Guder W G, Rupprecht A
Pflugers Arch. 1975;354(2):177-86. doi: 10.1007/BF00579947.
Isolated rat kidney cortex tubules were used as a model system to study the hormonal regulation of cyclic adenosine-3':5'-monophosphate (cAMP) levels in vitro. When incubated over 15 min, parathyroid hormone increased cAMP levels 4-fold in the absence of inhibitors of cAMP phosphodiesterase. Norepinephrine in a concentration of 5-10-7 M which had itself no effect on cAMP levels under this condition, inhibited the effect of parathyroid hormone by 50%. This effect of the catecholamines could be completely abolished by the addition of an alpha-receptor blocking agent, phentolamine. The addition of an inhibitor of cAMP phosphodiesterase, in a concentration sufficient to prevent the breakdown of extratubular cAMP, potentiated hormone effects on cAMP levels. The antagonism between catecholamines and parathyroid hormone on cAMP levels was however not abolished by this treatment. This indicated that catecholamines probably inhibited parathyroid hormone stimulated cAMP formation. Since most of the cAMP was found to be intratubular, it can be assumed that norepinephrine and parathyroid hormone interact in the same cell. Proximal tubular sodium reabsorption and renal gluconeogenesis are discussed as possible events of this hormone interaction.
分离的大鼠肾皮质肾小管被用作体外研究环磷腺苷(cAMP)水平激素调节的模型系统。在无cAMP磷酸二酯酶抑制剂的情况下孵育15分钟以上时,甲状旁腺激素可使cAMP水平增加4倍。在此条件下,浓度为5×10⁻⁷M的去甲肾上腺素本身对cAMP水平无影响,但可使甲状旁腺激素的作用降低50%。加入α受体阻断剂酚妥拉明可完全消除儿茶酚胺的这种作用。加入足以防止管外cAMP分解的cAMP磷酸二酯酶抑制剂可增强激素对cAMP水平的作用。然而,这种处理并未消除儿茶酚胺与甲状旁腺激素在cAMP水平上的拮抗作用。这表明儿茶酚胺可能抑制甲状旁腺激素刺激的cAMP形成。由于发现大部分cAMP存在于肾小管内,因此可以推测去甲肾上腺素和甲状旁腺激素在同一细胞中相互作用。近端肾小管钠重吸收和肾糖异生被作为这种激素相互作用的可能事件进行了讨论。