The effects of the phosphodiesterase inhibitors caffeine, theophylline, isobutylmethylxanthine (IBMX) and rolipram on spontaneous electrical activity (slow waves) were studied in the circular muscle of the guinea-pig gastric antrum. 2. All the inhibitors reduced slow wave frequency without changing the membrane potential and the slow wave configuration, but at higher concentrations they blocked the slow waves and caused membrane hyperpolarization. In the presence of the inhibitors a low level of irregular electrical activity could be observed in many preparations. 3. Isoprenaline, forskolin, dibutyryl cAMP and 8-bromo-cAMP all produced effects essentially similar to those of phosphodiesterase inhibitors. K+ (12 mM) and removal of K+ both depolarized the membrane and these were not affected by IBMX (1-3 microM). A decrease in frequency caused by IBMX was also not significantly affected by 12 mM K+ or K+ removal and only partially antagonized by TEA or 4-aminopyridine. 4. These results suggest that an increase in intracellular cAMP inhibits pacemaker activity of slow waves. An increase in K+ conductance does not seem to be a major factor in this inhibition. Slow waves appear to be a compound electrical activity in a group of muscle cells and are likely to be disintegrated by xanthine derivatives.
摘要
研究了磷酸二酯酶抑制剂咖啡因、茶碱、异丁基甲基黄嘌呤(IBMX)和咯利普兰对豚鼠胃窦环行肌自发性电活动(慢波)的影响。2. 所有抑制剂均降低慢波频率,而不改变膜电位和慢波形态,但在较高浓度时它们阻断慢波并引起膜超极化。在抑制剂存在的情况下,许多标本中可观察到低水平的不规则电活动。3. 异丙肾上腺素、福斯可林、二丁酰环磷腺苷和8-溴环磷腺苷产生的效应与磷酸二酯酶抑制剂基本相似。12 mM K⁺ 和去除K⁺ 均使膜去极化,且这些不受1 - 3 μM IBMX的影响。由IBMX引起的频率降低也不受12 mM K⁺ 或去除K⁺ 的显著影响,且仅部分被四乙铵或4 - 氨基吡啶拮抗。4. 这些结果表明细胞内cAMP增加会抑制慢波的起搏活动。K⁺ 电导增加似乎不是这种抑制的主要因素。慢波似乎是一组肌肉细胞中的复合电活动,并且很可能被黄嘌呤衍生物瓦解。