Division of Endocrinology, Diabetes and Hypertension, Department of Medicine, Brigham and Women's Hospital and Harvard Medical School, EBRC 223A, 221 Longwood Ave, Boston, MA 02115, United States.
Biochem Pharmacol. 2010 Aug 1;80(3):297-307. doi: 10.1016/j.bcp.2010.04.002. Epub 2010 Apr 9.
Calcimimetics, which activate the extracellular calcium (Ca(o)(2+))-sensing receptor in the parathyroid and other tissues participating in Ca(o)(2+) homeostasis, were the first described allosteric activators of a G-protein-coupled receptor. Cinacalcet, the only calcimimetic currently approved for human use, is used clinically for treating secondary hyperparathyroidism (e.g., overactivity of parathyroid glands) in patients being dialyzed for chronic kidney disease. By sensitizing the parathyroids to Ca(o)(2+), cinacalcet lowers the circulating parathyroid hormone (PTH) level. It also reduces serum calcium and phosphate, changes increasing the percentage of patients achieving the guidelines recommended by the National Kidney Foundation (NKF) for these minerals. Studies are underway addressing whether better adherence to these guidelines in patients receiving cinacalcet reduces cardiovascular disease and related mortality, which are both common is the dialysis population. The second approved use of cinacalcet is for treating hypercalcemia in patients with inoperable parathyroid carcinoma. In this setting, it provides the first medical therapy chronically lowering serum calcium concentration in this condition, albeit not to normal in most patients. Its effect on the long-term prognosis of these patients, if any, is presently unclear. "Off-label" administration of cinacalcet [i.e., not yet approved by the US Food and Drug Administration (FDA)] effectively lowers serum calcium and/or PTH in various other forms of hyperparathyroidism and increases serum phosphate in renal phosphate-wasting syndromes by reducing PTH-induced phosphaturia. In the future, the drug could conceivably be utilized to modulate the activity of the CaSR in other tissues (i.e., kidney, colon) in therapeutically desirable ways.
钙敏感受体激动剂可激活甲状旁腺和其他参与钙稳态的组织中的细胞外钙(Ca(o)(2+))感受器,是首批被描述的 G 蛋白偶联受体别构激活剂。西那卡塞是目前唯一获准用于人类的钙敏感受体激动剂,临床上用于治疗慢性肾脏病透析患者的继发性甲状旁腺功能亢进(例如甲状旁腺过度活跃)。通过使甲状旁腺对 Ca(o)(2+)敏感,西那卡塞降低循环甲状旁腺激素(PTH)水平。它还降低血清钙和磷,这些变化增加了达到美国国家肾脏基金会(NKF)为这些矿物质推荐的指南的患者比例。正在进行研究,以确定接受西那卡塞治疗的患者是否更好地遵守这些指南可以降低心血管疾病和相关死亡率,这在透析人群中很常见。西那卡塞的第二种批准用途是治疗无法手术的甲状旁腺癌引起的高钙血症。在这种情况下,它为这种情况下的慢性血清钙浓度提供了首次医学治疗,尽管大多数患者的血清钙浓度未降至正常。它对这些患者的长期预后的影响目前尚不清楚。西那卡塞的“超适应证”给药[即尚未获得美国食品和药物管理局(FDA)批准]可有效降低各种形式的甲状旁腺功能亢进症患者的血清钙和/或 PTH,并通过减少 PTH 诱导的尿磷排泄增加肾磷丢失综合征患者的血清磷。将来,该药物可能可以以治疗上期望的方式用于调节其他组织(即肾脏、结肠)中 CaSR 的活性。