Forte L R, Carnes D L, Nickols G A, Anast C S
J Supramol Struct. 1978;9(2):179-88. doi: 10.1002/jss.400090204.
Rats fed a diet deficient in vitamin D were found to exhibit a refractory cyclic AMP response of kidney slices to parathyroid hormone and a marked decrease in membrane parathyroid hormone-dependent adenylate cyclase activity. Both the characteristic calcium deficiency (hypocalcemia) and secondary elevation of circulating parathyroid hormone appeared before the first noticeable decrease in hormone-dependent enzyme activity. After repletion of D-deficient rats with vitamin D2, we found that serum calcium and parathyroid hormone were both restored to normal levels before the depressed enzyme response to the hormone was reversed. Moreover, infusion of parthyroid hormone into vitamin D-replete rats led to a marked reduction in parathyroid hormone-dependent adenylate cyclase activity, which was partly restored to control level 3 hours after discontinuing the hormone infusion. Taken as a whole, this study suggests that the elevated endogenous parathyroid hormone in the vitamin D-deficient rat is involved in the "down-regulation" of renal cyclic AMP responsiveness to the hormone. However, these experiments do not rule out the possibility that calcium deficiency and/or vitamin D per se participate in the regulation of the renal cyclic AMP response to parathyroid hormone.
研究发现,喂食缺乏维生素D饮食的大鼠,其肾切片对甲状旁腺激素呈现出难治性的环磷酸腺苷(cAMP)反应,且膜上依赖甲状旁腺激素的腺苷酸环化酶活性显著降低。在激素依赖性酶活性首次出现明显下降之前,特征性的钙缺乏(低钙血症)和循环甲状旁腺激素的继发性升高就已出现。在用维生素D2补充缺乏维生素D的大鼠后,我们发现血清钙和甲状旁腺激素在激素依赖性酶反应的抑制被逆转之前就已恢复到正常水平。此外,向维生素D充足的大鼠输注甲状旁腺激素会导致依赖甲状旁腺激素的腺苷酸环化酶活性显著降低,在停止激素输注3小时后,该活性部分恢复到对照水平。总体而言,这项研究表明,维生素D缺乏大鼠体内内源性甲状旁腺激素升高与肾脏对该激素的环磷酸腺苷反应性“下调”有关。然而,这些实验并未排除钙缺乏和/或维生素D本身参与调节肾脏对甲状旁腺激素的环磷酸腺苷反应的可能性。