Henry J G, Mitnick M, Dann P R, Stewart A F
Division of Endocrinology, Veterans Administration Connecticut Healthcare System, West Haven 06516, USA.
J Clin Endocrinol Metab. 1997 Mar;82(3):900-6. doi: 10.1210/jcem.82.3.3811.
PTH-related protein (PTHrP) is responsible for most cases of humoral hypercalcemia of malignancy (HHM). It mimics the actions of PTH as a result of its structural homology with PTH and its ability to bind to and signal via the PTH/PTHrP receptor in bone and kidney. PTHrP-(1-36) appears to be one of several secretory forms of PTHrP. This peptide has been administered iv to normal volunteers previously and has been shown to produce effects that are qualitatively and quantitatively the same as those produced by PTH-(1-34). To determine whether PTHrP-(1-36) could be used sc in humans as a diagnostic reagent for elucidating the differences between HHM and hyperparathyroidism, we performed a 12-h dose-finding study examining whether sc PTHrP-(1-36) could elicit effects on mineral homeostasis. PTHrP-(1-36) administered sc in three doses (0.82, 1.64, and 3.28 micrograms/kg) to 21 normal women produced increases in circulating PTHrP-(1-36), reductions in serum phosphorus and the renal phosphorus threshold, increments in fractional calcium excretion and nephrogenous cAMP excretion, and increases in plasma 1,25-dihydroxyvitamin D. These changes were highly significant in statistical terms and were observed at doses that had no effect on serum calcium or endogenous PTH. These studies demonstrate the feasibility of using PTHrP-(1-36) as a diagnostic probe for future studies aimed at elucidating the differing pathophysiologies of HHM and hyperparathyroidism.
甲状旁腺激素相关蛋白(PTHrP)是大多数恶性肿瘤体液性高钙血症(HHM)的病因。由于其与甲状旁腺激素(PTH)的结构同源性,以及它与骨和肾脏中的PTH/PTHrP受体结合并通过该受体发出信号的能力,PTHrP模拟了PTH的作用。PTHrP-(1-36)似乎是PTHrP的几种分泌形式之一。此前已将该肽静脉注射给正常志愿者,并已证明其产生的效应在定性和定量上与PTH-(1-34)产生的效应相同。为了确定PTHrP-(1-36)是否可在人体中皮下注射用作诊断试剂,以阐明HHM与甲状旁腺功能亢进之间的差异,我们进行了一项为期12小时的剂量探索研究,检查皮下注射PTHrP-(1-36)是否能引起对矿物质稳态的影响。对21名正常女性皮下注射三种剂量(0.82、1.64和3.28微克/千克)的PTHrP-(1-36)后,循环中的PTHrP-(1-36)增加,血清磷和肾磷阈值降低,钙排泄分数和肾源性环磷酸腺苷排泄增加,血浆1,25-二羟维生素D增加。这些变化在统计学上具有高度显著性,并且在对血清钙或内源性PTH无影响的剂量下观察到。这些研究证明了将PTHrP-(1-36)用作诊断探针用于未来旨在阐明HHM和甲状旁腺功能亢进不同病理生理学的研究的可行性。