Meisheri K D, McNeill J H
Am J Physiol. 1979 Nov;237(5):C257-63. doi: 10.1152/ajpcell.1979.237.5.C257.
The influence of alteration in the Ca2+ environment of the tissue on isoproterenol-induced increases in cAMP levels and relaxation was studied in rat uterus. In muscles depolarized with 47.5 mM K+ (with or without Na+), the ability of isoproterenol to increase cAMP levels and to produce relaxation was found to be inversely related to external calcium concentration. The pretreatment of the muscle with D600 or EGTA restored the cAMP response to isoproterenol in the depolarized uterus to a level observed in nondepolarized muscle. The study with Ro 20-1724, a phosphodiesterase (PDE) inhibitor indicated that the failure of isoproterenol to elevate cAMP levels in the depolarized uterus could not be related to the activation of PDE by Ca2+. The exposure of rat uterus to a zero-Ca2+ solution accentuated the increases in cAMP levels produced by isoproterenol. These results have raised the question of a possible regulatory role of Ca2+ in beta-adrenoceptor-induced increases in cAMP levels in uterine smooth muscle.
在大鼠子宫中研究了组织Ca2+环境改变对异丙肾上腺素诱导的cAMP水平升高和舒张的影响。在用47.5 mM K+(有或无Na+)使肌肉去极化的情况下,发现异丙肾上腺素升高cAMP水平和产生舒张的能力与细胞外钙浓度呈负相关。用D600或EGTA预处理肌肉可使去极化子宫中对异丙肾上腺素的cAMP反应恢复到在非去极化肌肉中观察到的水平。用磷酸二酯酶(PDE)抑制剂Ro 20-1724进行的研究表明,异丙肾上腺素在去极化子宫中未能升高cAMP水平与Ca2+激活PDE无关。将大鼠子宫暴露于零钙溶液中会加剧异丙肾上腺素引起的cAMP水平升高。这些结果提出了Ca2+在子宫平滑肌β-肾上腺素能受体诱导的cAMP水平升高中可能具有调节作用的问题。