Rosol T J, Capen C C
Department of Veterinary Pathobiology, Ohio State University, Columbus 43210.
Endocrinology. 1988 May;122(5):2098-102. doi: 10.1210/endo-122-5-2098.
In vitro bone resorption induced by tumor extract derived from a hypercalcemic canine adenocarcinoma was significantly inhibited by the PTH receptor antagonist, [Nle8,18,Tyr34]bovine (b) PTH-(3-34) amide. Dose-response curves were prepared for in vitro bone resorption induced in neonatal mouse calvaria by tumor extract, bPTH-(1-34), and prostaglandin E2. A 1:2000-fold ratio of bPTH-(1-34) to [Nle8,18,Tyr34]bPTH-(3-34) amide significantly inhibited bone resorption induced by bPTH-(1-34); however, a 1:10,000 ratio completely antagonized bone resorption. At equivalent potency (1.80-fold stimulation of in vitro bone resorption) of tumor extract compared to bPTH-(1-34), [Nle8,18,Tyr34]bPTH-(3-34) amide (5.0 microM) was capable of significantly reducing in vitro bone resorption. Bone resorption induced by tumor extract (1.35-fold stimulation) was inhibited by [Nle8,18,Tyr34]bPTH-(3-34) amide at concentrations of 5.0 and 1.0 microM. Bone resorption induced by prostaglandin E2 (300 nM) was not inhibited by [Nle8,18,Tyr34]bPTH-(3-34) amide (5.0 microM). These data indicate that [Nle8,18,Tyr34]bPTH-(3-34) amide antagonizes in vitro bone resorption induced by bPTH-(1-34) in a dose-dependent manner and significantly inhibits bone resorption induced by the canine adenocarcinoma model of humoral hypercalcemia of malignancy.
甲状旁腺激素(PTH)受体拮抗剂[Nle8,18,Tyr34]牛(b)PTH-(3-34)酰胺可显著抑制由高钙血症犬腺癌衍生的肿瘤提取物诱导的体外骨吸收。制备了肿瘤提取物、bPTH-(1-34)和前列腺素E2诱导新生小鼠颅骨体外骨吸收的剂量反应曲线。bPTH-(1-34)与[Nle8,18,Tyr34]bPTH-(3-34)酰胺的1:2000倍比例可显著抑制bPTH-(1-34)诱导的骨吸收;然而,1:10000的比例可完全拮抗骨吸收。与bPTH-(1-34)相比,当肿瘤提取物具有同等效力(体外骨吸收刺激1.80倍)时,[Nle8,18,Tyr34]bPTH-(3-34)酰胺(5.0 microM)能够显著降低体外骨吸收。肿瘤提取物诱导的骨吸收(刺激1.35倍)在浓度为5.0和1.0 microM时被[Nle8,18,Tyr34]bPTH-(3-34)酰胺抑制。前列腺素E2(300 nM)诱导的骨吸收未被[Nle8,18,Tyr34]bPTH-(3-34)酰胺(5.0 microM)抑制。这些数据表明,[Nle8,18,Tyr34]bPTH-(3-34)酰胺以剂量依赖性方式拮抗bPTH-(1-34)诱导的体外骨吸收,并显著抑制恶性肿瘤体液性高钙血症犬腺癌模型诱导的骨吸收。