De Mello W C
Eur J Pharmacol. 1977 Sep 15;45(2):153-63. doi: 10.1016/0014-2999(77)90085-1.
The influence of phosphodiesterase inhibitors, imidazole and dBcAMP on the action of histamine on peak tension, on rate of tension development and rate of relaxation of ventricular muscle of guinea pig's heart was investigated. It was found that theophylline plus dBcAMP enhanced the peak tension, (dF/dt)max and the rate of relaxation and increased the relaxing action of histamine. Imidazole, an activator of phosphodiesterase, also potentiated the action of histamine on peak tension, (dF/dt)max and rate of relaxation. Caffeine, a well-known inhibitor of phosphodiesterase, suppressed the relaxing action of histamine and epinephrine. These discrepant results could be explained by assuming the possibility that these drugs have effects other than those involving inhibition and activation of phosphodiesterase.
研究了磷酸二酯酶抑制剂、咪唑和二丁酰环磷腺苷(dBcAMP)对组胺作用于豚鼠心脏心室肌的峰值张力、张力发展速率和舒张速率的影响。结果发现,茶碱加dBcAMP增强了峰值张力、最大(dF/dt)和舒张速率,并增强了组胺的舒张作用。磷酸二酯酶激活剂咪唑也增强了组胺对峰值张力、最大(dF/dt)和舒张速率的作用。著名的磷酸二酯酶抑制剂咖啡因抑制了组胺和肾上腺素的舒张作用。这些不一致的结果可以通过假设这些药物除了具有抑制和激活磷酸二酯酶的作用外还具有其他作用来解释。