Elias A N, Vaziri N D, Deftos L J, Shinto R, Valenta L J
Gen Pharmacol. 1985;16(1):75-7. doi: 10.1016/0306-3623(85)90275-7.
The dopamine agonist, bromocriptine, was studied with respect to its effects on PTH secretion and calcium homeostasis in Sprague-Dawley rats made azotemic by either total or subtotal nephrectomy. The oral or intraperitoneal administration of 0.25 mg of bromocriptine resulted in a significant increase in the serum calcium concentration when compared to animals given placebo. Bromocriptine produced no significant change in the BUN or the serum concentrations of creatinine, inorganic phosphate or PTH. The mechanism of the hypercalcemic effect of bromocriptine in azotemic rats is unknown. The hypercalcemia may, however, be due to stimulation of PTH secretion, since PTH levels in the serum were inappropriately high for the corresponding levels of calcium.
研究了多巴胺激动剂溴隐亭对通过全肾切除或次全肾切除造成氮质血症的Sprague-Dawley大鼠甲状旁腺激素(PTH)分泌及钙稳态的影响。与给予安慰剂的动物相比,口服或腹腔注射0.25mg溴隐亭可使血清钙浓度显著升高。溴隐亭对血尿素氮(BUN)、血清肌酐、无机磷酸盐或PTH的浓度未产生显著影响。溴隐亭在氮质血症大鼠中产生高钙血症效应的机制尚不清楚。然而,高钙血症可能是由于刺激了PTH分泌,因为血清中PTH水平相对于相应的钙水平而言过高。