, Yamamoto A, Tanaka S
Shiraoka Research Station of Biological Science, Nissan Chemical Ind., Ltd., Saitama, Japan.
Eur J Pharmacol. 1991 Apr 3;195(3):389-94. doi: 10.1016/0014-2999(91)90480-e.
The relaxant effect of vasoactive intestinal peptide (VIP) was investigated in isolated guinea-pig trachea in the presence of the phosphodiesterase (PDE) inhibitors, papaverine and 3-isobutyl-1-methylxanthine (IBMX), and the results were compared to those obtained with the cyclic AMP-dependent bronchodilators, isoproterenol and prostaglandin E2 (PGE2). The relaxant effect of VIP was greater when the magnitude of the leukotriene D4 (LTD4)-induced contraction was smaller. A similar effect was also observed for the relaxation induced by isoproterenol but not by PGE2. In the presence of papaverine (1 microM) and IBMX (3 microM), which reduced the 30 nM LTD4-induced contraction to the same extent, the relaxant effect of VIP was not changed, whereas the relaxant effects of isoproterenol and PGE2 were significantly potentiated. The potentiating effect of PDE inhibitors was also observed for the relaxation induced by the adenylate cyclase activator, forskolin, but not for the relaxation induced by the guanylate cyclase activator, sodium nitroprusside. These results suggest that the relaxation induced by VIP is different from that induced by cyclic AMP-dependent bronchodilator in the guinea-pig trachea.
在磷酸二酯酶(PDE)抑制剂罂粟碱和3-异丁基-1-甲基黄嘌呤(IBMX)存在的情况下,研究了血管活性肠肽(VIP)对豚鼠离体气管的舒张作用,并将结果与环磷酸腺苷(cAMP)依赖性支气管扩张剂异丙肾上腺素和前列腺素E2(PGE2)的作用结果进行比较。当白三烯D4(LTD4)诱导的收缩幅度较小时,VIP的舒张作用更强。异丙肾上腺素诱导的舒张也观察到类似效应,但PGE2诱导的舒张未观察到。在罂粟碱(1 microM)和IBMX(3 microM)存在的情况下,二者将30 nM LTD4诱导的收缩降低到相同程度,此时VIP的舒张作用未改变,而异丙肾上腺素和PGE2的舒张作用显著增强。对于腺苷酸环化酶激活剂福斯可林诱导的舒张,也观察到PDE抑制剂的增强作用,但对于鸟苷酸环化酶激活剂硝普钠诱导的舒张则未观察到。这些结果表明,在豚鼠气管中,VIP诱导的舒张与cAMP依赖性支气管扩张剂诱导的舒张不同。